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Stef L M Bakker

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Cerebrovascular Diseases (Basel, Switzerland)|September 24, 2008

Assessment of feasibility of endovascular treatment of ruptured intracranial aneurysms with 16-detector row CT angiographyMathieu van der Jagt, H Zwenneke Flach, Hervé L J Tanghe, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|July 21, 2010

Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindredAntonetta M G Sas, Alessio Di Fonzo, Stef L M Bakker, et al.

Archives of Neurology|January 14, 2009

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Cerebrovascular Diseases (Basel, Switzerland)|September 24, 2008

Assessment of feasibility of endovascular treatment of ruptured intracranial aneurysms with 16-detector row CT angiographyMathieu van der Jagt, H Zwenneke Flach, Hervé L J Tanghe, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|July 21, 2010

Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindredAntonetta M G Sas, Alessio Di Fonzo, Stef L M Bakker, et al.

Archives of Neurology|January 14, 2009

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptakeBoukje de Vries, Hafsa Mamsa, Anine H Stam, et al.

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