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Cerebellar development and disease.
Curr Opin Neurobiol. 2008 Feb;18(1):12-9. doi: 10.1016/j.conb.2008.05.010. Epub 2008 May 29.
Curr Opin Neurobiol. 2008.
PMID: 18513948
Free PMC article.
Review.
The molecular control of cell-type specification within the developing cerebellum as well as the genetic causes of the most common human developmental cerebellar disorders have long remained mysterious. ...Indeed, several genes for congenital human cerebellar malformations …
The molecular control of cell-type specification within the developing cerebellum as well as the genetic causes of the most common hu …
[Carbohydrate-deficient glycoprotein syndrome and progression in electrophysiological results].
Bourcier F, Billard C, Toutain A, Delplace MP.
Bourcier F, et al.
J Fr Ophtalmol. 2002 Jun;25(6):584-9.
J Fr Ophtalmol. 2002.
PMID: 12223944
Review.
French.
PURPOSE: To document the progression of clinical and electrophysiological abnormalities in an infant with carbohydrate-deficient glycoprotein syndrome type Ia (CDGS Ia) over a period of 5 years. PATIENT AND METHODS: A 12-month-old male underwent clinical ophthalmic …
PURPOSE: To document the progression of clinical and electrophysiological abnormalities in an infant with carbohydrate-deficient glycoprotei …
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