Neudle.com: uncrossed pyramidal tract

Differential
(Click to cross reference)

abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abscess, intracerebral

abscess, spinal cord

abulia

aceruloplasminemia

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

activities of daily living

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

addiction, heroin

addiction, heroin-neurologic complications with

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

Africa

agenesis of corpus callosum

aggression

agitation

Aicardi-Goutieres syndrome

alcohol

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

altered states of consciousness

alternating rapid movement

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, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

ANA

anatomy of

anemia

anemia, megaloblastic

anesthesia, general

aneurysm, vertebral basilar system

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, neurologic complications with

anterior horn cell disease

anterior spinal artery

anterior tibial muscle weakness

anti GQ1b IgG antibody

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

asterixis, unilateral

atherosclerosis, generalized

atherosclerosis, premature

atlanto-axial subluxation

atrioventricular block

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autism

autoantibodies

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign in new born

baclofen

bacterial infection

bacterial infection, CNS

ballismus, bilateral

Barthel index

basal ganglia

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bedridden

behavioral disorder

Behcet's syndrome

Bickerstaff's brainstem encephalitis

blood dyscrasias, neurologic findings with

blood transfusion

bone marrow biopsy

bone marrow transplantation

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain biopsy, stereotaxic

brainstem

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hypoplasia

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

breast feeding

Brown Sequard syndrome

brucellosis

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar palsy

bulbar palsy, progressive

burning feet

burning paresthesia

CAG repeats

calcification, intracranial

calcifications, intracranial, punctate

CAT scan, demyelinating disease

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

CAT scan, serial

CAT scan, spinal cord

CAT scan, spine

cataracts

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar peduncle

cerebellar plaques, amyloid

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral folate deficiency syndrome

cerebral infarction

cerebral palsy

cerebral peduncle

cerebral venous thrombosis

cerebritis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, prognosis in

cerebrovascular accident, vascular territory involved

cerebrovascular disease

ceruloplasmin, serum

cervical spine

cervical spine injury, compression

cherry red spot-myoclonus syndrome

chilbran skin lesions

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

cirrhosis

claudication, intermittent of cauda equina

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

clonus

clonus, finger

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

cognition

Collier's sign

color vision, impaired

coma

complications

compression fracture

concentration, impaired

confusion

congenital bilateral perisylvian syndrome

congenital malformation

congenital malformation, non CNS

conjunctivitis

consanguinity

constipation

controversies in neurology

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cough

COVID-19

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

critical care unit

crossed adductor reflex

cry, abnormal

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyanide poison

cyst, epidermoid of CNS

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

decerebrate posture

decompressive spinal cord surgery

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

dementia, subcortical

dementia, thalamic

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

denture cream

depression

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

digits, abnormal

diplopia

disability, neurological

disorientation

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

Dravet syndrome

drooling

dropped head syndrome

drought

drowsiness

drug abuse

drug abuse, inhalation

drug abuse, neurologic complications of

dysarthria

dyskinesia

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, children

dystonia, focal

dystonia, treatment of

ear, abnormal

ears of the Lynx MR sign

electrical sensation

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram

ELISA

emergencies, neurologic

emergencies, neurosurgical

emergency room

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis

encephalitis lethargica

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

endemic area

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

erythema migrans

evoked potentials

exome sequencing

eye movement, disorders of

face, numbness of

facial anomalies

facial appearance, abnormal

facial nerve palsy

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

fatal familial insomnia

fatigue

fatty acid, elevated plasma content

feeding disorder

ferritin, elevated

ferritinemia

fetal alcohol syndrome

fetus

fever

fibrillations

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

fistula, arterio-venous, dural

folic acid deficiency

foot deformity

foot drop

fourth ventricle, enlargement of

fragile-X syndrome

frataxin

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

gadolinium

gag reflex, depressed

gamma amino butyric acid-mimetic drug

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric partitioning

gaze palsy

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

Gerstmann-Straussler-Scheinker disease

girdle sensation

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glutamine

Google

gram negative rod

granular osmiphilic material

granulomatosis with polyangiitis

granulomatous disease

grasp reflex

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hearing problems in children

heart block

heart block, complete

heel-knee-shin test

hemangioma

hemangioma, vertebral

hematoma, epidural-spinal

hematoma, intracerebral

hematopoietic tissue, extramedullary

hematuria, microscopic

hemianopia

hemiparesis

hemiplegia

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hemorrhage, putamenal

hemorrhage, thalamic

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

herniated disc

herniated disc, cervical

herpes virus

herpes virus infection

human immunodeficiency virus type 1

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

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

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperammonemic encephalopathy

hypercalcemia

hypercapnia

hypereosinophilic syndrome(HES)

