Neudle.com: distal muscle atrophy

Differential
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abdominal muscle paralysis

abductor pollicis brevis

abscess, vertebral

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

Addison's disease

adult polyglucosan body disease

advance directives

advances in neurology

adverse drug reaction

aggression

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

algorithm

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidurias

amyloid

amyloid angiopathy, cerebral

amyloidosis

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, cluster

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, conjugal

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, guamian type of

amyotrophic lateral sclerosis, hospitalization

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, myasthenic syndrome with

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, sensory symptoms in

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

analgesic

anatomy of

anemia

anemia, megaloblastic

anesthesia, general

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiitis

angiography, neurologic complications with

animal exposure

anisocoria

ankle reflex, absent

ankylosing spondylitis

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

anticoagulant, complications of

anticoagulant, treatment

apraxia of eye movements

arterial dissection, carotid

arthralgia

arthrogryposis multiplex

ascending paralysis

aspiration

asthma

asthma, poliomyelitis-like syndrome with

asymptomatic

ataxia

ataxia telangiectasia

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

autoantibodies

autoimmune disease

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion of

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavioral disorder

Bence Jones protein

benign congenital hypotonia

benign essential tremor

benzodiazepine

biologic markers

BiPAP

bitemporal visual field defect

bladder dysfunction

blink reflex

bone marrow biopsy

bone marrow suppression

border zone infarct

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bruit

bruit, supraclavicular

bulbar palsy

bulbar palsy, acute

bulbar palsy, progressive

calcification, intracranial

calcium channel dysfunction

campylobacter infection

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma

carcinoma of breast

cardiac catheterization, neurologic complications

cardiomegaly

cardiomyopathy

cardiovascular disease

caregiver

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

CAT scan, emission, abnormal

cataracts

cavernous sinus, syndrome

CD4 counts

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral ischemia

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, young adult

cervical band

cervical collar

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

cervical rib

cervical spine

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

Charcot-Marie-Tooth

cheiralgia paresthetica

chelation therapy

chest x-ray, abnormal

chromosomal abnormality

chronic polyneuritis, children

Chvostek sign

cimetidine

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

collagen vascular disease

coma

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

concussion

conduction block

confusion

confusional state, acute

congenital heart disease

congenital myopathy

congestive heart failure

constipation

contractures, joint

controversies in neurology

corneal reflex, abnormal

corneal reflex, absent

corona radiata

corpus callosum, infarction of

corpus callosum, lesion of

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

coxsackievirus, myopathy with

CPAP

cranial nerve palsies

craniopharyngioma

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

diarrhea

diet

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplegia, atonic

diplegia, brachial

diplopia

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

discitis

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine

drooling

dropped head syndrome

dystrophic calcification

dystrophin

edema, pedal

efficacy

electrical injury of nervous system

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

embolism

emotional lability

empyema, epidural-spinal

encephalitis

encephalitis, episodic

encephalocele

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

episodic neurologic deficits

evidence-based research

exercise-induced vascular symptoms

exome sequencing

exophthalmus

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

Fazio-Londe's disease

fever

fibrillations

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

football neurologic injuries

fracture, long bones, nerve injury with

fragile-X syndrome

free radical

Friedreich's ataxia

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

gait disorder

gait, spastic

gait, waddling

gammaglobulin therapy, intravenous

ganglion

gangliosides

Gantzer's muscle

gastrocnemius muscle weakness

gastroenteritis

gastrostomy

gastrostomy, percutaneous endoscopic

gaze palsy

gaze palsy, horizontal

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

granulomatous disease

growth retardation

guanidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

hallucination, auditory

Hand-Schuller-Christian disease

heart block, complete

heavy metal intoxication

hemangioma

hemidiaphragm, paralysis of

hemidystonia

hemiparesis

hemiplegia

hemiplegia, progressive

hemoglobinuria

hepatitis

hepatomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

herpes zoster

high arched feet

high arched palate

highly active antiretroviral therapy

histamine-2 receptor blockers

histochemistry

histochemistry of muscle

Hodgkin's disease, neurologic involvement with

Horner's syndrome

hospice

human immunodeficiency virus type 1

hyperhidrosis, palmar

hypokalemic periodic paralysis

hypoparathyroidism

hypopnea

hyporeflexia

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypoxic encephalopathy

iatrogenic neurologic disorders

immunoelectrophoresis, serum

immunologic disease

immunosuppression

immunosuppressive agents

immunotherapy

inability to sit up

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

incoordination

India

infant, evaluation of

infantile tremor syndrome

insomnia

insulinoma

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

internet

interosseous muscles

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

klippel feil syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic dehydrogenase(LDH)

