Results 111 to 120 of about 29,953 (181)

Genotypic Findings in Noonan and Non-Noonan RASopathies and Patient Eligibility for Growth Hormone Treatment. [PDF]

open access: yesJ Clin Med, 2023
Carcavilla A   +14 more
europepmc   +1 more source

Interrelaciones del perfil osteomineral y la obesidad en la edad pediátrica

open access: yes, 2014
1. Introducción o motivación de la tesis Desde una perspectiva epidemiológica, la obesidad se está convirtiendo en el principal enemigo de la salud pública en la mayoría de los países occidentales.
Romero Urrutia, Alicia
core  

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

open access: yesArch Endocrinol Metab
Faria AG   +17 more
europepmc   +1 more source

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

open access: yesBiomedica
Medina D   +8 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]

open access: yesEndocrinol Diabetes Nutr, 2022
Ariza Jimenez AB   +2 more
europepmc   +1 more source

Monitoring of the treatment of hypogonadotropic hypogonadism in the infant

open access: yesAnales de Pediatría (English Edition), 2019
María Álvarez Casaño   +1 more
doaj   +1 more source

Pruebas dinámicas en endocrinología pediátrica: pubertad precoz central

open access: yes, 2009
Precocious puberty is defined as the onset of puberty before the age of 8 years in girls and 9 years in boys; however, it may be affected by factors such as race, low birth weight and obesity.
Balthazar, Vital   +3 more
core  

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

open access: yesRev Med Inst Mex Seguro Soc
Contreras-Vargas LM   +9 more
europepmc   +1 more source

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

open access: yesHum Reprod Open
Carriço JN   +42 more
europepmc   +1 more source

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

open access: yesAdv Lab Med, 2023
Bravo Nieto D   +8 more
europepmc   +1 more source

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