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Juan Pedro López Siguero
Juan Pedro López Siguero
medico
Dirección de correo verificada de juntadeandalucia.es
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Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy
B Pandit, A Sarkozy, LA Pennacchio, C Carta, K Oishi, S Martinelli, ...
Nature genetics 39 (8), 1007-1012, 2007
7632007
Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome
M Tartaglia, LA Pennacchio, C Zhao, KK Yadav, V Fodale, A Sarkozy, ...
Nature genetics 39 (1), 75-79, 2007
6412007
Estudio transversal español de crecimiento 2008
A Carrascosa, ÁF Longás, JP López-Siguero, ES González, JMF García
Pfizer, 2008
511*2008
GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus
J Ludvigsson, D Krisky, R Casas, T Battelino, L Castaño, J Greening, ...
New England Journal of Medicine 366 (5), 433-442, 2012
3902012
No effect of the altered peptide ligand NBI-6024 on β-cell residual function and insulin needs in new-onset type 1 diabetes
M Walter, A Philotheou, F Bonnici, AG Ziegler, R Jimenez, ...
Diabetes care 32 (11), 2036-2040, 2009
1402009
Epidemiología de la diabetes mellitus tipo 1 en menores de 15 años en España
SC Barreiro, MR Rigual, GB Lozano, JPL Siguero, BG Pelegrín, MPR Val, ...
Anales de pediatría 81 (3), 189. e1-189. e12, 2014
1302014
Estudios españoles de crecimiento: situación actual, utilidad y recomendaciones de uso
ES González, AC Lezcano, JMF García, AF Longás, DL De Lara, ...
Anales de pediatría 74 (3), 193. e1-193. e16, 2011
1072011
The auditory threshold in a school-age population is related to iodine intake and thyroid function
F Soriguer, MC Millón, R Munoz, I Mancha, JPL Siguero, MJM Aedo, ...
Thyroid 10 (11), 991-999, 2000
992000
Evidence for genetic heterogeneity of pseudohypoaldosteronism type 1: identification of a novel mutation in the human mineralocorticoid receptor in one sporadic case and no …
M Viemann, M Peter, JP López-Siguero, G Simic-Schleicher, WG Sippell
The Journal of Clinical Endocrinology & Metabolism 86 (5), 2056-2059, 2001
842001
CDKN1C (p57Kip2) analysis in Beckwith–Wiedemann syndrome (BWS) patients: Genotype–phenotype correlations, novel mutations, and polymorphisms
V Romanelli, A Belinchon, S Benito‐Sanz, V Martínez‐Glez, ...
American Journal of Medical Genetics Part A 152 (6), 1390-1397, 2010
762010
Improvement in growth after two years of growth hormone therapy in very young children born small for gestational age and without spontaneous catch-up growth: results of a …
J Argente, R Gracia, L Ibánez, A Oliver, E Borrajo, A Vela, ...
The Journal of Clinical Endocrinology & Metabolism 92 (8), 3095-3101, 2007
742007
Prevalencia del síndrome metabólico y sus componentes en niños y adolescentes con obesidad
LT Ceballos, JPL Siguero, AJ Ortiz
Anales de Pediatría 67 (4), 352-361, 2007
692007
Estudios españoles de crecimiento 2008. Nuevos patrones antropométricos
A Carrascosa, JM Fernández, C Fernández, A Ferrández, ...
Endocrinología y Nutrición 55 (10), 484-506, 2008
612008
A novel dysfunctional growth hormone variant (Ile179Met) exhibits a decreased ability to activate the extracellular signal-regulated kinase pathway
MD Lewis, M Horan, DS Millar, V Newsway, TE Easter, L Fryklund, ...
The Journal of Clinical Endocrinology & Metabolism 89 (3), 1068-1075, 2004
592004
Spanish growth studies 2008. New anthropometric standards.
A Carrascosa, JM Fernandez, C Fernandez, A Ferrandez, ...
Endocrinologia y nutricion: organo de la Sociedad Espanola de Endocrinologia …, 2008
512008
SRD5A2 gene mutations and polymorphisms in Spanish 46,XY patients with a disorder of sex differentiation
M Fernández‐Cancio, L Audí, P Andaluz, N Torán, C Piró, M Albisu, ...
International journal of andrology 34 (6pt2), e526-e535, 2011
432011
Effect of recombinant growth hormone on leptin, adiponectin, resistin, interleukin-6, tumor necrosis factor-α and ghrelin levels in growth hormone-deficient children
JP López-Siguero, LF López-Canti, R Espino, E Caro, ...
Journal of endocrinological investigation 34, 300-306, 2011
432011
The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances
A Monteagudo-Sánchez, JR Hernandez Mora, C Simon, A Burton, ...
Nucleic acids research 48 (20), 11394-11407, 2020
412020
Adult height in children with idiopathic short stature treated with growth hormone
JP López-Siguero, Ε Garcia-Garcia, I Carralero, MJ Martlnez-Aedo
Journal of Pediatric Endocrinology and Metabolism 13 (9), 1595-1602, 2000
402000
Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing
A Maharaj, F Buonocore, E Meimaridou, G Ruiz-Babot, L Guasti, ...
Journal of the Endocrine Society 3 (1), 201-221, 2019
382019
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Artículos 1–20