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Biswadjiet Harhangi

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E J dos Santos Rubio; Biswadjiet S Harhangi; Johan M Kros; A J P E Vincent; Clemens M F Dirven
A primary extraosseous Ewing sarcoma in the cerebellopontine angle of a child: review of relevant literature and case report.
Biswadjiet S Harhangi; Erwin J O Kompanje; Frank W G Leebeek; Andrew I.R. Maas
Coagulation disorders after traumatic brain injury.
Vincenzo Bonifati; Guido J Breedveld; Ferdinando Squitieri; Nicola Vanacore; Pierluigi Brustenghi; Biswadjiet S Harhangi; Pasquale Montagna; Milena Cannella; Giovanni Fabbrini; Patrizia Rizzu; C.M. Duijn; Ben A Oostra; Giuseppe Meco; Peter Heutink
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.

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2010: E J dos Santos Rubio; Biswadjiet S Harhangi; Johan M Kros; A J P E Vincent; Clemens M F Dirven
A primary extraosseous Ewing sarcoma in the cerebellopontine angle of a child: review of relevant literature and case report.
Neurosurgery 2010;67(6):E1852-6.
2008: Biswadjiet S Harhangi; Erwin J O Kompanje; Frank W G Leebeek; Andrew I.R. Maas
Coagulation disorders after traumatic brain injury.
Acta neurochirurgica 2008;150(2):165-75; discussion 175.
2002: Vincenzo Bonifati; Guido J Breedveld; Ferdinando Squitieri; Nicola Vanacore; Pierluigi Brustenghi; Biswadjiet S Harhangi; Pasquale Montagna; Milena Cannella; Giovanni Fabbrini; Patrizia Rizzu; C.M. Duijn; Ben A Oostra; Giuseppe Meco; Peter Heutink
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.
Annals of neurology 2002;51(2):253-6.
2002: Enza Maria Valente; Francesco Brancati; Alessandro Ferraris; Elizabeth A Graham; Mary B Davis; Monique Breteler; Thomas Gasser; Vincenzo Bonifati; Anna Rita Bentivoglio; Giuseppe De Michele; Alexandra Dürr; Pietro Cortelli; Dietmar Wassilowsky; Biswadjiet S Harhangi; Nina Rawal; Viviana Caputo; Alessandro Filla; Giuseppe Meco; Ben A Oostra; Alexis Brice; Alberto Albanese; Bruno Dallapiccola; Nicholas W Wood
PARK6-linked parkinsonism occurs in several European families.
Annals of neurology 2002;51(1):14-8.
2001: Biswadjiet S Harhangi; Ben A Oostra; Peter Heutink; C.M. Duijn; Albert Hofman; Monique Breteler
CYP2D6 polymorphism in Parkinson's disease: the Rotterdam Study.
Movement disorders : official journal of the Movement Disorder Society 2001;16(2):290-3.
2000: Christoph B Lücking; Alexandra Dürr; Vincenzo Bonifati; J Vaughan; Giuseppe De Michele; Thomas Gasser; Biswadjiet S Harhangi; Giuseppe Meco; Patrice DENEFLE; Nicholas W Wood; Yves Agid; Alexis Brice
Association between early-onset Parkinson's disease and mutations in the parkin gene.
The New England journal of medicine 2000;342(21):1560-7.
2000: Biswadjiet S Harhangi; Maarten C de Rijk; C.M. Duijn; Christine Van Broeckhoven; Albert Hofman; Monique Breteler
APOE and the risk of PD with or without dementia in a population-based study.
Neurology 2000;54(6):1272-6.
1999: Biswadjiet S Harhangi; Ben A Oostra; Peter Heutink; C.M. Duijn; Albert Hofman; Monique Breteler
N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study.
Journal of neurology, neurosurgery, and psychiatry 1999;67(4):518-20.
1999: Biswadjiet S Harhangi; Matthew J Farrer; Sarah J Lincoln; Vincenzo Bonifati; Giuseppe Meco; Giuseppe De Michele; Alexis Brice; Alexandra Dürr; M Martinez; Thomas Gasser; Benjamin Bereznai; Jenny R Vaughan; Nicholas W Wood; John Hardy; Ben A Oostra; Monique Breteler
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
Neuroscience letters 1999;270(1):1-4.
1999: Nacer Abbas; Christoph B Lücking; Sylvain Ricard; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; S Bouley; Jenny R Vaughan; Thomas Gasser; Roberto Marconi; Emmanuel Broussolle; C Brefel-Courbon; Biswadjiet S Harhangi; Ben A Oostra; Edito Fabrizio; G A Böhme; Laurent Pradier; Nicholas W Wood; Alessandro Filla; Giuseppe Meco; Patrice DENEFLE; Yves Agid; Alexis Brice
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Human molecular genetics 1999;8(4):567-74.