Suchergebnisse - "Kieslich, Moritz"

PubPharm (10)

1

Sotrovimab in pediatric cardiac transplant recipients with SARS-CoV2 infection

enthalten in: The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation | 2022

von Weber, S. | Danne, F. | Kieslich, M. | +3

2

Soluble Receptor for Advanced Glycation End Products (sRAGE) Is a Sensitive Biomarker in Human Pulmonary Arterial Hypertension

enthalten in: International journal of molecular sciences | 2021

von Diekmann, F. | Chouvarine, P. | Sallmon, H. | +7

3

Severe infections of Panton-Valentine leukocidin positive Staphylococcus aureus in children

enthalten in: Medicine | 2019

von Hoppe, P. | Holzhauer, S. | Lala, B. | +22

4

Directed Alternative Splicing in Nijmegen Breakage Syndrome : Proof of Principle Concerning Its Therapeutical Application

enthalten in: Molecular therapy : the journal of the American Society of Gene Therapy | 2016

von Salewsky, B. | Hildebrand, G. | Rothe, S. | +9

5

Directed Alternative Splicing in Nijmegen Breakage Syndrome: Proof of Principle Concerning Its Therapeutical Application

enthalten in: Molecular therapy | 2016

von Radszewski, J. | Hildebrand, G. | Kieslich, M. | +9

6

Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)

enthalten in: BMC medical genetics | 2014

von Fröhler, S. | Kieslich, M. | Langnick, C. | +5

7

Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)

enthalten in: BMC medical genetics | 2014

von Fröhler, S. | Kieslich, M. | Langnick, C. | +5

8

Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2)

enthalten in: BMC medical genetics | 2014

von Fröhler, S. | Kieslich, M. | Langnick, C. | +5

9

Funktionelle Charakterisierung hypomorpher Proteinvarianten beim Nijmegen Breakage Syndrom

Erschienen: Berlin, Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2013

von Kieslich, M.

10

Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein

enthalten in: Nucleus (Austin, Tex.) | 2010

von Clayton, P. | Fischer, B. | Mann, A. | +18

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