Zobrazeno 1 - 10
of 16
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
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
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 (
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
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
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
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
Autor:
Sally Radovick, Mariam Gangat
Publikováno v:
Pituitary Disorders of Childhood ISBN: 9783030113384
This review will summarize pituitary development and function, as well as review defects in transcription factor genes PROP1 and POU1F1, which play a critical role in pituitary cell differentiation. These selected factors have been well described in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea920fba69cd0cf47b387ffee5f28a2d
https://doi.org/10.1007/978-3-030-11339-1_2
https://doi.org/10.1007/978-3-030-11339-1_2