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Peter Schneiderat

Showing results (1-10 of 20) with videos related to

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Advances in Experimental Medicine and Biology|September 9, 2010
Biobanking in rare disordersHanns Lochmüller, Peter Schneiderat
Orphanet Journal of Rare Diseases|April 9, 2013
miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factorsNaoe Harafuji, Peter Schneiderat, Maggie C Walter, et al.
Der Nervenarzt|July 29, 2025
[Severe disabling ballism after stroke-An interdisciplinary challenge for rehabilitation and outpatient neuropsychiatric care]Hans-Jürgen Gdynia, Peter Schneiderat, Martin Hinterseer, et al.
British Journal of Haematology|July 20, 2004
Functional analysis of apoptosis induction in acute myeloid leukaemia-relevance of karyotype and clinical treatment responseJan Braess, Peter Schneiderat, Claudia Schoch, et al.
Scientific Reports|April 4, 2017
Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle CellsCibely C Fontes-Oliveira, Maarten Steinz, Peter Schneiderat, et al.
Spinal Cord Series and Cases|November 11, 2024
Clinical features and rehabilitation outcome after surgical treatment of spinal meningiomaHans-Jürgen Gdynia, Peter Schneiderat, Andreas Gratzer, et al.
BMC Medical Genetics|September 18, 2013
Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromesOlivia Schreiber, Peter Schneiderat, Wolfram Kress, et al.
Neuromuscular Disorders : NMD|March 11, 2017
Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiencyBertold Schrank, Benedikt Schoser, Thomas Klopstock, et al.
Journal of Neurology|March 3, 2009
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexiaRita Horváth, Andreas Bender, Angela Abicht, et al.
Plos One|July 30, 2013
Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathiesElizabeth Stevens, Silvia Torelli, Lucy Feng, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|September 9, 2010
Biobanking in rare disordersHanns Lochmüller, Peter Schneiderat
Orphanet Journal of Rare Diseases|April 9, 2013
miR-411 is up-regulated in FSHD myoblasts and suppresses myogenic factorsNaoe Harafuji, Peter Schneiderat, Maggie C Walter, et al.
Der Nervenarzt|July 29, 2025
[Severe disabling ballism after stroke-An interdisciplinary challenge for rehabilitation and outpatient neuropsychiatric care]Hans-Jürgen Gdynia, Peter Schneiderat, Martin Hinterseer, et al.
British Journal of Haematology|July 20, 2004
Functional analysis of apoptosis induction in acute myeloid leukaemia-relevance of karyotype and clinical treatment responseJan Braess, Peter Schneiderat, Claudia Schoch, et al.
Scientific Reports|April 4, 2017
Bioenergetic Impairment in Congenital Muscular Dystrophy Type 1A and Leigh Syndrome Muscle CellsCibely C Fontes-Oliveira, Maarten Steinz, Peter Schneiderat, et al.
Spinal Cord Series and Cases|November 11, 2024
Clinical features and rehabilitation outcome after surgical treatment of spinal meningiomaHans-Jürgen Gdynia, Peter Schneiderat, Andreas Gratzer, et al.
BMC Medical Genetics|September 18, 2013
Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromesOlivia Schreiber, Peter Schneiderat, Wolfram Kress, et al.
Neuromuscular Disorders : NMD|March 11, 2017
Lifetime exercise intolerance with lactic acidosis as key manifestation of novel compound heterozygous ACAD9 mutations causing complex I deficiencyBertold Schrank, Benedikt Schoser, Thomas Klopstock, et al.
Journal of Neurology|March 3, 2009
Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNA(Val) causing MNGIE-like gastrointestinal dysmotility and cachexiaRita Horváth, Andreas Bender, Angela Abicht, et al.
Plos One|July 30, 2013
Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathiesElizabeth Stevens, Silvia Torelli, Lucy Feng, et al.
Pageof 2