laminectomy, cervical

laughing

laughing, pathologic

lead and the nervous system

lead poisoning

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

liver disease

liver function enzymes

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

Madonna facies

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

Martin-Gruber anastamosis

masseter muscle weakness

median nerve

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

Mees lines

memory, defect of recent

memory, impairment of

meningitis

mental retardation

mental status, abnormal

methotrexate

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

migraine

Millard Gubler syndrome

Mills syndrome

mimics

minimally conscious state

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

motor system

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

MRS

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle swelling

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, treatment of

myelopathy, chronic progressive

myocardial infarction

myopathy, carcinomatous

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, intracranial

neoplasm, intracranial, differential diagnosis of

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic disease, incurable

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, bicycle

neuropathy, demyelinating

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

newborn, evaluation of

next-generation sequencing

numbness, generalized

nusinersen

nystagmus

nystagmus, primary position of gaze

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

olivary degeneration, hypertrophic

Onufrowicz nucleus

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opiate

Oppenheim muscular dystrophy

opportunistic infection, CNS

orthopnea

osteomalacia

osteomyelitis

osteomyelitis, spinal

owl's eye sign of spinal cord

pain, management of chronic

paralysis, asymmetric

paranoia

paraoxonase

paraparesis

paraparesis, familial spastic

paraparesis, spastic

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, L-dopa nonresponsive

Parkinson disease, motor neuron disease with

Parkinson disease, treatment of

Parkinsonism syndrome

Parkinsonism-dementia complex

pathology

patient information and support

penicillamine

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

persistent vegetative state

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

Pick's disease

placebo

plasma cell dyscrasia

plasmacytoma

plasmapheresis

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

POEMS syndrome

poison, mercury

poison, neurologic problems with

poliomyelitis

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

porphyria

position sensation, abnormal

positive sharp waves

post polio syndrome

posterior column disease

posterior fossa

posterior fossa, differential diagnosis of lesions of

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

practice guidelines

precentral gyrus

preclinical

pregnancy, neurologic complications in

pressure sores

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

prisoners of war, neurologic complications in

progeria

prognosis

progranulin

progressive multifocal leucoencephalopathy

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

pronator syndrome

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudomyotonia

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary function tests

pure motor stroke

pyramidal tract

pyramidal tract dysfunction

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation therapy, salivary gland

radiculopathy

rapid onset dystonia parkinsonism

remote effect of cancer on the nervous system

renal stones

repetitive nerve stimulation

respirator

respiratory depression

respiratory failure

respiratory tract infection

retrovirus

reverse split hand sign

review article

RFLPs

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

right to die

riluzole

risk factors

risk-benefit assessment

salivation, excessive

sarcoidosis

sarcoidosis, CNS

scalenus anticus syndrome

schizophrenia

scissors gait

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

sedimentation rate, elevated

seizure

seizure, children

seizure, treatment of

sensorimotor stroke

sensory ganglia

sensory ganglia, abnormal

sensory level

sensory loss

sensory loss, cortical

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing

sensory testing, quantitative

serologic testing

serum alanine aminotransferase

short stature

shoulder, numbness

shoulder, pain in

shoulder, subluxation

shoveling

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep

sleep apnea

sleep pathology and physiology

slit lamp examination

small vessel disease

smell

Smell Identification Test

SMN1 gene

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, enlargement

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, intramedullary

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spirometry

spitting

splenium of corpus callosum

splenomegaly

spondylosis

spontaneous muscle activity

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

steppage gait

sternocleidomastoid muscle

steroid

steroid therapy, CNS treatment and complications with

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid hemorrhage

subclavian artery stenosis

survival motor neuron gene

swallow evaluation

sweating, abnormality of

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test

tensilon test, false positive

thoracic outlet syndromes

thromboangiitis obliterans cerebri

thyrotropin-releasing hormone

tongue, fasciculations of

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigeminal nerve, abnormality of

trinucleotide repeats

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

urine test in toxic screen

urine, dark

valium

vascular endothelial growth factor

vasculopathy

venous thrombosis, non-cerebral

vertebral erosion

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

visual evoked response

Waldenstrom's macroglobulinemia

walking frame

walking, delayed

walking, difficulty with

war

weakness

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

web sites

Weber's syndrome

weight loss

Werdnig-Hoffman disease

West disease

West Nile fever

wheelchair

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

workup

wrist drop

X-linked bulbospinal neuronopathy

yelling

zinc

Showing articles 550 to 600 of 4688 << Previous Next >>

A Novel, Blood-Based Diagnostic Assay for Limb Girdle Muscular Dystrophy 2B and Miyoshi Myopathy
Ann Neurol 51:129-133, Ho,M.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
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Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
JNNP 70:548-550, Pfeiffer,G.,et al, 2001

Clinical Study of 222 Patients with Pure Motor Stroke
JNNP 71:239-242, Arboix,A.,et al, 2001

A Blind Panic
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MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

Visual Manifestations of Giant Cell Arteritis
Medicine 79:283-292, Gonzalez-Gay,M.A.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Dysthyroid Orbitopathy
Semin Neurol 20:43-54, Jacobson,D.M., 2000

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

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

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Prader-Willi and Angelman Syndromes
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PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
Radiology 206:811-816, Lamer,S.,et al, 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

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

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Mononeuropathy of a Distal Branch of the Femoral Nerve in a Body Building Champion
JNNP 63:669-671, Padua,L.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Acute Focal Neuropathy in Male Weight Lifters
Muscle & Nerve 19:897-899996., Bird,S.J.&Brown,M.J., 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 1996

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

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

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