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

Year Number of Results
1989 2
1992 1
1993 1
2006 1
2007 1
2015 1
2019 1
2020 1
2021 1
2023 2
2024 2

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11 results

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Page 1
[Postoperative meralgia paresthetica].
Blanca Jover E, Olivares Sánchez L, Gómez Vida JM, Valenzuela Soria A, Broncano Lupiáñez S, Rodríguez Leal A. Blanca Jover E, et al. Among authors: gomez vida jm. An Pediatr (Barc). 2006 Nov;65(5):504. doi: 10.1157/13094253. An Pediatr (Barc). 2006. PMID: 17184614 Free article. Spanish. No abstract available.
Mild hypophosphatasia may be twice as prevalent as previously estimated: an effective clinical algorithm to detect undiagnosed cases.
González-Cejudo T, Villa-Suárez JM, Ferrer-Millán M, Andújar-Vera F, Contreras-Bolívar V, Andreo-López MC, Gómez-Vida JM, Martínez-Heredia L, González-Salvatierra S, de Haro Muñoz T, García-Fontana C, Muñoz-Torres M, García-Fontana B. González-Cejudo T, et al. Among authors: gomez vida jm. Clin Chem Lab Med. 2023 Jul 14;62(1):128-137. doi: 10.1515/cclm-2023-0427. Print 2024 Jan 26. Clin Chem Lab Med. 2023. PMID: 37440753 Free article.
Systemic effects of hypophosphatasia characterization of two novel variants in the ALPL gene.
Martínez-Heredia L, Muñoz-Torres M, Sanabria-de la Torre R, Jiménez-Ortas Á, Andújar-Vera F, González-Cejudo T, Contreras-Bolívar V, González-Salvatierra S, Gómez-Vida JM, García-Fontana C, García-Fontana B. Martínez-Heredia L, et al. Among authors: gomez vida jm. Front Endocrinol (Lausanne). 2024 Jan 3;14:1320516. doi: 10.3389/fendo.2023.1320516. eCollection 2023. Front Endocrinol (Lausanne). 2024. PMID: 38234425 Free PMC article.
Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study.
García Castaño A, Pérez de Nanclares G, Madariaga L, Aguirre M, Chocron S, Madrid A, Lafita Tejedor FJ, Gil Campos M, Sánchez Del Pozo J, Ruiz Cano R, Espino M, Gomez Vida JM, Santos F, García Nieto VM, Loza R, Rodríguez LM, Hidalgo Barquero E, Printza N, Camacho JA, Castaño L, Ariceta G; RenalTube Group. García Castaño A, et al. Among authors: gomez vida jm. Eur J Pediatr. 2015 Oct;174(10):1373-85. doi: 10.1007/s00431-015-2534-4. Epub 2015 Apr 23. Eur J Pediatr. 2015. PMID: 25902753
Epidemiological, Clinical and Genetic Study of Hypophosphatasia in A Spanish Population: Identification of Two Novel Mutations in The Alpl Gene.
García-Fontana C, Villa-Suárez JM, Andújar-Vera F, González-Salvatierra S, Martínez-Navajas G, Real PJ, Gómez Vida JM, de Haro T, García-Fontana B, Muñoz-Torres M. García-Fontana C, et al. Among authors: gomez vida jm. Sci Rep. 2019 Jul 2;9(1):9569. doi: 10.1038/s41598-019-46004-2. Sci Rep. 2019. PMID: 31267001 Free PMC article.
The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities.
Rica I, Luzuriaga C, Pérez de Nanclares G, Estalella I, Aragonés A, Barrio R, Bilbao JR, Carlés C, Fernández C, Fernández JM, Fernández-Rebollo E, Gastaldo E, Giralt P, Gomez Vida JM, Gutiérrez A, López Siguero JP, Martínez-Aedo MJ, Muñoz M, Prieto J, Rodrigo J, Vargas F, Castano L. Rica I, et al. Among authors: gomez vida jm. Diabet Med. 2007 Jul;24(7):707-13. doi: 10.1111/j.1464-5491.2007.02140.x. Epub 2007 May 8. Diabet Med. 2007. PMID: 17490422
[Familial thallium poisoning. Clinical and therapeutic considerations].
Ruiz Extremera A, Loscertales Abril M, del Moral García MT, Gómez Vida JM, Macías López FJ, Molina Font JA. Ruiz Extremera A, et al. Among authors: gomez vida jm. An Esp Pediatr. 1989 Feb;30(2):147-9. An Esp Pediatr. 1989. PMID: 2719419 Spanish. No abstract available.
11 results