Results 71 to 80 of about 651 (115)

Cyclophosphamide post-haploidentical stem cell transplantation experience in an infant with IPEX syndrome [PDF]

Biomedica
Medina D, Ariza-Insignares C, Restrepo A, Devia Á, Franco A, Lemus R, Olaya M, Milanés R, Pachajoa H.   +8 more
europepmc   +1 more source

Families' perspectives and the development of an educational program for diabetes in schools. [PDF]

J Pediatr (Rio J)
Cudizio L, Brambilla IR, Araújo KGM, Lot RG, Martins TO, Biasi RR, Galeote G, Costa-Riquetto AD, Salles JEN, Calliari LE.   +9 more
europepmc   +1 more source

[Likely impact of COVID-19 on referrals to pediatric endocrinology: Increased incidence of precocious puberty in a third-level hospital]. [PDF]

Endocrinol Diabetes Nutr, 2022
Ariza Jimenez AB, Aguilar Gomez-Cardenas FJ, de la Camara Moraño C.   +2 more
europepmc   +1 more source

Monitoring of the treatment of hypogonadotropic hypogonadism in the infant

Anales de Pediatría (English Edition), 2019
María Álvarez Casaño, Juan Pedro López Siguero   +1 more
doaj   +1 more source

[Brown tumor due to hyperparathyroidism secondary to chronic kidney disease: A clinical case]. [PDF]

Rev Med Inst Mex Seguro Soc
Contreras-Vargas LM, Sánchez-Cuevas M, Haro-Sandoval Y, Paque-Bautista C, González AP, Reyes-Sosa AM, Flores-Rodríguez R, Murguía-Pérez M, Guisao-Valencia CA, Sosa-Bustamante GP.   +9 more
europepmc   +1 more source

Genetic architecture of congenital hypogonadotropic hypogonadism: insights from analysis of a Portuguese cohort. [PDF]

Hum Reprod Open
Carriço JN, Gonçalves CI, Al-Naama A, Syed N, Aragüés JM, Bastos M, Fonseca F, Borges T, Pereira BD, Pignatelli D, Carvalho D, Cunha F, Saavedra A, Rodrigues E, Saraiva J, Ruas L, Vicente N, Martin Martins J, De Sousa Lages A, Oliveira MJ, Castro-Correia C, Melo M, Martins RG, Couto J, Moreno C, Martins D, Oliveira P, Martins T, Martins SA, Marques O, Meireles C, Garrão A, Nogueira C, Baptista C, Gama-de-Sousa S, Amaral C, Martinho M, Limbert C, Barros L, Vieira IH, Sabino T, Saraiva LR, Lemos MC.   +42 more
europepmc   +1 more source

Patient with adrenal insufficiency due to a de novo mutation in the NR0B1 gene. [PDF]

Adv Lab Med, 2023
Bravo Nieto D, García Fernández AS, Díaz Troyano N, Arnaiz MG, Arias García A, Fernández Álvarez P, Campos Martorell A, Ferrer Costa R, Clemente León M.   +8 more
europepmc   +1 more source

Transforming tallness: how sex steroids influence final height in Marfan syndrome. [PDF]

J Pediatr (Rio J)
Yamaguchi ABC, Siviero-Miachon AA, Okuda PMM, Oliveira E Silva LC, Bustamante TF, Spinola-Castro AM.   +5 more
europepmc   +1 more source

The impact of COVID-19 in children and adolescents with obesity in Brazil. [PDF]

Arch Endocrinol Metab, 2022
Pelicciari CR, Artioli TO, Longui CA, Monte O, Kochi C.   +4 more
europepmc   +1 more source

Pseudohipoaldosteronismo y aparente exceso de mineralocorticoides. Cara y ceca en dos pacientes pediátricos

Revista del Hospital Italiano de Buenos Aires
Los síndromes endocrinológicos con hipofunción o hiperfunción con niveles paradójicos de dosajes hormonales han sido bien caracterizados en los últimos años del siglo XX, a partir del desarrollo de técnicas genéticas y moleculares.
María Florencia Kuspiel, Guillermo Alonso   +1 more
doaj