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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

24 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
The exon 3-deleted growth hormone receptor is associated with better response to pegvisomant therapy in acromegaly.
Bernabeu I, Alvarez-Escolá C, Quinteiro C, Lucas T, Puig-Domingo M, Luque-Ramírez M, de Miguel-Novoa P, Fernandez-Rodriguez E, Halperin I, Loidi L, Casanueva FF, Marazuela M. Bernabeu I, et al. Among authors: quinteiro c. J Clin Endocrinol Metab. 2010 Jan;95(1):222-9. doi: 10.1210/jc.2009-1630. Epub 2009 Oct 22. J Clin Endocrinol Metab. 2010. PMID: 19850678
Analysis of IGF(CA)19 and IGFBP3-202A/C gene polymorphisms in patients with acromegaly: association with clinical presentation and response to treatments.
Ramos-Leví AM, Marazuela M, Paniagua A, Quinteiro C, Riveiro J, Álvarez-Escolá C, Lúcas T, Blanco C, de Miguel P, Martínez de Icaya P, Pavón I, Bernabeu I. Ramos-Leví AM, et al. Among authors: quinteiro c. Eur J Endocrinol. 2015 Feb;172(2):115-22. doi: 10.1530/EJE-14-0613. Epub 2014 Nov 10. Eur J Endocrinol. 2015. PMID: 25385818
Pituitary stalk dysgenesis-induced hypopituitarism in adult patients: prevalence, evolution of hormone dysfunction and genetic analysis.
Fernandez-Rodriguez E, Quinteiro C, Barreiro J, Marazuela M, Pereiro I, Peinó R, Cabezas-Agrícola JM, Dominguez F, Casanueva FF, Bernabeu I. Fernandez-Rodriguez E, et al. Among authors: quinteiro c. Neuroendocrinology. 2011;93(3):181-8. doi: 10.1159/000324087. Epub 2011 Feb 8. Neuroendocrinology. 2011. PMID: 21304225
High variability in CYP21A2 mutated alleles in Spanish 21-hydroxylase deficiency patients, six novel mutations and a founder effect.
Loidi L, Quinteiro C, Parajes S, Barreiro J, Lestón DG, Cabezas-Agrícola JM, Sueiro AM, Araujo-Vilar D, Catro-Feijóo L, Costas J, Pombo M, Domínguez F. Loidi L, et al. Among authors: quinteiro c. Clin Endocrinol (Oxf). 2006 Mar;64(3):330-6. doi: 10.1111/j.1365-2265.2006.02465.x. Clin Endocrinol (Oxf). 2006. PMID: 16487445
Genetic basis of short stature.
Castro-Feijóo L, Quinteiro C, Loidi L, Barreiro J, Cabanas P, Arévalo T, Diéguez C, Casanueva FF, Pombo M. Castro-Feijóo L, et al. Among authors: quinteiro c. J Endocrinol Invest. 2005;28(5 Suppl):30-7. J Endocrinol Invest. 2005. PMID: 16114273 Review.
24 results