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Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

abscess, brainstem

abscess, intracerebral

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome-related complex

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

addiction, heroin

addiction, heroin-neurologic complications with

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating rapid movement, impaired

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

aneurysm, abdominal aortic

aneurysm, aortic arch

aneurysm, intracranial

ankle reflex, absent

ankle, swelling of

anoctaminopathy

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti signal recognition particle antibody

antibodies to voltage-gated calcium channels

antiganglioside antibodies

antiviral agents

aorta, abdominal

aorta, abnormal

aspartate aminotransferase

ataxia, cerebellar

ataxia, progressive

atrioventricular block

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

bacterial infection

basophilic stippling of red blood cells

Behcet's syndrome

bent spine syndrome

Bing-Neel syndrome

biologic markers

bladder dysfunction

bone marrow biopsy

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain natriuretic peptide

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

brucellosis, nervous system involvement with

burning paresthesia

calf hypertrophy

campylobacter infection

carcinoma of bladder

carcinoma of lung

cardiovascular disease

carnitine deficiency myopathy

CAT scan, abdomen

CAT scan, abnormal

CAT scan, chest

CAT scan, muscle

cauda equina, enhancement

cauda equina, lesion of

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebral cortical atrophy

cerebral embolism

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, location of

cerebrovascular accident, recurrent

cerebrovascular accident, topographic pattern

cerebrovascular disease

Charcot-Marie-Tooth

chelation therapy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

choreoathetosis

chronic progressive external ophthalmoplegia

Churg-Strauss syndrome

Clinical Pathologic Conference(C.P.C.)

cold temperature

conduction block

congenital heart disease

congenital myopathy

contractures, joint

controversies in neurology

conversion reaction

copper deficiency

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cricopharyngeal bar

critical care unit

cyclic vomiting

cystoisospora belli

cytosine arabinoside

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

demyelinating disease

denervation of muscle

denervation potentials

dermatomyositis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diagnostic criteria

diaphragmatic paralysis

diarrhea, bloody

differential diagnosis

difficulty climbing stairs

diplegia, brachial

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

dropped head syndrome

drug abuse, neurologic complications of

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dystroglycanopathies

dystrophin associated proteins

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electronystagmography

electrophoretic pattern, serum

Emery-Dreifuss muscular dystrophy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, Powassan

encephalitis, Rasmussen's

encephalitis, viral

enzyme, muscle disease

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

episodic disorders

episodic neurologic deficits

exercise intolerance

exercise-related muscle strength increase

extraocular muscle lesion

eye movement, disorders of

facial nerve palsy

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

failure to thrive

fatigable chewing

fine motor function, impaired

Fisher's syndrome

flaccid paralysis

flu-like illness

foot drop, bilateral

foot drop, differential diagnoses of

F-wave response

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

geographic location

gliomatosis cerebri

glucose tolerance test, abnormal

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, variant forms of

hallucination, auditory

headache, positional

heart block, complete

heliotrope rash

hemiatrophy, cerebral

hemidiaphragm, paralysis of

hemiplegia, progressive

hemispherectomy

hemorrhagic diathesis

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex virus

herpes virus infection

herpes, genital

high arched feet

highly active antiretroviral therapy

histochemistry of muscle

HMGcoA reductase inhibitors

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

homocysteine, serum

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hydroxychloroquine

hyperhomocysteinemia

hypertension, intracranial causes of

hypertension, paroxysmal

hypoglycorrhachia

hypokalemic paralysis

hyponatremia with cerebral disorders

hypoosmolality of serum

hypopituitarism

hypotension, systemic

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

immunohistochemistry

immunomodulation

immunosuppressive agents

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

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

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infant, evaluation of

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles, wasting of

iododeoxyuridine

jaw jerk, abnormal

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, progressive

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limbic encephalitis

liver function enzymes

lung transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphadenopathy, paraaortic

lymphoma involving CNS

macroglobulinemia

malformation, vascular

malignant hyperpyrexia

malignant papulosis

Man-In-The-Barrel syndrome

masseter muscle wasting

mediastinum, mass of

medulla oblongata, lesion of

Melkersson's syndrome

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, basilar

meningoencephalitis

mental status, abnormal

methylmalonic acid, serum

methylmalonic acidemia

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, contrast enhanced

MRI, diffusion weighted

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

muscle stiffness

muscle strength, testing

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, intermediate onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, treatment of

myasthenic syndrome

mycobacterial infection

mycobacterium bovis

mycotic aneurysm

myelitis, longitudinal

myelogram, cervical

myeloneuropathy

myelopathy, chronic progressive

myeloradiculopathy

myopathy, amyloid

myopathy, autoimmune

myopathy, critically ill

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, steroid induced

myopathy, toxic

myopathy, vacuolar

myositis, ocular

myotonic discharges

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, intracranial assoc.with systemic hypertension

