Format
Items per page
Sort by

Send to:

Choose Destination

Search results

Items: 1 to 20 of 40

1.

Validity of a Spanish Version of the Leicester Cough Questionnaire in Children With Cystic Fibrosis.

Del Corral T, Percegona J, López N, Valiente A, Garriga M, Seborga M, Vilaró J.

Arch Bronconeumol. 2016 Feb;52(2):63-69. doi: 10.1016/j.arbres.2015.01.016. Epub 2015 Jul 9. English, Spanish.

2.

Impact of borderline minimum inhibitory concentration on the outcome of invasive infections caused by Enterobacteriaceae treated with β-lactams: a systematic review and meta-analysis.

Torres E, Delgado M, Valiente A, Pascual Á, Rodríguez-Baño J.

Eur J Clin Microbiol Infect Dis. 2015 Sep;34(9):1751-8. doi: 10.1007/s10096-015-2408-8. Epub 2015 Jun 2.

PMID:
26032669
3.

Correlation of myelodysplastic syndromes with i(17)(q10) and TP53 and SETBP1 mutations.

Adema V, Larráyoz MJ, Calasanz MJ, Palomo L, Patiño-García A, Agirre X, Hernández-Rivas JM, Lumbreras E, Buño I, Martinez-Laperche C, Mallo M, García O, Álvarez S, Blazquez B, Cervera J, Luño E, Valiente A, Vallespí MT, Arenillas L, Collado R, Pérez-Oteyza J, Solé F.

Br J Haematol. 2015 Oct;171(1):137-41. doi: 10.1111/bjh.13355. Epub 2015 Feb 25. No abstract available.

PMID:
25716545
4.

[Prevalence and genotype distribution changes in hepatitis C virus co-infection among human immunodeficiency virus-infected patients].

Cifuentes C, Mancebo-Hernández M, Pérez-Navarro E, Recio E, Monje-Agudo P, Valiente A, Pineda JA.

Enferm Infecc Microbiol Clin. 2015 Feb;33(2):110-2. doi: 10.1016/j.eimc.2014.05.010. Epub 2014 Dec 12. Spanish.

PMID:
25510595
5.

Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: different genetic mechanisms but equivalent poorer clinical outcome.

Puiggros A, Venturas M, Salido M, Blanco G, Fernandez-Rodriguez C, Collado R, Valiente A, Ruiz-Xivillé N, Carrió A, Ortuño FJ, Luño E, Calasanz MJ, Ardanaz MT, Piñán MÁ, Talavera E, González MT, Ortega M, Marugán I, Ferrer A, Gimeno E, Bellosillo B, Delgado J, Hernández JÁ, Hernández-Rivas JM, Espinet B; Grupo Cooperativo Español de Citogenética Hematológica (GCECGH); Grupo Español de Leucemia Linfática Crónica (GELLC).

Genes Chromosomes Cancer. 2014 Sep;53(9):788-97. doi: 10.1002/gcc.22188. Epub 2014 Jun 10.

PMID:
24915757
6.

Cervical IL-6 and pIGFBP-1 and the prediction of neonatal outcome in symptomatic preterm labour.

Brik M, Aguar M, Valiente A, Perales A.

J Matern Fetal Neonatal Med. 2014 Aug;27(12):1241-7. doi: 10.3109/14767058.2013.854326. Epub 2013 Nov 26.

PMID:
24111635
7.

Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukaemia: analysis of 627 patients with isolated 13q deletion.

Puiggros A, Delgado J, Rodriguez-Vicente A, Collado R, Aventín A, Luño E, Grau J, Hernandez JÁ, Marugán I, Ardanaz M, González T, Valiente A, Osma M, Calasanz MJ, Sanzo C, Carrió A, Ortega M, Santacruz R, Abrisqueta P, Abella E, Bosch F, Carbonell F, Solé F, Hernández JM, Espinet B; Grupo Cooperativo Español de Citogenética Hematológica (GCECGH) and Grupo Español de Leucemia Linfática Crónica (GELLC).

Br J Haematol. 2013 Oct;163(1):47-54. doi: 10.1111/bjh.12479. Epub 2013 Jul 19.

