Výsledky vyhledávání - "Brittany K. Wise-Oringer"

Salivary microbiome differences in prepubertal children with and without adrenal androgen excess

Autor: Anne-Catrin Uhlemann, Brittany K. Wise-Oringer, Sharon E. Oberfield, Heekuk Park, Richard J. Auchus, Anne Claire Burghard

Publikováno v: Pediatric research. 91(7)

Premature adrenarche is a condition of childhood adrenal androgen excess (AAE) in the absence of gonadotropin-dependent puberty, and has been linked to insulin resistance and progression to metabolic syndrome. Microbial dysbiosis is associated with p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9027cbfedf3ffed7ba5f12bdd19516
https://pubmed.ncbi.nlm.nih.gov/34341500

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The Unique Role of 11-Oxygenated C19 Steroids in Both Premature Adrenarche and Premature Pubarche

Autor: Richard J. Auchus, Ilene Fennoy, Renu Nandakumar, Sharon E. Oberfield, Aviva B. Sopher, Brittany K. Wise-Oringer, Patricia M Vuguin, Kristen M. Williams, Patrick O’Day, Abeer Hassoun, Anne Claire Burghard, Donald J. McMahon

Publikováno v: Horm Res Paediatr

Introduction: Recent studies have shown 11-oxygenated androgens (11oAs) are the dominant androgens in premature adrenarche (PA). Our objective was to compare 11oAs and conventional androgens in a well-defined cohort of children with PA or premature p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c963177085e17f74c75b6f697c00d12c
https://pubmed.ncbi.nlm.nih.gov/33530089

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OR27-06 11-Oxygenated C19 Steroids Are Alternative Markers of Androgen Excess in Children with Premature Adrenarche and Premature Pubarche

Autor: Brittany K. Wise-Oringer, Aviva B. Sopher, Patricia M Vuguin, Sharon E. Oberfield, Ilene Fennoy, Kristen M. Williams, Anne Claire Burghard, Abeer Hassoun, Renu Nandakumar, Patrick O’Day, Richard J. Auchus

Publikováno v: Journal of the Endocrine Society

Premature adrenarche (PA), the early onset of pubic hair and/or axillary hair/odor in children, is associated with elevated adrenal androgens and precursors in the absence of gonadotropin-dependent puberty. Laboratory data in PA classically demonstra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e6301e657ec9f72461c25d1963f618d
http://europepmc.org/articles/PMC7209282

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Thyroid Ultrasound: More Sensitive than Radioactive Iodine Imaging in Detecting Recurrence of Papillary Thyroid Cancer in Two Pediatric Patients

Autor: Brittany K. Wise-Oringer, Robert Rapaport, Michelle Klein, Josef Machac, Henrietta Kotlus Rosenberg, Marina Goldis, Molly O. Regelmann

Publikováno v: Hormone Research in Paediatrics. 90:66-72

Background: Papillary thyroid cancer (PTC) is an uncommon pediatric disease with an excellent prognosis. In follow-up surveillance, neck ultrasound (US), basal and thyroid-stimulating hormone-stimulated serum thyroglobulin (Tg) levels, and diagnostic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bed9f9d1428c6c1c420b7e7f07749ea8
https://doi.org/10.1159/000487436

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Familial X-Linked Acrogigantism: Postnatal Outcomes and Tumor Pathology in a Prenatally Diagnosed Infant and His Mother

Autor: Rebecca J Gordon, George Zanazzi, Sharon L. Wardlaw, Jeffrey H. Wisoff, Brittany K. Wise-Oringer, Raphael David, Christopher William, Wendy K. Chung, Brenda Kohn, Sharon E. Oberfield, Kwame Anyane-Yeboa

Publikováno v: J Clin Endocrinol Metab

ContextX-linked acrogigantism (X-LAG), a condition of infant-onset acrogigantism marked by elevated GH, IGF-1, and prolactin (PRL), is extremely rare. Thirty-three cases, including three kindreds, have been reported. These patients have pituitary ade

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c34404d70a00b0402121101b4c92f10
https://europepmc.org/articles/PMC6736216/

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SAT-463 Familial X-Linked Acrogigantism: Postnatal Outcomes and Tumor Pathology in a Prenatally Diagnosed Infant and His Affected Mother

Autor: Brenda Kohn, Christopher William, Brittany K. Wise-Oringer, Sharon L. Wardlaw, Rebecca J Gordon, George Zanazzi, Sharon E. Oberfield, Jeffrey H. Wisoff

Publikováno v: Journal of the Endocrine Society

Background: X-linked acrogigantism (X-LAG), a condition of infant-onset acrogigantism marked by elevated levels of GH, IGF-1, and PRL, is extremely rare with 33 cases reported in the literature (1), including 7 total familial cases from 3 kindreds. C

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e2d77504a812601e59579f49ee28e11
http://europepmc.org/articles/PMC6551907

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