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abdominal muscle paralysis

abductor pollicis brevis

abscess, vertebral

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

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

amyloid angiopathy, cerebral

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

anemia, megaloblastic

anesthesia, general

aneurysm, cavernous sinus

aneurysm, internal carotid artery

angiography, neurologic complications with

animal exposure

ankle reflex, absent

ankylosing spondylitis

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

antiviral agents

apraxia of eye movements

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arthrogryposis multiplex

ascending paralysis

asthma, poliomyelitis-like syndrome with

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

axonal degeneration

B 12 deficiency

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

biologic markers

bitemporal visual field defect

bladder dysfunction

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, atrophy

brainstem, infarction of

brainstem, lesion of

bright tongue sign

Brown Sequard syndrome

Brugada syndrome

bruit, supraclavicular

bulbar palsy, acute

bulbar palsy, progressive

bulging of biceps

burning paresthesia

calcification, intracranial

calcium channel dysfunction

calf amyotrophy

calf hypertrophy

campylobacter infection

carbon monoxide poisoning

carcinoembryonic antigen

carcinoma of breast

cardiac catheterization, neurologic complications

cardiovascular disease

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

carpo-pedal spasm

Castleman's disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cavernous sinus, syndrome

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

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 collar

cervical myelopathy

cervical osteoarthritis

cervical osteophyte

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

chewing, impaired

cholesterol, HDL

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

chronic polyneuritis, children

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cluster, geographic

cold temperature

collagen vascular disease

compartment syndrome

compartment syndrome, medial brachial fascial

compression neuropathy

conduction block

confusional state, acute

congenital heart disease

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

corneal reflex, abnormal

corneal reflex, absent

corpus callosum, infarction of

corpus callosum, lesion of

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical wrist drop

cost effectiveness

coxsackievirus, myopathy with

cranial nerve palsies

craniopharyngioma

creatine phosphokinase(CPK)elevated

crying, pathologic

Cushing's syndrome

cycad seed flour

cyclophosphamide

cyst, perineural

degenerative diseases of CNS

delay in diagnosis

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

denervation of muscle

denervation potentials

dentatorubral-pallidoluysian atrophy

dermatomyositis

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

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplegia, atonic

diplegia, brachial

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dropped head syndrome

drug interactions

dysferlinopathy

dystonia, focal

dystrophic calcification

electrical injury of nervous system

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electromyogram, decremental response

electron microscopy

electrophoretic pattern, serum

emotional lability

empyema, epidural-spinal

encephalitis, episodic

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, post anoxic

endocarditis, subacute bacterial

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erectile dysfunction

ethics in neurology

evidence-based research

evoked potentials

exercise intolerance

exercise-induced vascular symptoms

exome sequencing

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fatigable chewing

Fazio-Londe's disease

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

flaccid paralysis

flail arm syndrome

foot drop, bilateral

football neurologic injuries

fracture, long bones, nerve injury with

fragile-X syndrome

Friedreich's ataxia

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

gag reflex, depressed

gammaglobulin therapy, intravenous

Gantzer's muscle

gastrocnemius muscle weakness

gastroenteritis

gastrostomy, percutaneous endoscopic

gaze palsy, horizontal

gaze palsy, supranuclear

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

girdle sensation

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

Gulf War syndrome

hallucination, auditory

handcuff neuropathy

handlebar palsy

Hand-Schuller-Christian disease

health insurance

heart block, complete

heavy metal intoxication

hemidiaphragm, paralysis of

hemiplegia, progressive

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

high arched feet

high arched palate

highly active antiretroviral therapy

histamine-2 receptor blockers

histochemistry of muscle

history of neurology

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

human immunodeficiency virus type 1

Huntington's chorea

hyperadrenalism

hyperamylasemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperinsulinism

hyperparathyroidism

hypersegmented polys

hyperthyroidism

hypoglycemic coma

hypokalemic periodic paralysis

hypoparathyroidism

hypotension, systemic

hypothalamus, disturbance of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

immune complexes

immunodeficiency

immunoelectrophoresis, serum

immunologic disease

immunosuppression

immunosuppressive agents

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

infant, evaluation of

infantile tremor syndrome

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

internal capsule

interosseous muscles

intestinal pseudoobstruction

intracerebral hemorrhage

intrinsic hand muscles

intrinsic hand muscles, wasting of

Isaacs syndrome

islet cell tumor

Jackson's syndrome

Jakob-Creutzfeldt disease

jaw closure weakness

jaw jerk, abnormal

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, pathologic

lead and the nervous system

leg weakness, bilateral

leg weakness, unilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

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 function enzymes

locked-in syndrome

lumbar puncture

lumbrical muscles

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Man-In-The-Barrel syndrome

Martin-Gruber anastamosis

masseter muscle weakness

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

memory, defect of recent

memory, impairment of

mental retardation

mental status, abnormal

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

Millard Gubler syndrome

minimally conscious state

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

monoparesis, focal

Motor Band Sign

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gradient-echo

MRI, paramagnetic effect

MRI, peripheral nerve

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

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 diseases, characteristics of

muscle hypertrophy

muscle relaxant

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

myasthenic crisis

myasthenic syndrome

myelogram, cervical

myeloneuropathy

myelopathy, ischemic

myelopathy, chronic progressive

myocardial infarction

myocardial injury

myopathy, amyloid

myopathy, autoimmune

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

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myxedema, neurologic manifestations of

