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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 2
2009 1
2010 1
2012 2
2013 1
2014 1
2015 2
2016 3
2017 3
2018 4
2019 6
2021 4
2022 5
2023 5
2024 0

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35 results

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Page 1
Skewed X-inactivation in a Female Carrier with X-linked Chronic Granulomatous Disease.
López-Hernández I, Deswarte C, Alcantara-Ortigoza MÁ, Saez-de-Ocariz MDM, Yamazaki-Nakashimada MA, Espinosa-Padilla SE, Bustamante J, Blancas-Galicia L. López-Hernández I, et al. Among authors: alcantara ortigoza ma. Iran J Allergy Asthma Immunol. 2019 Aug 17;18(4):447-451. doi: 10.18502/ijaai.v18i4.1425. Iran J Allergy Asthma Immunol. 2019. PMID: 31522453 Free article. Review.
Unusual Clinical Manifestations in a Mexican Patient with Sanfilippo B Syndrome.
Fernández-Hernández L, Reyna-Fabián ME, Alcántara-Ortigoza MA, Aláez-Verson C, Flores-Lagunes LL, Carrillo-Sánchez K, González-Del Angel A. Fernández-Hernández L, et al. Among authors: alcantara ortigoza ma. Diagnostics (Basel). 2022 May 19;12(5):1268. doi: 10.3390/diagnostics12051268. Diagnostics (Basel). 2022. PMID: 35626423 Free PMC article.
Newborn cystic fibrosis screening in southeastern Mexico: Birth prevalence and novel CFTR gene variants.
Ibarra-González I, Campos-Garcia FJ, Herrera-Pérez LDA, Martínez-Cruz P, Moreno-Graciano CM, Contreras-Capetillo SN, León-Burgos V, Maldonado-Solis FA, Alcántara-Ortigoza MA, González Del Angel A, Vela-Amieva M. Ibarra-González I, et al. Among authors: alcantara ortigoza ma. J Med Screen. 2018 Sep;25(3):119-125. doi: 10.1177/0969141317722808. Epub 2017 Oct 9. J Med Screen. 2018. PMID: 28992757
Case report of renal tubular acidosis and misdiagnosed.
Medeiros M, Enciso S, Hernández AM, García Hernández HR, Toussaint G, Pinto C, Navarrete Rodríguez EM, Del-Rio-Navarro BE, Saucedo-Ramírez OJ, Medina Bravo P, Miranda S, Worona L, Sosa G, Belmont Martinez L, Alcántara Ortigoza MÁ, Escobar L, Muñoz Arizpe R. Medeiros M, et al. Among authors: alcantara ortigoza ma. Nefrologia. 2016 May-Jun;36(3):323-5. doi: 10.1016/j.nefro.2015.10.012. Epub 2016 Feb 5. Nefrologia. 2016. PMID: 26857205 Free article. English, Spanish. No abstract available.
Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening.
Vela-Amieva M, Alcántara-Ortigoza MA, González-Del Angel A, Belmont-Martínez L, López-Candiani C, Ibarra-González I. Vela-Amieva M, et al. Among authors: alcantara ortigoza ma. Orphanet J Rare Dis. 2021 Feb 26;16(1):103. doi: 10.1186/s13023-021-01693-9. Orphanet J Rare Dis. 2021. PMID: 33637102 Free PMC article.
An Updated PAH Mutational Spectrum of Phenylketonuria in Mexican Patients Attending a Single Center: Biochemical, Clinical-Genotyping Correlations.
Vela-Amieva M, Alcántara-Ortigoza MA, Ibarra-González I, González-Del Angel A, Fernández-Hernández L, Guillén-López S, López-Mejía L, Carrillo-Nieto RI, Belmont-Martínez L, Fernández-Lainez C. Vela-Amieva M, et al. Among authors: alcantara ortigoza ma. Genes (Basel). 2021 Oct 23;12(11):1676. doi: 10.3390/genes12111676. Genes (Basel). 2021. PMID: 34828281 Free PMC article.
35 results