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Differential
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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abducens nerve paralysis, children

acanthocytosis

accomodation, abnormal

achilles tendon, enlarged

acoustic nerve

acquired immunodeficiency syndrome

acral sensory symptoms

ACTH, ectopic syndrome of

acute ataxia of childhood

acute intermittant porphyria

acute respiratory distress syndrome

acyl CoA dehydrogenase deficiency

Addison's disease

Adies pupil

adrenoleukodystrophy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

Alexanders disease

Alexanders disease, adult onset

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amenorrhea

aminoacidurias

ammonia

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

ANA

anal wink response

ANA-negative systemic lupus erythematosus

anemia

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anti MAG antibodies

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, treatment

anticonvulsants

anticonvulsants, untoward effects of

antidepressant

antiganglioside antibodies

apraxia of eye movements

Arnold Chiari malformation

aspartate aminotransferase

ataxia telangiectasia

atherosclerosis, premature

athetosis

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basilar impression

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

benign essential tremor

benzodiazepine

beriberi

bicaudate index

Bickerstaff's brainstem encephalitis

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow suppression

bone marrow transplantation

botulinum toxin

botulism

botulism antitoxin

botulism immune globulin

brain biopsy, false negative

brain scan, abnormal

brainstem

brainstem, atrophy

brainstem, dysfunction

brainstem, ischemia

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy

bulbar palsy, acute

bulbar palsy, acute-causes of

bulbar palsy, progressive

calcification, intracranial

calf hypertrophy

camptocormia

campylobacter infection

cancer, unknown origin

cane

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma of pancreas

carcinoma of stomach

carcinoma of unknown origin

cardiac arrest

cardiac arrest and resuscitation

cardiac transplantation

cardiomegaly

cardiomyopathy

cardiovascular disease

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous sinus

cavernous sinus syndrome, bilateral

cavernous sinus, syndrome

CD4 counts

celiac disease, childhood

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellar plaques, amyloid

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, carotid origin

cerebral infarction

cerebral palsy

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, young adult

cervical myelopathy

cervical spine

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chenodeoxycholic acid

chest pain

chest x-ray, abnormal

children

chills

Chinese paralytic syndrome

choreoathetosis, paroxysmal

choroid plexus

chromosomal abnormality

chronic graft versus host disease

chronic idiopathic anhidrosis

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

cimetidine

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clomipramine

clonazepam

clonus

cobalamin C deficiency

congenital deformities

congenital heart disease

congenital malformation

congenital malformation, non CNS

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

conus medullaris, lesion of

convergence, impaired

corneal reflex, abnormal

coronavirus

corpus callosum, atrophy of

corpus callosum, lesion of

cortical-basal ganglionic degeneration

cough

COVID-19

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

critical care unit

crossed adductor reflex

cystic fibrosis, neurologic complications with

cystoisospora belli

cytokines

cytomegalovirus infection

deafness

deep gray nuclei

deep tendon reflexes

degenerative cervical myelopathy

degenerative diseases of CNS

Dejerine-Sottas syndrome

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

denervation of muscle

denervation potentials

dental prostheses

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetic ophthalmoplegia

diagnosis

diagnostic criteria

dialysis

diamond on quadriceps

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

diplegia, brachial

diplopia

disability, neurological

dislocated hip, congenital

disorientation

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diuretic

diurnal variation

dizziness

dopa responsive dystonia

down-beat nystagmus

drowsiness

drug induced neurologic disorders

drug induced neurologic disorders in children

drug interactions

drug overdose

drug overdose, management of

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, focal

dystonia, treatment of

dystrophin

ear, abnormal

eclampsia

eclampsia, postpartum

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electrophoretic pattern, serum

electroretinograph

ELISA

emergencies, neurologic

emergency room

Emery-Dreifuss muscular dystrophy

emotional lability

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, progressive

endemic area

enteritis

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilic granulomatosis with polyangiitis

ependymal

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

Erdheim-Chester disease

extraocular muscle lesion

extrapyramidal movement disorder, progressive

eye closure

eye movement, disorders of

face, elongated

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial pain

facial sweating, unilateral

facial weakness

facial weakness, bilateral

failed medical management

fatty acid, elevated plasma content

feeding disorder

fever

fibrillations

fine motor function, impaired

finger nose finger test

finger numbness

fingernails, abnormal

Fisher C.M.

