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Differential
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abdominal distention

abdominal muscle paralysis

abducens nerve paralysis

abscess, intracranial

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

acyl CoA dehydrogenase deficiency

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agammaglobulinemia

airway obstruction

alcohol intolerance

alcohol intoxication

alcohol, blood level of

alcohol, neurologic complications with

alcoholic blackout

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

alkylating agents

alpha glucosidase

alpha-fetoprotein

altered states of consciousness

alternative medicine

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

aminoacidopathies

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, misdiagnosis

anesthesia, general

Angelman syndrome

angiofibroma, facial

angiomyolipomas

animal exposure

anterior horn cell disease

anterior tibial muscle weakness

antibodies to voltage-gated calcium channels

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, selection of

anticonvulsants, untoward effects of

apolipoprotein E

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, pulmonary

arthrogryposis multiplex

aspartate aminotransferase

Asperger's syndrome

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

atrial fibrillation

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autism, screening for

autoimmune disease

automatic implantable cardioverter-defibrillator

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

behavior, combative

behavioral disorder

benign essential tremor

bent spine syndrome

bicaudate index

black toenail sign

bleeding disorder

blood dyscrasias, neurologic findings with

bone marrow transplantation

botulinum toxin

bovine spongiform encephalopathy

brainstem, lesion of

brainstem, neoplasms of

calcification, intracranial

calcium channel dysfunction

calf hypertrophy

carcinoma of pancreas

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, chest

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, muscle

cataracts, congenital

caudate nucleus

caudate nucleus, atrophy

central core disease

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemangioma

cerebellum, neoplasms of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral ischemia

cerebro hepato renal syndrome

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot-myoclonus syndrome

chewing, impaired

chloride channel dysfunction

chorea, familial

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

collagen vascular disease

compression neuropathy

conduction block

confidentiality

congenital heart disease

congenital heart disease, CNS complications with

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

contractures, joint

conversion reaction

cornea, abnormal

corneal dystrophy

corpus callosum

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyclic vomiting

cyst, peritumoral

cyst, neoplastic cerebellum

cyst, parenchymal

cytochrome c oxidase

cytochrome c oxidase, deficiency

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

dementia, familial

dementia, rapidly progressive

dementia, transmissible

demyelinating disease

dentatorubral-pallidoluysian atrophy

dermatomyositis

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

digits, abnormal

dilantin, hypersensitivity to

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dropped head syndrome

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dyschromatopsia

dysferlinopathy

dystonia, cervical

dystonia, etiology of

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystroglycanopathies

dystrophin associated proteins

eating disorder

edema, periorbital

Ehlers-Danlos syndrome

Ehlers-Danlos syndrome, classification

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

electronystagmography

electroretinograph

embolism, paradoxical

embolism, septic

Emery-Dreifuss muscular dystrophy

encephalomalacia

encephalopathy, anoxic

encephalopathy, neonatal

encephalopathy, progressive

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

epistaxis, recurrent

erectile dysfunction

esophageal varices

ethics in neurology

evoked potentials

exercise intolerance

exercise-induced neurologic dysfunction

extraocular muscle lesion

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

facial nerve palsy, bilateral

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

familial hemiplegic migraine

family planning

fatty acid, elevated plasma content

Fazio-Londe's disease

feeding disorder

fetal alcohol syndrome

fibroma, ungual

fine motor function, impaired

fistula, arterio-venous, pulmonary

foot drop, bilateral

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal balding

fundus, abnormality of

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

Gaucher's disease

gaze palsy, supranuclear

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glucocerebrosidase

glycogen storage disease

glycosyltransferase

gonadal dysgenesis

Gowers maneuver

growth hormone deficiency

Guillain Barre syndrome

gyrus, abnormal

Hallervorden Spatz disease

Hallgren's syndrome

head circumference

headache, positional

heart block, complete

heavy metal intoxication

hemangioblastoma

hematuria, gross

hemianopia, homonymous

hemidiaphragm, paralysis of

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

hereditary myopathy with early respiratory failure

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hexosaminidase-A

high arched feet

high arched palate

histochemistry of muscle

hormone replacement

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

Hurler's syndrome

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperkalemic periodic paralysis

