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Journal of Cellular Biochemistry|April 23, 2002
Augmented synthesis and differential localization of heparan sulfate proteoglycans in Duchenne muscular dystrophyKarin Alvarez, Ricardo Fadic, Enrique Brandan
Journal of Genetic Counseling|June 8, 2013
Medical genetics and genetic counseling in ChileSonia B Margarit, Mónica Alvarado, Karin Alvarez, et al.
Journal of Cellular and Molecular Medicine|September 23, 2006
Increase in decorin and biglycan in Duchenne Muscular Dystrophy: role of fibroblasts as cell source of these proteoglycans in the diseaseRicardo Fadic, Valeria Mezzano, Karin Alvarez, et al.
The Journal of Biological Chemistry|October 16, 2003
PIASgamma represses the transcriptional activation induced by the nuclear receptor Nurr1Danny Galleguillos, Andrea Vecchiola, José Antonio Fuentealba, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 27, 2015
Pyruvate dehydrogenase deficiency presenting as isolated paroxysmal exercise induced dystonia successfully reversed with thiamine supplementation. Case report and mini-reviewClaudia Castiglioni, Daniela Verrigni, Cecilia Okuma, et al.
Revista Medica De Chile|September 5, 2008
[Hereditary non-polyposis colorectal cancer. Report of four siblings]Alejandro Zárate, Karin Alvarez, Ana María Wielandt, et al.
American Journal of Medical Genetics. Part A|July 1, 2014
Activating PIK3CA somatic mutation in congenital unilateral isolated muscle overgrowth of the upper extremityClaudia Castiglioni, Enrico Bertini, Paulina Orellana, et al.
Diseases of the Colon and Rectum|March 23, 2010
Spectrum of MLH1 and MSH2 mutations in Chilean families with suspected Lynch syndromeKarin Alvarez, Claudia Hurtado, Montserrat A Hevia, et al.
Revista Medica De Chile|May 17, 2013
[Homozygous germline mutation in MUTYH gene in familial adenomatous polyposis]Karin Alvarez, Marjorie de la Fuente, Paulina Orellana, et al.
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