Hospital Universitario Nuestra Seora de Candelaria

Unidad de Investigacin
Publicaciones
  • Claverie-Martn F, Garca-Nieto V, Loris, C, Ariceta G, Nadal I, Espinosa L, Fernndez-Maseda M A, Antn-Gamero M, vila A, Madrid A, Gonzlez-Acosta H, Crdoba-Lanus E, Santos F, Gil-Calvo M, Espino M, Garca-Martnez E, Snchez A, Muley R F, for the RenalTube Group. Claudin-19 mutations and clinical phenotype in Spanish patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis (PLoS ONE, aceptado).
  • Luque de Pablos A, Garca-Nieto V, Lpez-Menchero J C, Ramos-Trujillo E, Gonzlez-Acosta H, Claverie-Martn F. Severe manifestation of Bartter syndrome type IV caused by a novel insertion mutation in the BSND gene (Clin Nephrol, aceptado).

  • Meja N, Santos F, Claverie-Martn F, Garca-Nieto V, Ariceta G, Castao L & Renaltube group. RENALTUBE: A network tool for clinical and genetic diagnosis of primary tubulopathies (enviado).
  • Gonzalez-Paredes F J, Ramos-Trujillo E, Claverie-Martin F. Aberrant pre-mRNA splicing in PKD1 due to presumed missense mutation R3719Q causing autosomal dominant polycystic disease (en preparacin).
  • Ramos-Trujillo E, Gonzalez-Paredes F J, Gonzalez-Acosta H, Claverie-Martin F. A mechanism for the exon skipping caused by an Alu insertion in the CLCN5 gene of a patient with Dent disease (en preparacin).
  • Claverie-Martn F, Ramos-Trujillo E, Garca-Nieto V (2011) Dent's disease: clinical features and molecular basis. Pediatr Nephrol 26:693-704. PubMed http://www.ncbi.nlm.nih.gov/pubmed/20936522
  • Garca Nieto V, Luis Yanes M I, Claverie Martn F (2011) Sndrome de Bartter y enfermedades afines. Nefrologia Sup Ext 2. doi:10.3265
  • Claverie-Martn F, Ramos-Trujillo E (2010) Estudios genticos. En Nefrologa Peditrica: Manual Prctico. Editorial Medica Panamericana, p. 89-94
  • de-Misa RF, Pérez-Méndez LI, Hernández-Jiménez JG, Rodríguez Mdel C, Vilar MC, Suárez J, Claveríe-Martín F. (2008) Main pigmentary features and melanocortin 1 receptor (MC1R) gene polymorphisms in the population of the Canary Islands. Int J Dermatol. 47:806-11. PubMed http://www.ncbi.nlm.nih.gov/pubmed/18717860
  • F-de-Misa R, Hernández-Jimenez JG, Carretero Hernández G, Pérez-Méndez L, Aguirre-Jaime A, Flores C, Suárez Hernández J, Perera Molinero A, Claveríe-Martín F. (2008) The D84E variant of the alpha-MSH receptor 1 gene is associated with cutaneous malignant melanoma early onset. J Dermatol Sci. 52:186-92. PubMed http://www.ncbi.nlm.nih.gov/pubmed/18657399
  • Ramos-Trujillo E, Garcia-Nieto V, Gonzalez-Acosta H, Vara J, Pérez-Diaz V, Nadal I, Oliveros R, Claverie-Martin, F (2007) Molecular analysis of the CLCN5 gene in Dent’s disease: First mutation identified in a patient from South America. Clin Nephrol 68: 367-372.   PubMed http://www.ncbi.nlm.nih.gov/pubmed/18184518
  • Ramos-Trujillo E, Gonzalez-Acosta H, Flores C, Garcia-Nieto V, Guillen E, Gracia S, Vicente C, Espinosa L, Maseda MA, Santos F, Camacho JA, Claverie-Martin F (2007). 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. J Hum Genet 52:255-261. PubMed    http://www.ncbi.nlm.nih.gov/pubmed/17262170
  • García-Nieto V, Flores C, Luis-Yanes M I, Gallego E, Villar J, Claverie-Martín, F (2006) Mutation G47R in the barttin gene causes Bartter syndrome with sensorineural deafness in two families from the Canary Islands. Pediatr Nephrol 21: 643-648. PubMed    http://www.ncbi.nlm.nih.gov/pubmed/16572343
  • Garcia Nieto V, Claverie-Martin F (2006) Urolithiasis, idiopathic hypercalciuria and insularity. Pediatr Nephrol 21:1331-1332. PubMedhttp://www.ncbi.nlm.nih.gov/pubmed/16721584
  • Claverie-Martín F, Vega-Hernández M. C. (2006). Aspartic porteases involved in milk-clotting. In “Industrial Ezyimes: Structure, Function and Applications”. Ed.: J. Polaina and A.P. MacCabe. Ed. Springer. (pp. 207-219).
  • Claverie-Martín F, García- Nieto V. (2006). Enfermedad de Dent. In “Nefrología Pediátrica”. 2ª Edición. Editores: V. García Vieto, F. Santos, B. Rodríguez-Iturbe. Ed. Grupo Aula Médica Madrid. pp. 135-149.
