Marco Spinazzi
mitovasc.univ-angers.fr
0000-0003-0048-9558
27 papers found
Refreshing results…
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function
Cardioembolic stroke in Danon disease
Severe dysphagia in lower cranial nerve involvement as the initial symptom of Wegener's granulomatosis
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A
Myelo-optico-neuropathy in copper deficiency occurring after partial gastrectomy
Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease
Molecular diagnosis in LGMD2A: Mutation analysis or protein testing?
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