Fisher's syndrome

Fisher's syndrome, atypical

fluorescent treponema antibody absorption(FTA-ABS)

Friedreich's ataxia, late onset

fucosidosis

fundus, abnormality of

F-wave response

gadolinium

gag reflex, depressed

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastroparesis

Gaucher's disease

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

general paresis of the insane

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucocerebrosidase

glucose tolerance test, abnormal

glutamic acid decarboxylase, antibody

gluten-free diet

glycoprotein

GM1 ganglioside antibodies

gout

Gowers maneuver

granular osmiphilic material

granuloma, eosinophilic

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, neuropathology of inflammatory lesion of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

gynecomastia

hairline, abnormal

Hallervorden Spatz disease

hallucination

hallucination, auditory

hallucination, visual

head retraction reflex

heart block, complete

heart murmur

heat intolerance

heatstroke

heavy metal intoxication

heel swelling

heel-knee-shin test

helminthic infection of CNS

hemianopia

hemidiaphragm, paralysis of

hemiparesis

hemoglobinuria

hemorrhagic diathesis

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc

herniated disc, cervical

herpes simplex virus

herpes virus

herpes virus infection

herpes, genital

high arched feet

high arched palate

highly active antiretroviral therapy

hip flexor weakness

histamine-2 receptor blockers

histiocytosis

histochemistry of muscle

HLA

hoarseness

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

human diploid cell rabies vaccine

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's disease, children

hydrocephalus

hydrocephalus, communicating

hyperemisis gravidarum

hyperpigmentation of skin

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hyponatremia

hypoosmolality of serum

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophonia

hypophosphatemia

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

iatrogenic neurologic disorders

immune checkpoint inhibitors

immunoelectrophoresis, serum

immunofluorescence

immunofluorescent"band"test

immunomodulation

immunosuppression

immunosuppressive agents

implantable cardioverter defibrillator

impotence

inability to sit up

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inappropriate behavior

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incontinence, fecal

incontinentia pigmenti

incoordination

infant, evaluation of

infantile neuronal degeneration

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal obstruction

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

intraneural hemorrhage

intrathecal chemotherapy

intrauterine

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy

laminectomy, cervical

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leprosy

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy with calcification and cysts

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

levitation

Lhermitte's sign

lid closure, weakness of

life expectancy

light-near dissociation, causes of

limb-girdle weakness

limbic encephalitis

lip, biting

lipid storage disorder of CNS

lissencephaly

lithium

liver disease

liver function enzymes

lumbosacral radiculopathy

lymphadenopathy, axillary

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

macrocephaly

Maghreb

magnetic stimulation

magnetic stimulation, brain

malabsorption

malabsorption syndrome

malformation, CNS, congenital

malignancy, occult

malignant hyperpyrexia

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata, lesion of

Mees lines

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningitis, elderly

meningitis, eosinophilic

meningitis, leukemic

meningitis, lupus

meningitis, lymphomatous

meningitis, neutrophilic

meningitis, recurrent

meningitis, syphilitic

meningoencephalitis

meningoencephalopathy

mental retardation

mental status, abnormal

methylhydrazine derivatives

methylmalonic acid, serum

methylmalonic acidemia

metrizamide

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mills syndrome

Mini Mental Status Examination

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy multiplex

mononeuropathy, children

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, contrast enhanced, subependymal

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, emergent

MRI, high signal foci on

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, sulcal hyperintensity

multicore myopathy

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple organ failure

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, etiology of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

mycobacterium kansasii

mycoplasma

mycoplasma pneumoniae

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myelogram

myelogram, cervical

myelogram, complications of

myelogram, metrizamide

myeloma, osteosclerotic

myelomalacia

myeloneuropathy

myelopathy

myelopathy, carcinomatous

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, toxic

myopathy, vacuolar

myositis

myositis, acute of childhood

myositis, post infectious

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal abstinence syndrome

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuritis, causes of

neuritis, heavy metals causing

neuroaxonal dystrophy

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, abnormal

neurologic signs

neurologic symptoms

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronal loss

neuronopathy

neuronopathy, sensory

neuropathology

neuropathology, brain

neuropathology, peripheral nerves

neuropathy

neuropathy, acute

neuropathy, asymptomatic

neuropathy, ataxic

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuroprotective agents

neuropsychiatry

neurosyphilis

neurotoxin

next-generation sequencing

nonsteroidal anti-inflammatory drug

NOTCH2NLC

numbness, ascending

numbness, extremity

numbness, generalized

nusinersen

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

obesity

occupational neurologic disorders

oculovestibular reflex

odontoid process

old age, neurology of

one and a half syndrome

opened mouth

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

opportunistic infection

opportunistic infection, CNS

opsoclonus

optic atrophy

optic nerve

optic nerve, enhancement

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optical coherence tomography