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve root biopsy

nerve root enhancement

nerve root hypertrophy

neuroendocrinology

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuronal intranuclear inclusion disease

neuropathy, acute

neuropathy, asymptomatic

neuropathy, hereditary peripheral

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

newborn, evaluation of

next-generation sequencing

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

ocular motility, disorders of

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

oral contraceptives

overlap syndrome

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

pain, total body

paralysis, acute

paralysis, asymmetric

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

PAS positive material in the brain

pedicles of vertebrae, erosion of

periarteritis nodosa

peripheral blood smear

pernicious anemia

personality change

pheochromocytoma

phosphorylase b kinase deficiency

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleural effusion

polyglucosan body

polyglucosan body disease

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, subacute idiopathic demyelinating

pons, infarction of

positive sharp waves

posterior column disease

postural abnormality

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

proprioception, abnormal

protozoan infection

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary embolism

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriparesis, acute

quadriparesis, progressive

quadriplegia, transient

quality of life

rabies, nervous system involvement with

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

regional enteritis

release phenomena

remote effect of cancer on the nervous system

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

retinal hemorrhages

retroperitoneal mass

reversible neurologic disorder

riboflavin transporter deficiency

sarcoidosis, CNS

sclerosis, bone

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, intractable

seizure, repetitive

seizure, surgical treatment of

seizure, treatment of

sensorineural hearing loss

sensory loss, band distribution

sensory loss, patchy

serum alanine aminotransferase

sex reassignment surgery

Sheehan's syndrome

shoulder, pain in

skin, lesions in neurologic disorders

sloped shoulders

slow virus infection of CNS

small vessel disease

small vessel vasculitis

small-bowel resection

solitary scerlosis

speech disorder, childhood

speech, delayed development of

spinal cord, cervical

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, intramedullary

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

standing difficulty

steroid therapy, CNS treatment and complications with

stooped posture

stroke, progression of

subarachnoid hemorrhage

suspended sensory loss

systemic illness

systemic lupus erythematosus

temporalis muscle wasting

thymus and neuromuscular function

tick-borne encephalitis

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

tonsillar herniation of cerebellum

transient ischemic attack

transverse smile

treatment of neurologic disorder

treatment, empirical

tremor, postural

ulcerative colitis

unconsciousness

upgaze, paralysis of

urinary incontinence

urine osmolality, elevated

vectors of infection

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

vitamin deficiency

Waldenstrom's macroglobulinemia

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, congenital

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

white matter disease

wide based gait

winging of scapula

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 50 to 100 of 3889 << Previous Next >>

Solitary Sclerosis
Neurol 78:540-544, Schmalstieg,W.F.,et al, 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Clinical Reasoning: A Middle-Aged Woman with Progressive Symmetric Weakness and a CSF Pleocytosis
Neurol 78:e88-e92, Marks,D.,et al, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
Neurol 78:1527-1532, Matthews,E.,et al, 2012

Guillain-Barre Syndrome
NEJM 366:2294-2304, Yuki, N. & Hartung, H.P., 2012

Bilateral Foot Drop in Polyarteritis Nodosa
NEJM 367:e9, Souza Neves, F. & Lin, K., 2012

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

Trapped in Bed (After 32 Years of a Blocked Nose)
Lancet 372:1606, Imtiaz,K.E.,et al, 2008

A 16-Year-Old Girl With Progressive Weakness of the Left Leg
Neurol 69:84-90, Hahn,A.F.,et al, 2007

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

IV Immunoglobulin in Patients With Myasthenia Gravis
Neurol 68:837-841,803, Zinman,L., et al, 2007

Clinicopath Conf., Chronic Inflammatory Demyelinating Polyneuropathy
NEJM 348:735-743, Case 6-2003, 2003

Lacunar Stroke Is the Major Cause of Progressive Motor Deficits
Stroke 33:1510-1516,1443, Steinke,W. &Ley,S.C., 2002

Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
Neurol 55:296-198, Peng,A. et al, 2000

A Woman Who Left Her Wheelchair
Lancet 353:806, Mingrone,G.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

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

Morvan's Fibrillary Chorea: A Paraneoplastic Manifestation of Thymoma
JNNP 65:857-862, Lee,E.K.,et al, 1998

Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
Ann Neurol 41:548-551, Argov,Z.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Therapeutic Dilemma of Inclusion Body Myositis
Neurol 48:567-568, Barohn,R.J., 1997

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

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

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

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

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin
Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Generalized Myositis in Behcet Disease:TReatment with Cyclosporine
Ann Int Med 116:651-653, Lingenfelser,T.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

Clinicopath Conf
Case 40-1991, Inclusion-Body Myositis, NEJM 325:1026-1035991., , 1991

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Hyponatremia and Inappropriate Secretion of Vasopressin (Antidiuretic Hormone) in Patients with Hypopituitarism
NEJM 321:492-496, 5381989., Oelkers,W., 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Showing articles 50 to 100 of 3889 << Previous Next >>