PMID:
23869550
8.

Propionic acidemia and optic neuropathy: a report of two cases.

Arias C, Raimann E, Peredo P, Cabello JF, Castro G, Valiente A, de la Parra A, Bravo P, Okuma C, Cornejo V.

JIMD Rep. 2014;12:1-4. doi: 10.1007/8904_2013_234. Epub 2013 Jul 2.

9.

[Systematic review of the Genomewide Association Studies (GWAS) in schizophrenia].

Valiente A, Lafuente A, Bernardo M.

Rev Psiquiatr Salud Ment. 2011 Oct;4(4):218-27. doi: 10.1016/j.rpsm.2011.09.003. Epub 2011 Nov 25. Spanish.

10.

Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: a worldwide collaborative project.

McHugh D, Cameron CA, Abdenur JE, Abdulrahman M, Adair O, Al Nuaimi SA, Åhlman H, Allen JJ, Antonozzi I, Archer S, Au S, Auray-Blais C, Baker M, Bamforth F, Beckmann K, Pino GB, Berberich SL, Binard R, Boemer F, Bonham J, Breen NN, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Bryant SC, Caggana M, Caldwell SG, Camilot M, Campbell C, Carducci C, Cariappa R, Carlisle C, Caruso U, Cassanello M, Castilla AM, Ramos DE, Chakraborty P, Chandrasekar R, Ramos AC, Cheillan D, Chien YH, Childs TA, Chrastina P, Sica YC, de Juan JA, Colandre ME, Espinoza VC, Corso G, Currier R, Cyr D, Czuczy N, D'Apolito O, Davis T, de Sain-Van der Velden MG, Delgado Pecellin C, Di Gangi IM, Di Stefano CM, Dotsikas Y, Downing M, Downs SM, Dy B, Dymerski M, Rueda I, Elvers B, Eaton R, Eckerd BM, El Mougy F, Eroh S, Espada M, Evans C, Fawbush S, Fijolek KF, Fisher L, Franzson L, Frazier DM, Garcia LR, Bermejo MS, Gavrilov D, Gerace R, Giordano G, Irazabal YG, Greed LC, Grier R, Grycki E, Gu X, Gulamali-Majid F, Hagar AF, Han L, Hannon WH, Haslip C, Hassan FA, He M, Hietala A, Himstedt L, Hoffman GL, Hoffman W, Hoggatt P, Hopkins PV, Hougaard DM, Hughes K, Hunt PR, Hwu WL, Hynes J, Ibarra-González I, Ingham CA, Ivanova M, Jacox WB, John C, Johnson JP, Jónsson JJ, Karg E, Kasper D, Klopper B, Katakouzinos D, Khneisser I, Knoll D, Kobayashi H, Koneski R, Kozich V, Kouapei R, Kohlmueller D, Kremensky I, la Marca G, Lavochkin M, Lee SY, Lehotay DC, Lemes A, Lepage J, Lesko B, Lewis B, Lim C, Linard S, Lindner M, Lloyd-Puryear MA, Lorey F, Loukas YL, Luedtke J, Maffitt N, Magee JF, Manning A, Manos S, Marie S, Hadachi SM, Marquardt G, Martin SJ, Matern D, Mayfield Gibson SK, Mayne P, McCallister TD, McCann M, McClure J, McGill JJ, McKeever CD, McNeilly B, Morrissey MA, Moutsatsou P, Mulcahy EA, Nikoloudis D, Norgaard-Pedersen B, Oglesbee D, Oltarzewski M, Ombrone D, Ojodu J, Papakonstantinou V, Reoyo SP, Park HD, Pasquali M, Pasquini E, Patel P, Pass KA, Peterson C, Pettersen RD, Pitt JJ, Poh S, Pollak A, Porter C, Poston PA, Price RW, Queijo C, Quesada J, Randell E, Ranieri E, Raymond K, Reddic JE, Reuben A, Ricciardi C, Rinaldo P, Rivera JD, Roberts A, Rocha H, Roche G, Greenberg CR, Mellado JM, Juan-Fita MJ, Ruiz C, Ruoppolo M, Rutledge SL, Ryu E, Saban C, Sahai I, García-Blanco MI, Santiago-Borrero P, Schenone A, Schoos R, Schweitzer B, Scott P, Seashore MR, Seeterlin MA, Sesser DE, Sevier DW, Shone SM, Sinclair G, Skrinska VA, Stanley EL, Strovel ET, Jones AL, Sunny S, Takats Z, Tanyalcin T, Teofoli F, Thompson JR, Tomashitis K, Domingos MT, Torres J, Torres R, Tortorelli S, Turi S, Turner K, Tzanakos N, Valiente AG, Vallance H, Vela-Amieva M, Vilarinho L, von Döbeln U, Vincent MF, Vorster BC, Watson MS, Webster D, Weiss S, Wilcken B, Wiley V, Williams SK, Willis SA, Woontner M, Wright K, Yahyaoui R, Yamaguchi S, Yssel M, Zakowicz WM.

