Peri-ictal Water Drinking Lateralizes Seizure Onset to the Nondominant Temporal Lobe
Neurol 60:873-876, Trinka,E.,et al, 2003
Underestimation of Time Perception After Repetitive Transcranial Magnetic Stimulation
Neurol 60:1844-1846, Koch,G.,et al, 2003
Early Visual Function Impairment in CADASIL
Neurol 60:2008-2010, Parisi,V.,et al, 2003
Lack of Hemispheric Dominance for Consciousness in Acute Ischaemic Stroke
JNNP 74:889-892, Cucchiara,B.,et al, 2003
Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003
Cerebral Microbleeds in CADASIL
Stroke 33:67-71, Dichgans,M.,et al, 2002
Ptosis in Patients with Hemispheric Strokes
Neurol 58:620-624, Averbuch-Heller,L.,et al, 2002
Monitoring Disease Progression in CADASIL With Diffusion Magnetic Resonance Imaging
Stroke 33:2902-2908, Molko,N.,et al, 2002
Language Lateralization in Left-Handed and Ambidextrous People
Neurol 59:238-244, Szaflarski,J.P.,et al, 2002
Subcortical Lacunar Lesions:An MR Imaging Finding in Patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Radiology 224:791-796, van den Boom, R., et al, 2002
CADASIL Mimicking Primary Angiitis of the Central Nervous System
Arch Neurol 59:1480-1483, Engelter,S.T.,et al, 2002
Diagnostic Strategies in CADASIL
Neurol 59:1134-1138, Markus,H.S.,et al, 2002
Schizophrenia in a Patient with Cerebral Autosomally Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (CADASIL Disease)
Nord J Psychiatry 55:41-42, Lagas,P.A. &Juvonen,V., 2001
Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001
Cerebral Microbleeds in CADASIL
Neurol 57:1066-1070, Lesnik,S.A.J.,et al, 2001
Gluten Sensitivity in Sporadic and Hereditary Cerebellar Ataxia
Ann Neurol 49:540-543, Bushara,K.O.,et al, 2001
Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001
MRI Hyperintensities of the Temporal Lobe and External Capsule in Patients with CADASIL
Neurol 56:628-634, O'Sullivan,M.,et al, 2001
The Differential Diagnosis of Multiple Sclerosis
JNNP 71(suppl II):ii9-ii15, Scolding, N., 2001
Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000
Cranial MR Imaging of Osteopetrosis
AJNR 21:1110-1115, Cure,J.K.,et al, 2000
De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000
Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000
Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000
Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance
Neurol 52:1361-1367, Dichgans,M.,et al, 1999
Cerebrospinal Fluid Findings in CADASIL
Neurol 53:233, Dichgans,M.,et al, 1999
Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999
Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998
CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998
Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998
The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998
Metabolic Abnormalities in Development Dyslexia Detected by 1H Magnetic Resonance Spectroscopy
Lancet 351:1849-1852, Rae,C.,et al, 1998
Patterns of MRI Lesions in Cadasil
Neurol 51:452-457, Chabriat,H.,et al, 1998
Intellectual Decline After Stroke, The Framingham Study
Stroke 29:805-812, Kase,C.S.,et al, 1998
Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998
Effects of Resective Surgery for Left-Sided Intracranial Tumors on Language Function:A Prospective Study
Lancet 351:1014-1018, Whittle,I.R.,et al, 1998
Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998
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
Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997
Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997
Pain After Thalamic Stroke:Right Diencephalic Predominance and Clinical Features in 180 Patients
Neurol 48:1196-1199, Nasreddine,Z.S.&Saver,J.L., 1997
"Gourmand Syndrome":Eating Passion Associated with Right Anterior Lesions
Neurol 48:1185-1190, Regard,M.&Landis,T., 1997
Localization of Lesion in Denial of Hemiplegia After Acute Stroke
Stroke 28:67-71, Ellis,S.&Small,M., 1997
Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997
The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996
Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996
Bilateral Ptosis and Upgaze Palsy with Right Hemispheric Lesions
Ann Neurol 40:465-468, Averbuch-Heller,L.,et al, 1996
Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995
Subjective Experiences of 24 Patients Dramatically Recovering from Stroke
Stroke 26:1285-1288, Grotta,J.&Bratina,P., 1995