Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lindsey A. Loomba-Albrecht"'
The process of puberty is part of an ongoing process that begins during fetal development and ends with sexual maturity. Early in gestation, GnRH secreting neurons gain functionality as a GnRH pulse generator. Pulsatile GnRH secretion results in puls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be02e9ebcdd2bc179ac829b3d8dfa6d1
https://doi.org/10.1016/b978-0-12-801238-3.65353-9
https://doi.org/10.1016/b978-0-12-801238-3.65353-9
Publikováno v:
Hormone Research in Paediatrics. 73:482-486
Background/Aims: Autosomal dominant pseudohypoaldosteronism type 1 is caused by mutations in the mineralocorticoid receptor (NR3C2) gene, often leading to life-threatening hyponatremia and hyperkalemia in the newborn period. We report a novel mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f89bb25f61c04af554bbec6e9deec6
https://doi.org/10.1159/000281290
https://doi.org/10.1159/000281290
Publikováno v:
Clinical Therapeutics. 31:816-820
Background: Neonatal diabetes mellitus (NDM) is rare, with a prevalence of ∼1 in 500,000 infants worldwide. NDM may be caused by several different genetic abnormalities, and might either be transient (TNDM) or permanent. Until recently, clinical ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10e369891f6b892607387eea77ebf558
https://doi.org/10.1016/j.clinthera.2009.04.003
https://doi.org/10.1016/j.clinthera.2009.04.003
Publikováno v:
Endocrinology and metabolism clinics of North America. 43(3)
Endocrine changes (including adrenal insufficiency, disorders of growth and puberty, thyroid dysfunction, metabolic abnormalities and osteopenia) accompany human immunodeficiency virus (HIV) infection in pediatric patients. The cause of these changes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1e4f473db379c1a9a6a98919cf7b34
https://pubmed.ncbi.nlm.nih.gov/25169569
https://pubmed.ncbi.nlm.nih.gov/25169569
Publikováno v:
Diabetes Research and Clinical Practice. 87:e23-e25
Maturity-onset diabetes of the young (MODY) is a group of disorders accounting for 2–5% of diabetes; MODY2 is caused by inactivating GCK mutations. We report a case of MODY2 caused by a novel GCK mutation and demonstrate differential glycemic/C-pep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dcc8ae39826fae567f27acb2f4d2a64
https://doi.org/10.1016/j.diabres.2009.11.013
https://doi.org/10.1016/j.diabres.2009.11.013
Publikováno v:
World journal of pediatrics : WJP. 9(2)
Puberty is a complex and dynamic period in development during which individuals transition from the juvenile to adult state. Regulated by multiple genetic and endocrine controls, it is characterized by somatic growth and sexual maturation. Sexual pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a467c53816403b7b7d91bb4a142a05
https://pubmed.ncbi.nlm.nih.gov/23677828
https://pubmed.ncbi.nlm.nih.gov/23677828
Publikováno v:
Pediatric annals. 41(4)
Puberty is a complex process of developmental change regulated by multiple genetic and endocrine controls. Abnormal pubertal development (both precocious and delayed puberty) can cause significant distress to the patient and may in some instances be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60fe2b95fc84cba534a33da40c255737
https://pubmed.ncbi.nlm.nih.gov/22494212
https://pubmed.ncbi.nlm.nih.gov/22494212
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 24(3-4)
OBJECTIVE Descriptive data characterizing the frequency of various chief complaints and presenting symptomatology in children with hyperthyroidism are lacking. Furthermore, difficulties in recognizing atypical presentations may delay diagnosis and in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2148f82db7878a9e707cd3f253195681
https://pubmed.ncbi.nlm.nih.gov/21648275
https://pubmed.ncbi.nlm.nih.gov/21648275