Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jaime A. López-Valdez"'
Autor:
Janeth E. Araujo-Cárdenas, Miguel A. Rodríguez-Ruiz, Jaime A. López-Valdez, Rosa I. Rodríguez-Téllez, Yanelly Garfias-Gómez, Israel Parra-Ortega, Genaro Patiño-López
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 80, Iss 2 (2023)
Background: Myosin 1g (Myo1g) has recently been identified as a potential diagnostic biomarker in childhood acute lymphocytic leukemia (ALL). Case report: We describe the case of a 1-year-old Mexican female patient. Although initially studied for hep
Externí odkaz:
https://doaj.org/article/606d1b5c908b4e068be71ad0f0a320ff
Autor:
Jaime A. López-Valdez, Luis A. Aguilar-Alonso, Vanessa Gándara-Quezada, Gabriel E. Ruiz-Rico, Juana M. Ávila-Soledad, Adriana A. Reyes, Fernando D. Pedroza-Jiménez
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 78, Iss 6 (2021)
Cystic fibrosis is an autosomal recessive genetic disease, mainly in Caucasian children and young adults. It is caused by pathogenic variants in the CFTR (cystic fibrosis transmembrane conductance regulator) gene, which results in increased viscosity
Externí odkaz:
https://doaj.org/article/796048c95bff4bddb9937f87c66a3034
Autor:
Mónica Aguinaga-Ríos, Higinio Estrada-Juárez, Elsa Romelia Moreno-Verduzco, Jaime Asael López-Valdez
Publikováno v:
Fetal and pediatric pathology. 32(2)
Sirenomelia is the most severe malformation complex affecting the human caudal pole, although its etiology is unclear, a primary defect of blastogenesis has been proposed. Studies consider sirenomelia as the most severe form of caudal dysgenesis, VAC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5df18a377685026842b5852ac10e2eea
https://pubmed.ncbi.nlm.nih.gov/22643051
https://pubmed.ncbi.nlm.nih.gov/22643051