Showing results (291-300 of 595) with videos related to
Sort By:
Pageof 60
Diagnostics (Basel, Switzerland)|December 30, 2025
Diagnostic Value of Muscle Biopsy for the Evaluation of Adult Myopathy in Daily Clinical PracticeVera E A Kleinveld, Julia Wanschitz, Anna Hotter, et al.American Journal of Human Genetics|December 14, 2011
Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevationJohannes A Mayr, Franz A Zimmermann, Christine Fauth, et al.Discovery Medicine|June 3, 2010
Stereotactic body radiation therapy for hepatocellular carcinomaSimon S Lo, Laura A Dawson, Edward Y Kim, et al.Mitochondrion|January 14, 2015
From ventriculomegaly to severe muscular atrophy: expansion of the clinical spectrum related to mutations in AIFM1Matthias Kettwig, Max Schubach, Franz A Zimmermann, et al.The Laryngoscope|February 27, 2001
Esthesioneuroblastoma: the University of Iowa experience 1978-1998J H Simon, W Zhen, T M McCulloch, et al.The EMBO Journal|December 15, 1994
p53 oligomerization and DNA looping are linked with transcriptional activationJ E Stenger, P Tegtmeyer, G A Mayr, et al.Neuromuscular Disorders : NMD|October 24, 2006
A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intoleranceJohannes A Mayr, Ali-Reza Moslemi, Holger Förster, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 30, 2016
MELAS Syndrome and Kidney Disease Without Fanconi Syndrome or Proteinuria: A Case ReportMichael Rudnicki, Johannes A Mayr, Johannes Zschocke, et al.Journal of Inherited Metabolic Disease|December 12, 2023
Complex I, V, and MDH2 deficient human skin fibroblasts reveal distinct metabolic signatures by 1 H HR-MAS NMRChristoph Meyer, Damian Hertig, Janine Arnold, et al.AJNR. American Journal of Neuroradiology|January 1, 1993
Metastatic lesions involving the cerebellopontine angleW T Yuh, N A Mayr-Yuh, T M Koci, et al.Pageof 60