Results 111 to 120 of about 5,091 (183)

Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series. [PDF]

Arch Endocrinol Metab
Faria AG, Montenegro LR, Jorge AAL, Martin RM, Fragoso MCBV, Tinano FR, Seraphim CE, Canton APM, Gomes LG, Martos-Moreno GA, García IT, Carcavilla A, Tirado-Capistros M, Souza-Pinto NC, Argente J, Latronico AC, Mendonca BB, Brito VN.   +17 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

[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

Bringing the Pediatric Endocrine Spanish Speaking Community Together: First Virtual Pediatric Endocrine Meeting in Low- and Middle-Income Countries in Central and South America.

Interact J Med Res, 2023
Bogarin R, Elizondo L, Kalaitzoglou E, Popovic J, Rogol A, Richmond E, Chanoine JP, Lopez-Pedrosa JM, Ruiz Salazar F, Vuguin P.   +9 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  

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

Lessons of screening two million newborns for congenital adrenal hyperplasia: 10-year experience of the Minas Gerais Public Health Program. [PDF]

J Pediatr (Rio J)
Botelho Barra C, Souza Sena G, Pereira Oliveira H, de Paula Gonzaga ALAC, Ferreira Araújo R, Ramos Villela T, Machado Mantovani R, Nélio Januário J, Novato Silva I.   +8 more
europepmc   +1 more source