Anjan Chatterjee < Anjum Misbahuddin < Anke A. Dijkstra

Facettes :

List of bibliographic references indexed by Anjum Misbahuddin

Number of relevant bibliographic references: 5.

Ident.	Authors (with country if any)	Title
000B95 (2012)	Laura L. Kilarski [Royaume-Uni] ; Justin P. Pearson ; Victoria Newsway ; Elisa Majounie ; M Duleeka W. Knipe ; Anjum Misbahuddin ; Patrick F. Chinnery ; David J. Burn ; Carl E. Clarke ; Marie-Helene Marion ; Alistair J. Lewthwaite ; David J. Nicholl ; Nicholas W. Wood ; Karen E. Morrison ; Caroline H. Williams-Gray ; Jonathan R. Evans ; Stephen J. Sawcer ; Roger A. Barker ; Mirdhu M. Wickremaratchi ; Yoav Ben-Shlomo ; Nigel M. Williams ; Huw R. Morris	Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
000F67 (2012)	Laura L. Kilarski [Royaume-Uni] ; Justin P. Pearson [Royaume-Uni] ; Victoria Newsway [Royaume-Uni] ; Elisa Majounie [Royaume-Uni] ; M. Duleeka W. Knipe [Royaume-Uni] ; Anjum Misbahuddin [Royaume-Uni] ; Patrick F. Chinnery [Royaume-Uni] ; David J. Burn [Royaume-Uni] ; Carl E. Clarke [Royaume-Uni] ; Marie-Helene Marion [Royaume-Uni] ; Alistair J. Lewthwaite [Royaume-Uni] ; David J. Nicholl [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Karen E. Morrison [Royaume-Uni] ; Caroline H. Williams-Gray [Royaume-Uni] ; Jonathan R. Evans [Royaume-Uni] ; Stephen J. Sawcer [Royaume-Uni] ; Roger A. Barker [Royaume-Uni] ; Mirdhu M. Wickremaratchi [Royaume-Uni] ; Yoav Ben-Shlomo [Royaume-Uni] ; Nigel M. Williams [Royaume-Uni] ; Huw R. Morris [Royaume-Uni]	Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in Early-Onset Parkinson's Disease
002D28 (2007)	Anjum Misbahuddin [Royaume-Uni] ; Mark Placzek [Royaume-Uni] ; Graham Lennox [Royaume-Uni] ; Jan-Willem Taanman [Royaume-Uni] ; Thomas T. Warner [Royaume-Uni]	Myoclonus–dystonia syndrome with severe depression is caused by an exon‐skipping mutation in the ε‐sarcoglycan gene
003835 (2005)	Anjum Misbahuddin [Royaume-Uni] ; Mark R. Placzek [Royaume-Uni] ; Jan-Willem Taanman [Royaume-Uni] ; Steve Gschmeissner [Royaume-Uni] ; Giampietro Schiavo [Royaume-Uni] ; J. Mark Cooper [Royaume-Uni] ; Thomas T. Warner [Royaume-Uni]	Mutant torsinA, which causes early‐onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH‐SY5Y cells
004179 (2003)	Enza-Maria Valente [Italie] ; Anjum Misbahuddin [Royaume-Uni] ; Francesco Brancati [Italie] ; Mark R. Placzek [Royaume-Uni] ; Barbara Garavaglia [Italie] ; Sergio Salvi [Italie] ; Andrea Nemeth [Royaume-Uni] ; Charles Shaw-Smith [Royaume-Uni] ; Nardo Nardocci [Italie] ; Anna-Rita Bentivoglio [Italie] ; Alfredo Berardelli [Italie] ; Roberto Eleopra [Italie] ; Bruno Dallapiccola [Italie] ; Thomas T. Warner [Royaume-Uni]	Analysis of the ϵ‐sarcoglycan gene in familial and sporadic myoclonus‐dystonia: Evidence for genetic heterogeneity

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