Hendrik Rosewich

Hendrik Rosewich

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Hendrik Rosewich

Hendrik Rosewich

Publications by authors named "Hendrik Rosewich"

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21Publications

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Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes.

Sci Rep 2018 May 17;8(1):7809. Epub 2018 May 17.

Department of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, Georg August University Göttingen, Robert-Koch-Strasse 40, 37075, Göttingen, Germany.

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May 2018

Research conference summary from the 2014 International Task Force on -Related Disorders.

Neurol Genet 2017 Apr 2;3(2):e139. Epub 2017 Mar 2.

Department of Pediatrics and Pediatric Neurology (H.R.), Georg August University, Göttingen, Germany; Division of Clinical Genetics (L.V.), Department of Pediatrics (T.N., M.T.S.) and Department of Neurology (M.T.S.), University of Utah, Salt Lake City; Center for Human Genetics (S.D.), University Hospitals and Case Western Reserve University, Cleveland, OH; Division of Pediatric Neurology (K.E.), Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN; Center for Human Genetics Research (L.O., M.M., K. Swoboda), Department of Neurology, Massachusetts General Hospital, Boston; Neurogenetics Unit (E.A.) and Epilepsy Research Group (E.A., F.A.), Montreal Neurological Hospital and Institute; Department of Neurology and Neurosurgery (E.A., F.A.), Department of Human Genetics (E.A.), and Department of Pediatrics (F.A.), McGill University, Quebec, Canada; Alternating Hemiplegia of Childhood Foundation (G.A., S.C., L.E., V.P.), Southfield, MI; BCBA (A. Belgrade), Belgrade Behavior Consulting, Chicago, IL; Department of Neurology (A. Brashear), Wake Forest School of Medicine, Winston-Salem, NC; Department of Pharmacology (A.L.G.), Northwestern University Feinberg School of Medicine, Chicago, IL; Department of Pediatrics (A.L.), University of Florida College of Medicine, Jacksonville; Integrative Neuropsychology (J.M.), Fairlawn, OH; Association Française de l'Hémiplégie Alternante (D.P.), Paris, France; Rare Disease Innovation Unit (S.R.), Clinical Development Program, Biogen, Cambridge, MA; Department of Child Neurology (M.S.), National Center of Neurology and Psychiatry, Kodaira, Japan; Swedish Neuroscience Institute (M.S.d.M.), Swedish Medical Center, Seattle, WA; Department of Neurosurgery (K. Sweadner), Massachusetts General Hospital and Harvard Medical School, Boston; Neuroscience Institute (M.Z.), Children's Hospital of Orange County, CA; and Departments of Pediatrics and Neurology (K. Silver), University of Chicago and Comer Children's Hospital, Chicago, IL.

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April 2017

Peroxisomal protein PEX13 functions in selective autophagy.

EMBO Rep 2017 01 8;18(1):48-60. Epub 2016 Nov 8.

Center for Autophagy Research, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA

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January 2017

Absence of biochemical evidence at an early age delays diagnosis in a patient with a clinically severe peroxisomal biogenesis disorder.

Eur J Paediatr Neurol 2016 Mar 1;20(2):331-335. Epub 2015 Dec 1.

Department of Pediatric Neurology, Goethe University Hospital, Frankfurt, Germany.

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March 2016

Clinical utility gene card for: Zellweger syndrome spectrum.

Eur J Hum Genet 2015 Aug 19;23(8). Epub 2014 Nov 19.

Department of Paediatrics and Adolescent Medicine, Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University, Göttingen, Germany.

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August 2015

Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome.

Neurology 2014 Aug 23;83(9):861-3. Epub 2014 Jul 23.

From the Interdisciplinary Pediatric Center for Children with Developmental Disabilities and Severe Chronic Disorders and the Division of Pediatric Neurology, Department of Pediatrics and Adolescent Medicine, University Medical Center Göttingen, Georg August University, Germany.

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August 2014

A novel ATP1A3 mutation with unique clinical presentation.

J Neurol Sci 2014 Jun 25;341(1-2):133-5. Epub 2014 Mar 25.

Interdisciplinary Pediatric Center for Children with Developmental Disabilities and Severe Chronic Disorders, University Medical Center, Georg August University, Göttingen, Germany. Electronic address:

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June 2014

The expanding clinical and genetic spectrum of ATP1A3-related disorders.

Neurology 2014 Mar 12;82(11):945-55. Epub 2014 Feb 12.

From the Department of Pediatrics and Adolescent Medicine (H.R., A.O., P.H., L.S., R.S., J.G., K.B.), Division of Pediatric Neurology, University Medical Center Göttingen, Georg August University; Department of Pediatrics (M.B.), Hospital Dritter Orden, Munich, Germany; Departments of Pediatric Neurology (I.C.), Hospital Maria Pia do Centro Hospitalar do Porto, Portugal; 4IRCCS Stella Maris (S.F.), Calambrone, Pisa; Department of Clinical and Experimental Medicine (S.F.), University of Pisa, Italy; Neurogenetics Unit (C.M.L.), Department of Neurology, School of Medicine of Ribeirao Preto, University of Sao Paulo, Brazil; and Children's Hospital of Eastern Ontario (S.S.), Ottawa, Canada.

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March 2014

Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders.

JIMD Rep 2011 22;1:29-36. Epub 2011 Jun 22.

Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, Georg August University, Robert-Koch-Strasse 40, 37075, Göttingen, Germany,

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February 2013

Identification of a new fatty acid synthesis-transport machinery at the peroxisomal membrane.

J Biol Chem 2012 Jan 1;287(1):210-21. Epub 2011 Nov 1.

Department of Pediatrics and Pediatric Neurology, Faculty of Medicine, Georg August University, 37075 Göttingen, Germany.

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January 2012

Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients.

BMC Med Genet 2011 Aug 16;12:109. Epub 2011 Aug 16.

Department of Pediatrics and Pediatric Neurology, University Medical Center, University of Göttingen, Robert Koch Str, 40, 37099 Göttingen, Germany.

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August 2011

Rational diagnostic strategy for Zellweger syndrome spectrum patients.

Eur J Hum Genet 2009 Jun 14;17(6):741-8. Epub 2009 Jan 14.

Department of Pediatrics and Pediatric Neurology, Faculty of Medicine, Georg August University, Göttingen, Germany.

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June 2009

Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.

Hum Mutat 2006 Nov;27(11):1157

Department of Pediatrics and Pediatric Neurology, Georg August University, Göttingen, Germany.

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November 2006

Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis.

Eur J Pediatr 2005 May 22;164(5):306-10. Epub 2005 Feb 22.

Department of Paediatrics and Paediatric Neurology, Georg August University, Faculty of Medicine, Robert-Koch-Strasse 40, 37075 Göttingen, Germany.

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May 2005