Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page


My NCBI Filters

Results by year

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

Year Number of Results
2006 1
2007 1
2008 3
2009 1
2010 1
2011 3
2012 3
2013 2
2014 4
2015 4
2016 2
2017 4
2018 7
2019 9
2020 4
2021 6
2022 6
2023 5
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

56 results

Results by year

Filters applied: . Clear all
Page 1
[Cystic fibrosis: molecular update and clinical implications].
Orozco L, Chávez M, Saldaña Y, Velázquez R, Carnevale A, González-del Angel A, Jiménez S. Orozco L, et al. Among authors: gonzalez del angel a. Rev Invest Clin. 2006 Mar-Apr;58(2):139-52. Rev Invest Clin. 2006. PMID: 16827266 Review. Spanish.
Kapur-Toriello syndrome: further delineation.
Yokoyama E, Martínez A, González-Del Angel A. Yokoyama E, et al. Among authors: gonzalez del angel a. Am J Med Genet A. 2008 Nov 1;146A(21):2791-3. doi: 10.1002/ajmg.a.32369. Am J Med Genet A. 2008. PMID: 18831061
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: gonzalez del angel a. Diagnostics (Basel). 2022 May 19;12(5):1268. doi: 10.3390/diagnostics12051268. Diagnostics (Basel). 2022. PMID: 35626423 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: gonzalez del angel a. Genes (Basel). 2021 Oct 23;12(11):1676. doi: 10.3390/genes12111676. Genes (Basel). 2021. PMID: 34828281 Free PMC article.
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: gonzalez del angel a. 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.
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: gonzalez del angel a. J Med Screen. 2018 Sep;25(3):119-125. doi: 10.1177/0969141317722808. Epub 2017 Oct 9. J Med Screen. 2018. PMID: 28992757
56 results