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Differential
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acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
adrenal mass
advances in neurology
Alzheimer's disease
amniocentesis
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
areflexia
arrhythmia, cardiac
astrocytoma
ataxia
atrial myxoma
autonomic dysfunction
cafe au lait spots
carcinoma
cardiomyopathy
CAT scan, abdomen
CAT scan, abnormal
cataracts
catecholamine
cavernous hemangioma
cerebral embolism
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
children
chromosomal abnormality
chromosome 17
chromosome 22
coagulopathy
constipation
cranial nerve tumor
deafness
developmental retardation
differential diagnosis
DNA probes
Ehlers-Danlos syndrome
ependymoma
Fabry's disease
familial
fibromuscular dysplasia
gadolinium
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
hamartoma
headache
hearing loss
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
homocystinuria
Huntington's chorea
hypertension
intellectual deficit
intracerebral hemorrhage
intracerebral hemorrhage, young adult
iris, abnormal
karyotyping
learning disability
learning disability, in children
Legius syndrome
life expectancy
Lisch nodules
long bone lesion
lymphoma
macrocephaly
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
meningioma
meningioma, familial
meningioma, multiple
merlin
migraine
migraine, hemiplegic
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
moyamoya
MRI
MRI, abnormal
MRI, spine
multiple endocrine neoplasia
muscular dystrophy
muscular dystrophy, Duchenne
myotonia dystrophica
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-familial occurrence
nerve growth factor
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease, diagnoses of
neurologic signs
neuropathy
NF1 gene
optic glioma
palpitations
patient information and support
pheochromocytoma
polycythemia, primary
precocious puberty
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
protein C deficiency
pruritus
pseudarthrosis
pseudoxanthoma elasticum
recombinant DNA
review article
RFLPs
Riley-Day syndrome
root lesion, nerve
schwannoma
scoliosis
seizure
sensory ganglia
sensory ganglia, abnormal
Shy-Drager syndrome
sickle cell disease
skin, lesions in neurologic disorders
skull x-ray, abnormal
skull x-ray, bony defect on
slit lamp examination
speech disorder
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary intradural
spinal cord, neoplasm, intramedullary
spinal cord, neoplasm, neurofibroma
SPRED1 mutation
sweating
thrombocytopenia
tinnitus
treatment of neurologic disorder
tuberous sclerosis
urinary catecholamines
Von Hippel Lindau
web sites
weight loss
white freckles
Showing articles 1100 to 1150 of 1738 << Previous Next >>

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992

Detecting Susceptibility to Malignant Hyperthermia
BMJ 304:791-792, Ellis,F.R., 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Midbrain Myasthenia:Fatigable Ptosis, 'Lid Twitch'Sign, and Ophthalmoparesis From a Dorsal Midbrain Glioma
Neurol 42 917-919, Ragge,N.K.&Hoyt,W.F., 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

Familial Cluster Headache:Occurrence in Three Generations
Neurol 42:1399-1400, Spierings,E.L.H.&Vincent,A.J.P.E., 1992

Migraine:Theories of Pathogenesis
Lancet 339:1202-1207, Blau,J.N., 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

A Study of Twins and Stroke
Stroke 23:221-223, Brass,L.M.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

The Chiari Type I Malformation in Two Monozygotic Twins and First-Degree Relatives
Ann Neurol 31:220-222, Stovner,L.J.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Prion Disease
NEJM 326:486-487, Johnson,R.T., 1992

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Erythromelalgia:Review of Clinical Characteristics and Pathophysiology
Am J Med 91:416-422, Jurzrock,R.&Cohen,P.R., 1991

More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
Lancet 338:1562-1563, , 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

The Phenotype of the X-Linked Dystonia-Parkinsonism Syndrome, An Assessment of 42 Cases in the Philippines
Medicine 70:179-187, Lee,J.V.,et al, 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991

Clinical Genetics and Genetic Counseling in Alzheimer Disease
Ann Int Med 115:601-606, Breitner,J.C.S., 1991

Discordance and Concordance of Dementia of the Alzheimer Type (DAT) in Monozygotic Twins
Neurol 41:1549-1553, Rapoport,S.I.,et al, 1991

Cerebral Haemorrhage and Berry Aneurysm:Evidence from a Family for a Pattern of Autosomal Dominant Inheritance
JNNP 54:838-840, Shinton,R.,et al, 1991

Familial Association of Intracranial Aneurysms and Cervical Artery Dissections
Stroke 22:1426-1430, Schievink,W.I.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991

Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
Neurol 41:1313-1315, Visy,J.M.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers
Neurol 41:992-999, Farrer,L.A.,et al, 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991



Showing articles 1100 to 1150 of 1738 << Previous Next >>