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.

Https

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

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

24 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
AUTOSOMAL DOMINANT MÜLLER CELL SHEEN DYSTROPHY: Clinical, Histopathologic, and Genetic Assessment in an Extended Family With Long Follow-Up.
Dalma-Weiszhausz J, Chacón-Camacho O, Chevez-Barrios P, Zenteno JC, Franco-Cárdenas V, García-Montaño LA, Pérez-Bravo J, García-Montalvo IA, Jiménez-Sierra JM, Dalma A. Dalma-Weiszhausz J, et al. Among authors: garcia montalvo ia. Retina. 2022 May 1;42(5):981-991. doi: 10.1097/IAE.0000000000003413. Retina. 2022. PMID: 35125479
Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing.
Matías-Pérez D, García-Montaño LA, Cruz-Aguilar M, García-Montalvo IA, Nava-Valdéz J, Barragán-Arevalo T, Villanueva-Mendoza C, Villarroel CE, Guadarrama-Vallejo C, la Cruz RV, Chacón-Camacho O, Zenteno JC. Matías-Pérez D, et al. J Hum Genet. 2018 Nov;63(11):1169-1180. doi: 10.1038/s10038-018-0504-1. Epub 2018 Sep 4. J Hum Genet. 2018. PMID: 30181649
Mutational screening of FOXE3, GDF3, ATOH7, and ALDH1A3 in congenital ocular malformations. Possible contribution of the FOXE3 p.VAL201MET variant to the risk of severe eye malformations.
Garcia-Montalvo IA, Pelcastre-Luna E, Nelson-Mora J, Buentello-Volante B, Miranda-Duarte A, Zenteno JC. Garcia-Montalvo IA, et al. Ophthalmic Genet. 2014 Sep;35(3):190-2. doi: 10.3109/13816810.2014.903983. Epub 2014 Apr 1. Ophthalmic Genet. 2014. PMID: 24689660 No abstract available.
PCSK9 Gene Participates in the Development of Primary Dyslipidemias.
Matías-Pérez D, Pérez-Santiago AD, Sánchez Medina MA, Alpuche Osorno JJ, García-Montalvo IA. Matías-Pérez D, et al. Among authors: garcia montalvo ia. Balkan J Med Genet. 2021 Jul 27;24(1):5-14. doi: 10.2478/bjmg-2021-0009. eCollection 2021 Jun. Balkan J Med Genet. 2021. PMID: 34447653 Free PMC article.
[A GENETIC VIEW OF FAMILIAL HYPERCHOLESTEROLEMIA].
Matías-Pérez D, Pérez-Campos E, García-Montalvo IA. Matías-Pérez D, et al. Nutr Hosp. 2015 Dec 1;32(6):2421-6. doi: 10.3305/nh.2015.32.6.9885. Nutr Hosp. 2015. PMID: 26667688 Free article. Review. Spanish.
Corrigendum to "Molecules in seminal plasma related to platelets in preeclampsia" [Med. Hypotheses 93 (2016) 27-29].
García-Montalvo IA, Andrade GM, Mayoral LP, Canseco SP, Cruz RM, Martínez-Cruz M, Zenteno E, Mayoral EP, Gallegos Velasco I, Hernandez-Huerta MT, Matias-Perez D, Pérez-Campos E. García-Montalvo IA, et al. Med Hypotheses. 2017 Mar;100:1. doi: 10.1016/j.mehy.2016.12.014. Epub 2017 Jan 16. Med Hypotheses. 2017. PMID: 28236838 No abstract available.
24 results