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

Year Number of Results
2003 1
2005 4
2006 3
2007 1
2008 1
2009 1
2010 1
2012 1
2014 1
2015 2
2017 1
2019 1
2020 2
2022 1
2023 1
2024 0

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19 results

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Page 1
Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment.
Carcavilla A, Cambra A, Santomé JL, Seidel V, Cruz J, Alonso M, Pozo J, Valenzuela I, Guillén-Navarro E, Santos-Simarro F, González-Casado I, Rodríguez A, Medrano C, López-Siguero JP, Ezquieta B. Carcavilla A, et al. Among authors: alonso m. J Clin Med. 2023 Jul 29;12(15):5003. doi: 10.3390/jcm12155003. J Clin Med. 2023. PMID: 37568403 Free PMC article.
Biallelic cGMP-dependent type II protein kinase gene (PRKG2) variants cause a novel acromesomelic dysplasia.
Díaz-González F, Wadhwa S, Rodriguez-Zabala M, Kumar S, Aza-Carmona M, Sentchordi-Montané L, Alonso M, Ahmad I, Zahra S, Kumar D, Kushwah N, Shamim U, Sait H, Kapoor S, Roldán B, Nishimura G, Offiah AC, Faruq M, Heath KE. Díaz-González F, et al. Among authors: alonso m. J Med Genet. 2022 Jan;59(1):28-38. doi: 10.1136/jmedgenet-2020-107177. Epub 2020 Oct 26. J Med Genet. 2022. PMID: 33106379
Pulmonary function in children with type 1 diabetes mellitus.
Martín-Frías M, Lamas A, Lara E, Alonso M, Ros P, Barrio R. Martín-Frías M, et al. Among authors: alonso m. J Pediatr Endocrinol Metab. 2015 Jan;28(1-2):163-9. doi: 10.1515/jpem-2014-0147. J Pediatr Endocrinol Metab. 2015. PMID: 25153374
[Dermatomyositis, lipodystrophy and insulin resistance].
Vidal A, Alonso M. Vidal A, et al. Among authors: alonso m. Med Clin (Barc). 2006 Apr 8;126(13):515. doi: 10.1157/13086854. Med Clin (Barc). 2006. PMID: 16624235 Spanish. No abstract available.
An XX male with an intratubular undifferentiated germ cell neoplasia.
Carcavilla A, Alonso M, Ezquieta B, García-Galloway E, Barrio R, Nistal M. Carcavilla A, et al. Among authors: alonso m. Fertil Steril. 2008 Nov;90(5):2005.e3-5. doi: 10.1016/j.fertnstert.2008.07.001. Epub 2008 Aug 13. Fertil Steril. 2008. PMID: 18701099 Free article.
Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1.
Martínez de LaPiscina I, Mahmoud RA, Sauter KS, Esteva I, Alonso M, Costa I, Rial-Rodriguez JM, Rodríguez-Estévez A, Vela A, Castano L, Flück CE. Martínez de LaPiscina I, et al. Among authors: alonso m. Int J Mol Sci. 2020 Nov 13;21(22):8554. doi: 10.3390/ijms21228554. Int J Mol Sci. 2020. PMID: 33202802 Free PMC article.
Alterations in RAS-MAPK genes in 200 Spanish patients with Noonan and other neuro-cardio-facio-cutaneous syndromes. Genotype and cardiopathy.
Ezquieta B, Santomé JL, Carcavilla A, Guillén-Navarro E, Pérez-Aytés A, Sánchez del Pozo J, García-Miñaur S, Castillo E, Alonso M, Vendrell T, Santana A, Maroto E, Galbis L. Ezquieta B, et al. Among authors: alonso m. Rev Esp Cardiol (Engl Ed). 2012 May;65(5):447-55. doi: 10.1016/j.recesp.2011.12.016. Epub 2012 Mar 31. Rev Esp Cardiol (Engl Ed). 2012. PMID: 22465605 English, Spanish.
19 results