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Endocrinologia, Diabetes Y Nutricion|May 15, 2022
Perinatal factors influence on the neurocognitive development of children born small for gestational age (SGA) during the first 2 years of lifeMaría García Ventura, Antonio de Arriba Muñoz, Beatriz Puga González, et al.International Journal of Molecular Sciences|November 12, 2016
Association between Interleukin-6 Promoter Polymorphism (-174 G/C), Serum Interleukin-6 Levels and Mortality in Severe Septic PatientsLeonardo Lorente, María M Martín, Antonia Pérez-Cejas, et al.Clinical Case Reports|March 8, 2017
A case of congenital dyserythropoietic anemia type IVSilvia de-la-Iglesia-Iñigo, María-Isabel Moreno-Carralero, Angelina Lemes-Castellano, et al.Nature Plants|October 14, 2020
A scoping review of feed interventions and livelihoods of small-scale livestock keepersIsabelle Baltenweck, Debbie Cherney, Alan Duncan, et al.Anales De Pediatria (Barcelona, Spain : 2003)|December 21, 2010
[Different expression of the Asn264LysfsX35 mutation of the GNAS gene in a family with pseudohypoparathyroidism.]A de Arriba Muñoz, J I Labarta Aizpún, E Mayayo Dehesa, et al.Anales De Pediatria (Barcelona, Spain : 2003)|March 6, 2014
[Congenital adrenal hyperplasia due to lack of 17α-hydroxylase: a report of a new mutation in the gene CYP17A1]J I Perales Martínez, B Pina Marqués, A de Arriba Muñoz, et al.European Journal of Endocrinology|July 19, 2012
Individualised vs fixed dose of oral 17β-oestradiol for induction of puberty in girls with Turner syndrome: an open-randomised parallel trialJosé I Labarta, Maria L Moreno, Juan P López-Siguero, et al.Hormone Research in Paediatrics|August 17, 2016
Changes in Body Mass Index in Girls with Idiopathic Central Precocious Puberty under Gonadotropin-Releasing Hormone Analogue Therapy: The Spanish RegistryRaquel Corripio, Leandro Soriano-Guillén, Francisco-Javier Herrero, et al.Plos One|June 13, 2015
The 4G/4G Genotype of PAI-1 Polymorphism Is Associated with Higher Plasma PAI-1 Concentrations and Mortality in Patients with Severe SepsisLeonardo Lorente, María M Martín, Juan M Borreguero-León, et al.Anales De Pediatria (Barcelona, Spain : 2003)|March 4, 2014
[Type 1 polyglandular autoimmune syndrome associated with C322fsx372 mutation]P Roncalés-Samanes, A de Arriba Muñoz, G M Lou Francés, et al.Pageof 33