Intellectual Decline After Stroke, The Framingham Study
Stroke 29:805-812, Kase,C.S.,et al, 1998
Cranial Computed Tomographic Ovservations in Multi-Infarct Dementia
Stroke 23:804-811, Gorelick,P.B.,et al, 1992
Apraxia in Alzheimer's Disease
Neurol 39:664-668, Rapcsak,S.Z.,et al, 1989
Cerebral Lateralizaion, Biological Mechanisms, Associations, & Pathology:III
Arch Neurol 42:634-654, Geschwind,N.&Galaburda,A.M., 1985
Left-handedness in Early & Late Onset Dementia
Neurol 34:367-369, Seltzer,B.,et al, 1984
Capgras Syndrome:A Reduplicative Phenomenon
Neurol 29:334-339, Alexander,M.P.,et al, 1979
Bihemispheric Decreases of Regional Cerebral Blood Flow in Dementia:Correlation with Age-Matched Normal Controls
Ann Neurol 4:445-450, Lavy,S.,et al, 1978
A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019
Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003
Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998
Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995
Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985
Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985
A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980
Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978