hypersensitivity reaction

hyperthyroidism

hypertrophic cardiomyopathy

hypoglycemic coma

hypokalemic periodic paralysis

hypopigmentation of skin

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immunodeficiency

immunohistochemistry

immunology and the nervous system

inability to sit up

inability to stand on tiptoes

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

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infantile spasm

informed consent

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial pressure, increased

intrauterine infection

intrinsic hand muscles, wasting of

ischemic exercise test

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

joint hypermobility

Kearns-Sayre syndrome

klippel feil syndrome

Korsakoff's psychosis

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

Lafora's disease

laminar necrosis, cortical

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

leg spasms, painful

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lens, dislocation of

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

lid closure, weakness of

life expectancy

limb-girdle weakness

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

lymphadenopathy

lymphangiomyomatosis

lymphocyte capping, diminished

lysosomal storage disease

lysosomes, abnoral

macular degeneration

magnetoencephalography

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

McArdle's disease

McLeod syndrome

medical-legal aspects of neurology

meningeal enhancement

meningoencephalopathy

mental retardation

mental retardation, familial

metabolic acidosis

metabolic disorder, primary

methylhydrazine derivatives

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

Miller-Dieker syndrome

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

monoamine oxidase inhibitors

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, gyral swelling

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

mucopolysaccharidoses

multicore myopathy

multiminicore disease

multiple sclerosis, misdiagnosis

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle phosphorylase deficiency

muscle stiffness

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

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, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

muscular dystrophy, lymphocyte capping, diminished

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

muscular dystrophy, systemic membrane defect

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, differential diagnosis

myasthenia gravis, distal weakness

myasthenia gravis, familial incidence of

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, receptor site in

myasthenia gravis, seronegative

myasthenic crisis

myasthenic syndrome

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, alcoholic

myopathy, carcinomatous

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, genetic

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, thyroid disease causing

myopathy, vacuolar

myotonia congenita

myotonia dystrophica

myotonia dystrophica, classification

myotonic discharges

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-surgical treatment of

nerve conduction studies

nerve growth factor

nerve hypertrophy

neuritis, causes of

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurogenic vs.myopathic atrophy

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination, focal

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathy, amyloid

neuropathy, ataxia, retinitis pigmentosa

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, peripheral

newborn, evaluation of

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

Noonan Syndrome

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy, hereditary

optic disc edema

optic nerve, compression of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

orthostatic hypotension

pacemaker, cardiac-transvenous

pain, abdominal

paralysis, acute areflexic

paramyotonia congenita

paraparesis, familial spastic

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

pectus excavatum

percussion induced muscle contraction

periodic paralysis

periodic paralysis, thyrotoxic

peroxisomal disease

personality change

pheochromocytoma

phosphorylase b kinase deficiency

pigmentary retinopathy

pituitary, hormones of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polycystic kidneys

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

Pompe's disease of glycogen storage

Pompe's disease, infantile

portal caval shunt

positive sharp waves

postural abnormality

potassium channel antibodies

potassium channel dysfunction

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prevention of neurologic disorders