oral contraceptives

organ transplantation

organomegaly

oropharyngeal weakness

orthopnea

orthostatic hypotension

oscillopsia

osmotic demyelination syndrome

osteomalacia

overlap syndrome

pacemaker, cardiac-transvenous

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic ganglionopathy

paranoia

paraparesis

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraparesis, spastic, tropical

parenteral alimentation

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, hemiparesis in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

paroxysmal neurologic disorder

pericardial friction rub

pericarditis

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

perivascular enhancement

pernicious anemia

personality change

pes cavus

phenothiazine, dyskinesia associated with

phenylketonuria

photophobia

photosensitivity, skin

pituitary stalk

pituitary stalk, lesion of

plasma cell dyscrasia

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poliomyelitis-like illness

POLR3B

polycystic kidneys

polyglucosan body disease

polymerase chain reaction

polymerase chain reaction, false negative

polymyositis

polyneuritis

polyneuritis, acute sensory

polyneuropathy

polyneuropathy, acute sensory

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyneuropathy, familial

polyneuropathy, lymphomatous

polyneuropathy, subacute idiopathic demyelinating

polyneuropathy, uremic

polypharmacy

polyradiculoneuropathy

position sensation, abnormal

positional head-hanging test

positive sharp waves

post transplant lymphoproliferative disease

posterior column disease

posterior leukoencephalopathy syndrome

postinfectious

postoperative neurologic complications

postpartum

postural abnormality

potassium

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

primary lateral sclerosis

primitive neuroectodermal tumors

prion disease

procarbazine

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

prolactin, elevated

proprioception

proprioception, abnormal

proteinuria

protozoan infection

proximal muscle atrophy

pruritus

pseudoathetosis

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pulmonary nodules

pupil

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, episodic

pupil, dilated, unilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriparesis

quadriparesis, progressive

quadriplegia

quadriplegia, transient

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading disorder, acquired

real-time quaking-induced conversion

remote effect of cancer on the nervous system

renal failure

renal failure, acute

renal stones

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

reticular activating system

reticulum cell sarcoma

reversible neurologic disorder

review article

rhabdomyolysis

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin

riboflavin transporter deficiency

rippling muscle disease

saccadic eye movements, abnormal

scoliosis, neurologic association with

sedimentation rate, elevated

segmental demyelination

seizure

seizure, children

seizure, withdrawal

selective serotonin reuptake inhibitors

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, cortical

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

serum alanine aminotransferase

serum gamma glutamyl transferase

serum lipase, elevated

severe acute respiratory syndrome

shivering

short neck

short stature

shunt procedure, ventricular

Shy-Drager syndrome

simvastatin

sinemet

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep

sleep apnea

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

slurred speech

small vessel vasculitis

SMN1 gene

snout reflex

sodium valproate

somatosensory evoked potentials

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, dorsal subpial enhancement