hyperhidrosis

hyperhomocysteinemia

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypoglycorrhachia, causes of

hypogonadism

hypomyelination

hypopigmentation of skin

hyporeflexia

hypothalamus

hypothalamus, disturbance of

hypothermia

hypothermia, causes of

hypothyroidism

hypotonia

iatrogenic neurologic disorders

imbalance

immunosuppression

immunosuppressive agents

impotence

impulsivity

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

interferon alpha

internal capsule

internet

internuclear ophthalmoplegia

interobserver agreement

intracerebral hemorrhage

intrathecal antispasticity drugs

intrauterine

intrinsic hand muscles, wasting of

introverted

intubation

ipsilateral hemiplegia

iron, brain

iron, serum, low

irritability

Jakob-Creutzfeldt disease

Jamaica ginger paralysis

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

lacunar infarction

laminectomy, cervical

left-right orientation

leg numbness

leg spasms, painful

leg weakness, bilateral

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leptospirosis

lethargy

leukemia

leukemia, neurologic findings assoc.with

leuko-araiosis

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

Lhermitte's sign

life expectancy

limbic system

lipid storage disorder of CNS

lymphadenopathy, hilar

lymphocytic pneumonitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatoid granulomatosis

lysosomal storage disease

Maghreb

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

malformation, vascular, treatment of

meconium staining

medial lemniscus

mediastinum, lymph-node biopsy

mediastinum, mass of

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meninges

meningitis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, TB

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

meningomyelitis

meningovascular syphilis

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, late-infantile

methyl benzene

methylmalonic acid, serum

methylmalonic acidemia

methylmalonic aciduria

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mills syndrome

mimics

misdiagnosis

mitochondrial disease

molecular genetics

mononeuropathy multiplex

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, negative

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, ring sign

MRI, serial

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, target sign

MRS

mucopolysaccharidoses

multinucleated giant cell

multiple sclerosis

multiple sclerosis, chronic progressive

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, prognosis

multiple sclerosis, spinal form

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

mutism

mycoplasma

mycoplasma pneumoniae

myelitis

myelitis, longitudinal

myelitis, post infectious

myelopathy, ascending

myelopathy, chronic progressive

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

nerve culture

nerve root enhancement

nerve root hypertrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neuroendocrinology

neurogenic bladder

neuroichthyosis

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

neuropathy, sensory

neuropathy, vasculitic, systemic

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

occupational neurologic disorders

ochronosis

ocular dysmetria

ocular flutter

ocular motility, disorders of

oculodentodigital dysplasia

oculogyric crisis

odontoid process

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opisthotonus

opportunistic infection

opsoclonus

optic ataxia

optic atrophy

optic atrophy, hereditary

optic chiasm, enlarged

optic nerve

optic nerve, enlarged

optic nerve, lesion of

orthostatic hypotension

oscillopsia

osteoarthrosis

osteomyelitis

osteomyelitis, spinal

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, painful

paraparesis, spastic

paraparesis, spastic, tropical

paraplegia

paraplegia, progressive

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive

PAS positive material in the brain

perivascular enhancement

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

phenylketonuria, adult onset

phlebotomy

pinealoma

pituitary stalk

pituitary stalk, lesion of

plantar reflex

pleocytosis of cerebrospinal fluid

poison, organophosphate

polycythemia, primary

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymicrogyria

polyneuropathy

polyneuropathy, familial

position sensation, abnormal

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

posterior longitudinal ligament, ossification of

postictal neurologic deficits

postural abnormality

precentral gyrus

precipitating factors

precocious puberty

prenatal

prenatal diagnosis by amniocentesis

primary lateral sclerosis

prion disease

prisoners of war, neurologic complications in

progeria

prognosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

proteinuria

pseudobulbar palsy

pseudomonas aeruginosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pure dysarthria

pursuit eye movements, abnormal

pyramidal

pyramidal tract

pyramidal tract dysfunction

pyramidal tract dysfunction, unilateral

pyramidal tract, uncrossed

pyruvate metabolism, abnormality of

quadriparesis

quadriparesis, progressive

quadriplegia

radiation encephalopathy, delayed

radiation therapy, CNS treatment and complications with

respiratory dyskinesias

respiratory failure

respiratory tract infection

reticulum cell sarcoma

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rubella encephalitis, progressive

