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Neurology|July 23, 1998
Familial multiple symmetric lipomatosis associated with the A8344G mutation of mitochondrial DNAJ Gámez, A Playán, A L Andreu, et al.Human Mutation|January 16, 2007
A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patientsJuan C Rubio, Ines Garcia-Consuegra, Gisela Nogales-Gadea, et al.Archivos De Bronconeumologia|June 24, 2026
Mitochondrial Dysfunction and Telomeric Shortening as Long-term Complications After COVID-19Alba Mulet, Jaime Signes-Costa, Estrella Fernández-Fabrellas, et al.Journal of the National Cancer Institute|May 1, 1984
Caffeine consumption and fibrocystic breast disease: a case-control epidemiologic studyC A Boyle, G S Berkowitz, V A LiVolsi, et al.Journal of the National Cancer Institute|November 5, 1997
Concordance of genetic alterations in poorly differentiated colorectal neuroendocrine carcinomas and associated adenocarcinomasA O Vortmeyer, I A Lubensky, M J Merino, et al.Cancer Research|January 15, 1992
Molecular and cellular characterization of human renal cell carcinoma cell linesP Anglard, E Trahan, S Liu, et al.Fertility and Sterility|July 9, 2004
CD10 immunohistochemical staining enhances the histological detection of endometriosisClariss Potlog-Nahari, Andrew L Feldman, Pamela Stratton, et al.Endocrine Regulations|October 28, 2009
Animal model of metastatic pheochromocytoma: evaluation by MRI and PETL Martiniova, E W Lai, D Thomasson, et al.Acta Neuropathologica|December 10, 2002
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunctionKurenai Tanji, Josep Gamez, Carles Cervera, et al.Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.Pageof 279