Hortensia Alonso-Navarro < Hoskote S. Chandrashekar < Hossein Najmabadi

Facettes :

List of bibliographic references indexed by Hoskote S. Chandrashekar

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
000902 (2013)	Ignacio Rubio-Agusti [Royaume-Uni] ; Miryam Carecchio ; Kailash P. Bhatia ; Maja Kojovic ; Isabel Parees ; Hoskote S. Chandrashekar ; Emma J. Footitt ; Derek Burke ; Mark J. Edwards ; Robin H L. Lachmann ; Elaine Murphy	Movement disorders in adult patients with classical galactosemia.
000E52 (2012)	Ignacio Rubio-Agusti [Royaume-Uni] ; Maja Kojovic ; Hoskote S. Chandrashekar ; Mark J. Edwards ; Kailash P. Bhatia	Cervical dystonia and joint hypermobility syndrome: a dangerous combination.
000E76 (2012)	Ignacio Rubio-Agusti [Royaume-Uni] ; Maja Kojovic ; Mark J. Edwards ; Elaine Murphy ; Hoskote S. Chandrashekar ; Robin H. Lachmann ; Kailash P. Bhatia	Atypical parkinsonism and cerebrotendinous xanthomatosis: report of a family with corticobasal syndrome and a literature review.
001175 (2012)	Ignacio Rubio-Agusti [Royaume-Uni, Espagne] ; Maja Kojovic [Royaume-Uni] ; Hoskote S. Chandrashekar [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Cervical Dystonia and Joint Hypermobility Syndrome: A Dangerous Combination
001200 (2012)	Ignacio Rubio-Agusti [Royaume-Uni, Espagne] ; Maja Kojovic [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Elaine Murphy [Royaume-Uni] ; Hoskote S. Chandrashekar [Royaume-Uni] ; Robin H. Lachmann [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni]	Atypical Parkinsonism and Cerebrotendinous Xanthomatosis: Report of a Family With Corticobasal Syndrome and a Literature Review
001E55 (2010)	Marianne J. U. Novak [Royaume-Uni] ; Mary G. Sweeney [Royaume-Uni] ; Abi Li [Royaume-Uni] ; Colm Treacy [Royaume-Uni] ; Hoskote S. Chandrashekar [Royaume-Uni] ; Paola Giunti [Royaume-Uni] ; Robert G. Goold [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Sarah J. Tabrizi [Royaume-Uni]	An ITPR1 gene deletion causes spinocerebellar ataxia 15/16: A genetic, clinical and radiological description

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