Genetic determinism < Genetic disease < Genetic factors

Facettes :

List of bibliographic references indexed by Genetic disease

Number of relevant bibliographic references: 31.
[20-40] [0 - 20][0 - 31]

Ident.	Authors (with country if any)	Title
006212 (1991)	A. Berardelli ; P. D. Thompson ; M. Zaccagnini ; O. Giardini ; P. D'Eufemia ; R. Massoud ; M. Mandredi	Two sisters with generalized dystonia associated with homocystinuria
006233 (1991)	S. Fahn ; O. Sjaastad	Hereditary essential myoclonus in a large Norwegian family
006376 (1990)	A. Berardelli ; M. Inghilleri ; A. Priori ; P. D. Thompson ; S. Fabri ; C. Fieschi ; M. Manfredi	Involvement of corticospinal tract in Wilson's disease : a study of three cases with transcranial stimulation
006378 (1990)	J. B. Jr Penney ; A. B. Young ; I. Shoulson ; S. Starosta-Rubenstein ; S. R. Snodgrass ; J. Sanchez-Ramos ; M. Ramos-Arroyo ; F. Gomez ; G. Penchaszadeh ; J. Alvir ; J. Esteves ; I. Dequiroz ; N. Marsol ; H. Moreno ; P. M. Conneally ; E. Bonilla ; N. S. Wexler	Huntington's disease in Venezuela: 7 years of follow-up on symptomatic and asymptomatic individuals
006414 (1989)	C. D. Marsden [Royaume-Uni] ; J. A. Obeso [Espagne]	Viewpoints on the Ramsay Hunt syndrome. The Ramsay Hunt syndrome is a useful clinical entity
006487 (1989)	F. Andermann ; S. Berkovic ; S. Carpenter ; E. Andermann	Viewpoints on the Ramsay hunt syndrome. II: The Ramsay Hunt syndrome is no longer a useful diagnostic category
006488 (1989)	A. E. Harding	Viewpoints on the Ramsay Hunt syndrome. III: Ramsay Hunt syndrome, Unverricht-Lundborg disease, or what?
006526 (1988)	R. J. Coleman [Royaume-Uni] ; S. A. Robb [Royaume-Uni] ; B. D. Lake [Royaume-Uni] ; E. M. Brett [Royaume-Uni] ; Harding [Royaume-Uni]	The diverse neurological features of Niemann‐Pick disease type C: A report of two cases
006556 (1988)	R. Agostino ; Berardelli ; G. Cruccu ; G. Pauletti ; F. Stocchi [Italie] ; M. Manfredi	Correlation between facial involuntary movements and abnormalities of blink and corneal reflexes in Huntington's chorea
006574 (1988)	R. L. Albin ; A. B. Young	Somatosensory phenomena in Huntington's disease
006649 (1987)	R. Kurlan ; J. Behr ; I. Shoulson	Hereditary myoclonus and chorea: the spectrum of hereditary nonprogressive hyperkinetic movement disorders

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