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Differential
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aminoacidopathies
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, iatrogenic
antibodies to voltage-gated calcium channels
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
autism
B 12 deficiency
behavioral disorder
CAG repeats
calcium channel dysfunction
central core disease
cerebellar ataxia, hereditary
cerebellar ataxia, primary
children
chloride channel dysfunction
chromosomal abnormality
chromosome 6
dementia
diagnostic criteria
dural graft, cadaveric
dysarthria
dystonia
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
enzyme, defect
episodic neurologic deficits
eye movement, disorders of
familial
familial hemiplegic migraine
Friedreich's ataxia
gene
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
hallucination
hyporeflexia
hypotonia
iatrogenic neurologic disorders
inborn errors of metabolism
intracerebral hemorrhage
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
L-dopa
malignant hyperpyrexia
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
migraine
molecular genetics
MRI
MRI, abnormal
myotonia congenita
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuropathology
nystagmus
ocular motility, disorders of
ophthalmoplegia
paramyotonia congenita
Parkinson disease, fluctuations in
Parkinson disease, freezing phenomena in
Parkinson disease, young onset
Parkinsonism syndrome
paroxysmal neurologic deficits
periodic paralysis
potassium channel antibodies
potassium channel dysfunction
PRKN gene
psychomotor retardation
pyramidal tract dysfunction
pyridoxine
pyridoxine deficiency
review article
seizure
seizure, children
seizure, neonatal
seizure, pyridoxine dependent
self-mutilation
semialdehyde dehydrogenase deficiency
sensory loss
sodium channel dysfunction
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
tonic foot response
tremor
trinucleotide repeats
urine test for metabolic disorders
Showing articles 1000 to 1050 of 1343 << Previous Next >>

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Tourette Syndrome
Editorial, Lancet 1:3081987., , 1987

Dementia of the Alzheimer Type:Clinical & Family Study of 22 Twin Pairs
Neurol 37:359-363, Nee,L.E.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Benign Sexual Headach within a Family
Arch Neurol 43:1158-1160, Johns,D.R., 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986

Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986

The Inheritance of Gilles De La Tourette's Syndrome & Associated Behaviors
NEJM 315:993-997, Pauls,D.L.&Leckman,J.F., 1986

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986

Familial Myoclonic Dementia Masquerading as Creutzfeldt-Jakob Disease
Ann Neurol 20:231-239, Little,B.W.,et al, 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

A Population-Based Study of Multiple Sclerosis in Twins
NEJM 315:1638-1642, Ebers,G.C.,et al, 1986

Familial Hyperlipidemia in Stroke in the Young
Stroke 17:1142-1145, Bansal,B.C.,et al, 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986

On Heredity, Twins, & Parkinson's Disease
Ann Neurol 19:409-411, Duvoisin,R.C., 1986

Parkinson's Disease in Monozygotic Twins
Ann Neurol 19:405-408, Jankovic,J.&Reches,A., 1986

Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

Cerebrospinal Fluid Findings in Healthy Siblings of Multiple Sclerosis Patients
Neurol 36:727-729, Duquette,P.&Charest,L., 1986

Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986

Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986

Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
Neurol 36:687-692, Yasuda,Y.,et al, 1986

Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986

Myasthenia Gravis in Identical Twins
Neurol 36:78-80, Murphy,J.&Murphy,S.F., 1986

Clinicopathological Conference
Paget's Disease of Bone, Giant-Cell Reparative Granuloma, Case 1-1986, NEJM 314:105-11386., , 1986

Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986

Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986

Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986

Preventive Screening for the Fragile X Syndrome
NEJM 315:607-609, Turner,G.,et al, 1986



Showing articles 1000 to 1050 of 1343 << Previous Next >>