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Biochimica Et Biophysica Acta|September 5, 2006
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspectsJohannes Berger, Jutta GärtnerJournal of Medical Genetics|May 15, 2012
First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypesS Thoms, Jutta GärtnerJournal of Child Neurology|October 18, 2005
Molecular diagnosis of Rett syndromePeter Huppke, Jutta GärtnerJournal of Neurology|March 21, 2009
Paediatric multiple sclerosis: the experience of the German Centre for Multiple Sclerosis in Childhood and AdolescenceWiebke Stark, Peter Huppke, Jutta GärtnerTrends in Molecular Medicine|June 30, 2009
Organelle interplay in peroxisomal disordersSven Thoms, Sabine Grønborg, Jutta GärtnerEuropean Journal of Human Genetics : EJHG|January 15, 2009
Rational diagnostic strategy for Zellweger syndrome spectrum patientsCindy Krause, Hendrik Rosewich, Jutta GärtnerThe Journal of Biological Chemistry|October 9, 2001
Two different targeting signals direct human peroxisomal membrane protein 22 to peroxisomesUte Brosius, Thomas Dehmel, Jutta GärtnerBiochimica Et Biophysica Acta|April 10, 2012
Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disordersBwee Tien Poll-The, Jutta GärtnerNeuropediatrics|May 22, 2019
Opening New Horizons in the Treatment of Childhood Onset LeukodystrophiesStina Schiller, Marco Henneke, Jutta GärtnerThe Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 20, 2006
Detection of tripeptidyl peptidase I activity in living cells by fluorogenic substratesRobert Steinfeld, Jens C Fuhrmann, Jutta GärtnerPageof 17