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

proximal muscle atrophy

proximal myotonic myopathy

pseudomyasthenia

pseudoretinitis pigmentosa

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis, acute

psychosocial aspects

ptosis, bilateral

ptosis, familial

pulmonary hypertension

pulmonary infection

pulmonary stenosis

quadriceps atrophy

quadriceps weakness

quality of life

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

ragged-red fibers

rapidly progressing neurologic illness

real-time quaking-induced conversion

recombinant DNA

refractive errors

Refsum's disease

renal cell carcinoma

repetitive nerve stimulation

respiratory depression

respiratory failure

respiratory tract infection

retina, abnormal

retinal degeneration

retinal hamartoma

retinal hemangioma

retinitis pigmentosa

reversible neurologic disorder

rhabdomyosarcoma of heart

rigid spine syndrome

rippling muscle disease

saccadic eye movements, abnormal

sarcoglycanopathy

scoliosis, neurologic association with

second wind phenomena

seizure, children

seizure, familial

seizure, injury following

seizure, intractable

seizure, neonatal

seizure, paradoxical

seizure, treatment of

self-mutilation

sensorineural hearing loss

shoulder, pain in

sick sinus syndrome

single photon emission computed tomography

skin, darkening of

skin, hyperextensible

skin, lesions in neurologic disorders

skin, translucent

skull x-ray, abnormal

slit lamp examination

sloped shoulders

sodium channel dysfunction

speech disorder

speech, delayed development of

sphingolipodoses

Spielmeyer Vogt syndrome

spinal cord, neoplasm

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

spinocerebellar ataxia type 2

spinocerebellar ataxia type 6

spinocerebellar degeneration

spongy degeneration of brain

spontaneous remission

standing difficulty

stereotaxic surgery

stereotyped behavior, drug induced

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

storage disease of CNS

striatum, lesion of

strokelike episodes

subarachnoid hemorrhage

subependymal nodules

succinate dehydrogenase deficiency

survival motor neuron gene

symmetric brain lesions

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

tapetoretinal degeneration

Tay-Sachs disease

telangiectases, retinal

temper tantrums

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular atrophy

testicular enlargement

thalamus, lesion of-bilateral

thyroid function tests

tissue plasminogen activator, intravenous

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

torticollis, post traumatic

transient neurologic deficit

transverse smile

treatment of neurologic disorder

tremor, postural

tricresylphosphate

trinucleotide repeats

tuberous sclerosis

tuberous sclerosis, screening for

type 1 muscle fiber

Unverricht-Lundborg disease

upgaze, paralysis of

Usher's syndrome

very long chain fatty acids

vincristine neurotoxicity

visceral neuropathy

vision, failure of in childhood

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss, progressive

vocal cord paralysis

vomiting, recurrent

Von Hippel Lindau

walking, difficulty with

weakness, acute

weakness, chronic

weakness, episodic

weakness, fatiguable

weakness, fluctuating

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Werdnig-Hoffman disease

Wernicke's encephalopathy

Western immunoblot test

white matter disease

white matter disease, pattern

wide based gait

winging of scapula

wound healing, poor

X-linked bulbospinal neuronopathy

x-linked hydrocephalus

x-linked mental retardation

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 1100 to 1150 of 2683 << Previous Next >>

Creutzfeldt-Jacob Disease in a Husband and Wife
Neurol 50:684-688, Brown,P.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

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

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
Neurol 50:1441-1445, Antonini,G.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

A Rash, Circulating Anticoagulant, Then Meningitis
Lancet 351:1856, Schanen,A.,et al, 1998

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

Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
Neurol 50:764-767, Levin,M.I.,et al, 1998

Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
Neurol 50:526-529, Al-Lozi,M.T.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

MR of Hereditary Hemorrhagic Telangiectasia:Prevalence and Spectrum of Cerebrovascular Malformations
AJNR 19:477-484, Fulbright,R.K.,et al, 1998

Acute Myopathy After Liver Transplantation
Neurol 50:46-53, Campellone,J.V.,et al, 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
Neurol 51:1226-1227, Wasay,M.,et al, 1998

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

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

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

A News Locus for Hemiplegic Migraine Maps to Chromosome 1q31
Neurol 49:1231-1238, 11931997., Gardner,K.,et al, 1997

Comparison of First Degree Relatives and Spouses of Poeple with Chronic Tension Headache
BMJ 314:1092-1093, Ostergaard,S.,et al, 1997

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Clinicopath Conf
Genetic Hemochromatosis, Micronodular Cirrhosis of Liver, Case 10-1997, NEJM 336:939-94797., , 1997

Focal Myositis Mimicking Acute Psoas Abscess, An Unusual Presentation of Systemic Lupus Erythematosus
BMJ 31:805-808, Lawson,T.M.,et al, 1997

The Diagnostic Evaluation & Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2
JAMA 278:51-57, Gutmann,D.H.,et al, 1997

Endolymphatic Sac Tumors, A Source of Morbid Hearing Loss in von Hippel-Lindau Disease
JAMA 277:1461-1466, Manski,T.J.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Acute Corticosteroid Myopathy in Intensive Care Patients
Muscle & Nerve 20:1371-1380997., Hanson,P.,et al, 1997

Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
Arch Neurol 54:1420-1422, Sun,D.Y.,et al, 1997

Idiopathic Granulomatous Angiitis of the CNS Manifesting as Diffuse White Matter Disease
Neurol 49:1696-1699, Finelli,P.F.,et al, 1997

Complete Genomic Screen in Late-Onset Familial Alzheimer Disease, Evidence for a New Locus on Chromosome 12
JAMA 278:1237-1241, 12821997., Pericak-Vance,M.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Painful Proximal Diabetic Neuropathy:Inflammatory Nerve Lesions and Spontaneous Favorable Outcome
Ann Neurol 41:762-770, Said,G.,et al, 1997

Clinicopath Conf
Skeletal-Muscle Infarction Associated with Diabetes Mellitus, Case 29-1997, NEJM 337:839-845997., , 1997

Acute Intermittent Porphyria:Clinicopathologic Correlation
Neurol 48:1678-1683, Suarez,J.I.,et al, 1997

A Gene for Parkinson Disease
Arch Neurol 54:1156-1157, Chase,T.N., 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Predictors of Recurrent Febrile Seizures
Arch Pediatr Adolesc Med 151:371-378, Berg,A.T.,et al, 1997

The Expansion of the CAG Repeat in Ataxin-2 is a Frequent Cause of Autosomal Dominant Spinocerebellar Ataxia
Neurol 49:1009-1013, Lorenzetti,D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Showing articles 1100 to 1150 of 2683 << Previous Next >>