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Lancet 400:1363-1380, Feldman, E.L.,et al, 2022
A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
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Cranial Cavernous Malformations
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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NEJM 390:1022-1028, Smith,E.R., 2024
Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Thyrotoxic Periodic Paralysis
UptoDate Jan, Gutmann, L. & Conwit, R., 2022
Recurrent Cerebral Ischemia During Pregnancies
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Neuromyelitis Optica Spectrum Disorders
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Lancet 383:896-910, Lai, M.C.,et al, 2014
Familial Risk of Cerebral Palsy: Population Based Cohort Study
BMJ 349:g4294, g4514, Tollanes, M.C.,et al, 2014
Degenerative Diseases of the Nervous System, Parkinson Disease
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Familial Neuromyelitis Optica
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Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,et al, 2010
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Familiality in Brain Tumors
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Neurol 69:586-595, Fertleman,C.R.,et al, 2007
Parental Transmission of MS in a Population-Based Canadian Cohort
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Seizures on Hearing the Alarm Clock
Lancet 370:2172, Vollmar,C.,et al, 2007
Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
Stroke 37:2924-2929, Martin,J.J.,et al, 2006
Migraine and Cerebral White Matter Lesions
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Pathogenetic Mechanisms of Parkin in Parkinson's Disease
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Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004
Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003
Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002
Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
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Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000
De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000
Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
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The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998
Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Recurrent Spontaneous Arterial Dissections-Risk in Familial Vs Nonfamilial Disease
Stroke 27:662-624, Schievink,W.,et al, 1996
Evidence for Genetic Basis of Multiple Sclerosis
Lancet 347:1728-1730, Sadovnick,A.D.,et al, 1996