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amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
antibodies to voltage-gated calcium channels
arrhythmia, cardiac
arteriopathy
ataxia
ataxia, hereditary
ataxia, paroxysmal
atrial myxoma
benign essential tremor
calcium antagonist
calcium channel dysfunction
cardiomyopathy
CAT scan
cavernous hemangioma
central core disease
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral embolism
cerebrovascular accident
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cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
children
chloride channel dysfunction
chromosomal abnormality
chromosome 19
coagulopathy
complicated migraine
dementia
dementia, subcortical
Ehlers-Danlos syndrome
electroencephalogram, pediatric patients
eye movement, disorders of
Fabry's disease
familial
familial hemiplegic migraine
familial periodic ataxia
fibromuscular dysplasia
gene
gene mutation
genetic neurologic disorders
headache
hemiparesis
hemiparesis, transient
hemiplegia
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
homocystinuria
hypokalemic periodic paralysis
intracerebral hemorrhage
intracerebral hemorrhage, young adult
leukoencephalopathy
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malignant hyperpyrexia
migraine
migraine, EEG in
migraine, hemiplegic
migraine, treatment of
mitral valve prolapse
moyamoya
MRI
MRI, abnormal
myasthenic syndrome
myotonia congenita
neurocutaneous disease
neurofibromatosis 1
neurologic disease
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neuroophthalmology
nystagmus
paramyotonia congenita
paroxysmal neurologic deficits
periodic paralysis
polycythemia, primary
potassium channel antibodies
potassium channel dysfunction
protein C deficiency
pseudobulbar palsy
pseudoxanthoma elasticum
pursuit eye movements, abnormal
quadriparesis
review article
seizure
sickle cell disease
sodium channel dysfunction
spinal cord, infarction of
spinocerebellar ataxia
spinocerebellar ataxia type 6
thrombocytopenia
transient neurologic deficit
treatment of neurologic disorder
tremor
tuberous sclerosis
verapamil
Von Hippel Lindau
Showing articles 50 to 100 of 3783 << Previous Next >>

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
Radiology 214:209-216, Brunereau,L.,et al, 2000

Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
AJNR 21:1016-1020, Matsubara,S.,et al, 2000

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Migraine and Stroke in Young Women:Case-Control Study
BMJ 318:13-18, Chang,C.L.,et al, 1999

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

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

Basilar Artery Migraine and Reversible Imaging Abnormalities
AJNR 19:1116-1119, Maytal,J.,et al, 1998

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

Clin Features of Early-Onset Alzheimer Disease in Large Kindred with an E280A Presenilin-1 Mutation
JAMA 277:793-799, Lopera,F.,et al, 1997

Familial Acephalgic Migraines
Neurol 48:776-777, Shevell,M.I., 1997

Familial Migraine with Vertigo and Essential Tremor
Neurol 46:458-460, Baloh,R.W.,et al, 1996

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Familial Acephalgic Migraine
Neurol 45:2293-2294, Ziegler,D.K., 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

'Complicated Migraine-like Episodes'in Children Following Cranial Irridiation and Chemotherapy
Neurol 45:1837-1840, Shuper,A.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Benign Familial Nocturnal Alternating Hemiplegia of Childhood
Neurol 44:1812-1814, Andermann,E.,et al, 1994

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994

Validity of Family History Data on Severe Headache and Migraine
Neurol 43:1954-1960, Ottman,R.,et al, 1993

Migraine Madness:Recurrent Psychosis after Migraine
JNNP 56:416-418, Fuller,G.N.,et al, 1993

Migraine and Migranous Stroke:Risk Factors and Prognosis
Neurol 43:2473-2476, Rothrock,J.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Hemiplegic Migraine and Moyamoya Disease
Am J Dis Child 147:718-719, Bernstein,A.L., 1993

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

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

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Migraine and Vertebrobasilar Ischemia
Neurol 41:55-61, Caplan,L.R., 1991

Recurrent Prolonged Coma Due to Basilar Artery Migraine:A Case Report
Headache 31:75-81, Frequin,S.T.F.M.,et al, 1991

The First Report of Cluster Headache in Identical Twins
Neurol 41:761, Couturier,E.G.M.,et al, 1991

Permanent Cerebral Diplopia in a Migraineur
Neurol 40:1138-1139, Sinoff,S.E.&Rosenberg,M., 1990

Migraine-Related Stroke in the Context of the International Headache Society Classification of Head Pain
Arch Neurol 47:458-462, Welch,K.M.A.&Levine,S.R., 1990

Migraine with Vasospasm and Delayed Intracerebral Hemorrhage
Arch Neurol 47:53-56, Cole,A.J.&Aube,M., 1990

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Migraine Stroke
Neurol 38:223-227, Bogousslavsky,J.,et al, 1988

Migrainous Stroke
Arch Neurol 45:63-67, Rothrock,J.F.,et al, 1988

Intracerebral Hemorrhage Revisited
Neurol 38:624-627, Caplan,L., 1988

Bilateral Posterior Cerebral Artery Strokes in a Young Migraine Sufferer
Stroke 19:525-528, Moen,M.,et al, 1988

Clinicopath Conf
Mastoiditis with Right Transverse-Sinus and Sigmoid-Sinus Thrombosis, Case Record 20-1988, NEJM 318:, 321328,1988., 1988

Cheiro-Oral Syndrome: Does It Have a Specific Localizing Value?
Eur Neurol 28:326-330, Holter,J.T. &Tijssen,C., 1988

Migraine-Related Strokes, Clinical Profile & Prognosis in 20 Patients
Arch Neurol 44:868-871, Broderick,J.P.&Swanson,J.W., 1987

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

Unusual Acute Neurologic Presentations with Epstein-Barr Virus Infection
Arch Neurol 43:186-188, Leavell,R.,et al, 1986

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986

Transient & Persistent Neurological Manifestations of Migraine
Stroke 15:383-386, Bartleson,J.D., 1984

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984



Showing articles 50 to 100 of 3783 << Previous Next >>