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, classification

spinal stenosis

spinal stenosis, familial

spinal xanthomatosis

spine, metastasis to

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

spontaneous remission

stem cell transplantation

steppage gait

steroid

steroid therapy, CNS treatment and complications with

striatonigral degeneration

striatonigral degeneration, infantile

superior cerebellar peduncle

superior oblique palsy

suspended sensory loss

sweating

sweating, abnormality of

symmetric brain lesions

syncope

synucleinopathy

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

teeth, number of in infants

telangiectases

temporal lobe, lesion

temporal lobe, lesion, bilateral

tenderness

tendon, enlarged

tensilon test

tensilon test, false positive

term infant

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thyroid function tests

tick-borne encephalitis

tomaculous neuropathy

tongue, atrophy

tongue, biting

tongue, fasciculations of

tongue, impaired movements of

tonsillar herniation of cerebellum

toxic encephalopathy

toxins, nervous system

transient neurologic deficit

transverse smile

trauma

trazodone

treatment of neurologic disorder

tricyclic antidepressant

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal neuropathy

trinucleotide repeats

tripping

trismus

tyrosine hydroxylase deficiency

ulcerative colitis

ulnar neuropathy

ultrasonography, nerve

unconsciousness

unconsciousness, transient

undiagnosed

upgaze

upgaze, paralysis of

urea-cycle enzymopathies

urine osmolality, elevated

urine test for metabolic disorders

urine test in toxic screen

urine, dark

useless hand

vaccination, neurologic complications with

valium

vascular endothelial growth factor

vasculitides

vectors of infection

vecuronium

Venereal Disease Research Laboratory test

venous thrombosis, non-cerebral

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vibratory sensation, abnormal

vinblastine

vincristine neurotoxicity

visual acuity, decreased

visual evoked response

visual loss

visual loss, progressive

vitamin supplementation

vitiligo

vocal cord paralysis

vocalizations

voice, abnormality of

Waldenstrom's macroglobulinemia

walking

walking frame

walking, delayed

walking, difficulty with

Watson-Schwartz reaction

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weakness, severe

weaning from respirator, failure to

web sites

weight gain

weight loss

Wernicke's encephalopathy

X-linked bulbospinal neuronopathy

x-linked mental retardation

x-ray, cervical spine

x-ray, spine

zinc

Showing articles 150 to 200 of 332 << Previous Next >>

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

A Poliomyelitis-like Syndrome from West Nile Virus Infection
NEJM 347:1279-1280, Leis,A.A., et al, 2002

A Reversible Paralysis
Lancet 360:1160, Maury,E.,et al, 2002

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Sensory Guillain-Barre Syndrome
Neurol 56:82-86, Oh,S.J.,et al, 2001

Nonpoliovirus Poliomyelitis Simulating Guillain-Barre Syndrome
Arch Neurol 58:1460-1464, Gorson,K.C.&Ropper,A.H., 2001

Clinicopath Conf,Pulmonary Mycobacterial Infection and Transverse Myelitis
NEJM 345:1263-1269, Case 33-2001, 2001

A Six-Year-Old Girl with Tick paralysis
NEJM 342:90-94, Felz,M.W.,et al, 2000

Nitrous Oxide Anesthesia-Associated Myelopathy
ArchNeurol 57:380-382, Marie,R.,et al, 2000

Clinical Features of Nipah Virus Encephalitis Among Pig Farmers in Malaysia
NEJM 342:1229-1235, Goh,K.J.,et al, 2000

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Serotonin Sydrome
Medicine 79:201-209, Mason,P.J. et al, 2000

Holmes-Adie Syndrome
Lancet 356:1760-1761, Martinelli,P., 2000

Acute Renal Failure with Neurological Involvement in Adults Associated with Measles Virus Isolation
Lancet 354:992-995, Wairagkar,N.S.,et al, 1999

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Benign Acute Childhood Myositis, Laboratory and Clinical Features
Neurol 53:2127-2131, Mackay,M.T.,et al, 1999

Secondary Hyperkalaemic Paralysis
JNNP 64:249-252, Evers,S.,et al, 1998

Guillain-Barre Syndrome
Lancet 352:635-641, Hahn,A.F., 1998

Clinicopath Conf
Chronic Inflammatory Demyelinating Polyneuropathy, Case 13-1998, NEJM 338:1212-1219998., , 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

Pregnant,Vomiting,and Going Blind
Lancet 352:1594, Tesfaye,S.,et al, 1998

Hypophosphatemia-Induced Neuropathy: Clinical and Electrophysiologic Findings
Muscle Nerve 21:650-652, Siddiqui,M.F. &Bertorini,T.E., 1998

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,et al, 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Site of Autonomic Dysfunction in a Patient with Ross'Syndrome and Postganglionic Horner's Syndrome
Neurol 45:2094-2096, Wolfe,G.I.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Acute Lumbosacral Polyradiculopathy in Acquired Immunodeficiency Syndrome:Experience in 23 Patients
Ann Neurol 35:53-58, So,Y.T.&Olney,R.K., 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Showing articles 150 to 200 of 332 << Previous Next >>