N-acetyl-L-aspartic acid

narcotic analgesics

nausea and vomiting

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 conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

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

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory and motor

neuroophthalmology

neuropathology, brain

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

neurotransmitter

newborn, evaluation of

next-generation sequencing

night blindness

NMDA antagonists

numbness, ascending

numbness, extremity

numbness, generalized

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

Oppenheim muscular dystrophy

opportunistic infection, CNS

osteomyelitis, spinal

owl's eye sign of spinal cord

pain, abdominal

pain, interscapular

pain, management of chronic

palatal myoclonus

palliative care

paracentral lobule

paralysis, asymmetric

paraparesis, familial spastic

paraparesis, spastic

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

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

patient information and support

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

persistent vegetative state

personality change

pheochromocytoma

phrenic nerve pacemaker

physical activity

physical therapy

physician assisted suicide

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poison, mercury

poison, neurologic problems with

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

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

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

pregnancy, neurologic complications in

prevention of neurologic disorders

primary aldosteronism

primary lateral sclerosis

prisoners of war, neurologic complications in

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

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, unilateral

pulmonary embolism

pulmonary function tests

pure motor stroke

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

quality of life

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation hypersensitivity

radiation therapy, salivary gland

rapid onset dystonia parkinsonism

Raynaud's phenomenon

recruitment, reduced

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory depression

respiratory failure

respiratory tract infection

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

risk-benefit assessment

Rolandic artery

root lesion, nerve

salivation, excessive

sarcoidosis, CNS

scalenus anticus syndrome

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, treatment of

sensorimotor stroke

sensory ganglia

sensory ganglia, abnormal

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

shoulder, numbness

shoulder, pain in

shoulder, subluxation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

small vessel disease

Smell Identification Test

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

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

splenium of corpus callosum

spontaneous muscle activity

sports medicine, neurology of

standing difficulty

stem cell tourism

stem cell transplantation

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

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

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

subarachnoid hemorrhage

subclavian artery stenosis

subdural hematoma

superoxide dismutase

survival motor neuron gene

swallow evaluation

sweating, abnormality of

systemic illness

tandem gait, ataxic

Tangier's disease

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

tensilon test, false positive

testicular atrophy

thallium poisoning

thoracic outlet syndromes

thromboangiitis obliterans cerebri

thrombocytopenia

thrombophlebitis

thyrotropin-releasing hormone

Tolosa Hunt syndrome

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, swelling

tongue, weakness

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

tremor, postural

triangle of Guillain and Mollaret

tricresylphosphate

trigeminal nerve, abnormality of

trinucleotide repeats

Trousseau's sign

tuberous sclerosis

ulcers, fingertip

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

ulnar neuropathy

ultrasonography

unconsciousness

upgaze, paralysis of

urinary incontinence

urine test in toxic screen

vascular endothelial growth factor

venous thrombosis, non-cerebral

vertebral erosion

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

visual evoked response

vitamin E deficiency

Volkmann's ischemia

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Weber's syndrome

Werdnig-Hoffman disease

West Nile fever

whistle, inability to

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 500 to 550 of 4688 << Previous Next >>

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,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

Pure Motor Monoparesis Due to Ischemic Stroke
The Neurologist 17:301-308, Hiraga, A., 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

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

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

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

Diagnosis and New Treatments in Muscular Dystrophies
JNNP 80:706-714, Manzur,A.Y. &Muntoni,F., 2009

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

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Polymyalgia Rheumatica and Giant-Cell Arteritis
Lancet 372:234-245, Salvarani,C.,et al., 2008

Proximal Paresis of the Upper Extremity in Patients With Stroke
Neurol 69:348-355, Hatakenaka,M.,et al, 2007

Neurologic Complications of Gastric Bypass Surgery for Morbid Obesity
Neurol 68:1843-1850, Juhasz-Pocsine,K.,et al, 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Hanging Leg Syndrome: Combined Bilateral Femoral and Sciatic Neuropathies
Neurol 66:1124-1125, Scherer,K.,et al, 2006

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
Neurol 65:681-689, 662, Sahenk,Z.,et al, 2005

Quality of Life in Patients with Charcot-Marie-Tooth Disease
Neurol 65:922-924, Vinci,P.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Isolated Monoparesis Following Stroke
JNNP 76:805-807, Paciaroni,M.,et al, 2005

Pure Monoparesis
Arch Neurol 62:1221-1224, Maeder-Ingvar,M.,et al, 2005

Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
Neurol 64:2033-2039,2001, Josephs,K.A.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Diagnosing Suprascapular Neuropathy in Patients with Shoulder Dysfunction: A Report of 5 Cases
Physther 84:359-372, Walsworth, M.K.,et al, 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Recent Developments in Thyroid Eye Disease
BMJ 329:385-390, Cawood,T.,et al, 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Bilateral Extraocular Muscle Atrophy in Myotonic Dystrophy Type 1
Neurol 63:759-760, Yamashita,T.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Isolated Shoulder Paresis Caused by a Small Cortical Infarction
Neurol 61:1457, Komatsu,K.,et al, 2003

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Asymmetric Flaccid Paralysis: A Neuromuscular Presentation of West Nile Virus Infection
Ann Neurol 53:703-710,691, Li,J.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

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

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