Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mariam, Gangat"'
Publikováno v:
Endocrines, Vol 3, Iss 4, Pp 736-744 (2022)
Short stature is a common reason for a child to visit the endocrinologist, and can be a variant of normal or secondary to an underlying pathologic cause. Pathologic causes include growth hormone deficiency (GHD), which can be congenital or acquired l
Externí odkaz:
https://doaj.org/article/11b73ddea4c64117a4e5a1afdb3aa23e
Autor:
Youn Hee Jee, Mariam Gangat, Olga Yeliosof, Adrian G. Temnycky, Selena Vanapruks, Philip Whalen, Evgenia Gourgari, Cortney Bleach, Christine H. Yu, Ian Marshall, Jack A. Yanovski, Kathleen Link, Svetlana Ten, Jeffrey Baron, Sally Radovick
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
PurposeCongenital hypopituitarism usually occurs sporadically. In most patients, the etiology remains unknown.MethodsWe studied 13 children with sporadic congenital hypopituitarism. Children with non-endocrine, non-familial idiopathic short stature (
Externí odkaz:
https://doaj.org/article/773e06597021478bb0b5917abde9cc0c
Autor:
Kathryn M. Sumpter, Sadana Balachandar, Janine Sanchez, Robert Rapaport, Anastasia Albanese-O'Neill, Catherina T. Pinnaro, Srinath Sanda, Alissa J. Roberts, Jenise C. Wong, Saketh Rompicherla, Shideh Majidi, Mary Pat Gallagher, Mariam Gangat, Osagie Ebekozien, Abha Choudhary, Tossaporn Seeherunvong, Brynn E. Marks, Ana L. Creo, Liana Gabriel, Meredith Wilkes, Guy T. Alonso, Jamie R. Wood, Anna Cymbaluk, Sarah K. Lyons, Neha S. Patel, Jose Jimenez-Vega
Publikováno v:
Journal of diabetes, vol 13, iss 8
Journal of Diabetes
Journal of Diabetes
Background Diabetes is a risk factor for poor COVID‐19 outcomes, but pediatric patients with type 1 diabetes are poorly represented in current studies. Methods T1D Exchange coordinated a US type 1 diabetes COVID‐19 registry. Forty‐six diabetes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71fd0657e9ca7e8412e91b65699b4676
https://doi.org/10.1111/1753-0407.13184
https://doi.org/10.1111/1753-0407.13184
Autor:
Youn Hee Jee, Mariam Gangat, Benjamin Hauser, Bethany Mancuso, Jennifer Miller, Sally Radovick
Publikováno v:
Journal of the Endocrine Society. 6:A579-A580
Splicing variants in the exon-intron boundaries of the GH1 gene have been reported to cause autosomal dominant growth hormone deficiency (GHD type 2). However, whether variants in the intron consensus sequence (XGGG repeats) have an important role in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e21d8418db0f0689171155701b12912
https://doi.org/10.1210/jendso/bvac150.1201
https://doi.org/10.1210/jendso/bvac150.1201
Autor:
Evgenia Gourgari, Olga Yeliosof, Adrian G. Temnycky, Selena Vanapruks, Philip Whalen, Jack A. Yanovski, Christine Yu, Sally Radovick, Kathleen Link, Svetlana Ten, Jeffrey Baron, Cortney C. Bleach, Ian Marshall, Youn Hee Jee, Mariam Gangat
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in Genetics
PurposeCongenital hypopituitarism usually occurs sporadically. In most patients, the etiology remains unknown.MethodsWe studied 13 children with sporadic congenital hypopituitarism. Children with non-endocrine, non-familial idiopathic short stature (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c4a5b8d6e32eb920035807a509a6d6
https://www.frontiersin.org/articles/10.3389/fgene.2021.697549/full
https://www.frontiersin.org/articles/10.3389/fgene.2021.697549/full
Autor:
Mariam GANGAT, Sally RADOVICK
Publikováno v:
Minerva pediatrica. 72(6)
Precocious puberty (PP) is a common reason for referral to pediatric endocrinology clinics, with a strong female predominance. PP is a broad term encompassing benign variants of normal development, gonadotropin-dependent precious puberty (GDPP), and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43cd83a73abd7f23300e92b879651f6f
https://pubmed.ncbi.nlm.nih.gov/32748611
https://pubmed.ncbi.nlm.nih.gov/32748611
Autor:
Youn Hee Jee, Kathleen Link, Selena Vanapruks, Jeffrey Baron, Svetlana Ten, Sally Radovick, Mariam Gangat, Evgenia Gourgari, Jack A. Yanovski, Adrian G. Temnycky, Olga Yeliosof
Publikováno v:
Journal of the Endocrine Society
Congenital hypopituitarism usually occurs in a child without a family history of pituitary disease. Explanations for such sporadic occurrence include: 1) monogenic inheritance (recessive or de novo), 2) digenic/oligogenic inheritance, and/or 3) nonge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a1cde0a6bf6b086489a35c0897cd2d0
https://doi.org/10.1210/jendso/bvaa046.1477
https://doi.org/10.1210/jendso/bvaa046.1477
Autor:
Mariam Gangat, Sadana Balachandar, Stacey Johnson, Kandy Bahadur, Joann Carlson, Benjamin Lentzner
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:469-472
Background: Subcutaneous fat necrosis (SCFN) is a rare, self-limiting condition that has been associated with several complications including hypercalcemia. Case presentation: We present the case of a 6-week-old male who presented to his pediatrician
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e2437caed01830fe311fa47c1edff03
https://doi.org/10.1515/jpem-2017-0365
https://doi.org/10.1515/jpem-2017-0365
Autor:
Mariam, Gangat, Sally, Radovick
Publikováno v:
Endocrinology and Metabolism Clinics of North America. 46:247-257
This article summarizes pituitary development and function as well as specific mutations of genes encoding the following transcription factors: HESX1, LHX3, LHX4, POU1F1, PROP1, and OTX2. Although several additional genetic defects related to hypopit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e631d57b9ca2381e3b33d1ef8b24a87
https://doi.org/10.1016/j.ecl.2017.01.003
https://doi.org/10.1016/j.ecl.2017.01.003
Autor:
Mariam Gangat, Olga Yeliosof
Publikováno v:
Current opinion in pediatrics. 31(4)
This review summarizes pituitary function, and the clinical presentation and treatment of hypopituitarism.Updates in the field include new guidelines and meta-analyses on the diagnosis and treatment of select hormone deficiencies, novel treatment opt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ec6a05e3c2e92bd54fc484935e3875
https://pubmed.ncbi.nlm.nih.gov/31082937
https://pubmed.ncbi.nlm.nih.gov/31082937