Neudle.com: hand posture

Differential
(Click to cross reference)

abdominal distention

abulia

accommodation

accomodation, abnormal

acetazolamide

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acromicria

acute ataxia of childhood

acute cerebellar ataxia

acute disseminated encephalomyelitis

Addison's disease

adolescent medicine

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alexia without agraphia

algorithm

alien hand syndrome

allodynia

alternating rapid movement

alternating rapid movement, impaired

amphiphysin antibodies

anemia, megaloblastic

anterior tibial muscle weakness

anterocollis

anti citrullinated antibody

anti IgLON5

anti MAG antibodies

anticonvulsants

anticonvulsants, untoward effects of

antiviral agents

anxiety

aphasia

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

aspartate aminotransferase

ataxia telangiectasia

ataxia, truncal, associated with ocular oscillations

ataxic gait

ataxic-dystonia syndromes

athetosis

athetosis, causes of

atrial fibrillation

attention deficit disorder with hyperactivity

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

benign essential tremor

benzodiazepine

beta adrenergic blocker

bone marrow suppression

botulinum toxin

botulinum toxin, complications of

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

calcification, intracranial

CAT scan, emission, abnormal

cauda equina, enhancement

CD4 counts

central cord syndrome

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral palsy

cerebral palsy, associated problems with

cerebral peduncle

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, complications with

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 14

chromosome 15

chromosome 6

chronic progressive external ophthalmoplegia

cirrhosis

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

concentration, impaired

convergence, impaired

conversion reaction

copper

copper metabolism, abnormal

cornea, abnormal

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

cryptococcal meningitis

cryptorchidism

cultured skin fibroblasts

cytokines

cytomegalovirus infection

decerebrate posture

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dental procedure, neurologic complications with

dentate nuclei

dentate nuclei, lesion of

depression

dermatitis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

dilantin

dilantin, toxicity

diplopia

disability rating scale, neurological

disability, neurological

distal muscle atrophy

distal muscle weakness

diurnal variation

dizziness

dopa responsive dystonia

dopamine antagonist

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze

drooling

drug abuse

drug abuse, inhalation

drug induced neurologic disorders

dysarthria

dysarthria-clumsy hand syndrome

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, focal lesion causing

dystonia, focal task specific

dystonia, laryngeal

dystonia, post traumatic

dystonia, psychogenic

dystonia, symptomatic

dystonia, treatment of

dystonic reaction, acute

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

embolism

embolism, fat

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, episodic

encephalitis, focal

encephalitis, human immunodeficiency virus type 1

encephalitis, St.Louis

encephalitis, viral

encephalomyelitis, paraneoplastic

encephalopathy

encephalopathy, parainfectious

encephalopathy, progressive

enzyme, defect

eosinophilia

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

executive dysfunction

exome sequencing

eye color

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

facial expression abnormality

fetal movements, reduced

fetus

fever

fine motor function, impaired

finger naming

finger nose finger test

finger numbness

finger tapping

fingernails, abnormal

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

gammaglobulin therapy, intravenous

ganglionitis

gastric biopsy

gastritis

gastrocnemius muscle weakness

gastroenteritis

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

globoid cells

globus pallidus

globus pallidus, lesion of

glycogen storage disease

granular osmiphilic material

grasp reflex

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallervorden Spatz disease

hallucination

hallucination, visual

heavy metal intoxication

hemiakathisia

hemianopia

hemianopia, homonymous

hepatic encephalopathy

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniated disc

herniated disc, central

herniated disc, cervical

herniation syndromes, intracranial

hiccoughs

high arched feet

highly active antiretroviral therapy

hip flexor weakness

histochemistry

histochemistry of muscle

HIV CSF viral escape syndrome

human immunodeficiency virus type 1

human immunodeficiency virus type 1, asymptomatic

human immunodeficiency virus type 1, pathogenesis

hypogonadism, hypogonadotropic

hyponatremia

hypophonia

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

impulsivity

inability to stand on tiptoes

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

incoordination

industrial neurologic disorders

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracranial pressure, increased

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

jaw jerk, abnormal

Jewish

Kayser-Fleischer ring

kinesia paradoxica

Krabbe's disease

lactic acidemia

lacunar infarction, differential diagnosis of

laminectomy

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukoencephalopathy, differential diagnosis

leukoencephalopathy, hereditary diffuse

lipid storage disorder of CNS

liver biopsy

liver disease

liver function enzymes

liver transplantation

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

medical-legal aspects of neurology

Mees lines

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis

meningoencephalitis

meningoencephalitis, amoebic

mental retardation

mental status, abnormal

merosin

metabolic disorder, primary-screening tests

methylmalonic acid, serum

methylmalonic acidemia

midbrain, infarction of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

mimics

misdiagnosis

mitochondrial disease

molecular genetics

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy multiplex

mortality

motor dysfunction

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MPTP

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, hypointense signal foci on

