Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 14

1.

Generation of an integration-free iPSC line, ICCSICi005-A, derived from a Parkinson's disease patient carrying the L444P mutation in the GBA1 gene.

Rodríguez-Traver E, Rodríguez C, Díaz-Guerra E, Arenas F, Araúzo-Bravo M, Orera M, Kulisevsky J, Moratalla R, Vicario C.

Stem Cell Res. 2019 Sep 12;40:101578. doi: 10.1016/j.scr.2019.101578. [Epub ahead of print]

2.

A collection of four integration-free iPSC lines derived from diagnosed sporadic Alzheimer's disease patients with different APOE alleles.

Díaz-Guerra E, Moreno-Jiménez EP, de Rojas I, Rodríguez C, Rodríguez-Traver E, Arribas-González E, Orera M, Hernández I, Ruiz A, Vicario C.

Stem Cell Res. 2019 Aug;39:101522. doi: 10.1016/j.scr.2019.101522. Epub 2019 Aug 1.

3.

A collection of integration-free iPSCs derived from Parkinson's disease patients carrying mutations in the GBA1 gene.

Rodríguez-Traver E, Díaz-Guerra E, Rodríguez C, Fernández P, Arenas F, Araúzo-Bravo M, Orera M, Kulisevsky J, Moratalla R, Vicario C.

Stem Cell Res. 2019 Jul;38:101482. doi: 10.1016/j.scr.2019.101482. Epub 2019 Jun 6.

4.

PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.

Nevado J, Rosenfeld JA, Mena R, Palomares-Bralo M, Vallespín E, Ángeles Mori M, Tenorio JA, Gripp KW, Denenberg E, Del Campo M, Plaja A, Martín-Arenas R, Santos-Simarro F, Armengol L, Gowans G, Orera M, Sanchez-Hombre MC, Corbacho-Fernández E, Fernández-Jaén A, Haldeman-Englert C, Saitta S, Dubbs H, Bénédicte DB, Li X, Devaney L, Dinulos MB, Vallee S, Crespo MC, Fernández B, Fernández-Montaño VE, Rueda-Arenas I, de Torres ML, Ellison JW, Raskin S, Venegas-Vega CA, Fernández-Ramírez F, Delicado A, García-Miñaúr S, Lapunzina P.

Eur J Hum Genet. 2015 Dec;23(12):1615-26. doi: 10.1038/ejhg.2015.51. Epub 2015 Apr 8.

5.

Characterization of patients' requests and pharmacists' professional practice in oropharyngeal condition in Spain.

Hernández A, Garcia-Delgado P, Garcia-Cardenas V, Ocaña A, Labrador E, Orera ML, Martinez-Martinez F.

Int J Clin Pharm. 2015 Apr;37(2):300-9. doi: 10.1007/s11096-014-0053-4. Epub 2015 Feb 24.

PMID:
25708123
6.

NID2 and HOXA9 promoter hypermethylation as biomarkers for prevention and early detection in oral cavity squamous cell carcinoma tissues and saliva.

Guerrero-Preston R, Soudry E, Acero J, Orera M, Moreno-López L, Macía-Colón G, Jaffe A, Berdasco M, Ili-Gangas C, Brebi-Mieville P, Fu Y, Engstrom C, Irizarry RA, Esteller M, Westra W, Koch W, Califano J, Sidransky D.

Cancer Prev Res (Phila). 2011 Jul;4(7):1061-72. doi: 10.1158/1940-6207.CAPR-11-0006. Epub 2011 May 10.

7.

Quantitative abnormalities of peripheral blood distinct T, B, and natural killer cell subsets and clinical findings in obstetric antiphospholipid syndrome.

Carbone J, Gallego A, Lanio N, Navarro J, Orera M, Aguaron A, Fernandez-Cruz E, Sarmiento E.

J Rheumatol. 2009 Jun;36(6):1217-25. doi: 10.3899/jrheum.081079. Epub 2009 Mar 30.

PMID:
19332638
8.

An excess of chromosome 1 breakpoints in male infertility.

Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N.

Eur J Hum Genet. 2004 Dec;12(12):993-1000.

9.
10.

[Antiphospholipid syndrome updating].

Orts JA, Zúñiga A, Orera M.

Med Clin (Barc). 2003 Oct 11;121(12):459-71. Review. Spanish.

PMID:
14572372
11.

Molecular analysis of a gestation consisting of a complete hydatidiform mole and normal dizygotic twin.

Ruiz-Casares E, Henriques-Gil N, Orera M, Fernández-Pacheco RP, Aguarón A.

J Reprod Med. 2001 Dec;46(12):1041-5.

PMID:
11789083
12.

[Familial Pitt-Rogers-Danks: two new cases].

Cabrera López JC, Marti Herrero M, Fernández Burriel M, Toledo L, de Andrés-Cofiño R, Orera MA.

Rev Neurol. 2001 Sep 1-15;33(5):439-43. Review. Spanish.

13.

Polydactyly in 22q11 syndrome: should it be taken into account?

Sánchez-Ramón S, Bartolomé J, Sánchez-Luna M, Franco ML, Orera M, Fernández-Cruz E, Fernández-Pacheco RP, Gil J.

Clin Genet. 2000 Jul;58(1):84-5. No abstract available.

PMID:
10945670
14.

Immunological abnormalities in primary APS evolving into SLE: 6 years follow-up in women with repeated pregnancy loss.

Carbone J, Orera M, Rodríguez-Mahou M, Rodríguez-Pérez C, Sánchez-Ramón S, Seoane E, Rodríguez JJ, Zabay JM, Fernández-Cruz E.

Lupus. 1999;8(4):274-8.

PMID:
10413205

Supplemental Content

Support Center