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Tilkorn, Friederike Karin Marie Theres [Author] ; Zautner, Andreas [Degree supervisor]; Rosewich, Hendrik [Other]

Clostridioides-difficile-Isolate aus Kindern im ersten Lebensjahr: Typisierung, Antibiotikaempfindlichkeit und Toxinexpression

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2022
Tilkorn, Friederike Karin Marie Theres [Author] ; Zautner, Andreas [Degree supervisor]; Rosewich, Hendrik [Degree supervisor]

Clostridioides-difficile-Isolate aus Kindern im ersten Lebensjahr: Typisierung, Antibiotikaempfindlichkeit und Toxinexpression

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Göttingen, 2022
Porsche, Melissa [Author] ; Neeße, Albrecht [Degree supervisor]; Rosewich, Hendrik [Degree supervisor]

Einfluss der Nahrungsaufnahme auf die Lebersteifigkeit, gemessen mit 2D-Scherwellen-Elastographie (Gerät: LOGIQ E9) bei freiwilligen Probanden = Impact of Food Intake on Liver Stiffness Determined by 2D Shear Wave Elastography (LOGIQ E9): Prospective Interventional Study in 100 Healthy Patients

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Göttingen, 2020
Künanz, Johannes [Author] ; Gross, Oliver [Degree supervisor]; Rosewich, Hendrik [Degree supervisor]

Der langfristige Effekt einer RAAS-Blockade auf den Krankheitsverlauf bei heterozygoten Mutationsträgern des Alport-Syndroms = The long-term effect of RAAS blockade on the progression of disease in heterozygous mutation carriers of Alport syndrome

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Göttingen, 2020
Sümpelmann, Anne Esther [Author] ; Russo, Sebastian [Degree supervisor]; Rosewich, Hendrik [Degree supervisor]

Sonographische Untersuchung der Magenentleerung bei Kindern unter sechs Jahren = Ultrasound assessment of gastric emptying in healthy preschool children

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Göttingen, 2020
Künanz, Johannes [Author] ; Gross, Oliver [Degree supervisor]; Gross, Oliver [Other]; Rosewich, Hendrik [Other]

Der langfristige Effekt einer RAAS-Blockade auf den Krankheitsverlauf bei heterozygoten Mutationsträgern des Alport-Syndroms : Eine prospektive Vier-Jahres-Auswertung des Europäischen Alport-Registers

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020
Krefting, Dagmar [Author]; Tahar, Kais [Author]; Kesztyüs, Tibor [Author]; Rosewich, Hendrik [Author]; Hügel, Jonas [Author] ; Georg-August-Universität Göttingen

CORD-MI - Konsortien übergreifender Use Case Collaboration on Rare Diseases - Teilprojekt Uni Göttingen: Arbeitspapier zu besonderen Aspekten des Kerndatensatzes der Medizininformatik-Initiative bei seltenen Erkrankungen : Schlussbericht : Laufzeit: 01.07.2020-30.06.2023

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Göttingen: [Georg-August-Universität Göttingen], [2023?]
Sümpelmann, Anne Esther [Author] ; Russo, Sebastian G. [Degree supervisor]; Russo, Sebastian G. [Other]; Rosewich, Hendrik [Other]

Sonographische Untersuchung der Magenentleerung bei Kindern unter sechs Jahren

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020
Glonke, Niklas [Author] ; Gross, Oliver [Degree supervisor]; Gross, Oliver [Other]; Rosewich, Hendrik [Other]; Reiß, Jochen [Other]

Prospektive Verlaufsstudie über die Auswirkung der RAAS-Blockade bei Trägern des Alport-Syndroms

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Göttingen: Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2018
Krech, Lisa; Rosewich, Hendrik; Welkoborsky, Hans-Jürgen

Congenital sensorineural hearing loss in a 1-year-old twin with Zellweger syndrome: a case report

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Georg Thieme Verlag, 2022

Published in: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin (2022)
Krech, Lisa; Rosewich, Hendrik; Welkoborsky, Hans-Jürgen

Kongenitale Schallempfindungsschwerhörigkeit bei einem 1-Jahr alten Zwillingskind mit Zellweger Spektrum Erkrankung: Fallvorstellung

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Georg Thieme Verlag, 2022

Published in: Abstract- und Posterband - 93. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn Interface - Fokus Mensch im Zeitalter der technisierten Medizin (2022)
Krause, Cindy; Rosewich, Hendrik; Gärtner, Jutta

Rational diagnostic strategy for Zellweger syndrome spectrum patients

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Springer Science and Business Media LLC, 2009

Published in: European Journal of Human Genetics, 17 (2009) 6, Seite 741-748
Schiller, Stina; Rosewich, Hendrik; Grünewald, Stephanie; Gärtner, Jutta

Inborn errors of metabolism leading to neuronal migration defects

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Wiley, 2020

Published in: Journal of Inherited Metabolic Disease, 43 (2020) 1, Seite 145-155
Rosewich, Hendrik; Nessler, Stefan; Brück, Wolfgang; Gärtner, Jutta

B cell depletion can be effective in multiple sclerosis but failed in a patient with advanced childhood cerebral X-linked adrenoleukodystrophy

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SAGE Publications, 2019

Published in: Therapeutic Advances in Neurological Disorders, 12 (2019), Seite 175628641986813
Soliman, Kareem; Göttfert, Fabian; Rosewich, Hendrik; Thoms, Sven; Gärtner, Jutta

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

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Springer Science and Business Media LLC, 2018

Published in: Scientific Reports, 8 (2018) 1
Rosewich, Hendrik; Weise, Dagmar; Ohlenbusch, Andreas; Gärtner, Jutta; Brockmann, Knut

Phenotypic overlap of alternating hemiplegia of childhood and CAPOS syndrome

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Ovid Technologies (Wolters Kluwer Health), 2014

Published in: Neurology, 83 (2014) 9, Seite 861-863
Krause, Cindy; Rosewich, Hendrik; Woehler, Andrew; Gärtner, Jutta

Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis

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Oxford University Press (OUP), 2013

Published in: Human Molecular Genetics, 22 (2013) 19, Seite 3844-3857
Grønborg, Sabine; Krätzner, Ralph; Rosewich, Hendrik; Gärtner, Jutta

JIMD Reports: Lymphoblastoid Cell Lines for Diagnosis of Peroxisome Biogenesis Disorders

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Springer Berlin Heidelberg, 2011

Published in: JIMD Reports (2011), Seite 29-36
Krause, Cindy; Rosewich, Hendrik; Thanos, Melissa; Gärtner, Jutta

Identification of novel mutations inPEX2,PEX6,PEX10,PEX12, andPEX13in Zellweger spectrum patients

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Hindawi Limited, 2006

Published in: Human Mutation, 27 (2006) 11, Seite 1157-1157
Lex, Christiane; Minso, Rebecca; Alfeis, Nadine; Rosewich, Hendrik; Schucht, Sylvia; Tümmler, Burkhard

Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters

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Elsevier BV, 2022

Published in: Journal of Cystic Fibrosis, 21 (2022) 2, Seite 375-377

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