MRI, negative

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRS

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, limb-girdle

musicians

musician's dystonia

myelinolysis, extrapontine

myelitis, longitudinal

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myositis, acute of childhood

myositis, post infectious

neoplasm, intracranial

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-recurrent

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

neoplastic angioendotheliosis

nerve biopsy

nerve conduction studies

nerve conduction studies, sensory

nerve root biopsy

neuritis, heavy metals causing

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neuroleptic

neuroleptic malignant syndrome

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neurologic symptoms, unexplained

neuromuscular disease, electrodiagnosis of

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

next-generation sequencing

numb clumsy hands syndrome

numbness, extremity

numbness, generalized

nystagmus

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, vertical

obesity

occupational neurologic disorders

ocular motility, disorders of

Oculinum

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

opportunistic infection

opportunistic infection, CNS

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic chiasm, enlarged

optic nerve, enlarged

optic neuropathy

ornithine transcarbamylase deficiency

orthostatic hypotension

osmotic demyelination syndrome

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

parasitic infection, CNS

paresthesias

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, etiology of

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, prognosis of

Parkinson disease, psychogenic

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

paroxysmal nonkinesigenic dyskinesia

PAS positive

PAS positive material in the brain

past pointing

patient information and support

pelvic mass

penguin silhouette sign

penicillamine

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

photosensitivity, skin

pigmentary retinopathy

plasmacytoma

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

POEMS syndrome

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

pons, lesion of

position sensation

position sensation, abnormal

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior column disease

postoperative neurologic complications

postural abnormality

posturography

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary episodic ataxia

prion disease

PRKN gene

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

propranolol

proprioception

proprioception, abnormal

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pull test

pupil, dilated and fixed, bilateral

pure sensory stroke

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

quality of life

radiation therapy, CNS treatment and complications with

radiculopathy

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

rash, hand

real-time quaking-induced conversion

recurrent

Red flags

reflex sympathetic dystrophy

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

rheumatoid vasculitis

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

screaming

screening

sea-blue histiocytes

sedimentation rate, elevated

seizure, psychomotor-temporal lobe

self harm

sensorineural hearing loss

sensory loss

sensory loss, asymmetric

sensory loss, cortical

sensory tricks

sequencing difficulty

seroconversion

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slurred speech

snout reflex

sodium valproate

sodium valproate, toxicity

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

splenomegaly

spontaneous remission

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

storage disease of CNS

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuttering

subarachnoid hemorrhage

substantia nigra

suck reflex

suck, poor

superior cerebellar artery infarction

superior cerebellar artery syndrome

swallow evaluation

sweating

sweating, abnormality of

symmetric brain lesions

synovitis

syphilis, diagnosis and treatment

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, protrusion of

tonic foot response

tonic spasms

torticollis

torticollis, post traumatic

toxoplasmosis, CNS

transcutaneous electrical nerve stimulation

transient ischemic attack

transient neurologic deficit

transient neurologic deficit, benign syndrome in young adults

trauma

treatment failure

treatment of neurologic disorder

tremor, post traumatic

trientine dihydrochloride

trinucleotide repeats

tripping

typing

typist cramp

tyrosine hydroxylase deficiency

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

undiagnosed

upgaze, paralysis of

urea-cycle enzymopathies

uremia

uric acid, low

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

useless hand

uveitis

vascular endothelial growth factor

vasculitides

vegetarianism

ventricular enlargement

vertigo

vertigo, positional

vibratory sensation

vibratory sensation, abnormal

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual symptoms

visuospatial disturbance

voice, abnormality of

walking

walking frame

walking, delayed

walking, difficulty with

weakness

weakness, congenital

weakness, generalized

weakness, progressive

weight loss

Wernekinck commissure syndrome

word-finding difficulty

Showing articles 50 to 100 of 1461 << Previous Next >>

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

Degenerative Diseases of the Nervous System, Dystonia Musculorum Deformans
Adams & Victors Principles of Neurology, Chp 39, pg 1099, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Cerebellar Degeneration
Adams & Victors Principles of Neurology, Chp 39, pg 1105, Ropper, A.H.,et al, 2014

A Man with Tingling Fingers
BMJ 346:f1443, Larkman, M.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Parkin Disease
JAMA Neurol 70:571-579, Doherty, K.,et al, 2013

Long-Term Improvement of Musicians Dystonia after Stereotactic Ventro-Oral Thalamotomy
Ann Neurol 74:648-654,627, Horisawa, S.,et al, 2013

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

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

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

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

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

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

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
J Natl Cancer Inst 101:946-958, Armstrong,G.T.,et al, 2009

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

Deep Brain Stimulation
Neurologist 13:237-252, Kem,DS. &Kumar,R., 2007

Secondary Motor Disturbances in 101 Patients With Musicians Dystonia
JNNP 78:949-953, Rosset-Llobet,J.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Dystonia
NEJM 355:818-829, Tarsy,D. &Simon,D.K., 2006

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

TENS for the Treatment of Writers Cramp Dystonia:A Randomized, Placebo-Controlled Study
Neurol 64:1946-1948, Tinazzi,M.,et al, 2005

Botulinum toxin injections in the treatment of musician's dystonia
Neurol 64:341-343, Schuele, S., et al, 2005

Musician's dystonia
Neurol 64:186-187, Pullman, S.L. & Hristova, A.H., 2005

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

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

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

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

Limb Immobilization for the Treatment of Focal Occupational Dystonia
Neurol 57:405-409, Priori,A.,et al, 2001

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

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

Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998

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

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

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Tremor and Other Movement Disorders after Whiplash Type Injuries
JNNP 63:110-112, Ellis,S.J., 1997

Thalamic Tremor:Case Reports and Implications of the Tremor-Generating Mechanism
Neurol 46:75-79, Miwa,H.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 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

Post-Traumatic Movement Disorders in Survivors of Severe Head Injury
Neurol 47:1488-1492, Krauss,J.K.,et al, 1996

Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
JNNP 59:406-412, Factor,S.A.,et al, 1995

Showing articles 50 to 100 of 1461 << Previous Next >>