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma

scleroderma, neurologic involvement with

SCN1A gene

scoliosis

scoliosis, neurologic association with

scotoma

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, tonic-clonic

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

severe acute respiratory syndrome

single photon emission computed tomography

Sjogren-Larsson syndrome

Sjogren's syndrome

skin, darkening of

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

slurred speech

snout reflex

sodium channel dysfunction

somatosensory evoked potentials

spastic paraplegia, type 11

spastic paraplegia, type 15

spastic paraplegia, type 7

spasticity

spasticity, treatment of

spastin

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, biopsy

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, herniation

spinal cord, infarction of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, meningioma

spinal cord, pathologic exam of

spinal cord, vascular disorders Affecting

spinal cord, vascular malformation of

spinal stenosis

spinal stenosis, familial

spinal xanthomatosis

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spirochete infection

splenomegaly

spondylolysis

spongy degeneration of brain

spontaneous remission

steroid therapy, CNS treatment and complications with

stiff legs

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

subarachnoid hemorrhage

superior cerebellar artery infarction

superior sagittal sinus thrombosis

symmetric brain lesions

syncope

syndactyly

syphilis, meningomyelitis

syphilis, neurologic complications with

syringomyelia

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, lesion

temporal lobe, lesion, bilateral

tendon, enlarged

testicular atrophy

testicular enlargement

tetanus

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic foot response

toxins, nervous system

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

transposition of the great vessels

transsynaptic degeneration

trauma

treatment of neurologic disorder

trigeminal nerve, abnormality of

trinucleotide repeats

vaccination, neurologic complications with

valsalva maneuver

vasculitides

vegetarianism

ventricular enlargement

vertebral artery

vertebral artery occlusion

vertebral-basilar insufficiency

vertigo

vertigo, episodic

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

visual fields, constricted

Vogt-Koyanagi-Harada syndrome

walking frame

walking, delayed

walking, difficulty with

Wallerian degeneration

war

watershed infarcts

weakness

weakness, generalized

weakness, progressive

weaning from respirator, failure to

weight loss

Werner's syndrome

Western immunoblot test

wheelchair

white matter disease

white matter disease, periventricular

wide based gait

workup

xanthoma, tendon

x-linked hydrocephalus

x-linked mental retardation

x-ray, spine

x-ray, thoracic spine

zinc

zoonoses

Showing articles 50 to 100 of 535 << Previous Next >>

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

A Case of Slowly Progressive Painful Paraparesis
Neurol 82:1476-1479, Corbetto, M.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Tropical Spastic Paraparesis, HTLV-1 Infection
Adams & Victors Principles of Neurology, Chp 33, pg 762, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Familial Dementia with Spastic Paraparesis
Adams & Victors Principles of Neurology, Chp 39, pg 1081, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Longitudinally Extensive Transverse Myelitis in Neuro-Beh�et Disease
Neurol 80:e189-e190, Graham, D.,et al, 2013

Clinical Reasoning: A Case of Treatable Spastic Paraparesis
Neurol 79: e50-e53, McKinnon, J.H. & Bosch E.P., 2012

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

MR Imaging Findings in Hepatic Encephalopathy
AJNR 29:1612-1621, Rovira,A.,et al, 2008

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

Late-Onset Metachromatic Leukodystrophy: Genotype Strongly Influences Phenotype
Neurol 67:859-863, Rauschka,H.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

ALS Corticospinal Degeration on DWI
Neurol 62:1834, Cabello,J.P.,et al, 2004

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

Prevalence and Clinical Features of HTLV Neurologic Disease in the HTLV Outcomes Study
Neurol 61:1588-1594, Orland,J.R.,et al, 2003

The Hereditary Spastic Paraplegias
Arch Neurol 60:1045-1049, Fink,J.K., 2003

A Wallerian Degeneration Pattern in Patients at Risk for MS
Neurol 54:1155-1160, Simion,J.H.,et al, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Recurrent Reversible Paraplegia
Lancet 357:1092, Haran,M. & Ni,S., 2001

Dysarthria in Acute Ischemic Stroke
Neurol 56:1021-1027, Urban,P.P.,et al, 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

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

Hereditary Spastic Paraparesis: A Review of New Developments
JNNP 69:150-160, McDermott,C.J. et al, 2000

MR Imaging and Proton MR Spectorscopy in Adult Krabbe Disease
AJNR 21:1478-1482, Farina,L. et al, 2000

Ipsilateral Hemiparesis After Putaminal Hemorrhage Due to Uncrossed Pyramidal Tract
Neurol 54:1801-1805, Terakawa,H.,et al, 2000

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Granulomatous Compressive Thoracic Myelopathy as the Initial Manifestation of Wegener's Granulomatosis
Neurol 51:1769-1770, Kelly,P.J.,et al, 1998

Disequilibrium in Patients with Atherosclerosis; Relevance of Pontine Ischemic Rarefaction
Neurol 51:570-573, Kwa,V.I.H.,et al, 1998

Primary Central Nervous System Lymphoma Presenting as Diffuse Cerebral Infiltration
Radiat Med 16:137-140, Okamoto,F.T.,et al, 1998

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