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Histopathology|October 20, 1998
Male adnexal tumour of probable Wolffian origin occurring in a seminal vesicleL P Middleton, M J Merino, S M Popok, et al.Enfermedades Infecciosas Y Microbiologia Clinica|February 1, 1989
[Clinical and epidemiologic characteristics of diarrhea caused by Cryptosporidium]F J Merino, M T Pérez, C Ladrón de Guevara, et al.Journal of Personalized Medicine|July 27, 2022
Evaluating Translational Methods for Personalized Medicine-A Scoping ReviewVibeke Fosse, Emanuela Oldoni, Chiara Gerardi, et al.Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.Neurology|September 15, 2006
Infusion of platelets transiently reduces nucleoside overload in MNGIEM C Lara, B Weiss, I Illa, et al.Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.Neurology|November 18, 1998
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathyA L Andreu, C Bruno, S Shanske, et al.Revista De Neurologia|July 23, 2002
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)]A Playán, A Solano-Palacios, J B González de la Rosa, et al.Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.Journal of Cancer|October 27, 2010
Protein expression profiling in the spectrum of renal cell carcinomasVladimir A Valera, Elsa Li-Ning-T, Beatriz A Walter, et al.Pageof 279