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Springe zu: Zeitschriftenartikel
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]