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Page 1
New approach to osteopenia in phenylketonuric patients.
Pérez-Dueñas B, Cambra FJ, Vilaseca MA, Lambruschini N, Campistol J, Camacho JA. Pérez-Dueñas B, et al. Among authors: camacho ja. Acta Paediatr. 2002;91(8):899-904. doi: 10.1080/080352502760148603. Acta Paediatr. 2002. PMID: 12222712 Clinical Trial.
Biochemical follow-up in late-treated nephropathic cystinosis.
Vilaseca MA, Camacho JA, Briones P, Farré C, Mas A. Vilaseca MA, et al. Among authors: camacho ja. J Inherit Metab Dis. 1995;18(2):147-50. doi: 10.1007/BF00711751. J Inherit Metab Dis. 1995. PMID: 7564231 No abstract available.
[Neurologic presentation in haemolytic-uraemic syndrome].
Roche-Martínez A, Póo P, Maristany-Cucurella M, Jiménez-Llort A, Camacho JA, Campistol J. Roche-Martínez A, et al. Among authors: camacho ja. Rev Neurol. 2008 Aug 16-31;47(4):191-6. Rev Neurol. 2008. PMID: 18671208 Spanish.
Cysteamine (Cystagon®) adherence in patients with cystinosis in Spain: successful in children and a challenge in adolescents and adults.
Ariceta G, Lara E, Camacho JA, Oppenheimer F, Vara J, Santos F, Muñoz MA, Cantarell C, Gil Calvo M, Romero R, Valenciano B, García-Nieto V, Sanahuja MJ, Crespo J, Justa ML, Urisarri A, Bedoya R, Bueno A, Daza A, Bravo J, Llamas F, Jiménez Del Cerro LA. Ariceta G, et al. Among authors: camacho ja. Nephrol Dial Transplant. 2015 Mar;30(3):475-80. doi: 10.1093/ndt/gfu329. Epub 2014 Oct 26. Nephrol Dial Transplant. 2015. PMID: 25348508 Free PMC article.
A coordinated transition model for patients with cystinosis: from pediatrics to adult care.
Ariceta G, Camacho JA, Fernández-Obispo M, Fernández-Polo A, Gámez J, García-Villoria J, Lara E, Leyes P, Martín-Begué N, Perelló M, Pintos-Morell G, Torra R, Torregrosa JV, Torres-Sierra S, Vila-Santandreu A, Güell A; Grupo T-CiS.bcn. Ariceta G, et al. Among authors: camacho ja. Nefrologia. 2016 Nov-Dec;36(6):616-630. doi: 10.1016/j.nefro.2016.05.012. Epub 2016 Aug 30. Nefrologia. 2016. PMID: 27595514 Free article. English, Spanish.
Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
Santín S, García-Maset R, Ruíz P, Giménez I, Zamora I, Peña A, Madrid A, Camacho JA, Fraga G, Sánchez-Moreno A, Cobo MA, Bernis C, Ortiz A, de Pablos AL, Pintos G, Justa ML, Hidalgo-Barquero E, Fernández-Llama P, Ballarín J, Ars E, Torra R; FSGS Spanish Study Group. Santín S, et al. Among authors: camacho ja. Kidney Int. 2009 Dec;76(12):1268-76. doi: 10.1038/ki.2009.381. Epub 2009 Oct 7. Kidney Int. 2009. PMID: 19812541 Free article.
A missense mutation in the chloride/proton ClC-5 antiporter gene results in increased expression of an alternative mRNA form that lacks exons 10 and 11. Identification of seven new CLCN5 mutations in patients with Dent's disease.
Ramos-Trujillo E, González-Acosta H, Flores C, García-Nieto V, Guillén E, Gracia S, Vicente C, Espinosa L, Maseda MAF, Santos F, Camacho JA, Claverie-Martín F. Ramos-Trujillo E, et al. Among authors: camacho ja. J Hum Genet. 2007;52(3):255-261. doi: 10.1007/s10038-007-0112-y. Epub 2007 Jan 30. J Hum Genet. 2007. PMID: 17262170
74 results