Results 81 to 86 of about 199 (86)

Molecular Genetics of OXPHOS Disorders

, 2016
A. Blázquez, J. Arenas, Miguel Ángel Martín   +2 more
semanticscholar   +1 more source

Características audiométricas de la hipoacusia familiar transmitida por herencia mitocondrial (A1555G)

, 2002
C. Angulo, J. Terán, J. García-Mantilla, I. D. Castillo, Miguel Ángel Moreno Pelayo, F. Herrero   +5 more
semanticscholar   +1 more source

Síndrome de Leigh causado por la mutación G14459A del ADN mitocondrial en una familia mexicana

, 2009
A. Gutiérrez, A. Saldaña-Martínez, R. García-Ramírez, D. Rayo-Mares, M. Carreras, M. López-Pérez, E. Ruiz-Pesini, Julio Montoya, Montiel-Sosa Jf   +8 more
semanticscholar   +1 more source

Heterogeneidade Clínica de 6 Casos com a Mutação «MELAS» A3243G do DNA Mitocondrial

, 1999
L. Vilarinho, Lurdes Rodrigues, I. Coelho, H. Rocha, M. M. Pires, A. Guimarães   +5 more
semanticscholar   +1 more source

Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns‐Sayre syndrome, progressive externaI ophthalmoplegia and MEWS *

Neuropathology and Applied Neurobiology, 1995
M. Molnár, S. Neudecker, J. Schröder
semanticscholar   +1 more source

A Rare Case of Pearson's Syndrome with Predominant Hematological Manifestations and Novel Mitochondrial Deletion

, 2017
Parth Desai, A. Saksena, Prasad Dange, Richa Gupta, S. Kapoor, T. Singh   +5 more
semanticscholar   +1 more source