  • Claverie-Martín F, Flores C, Antón-Gamero M, González-Acosta H,  García-Nieto V. (2005) The Alu insertion in the CLCN5 gene of a patient with Dent disease leads to exon 11 skipping.  J. Hum Genet 50: 370-37. PubMed      http://www.ncbi.nlm.nih.gov/pubmed/16041495
  • Antón Gamero M, Claverie-Martín F, García-Nieto V, Vela-Enríquez F, García-Martínez E, Pérez-Navero J L (2005) Chloride and sodium renal tubular handling in Dent’s disease. Pediatr Nephrol 20: 1198-1199. PubMed http://www.ncbi.nlm.nih.gov/pubmed/15912380
  • García-Nieto, V., Claverie-Martín, F. (2005). Enfermedad de Bartter con sordera neurosensorial (Bartter tipo IV). Una entidad descrita hace solo diez años. Nefrología, 25: 596-601. PubMed http://www.ncbi.nlm.nih.gov/pubmed/16514898
  • Navarro J.,F, Milena, F.J., Mora, C, Leon, C., Claverie, F., Flores, C., Garcia, J. (2005). Tumor necrosis factor-alpha gene expression in diabetic nephropathy: Relationship with urinary albumin excretion and effect of angiotensin-converting enzyme inhibition. Kidney Int., 68(s99):S98-S102. PubMed http://www.ncbi.nlm.nih.gov/pubmed/16336586
  • Wolf M T F, Zalewski I, Claverie-Martin F, Ruf R, Muller D, Hennies H C, Schwarz S, Panther F, Attanasio M, Gonzalez-Acosta H, Imm A, Lucke B, Utsch B, Otto E, Nurnberg P, Garcia-Nieto V, Hildebrandt F (2005) Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage. Nephrol Dial Transplant  20:909-914. PubMed http://www.ncbi.nlm.nih.gov/sites/pubmed
  • Vega-Hernández MC, Gómez-Coello A, Villar J, Claverie-Martín F. (2004) Molecular cloning and expression in yeast of caprine prochymosin. J Biotechnol. 114:69-79. PubMed   http://www.ncbi.nlm.nih.gov/pubmed/15464600
  • Martín-López JV, Díez-Gil O, Morales M, Batista N, Villar J, Claverie-Martín F, Méndez-Alvarez S. (2004) Simultaneous PCR detection of ica cluster and methicillin and mupirocin resistance genes in catheter-isolated Staphylococcus. Int Microbiol. 7:63-6. PubMed http://www.ncbi.nlm.nih.gov/pubmed/15179609
  • Lorenzo-Díaz F, Delgado T, Reyes-Darias JA, Flores C, Méndez-Alvarez S, Villar J, Sierra A, Claverie-Martín F. (2004) Characterization of the first VanB vancomycin-resistant Enterococcus faecium isolated in a Spanish hospital. Curr Microbiol. 48:199-203. PubMed http://www.ncbi.nlm.nih.gov/pubmed/15057465
  • Müller D, Jaya Kausalya P, Claverie-Martin F, Meij I C, Eggert P, van Os C H, Garcia-Nieto V, Hunziker W (2003) A novel Claudin 16 mutation associated with childhood hypercalciuria abolishes binding to ZO-1 and results in lysosomal mistargeting. Am J Hum Genet 73: 1293-1301.   PubMed    http://www.ncbi.nlm.nih.gov/pubmed/14628289
  • Carballo-Trujillo I, Garcia-Nieto V, Méndez-Alvarez S, Antón Gamero M, Camacho F, Loris C, Claverie-Martín F (2003) Novel truncating mutations in the CLCN5 gene of patients with Dent’s disease. Nephrol Dial Transplant 18: 717-723. PubMed     http://www.ncbi.nlm.nih.gov/pubmed/12637640
  • Claverie-Martin F, González-Acosta H, Flores C, Antón-Gamero M, García-Nieto V (2003) De Novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent’s disease. Hum Genet 113: 480-485.  PubMed      http://www.ncbi.nlm.nih.gov/pubmed/14569459
  • García-Nieto, V., Cantabrana, A., Müller, D., Claverie-Martin, F. (2003). Condrocalcinosis e hipomagnesemia en un paciente portador de una nueva mutación en el gen del cotransportador de Cl-Na sensible a tiazidas. Nefrología 23: 504-509.  PubMed http://www.ncbi.nlm.nih.gov/pubmed/15002785
  • García Nieto V., Claverie-Martín, F. (2003). Enfermedad de Dent. Historia y causas genéticas de una "nueva" tubulopatía. Nefrología 23:1-5. PubMed http://www.ncbi.nlm.nih.gov/pubmed/12891933
  • Ramos-Trujillo E, Pérez-Roth E, Méndez-Alvarez S, Claverie-Martín F. (2003) Multiplex PCR for simultaneous detection of enterococcal genes vanA and vanB and staphylococcal genes mecA, ileS-2 and femB. Int Microbiol. 6:113-5. PubMed  http://www.ncbi.nlm.nih.gov/pubmed/12802618
  • Pérez-Hernández X, Méndez-Alvarez S, Delgado T, Moreno A, Reyes-Darias A, Sierra López A, Villar J, González A, Martín Sánchez M, Macía M, Claverie-Martín F. (2002) Low prevalence of vancomycin-resistant enterococci in clinical samples from hospitalized patients of the Canary Islands, Spain. Int Microbiol. 5:117-20. PubMed http://www.ncbi.nlm.nih.gov/pubmed/12207212
  • Müller D, Hoenderop JG, Vennekens R, Eggert P, Harangi F, Méhes K, Garcia-Nieto V, Claverie-Martin F, Os CH, Nilius B, J M Bindels R. (2002) Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria. Nephrol Dial Transplant. 17:1614-20. PubMed http://www.ncbi.nlm.nih.gov/pubmed/12198212