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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 6

Zeitschriftenartikel

Kroidl, Inge; Mecklenburg, Ingo; Schneiderat, Peter; Mueller, Katharina; Girl, Philipp; Woelfel, Roman; Sing, Andreas; Dangel, Alexandra; Wieser, Andreas und Hoelscher, Michael (2021): Vaccine breakthrough infection and onward transmission of SARS-CoV-2 Beta (B.1.351) variant, Bavaria, Germany, February to March 2021. In: Eurosurveillance, Bd. 26, Nr. 30

Schrank, Bertold; Schoser, Benedikt; Klopstock, Thomas; Schneiderat, Peter; Horvath, Rita; Abicht, Angela; Holinski-Feder, Elke und Augustis, Sarunas (2017): Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiency. In: Neuromuscular Disorders, Bd. 27, Nr. 5: S. 473-476

Fontes-Oliveira, Cibely C.; Steinz, Maarten; Schneiderat, Peter; Mulder, Hindrik und Durbeej, Madeleine (2017): Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle Cells. In: Scientific Reports, Bd. 7, 45272 [PDF, 6MB]

Zurita, Francisco; Galera, Teresa; Gonzalez-Paramos, Cristina; Moreno-Izquierdo, Ana; Schneiderat, Peter; Fraga, Mario F.; Fernandez, Agustin F.; Garesse, Rafael und Esther Gallardo, M. (2016): Generation of a human iPSC line from a patient with a defect of intergenomic communication. In: Stem Cell Research, Bd. 16, Nr. 1: S. 120-123 [PDF, 657kB]

Schreiber, Olivia; Schneiderat, Peter; Kress, Wolfram; Rautenstrauss, Bernd; Senderek, Jan; Schoser, Benedikt und Walter, Maggie C. (2013): Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A-evidence for "double trouble" overlapping syndromes. In: BMC Medical Genetics 14:92 [PDF, 1MB]

Harafuji, Naoe; Schneiderat, Peter; Walter, Maggie C. und Chen, Yi-Wen (2013): miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factors. In: Orphanet Journal of Rare Diseases 8:55 [PDF, 497kB]

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