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Hendrik Rosewich

Showing results (1-10 of 38) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 2009
Rational diagnostic strategy for Zellweger syndrome spectrum patientsCindy Krause, Hendrik Rosewich, Jutta Gärtner
Human Mutation|October 17, 2006
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patientsCindy Krause, Hendrik Rosewich, Melissa Thanos, et al.
JIMD Reports|February 23, 2013
Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disordersSabine Grønborg, Ralph Krätzner, Hendrik Rosewich, et al.
Therapeutic Advances in Neurological Disorders|August 28, 2019
B cell depletion can be effective in multiple sclerosis but failed in a patient with advanced childhood cerebral X-linked adrenoleukodystrophyHendrik Rosewich, Stefan Nessler, Wolfgang Brück, et al.
Journal of Inherited Metabolic Disease|November 21, 2019
Inborn errors of metabolism leading to neuronal migration defectsStina Schiller, Hendrik Rosewich, Stephanie Grünewald, et al.
Human Molecular Genetics|May 30, 2013
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesisCindy Krause, Hendrik Rosewich, Andrew Woehler, et al.
Seminars in Perinatology|September 13, 2025
The role of sleep in neonatal neurocritical care and the influence on long-term outcomeLeonie M Paciello, Mirja Quante, Hendrik Rosewich, et al.
Journal of the Neurological Sciences|April 10, 2014
A novel ATP1A3 mutation with unique clinical presentationHendrik Rosewich, Martina Baethmann, Andreas Ohlenbusch, et al.
Scientific Reports|May 19, 2018
Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomesKareem Soliman, Fabian Göttfert, Hendrik Rosewich, et al.
Pediatric Neurology|December 12, 2022
Association of Overweight and Obesity With Bell Palsy in ChildrenVivian Breitling, Andreas Leha, Stina Schiller, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|January 15, 2009
Rational diagnostic strategy for Zellweger syndrome spectrum patientsCindy Krause, Hendrik Rosewich, Jutta Gärtner
Human Mutation|October 17, 2006
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patientsCindy Krause, Hendrik Rosewich, Melissa Thanos, et al.
JIMD Reports|February 23, 2013
Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disordersSabine Grønborg, Ralph Krätzner, Hendrik Rosewich, et al.
Therapeutic Advances in Neurological Disorders|August 28, 2019
B cell depletion can be effective in multiple sclerosis but failed in a patient with advanced childhood cerebral X-linked adrenoleukodystrophyHendrik Rosewich, Stefan Nessler, Wolfgang Brück, et al.
Journal of Inherited Metabolic Disease|November 21, 2019
Inborn errors of metabolism leading to neuronal migration defectsStina Schiller, Hendrik Rosewich, Stephanie Grünewald, et al.
Human Molecular Genetics|May 30, 2013
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesisCindy Krause, Hendrik Rosewich, Andrew Woehler, et al.
Seminars in Perinatology|September 13, 2025
The role of sleep in neonatal neurocritical care and the influence on long-term outcomeLeonie M Paciello, Mirja Quante, Hendrik Rosewich, et al.
Journal of the Neurological Sciences|April 10, 2014
A novel ATP1A3 mutation with unique clinical presentationHendrik Rosewich, Martina Baethmann, Andreas Ohlenbusch, et al.
Scientific Reports|May 19, 2018
Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomesKareem Soliman, Fabian Göttfert, Hendrik Rosewich, et al.
Pediatric Neurology|December 12, 2022
Association of Overweight and Obesity With Bell Palsy in ChildrenVivian Breitling, Andreas Leha, Stina Schiller, et al.
Pageof 4