D. M. Kullmann < D. M. Maraganore < D. M. Mezzapesa

Facettes :

List of bibliographic references indexed by D. M. Maraganore

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
005181 (1998)	D. W. Anderson [États-Unis] ; W. A. Rocca [États-Unis] ; M. C. De Rijk [Pays-Bas] ; F. Grigoletto [Italie] ; M. O. Melcon [Argentine] ; M. B. Breteler [Pays-Bas] ; D. M. Maraganore [États-Unis]	Case ascertainment uncertainties in prevalence surveys of Parkinson's disease
005195 (1998)	R. B. Jr Dewey [États-Unis] ; D. M. Maraganore [États-Unis] ; J. E. Ahlskog [États-Unis] ; J. Y. Matsumoto [États-Unis]	A double-blind, placebo-controlled study of intranasal apomorphine spray as a rescue agent for off-states in Parkinson's disease
005624 (1996)	Elan D. Louis [États-Unis] ; Kenji Nakashima [Japon] ; Masayoshi Kusumi [Japon] ; Kazuro Takahashi [Japon] ; Yuichi Inoue [Japon] ; Ryan J. Uitti [États-Unis] ; J. Eric Ahlskog [États-Unis] ; D. M. Maraganore [États-Unis] ; Anthony E. Lang [Canada]	Letters to the editor
005A74 (1994)	V. Planté-Bordeneuve [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; D. M. Maraganore [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; Harding [Royaume-Uni]	Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
005C40 (1994)	V. Plante-Bordeneuve [Royaume-Uni] ; M. B. Davis ; D. M. Maraganore ; C. D. Marsden ; A. E. Harding	Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's disease
005F01 (1993)	R. J. Uitti [États-Unis] ; D. M. Maraganore	Adult onset familial cervical dystonia: report of a family including monozygotic twins
006080 (1992)	D. M. Maraganore [États-Unis] ; W. N. Folger ; J. W. Swanson ; J. E. Ahlskog	Movement disorders as sequelae of central pontine myelinolysis : report of three cases
006186 (1991)	D. M. Maraganore [États-Unis] ; Andrew Lees (neurologue) [Royaume-Uni] ; Marsden [Royaume-Uni]	Complex stereotypies after right putaminal infarction: A case report
006247 (1991)	D. M. Maraganore ; A. E. Harding ; C. D. Marsden	A clinical and genetic study of familial Parkinson's disease

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