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Stefan Wieczorek

Showing results (1-10 of 55) with videos related to

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The Journal of Rheumatology|December 7, 2007
Venous thromboembolism in Wegener's granulomatosisPeter Lamprecht, Konstanze Holl-Ulrich, Stefan Wieczorek
PPAR Research|December 18, 2009
Genetic Variation of PPARsMarie-Claude Vohl, Mostafa Badr, Stefan Wieczorek
Current Opinion in Rheumatology|October 30, 2009
Recent progress in the genetics of Wegener's granulomatosis and Churg-Strauss syndromeStefan Wieczorek, Julia U Holle, Jörg T Epplen
Rheumatic Diseases Clinics of North America|August 7, 2010
The future of ANCA-associated vasculitisJulia U Holle, Stefan Wieczorek, Wolfgang L Gross
Clinical and Experimental Rheumatology|April 24, 2010
Genetic association studies in ANCA-associated vasculitides: what we have learnt so far and what needs to be done in the futureJulia U Holle, Stefan Wieczorek, Wolfgang L Gross
Human Mutation|July 4, 2012
Spinocerebellar ataxias: an example of the challenges associated with genetic databases for dynamic mutationsJoanne E Martindale, Sara Seneca, Stefan Wieczorek, et al.
Journal of Human Genetics|February 24, 2006
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European populationStefan Wieczorek, Larissa Arning, Ingrid Alheite, et al.
Neuropediatrics|July 22, 2014
Xp21/A translocation: a rarely considered genetic cause for manifesting carriers of duchenne muscular dystrophyHeike Trippe, Stefan Wieczorek, Judith Kötting, et al.
Neuromuscular Disorders : NMD|July 29, 2008
Expanded HSAN4 phenotype associated with two novel mutations in NTRK1Stefan Wieczorek, Jonas Bergström, Maria Sääf, et al.
PPAR Research|February 19, 2009
Genetic variability of RXRB, PPARA, and PPARG in Wegener's granulomatosisStefan Wieczorek, Silvia Knaup, Wolfgang L Gross, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
The Journal of Rheumatology|December 7, 2007
Venous thromboembolism in Wegener's granulomatosisPeter Lamprecht, Konstanze Holl-Ulrich, Stefan Wieczorek
PPAR Research|December 18, 2009
Genetic Variation of PPARsMarie-Claude Vohl, Mostafa Badr, Stefan Wieczorek
Current Opinion in Rheumatology|October 30, 2009
Recent progress in the genetics of Wegener's granulomatosis and Churg-Strauss syndromeStefan Wieczorek, Julia U Holle, Jörg T Epplen
Rheumatic Diseases Clinics of North America|August 7, 2010
The future of ANCA-associated vasculitisJulia U Holle, Stefan Wieczorek, Wolfgang L Gross
Clinical and Experimental Rheumatology|April 24, 2010
Genetic association studies in ANCA-associated vasculitides: what we have learnt so far and what needs to be done in the futureJulia U Holle, Stefan Wieczorek, Wolfgang L Gross
Human Mutation|July 4, 2012
Spinocerebellar ataxias: an example of the challenges associated with genetic databases for dynamic mutationsJoanne E Martindale, Sara Seneca, Stefan Wieczorek, et al.
Journal of Human Genetics|February 24, 2006
Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European populationStefan Wieczorek, Larissa Arning, Ingrid Alheite, et al.
Neuropediatrics|July 22, 2014
Xp21/A translocation: a rarely considered genetic cause for manifesting carriers of duchenne muscular dystrophyHeike Trippe, Stefan Wieczorek, Judith Kötting, et al.
Neuromuscular Disorders : NMD|July 29, 2008
Expanded HSAN4 phenotype associated with two novel mutations in NTRK1Stefan Wieczorek, Jonas Bergström, Maria Sääf, et al.
PPAR Research|February 19, 2009
Genetic variability of RXRB, PPARA, and PPARG in Wegener's granulomatosisStefan Wieczorek, Silvia Knaup, Wolfgang L Gross, et al.
Pageof 6