Genet Med. 2011 Mar;13(3):230-54. doi: 10.1097/GIM.0b013e31820d5e67.

PMID:
21325949
11.

Past, present and future of newborn screening in Chile.

Cornejo V, Raimann E, Cabello JF, Valiente A, Becerra C, Opazo M, Colombo M.

J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S301-6. doi: 10.1007/s10545-010-9165-8. Epub 2010 Aug 4.

PMID:
20683669
12.

[Genetic screening to determine an etiologic diagnosis in children with mental retardation].

Alliende MA, Cámpora L, Curotto B, Toro J, Valiente A, Castillo M, Cortés F, Trigo C, Alvarado C, Silva M, Caru M.

Rev Med Chil. 2008 Dec;136(12):1542-51. doi: /S0034-98872008001200006. Epub 2009 Mar 23. Spanish.

13.

[Experience and results of acute lymphoblastic leukaemia treatment in children between 1989-2005 in Navarre].

Molina J, Molins T, Gil FJ, Sagaseta de Ilurdoz M, Ruipérez E, Guembero E, Sala F, Valiente A, Labaca MA.

An Sist Sanit Navar. 2007 Sep-Dec;30(3):363-71. Spanish.

PMID:
18227893
14.

Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models.

García-Alegría E, Ibáñez B, Mínguez M, Poch M, Valiente A, Sanz-Parra A, Martinez-Bouzas C, Beristain E, Tejada MI.

RNA. 2007 May;13(5):756-62.

15.

[Genetic mechanisms in the hereditary predisposition to colorectal cancer].

Alonso A, Moreno S, Valiente A, Artigas M, Pérez-Juana A, Ramos Arroyo MA.

An Sist Sanit Navar. 2006 Jan-Apr;29(1):59-76. Review. Spanish.

16.

Erythromycin resistance and genetic elements carrying macrolide efflux genes in Streptococcus agalactiae.

Marimón JM, Valiente A, Ercibengoa M, García-Arenzana JM, Pérez-Trallero E.

Antimicrob Agents Chemother. 2005 Dec;49(12):5069-74.

17.

Incidence and mutation rates of Huntington's disease in Spain: experience of 9 years of direct genetic testing.

Ramos-Arroyo MA, Moreno S, Valiente A.

J Neurol Neurosurg Psychiatry. 2005 Mar;76(3):337-42.

18.

[ACT/AA polymorphism could duplicate the APOE*epsilon4-associated Alzheimer's disease risk].

Hernández-Charro B, Moreno S, Valiente A, Manubens JM, Villar MD, Ramos-Arroyo MA.

Med Clin (Barc). 2004 Sep 4;123(7):251-4. Spanish.

PMID:
15482730
19.

Evaluation of reliability for urine mucopolysaccharidosis screening by dimethylmethylene blue and Berry spot tests.

Mabe P, Valiente A, Soto V, Cornejo V, Raimann E.

Clin Chim Acta. 2004 Jul;345(1-2):135-40.

PMID:
15193988
20.

[Phenylketonuria diagnosed during the neonatal period and breast feeding].

Cornejo V, Manríquez V, Colombo M, Mabe P, Jiménez M, De la Parra A, Valiente A, Raimann E.

Rev Med Chil. 2003 Nov;131(11):1280-7. Spanish.

PMID:
14743689
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk