Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Elka Jacobson-Dickman"'
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 02, Pp e243-e245 (2016)
Abstract Introduction Neonatal thyrotoxicosis is a life-threatening condition with potentially irreversible neurologic sequelae. Most cases are seen in neonates born to mothers with Graves' disease. Topical iodine–induced hypothyroidism has been
Externí odkaz:
https://doaj.org/article/836f914c8ce3404792cbc23a77e57b39
Autor:
Roja Motaghedi, Elka Jacobson-Dickman, Apoorva Ravindranath Waikar, Irina Kazachkova, Prabhsimranjot Singh, Ludovico Guarini, Sonali Malhotra
Publikováno v:
World Journal of Oncology
Adrenocortical carcinoma (ACC) is a rare malignancy and even rarer in infancy. Most of these tumors in pediatric age group are hormonally active and predominantly present with virilization. Cortisol hypersecretion presenting as Cushing syndrome is ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a42c6e0dc757b4a898d5481a5741053e
https://doi.org/10.14740/wjon1036w
https://doi.org/10.14740/wjon1036w
Publikováno v:
Pediatric Emergency Care. 33:e27-e29
Herein, we report a case of a 12-year-old girl who presented with diabetic ketoacidosis and a leukemoid reaction. Although this association has been described in a few adult patients, pediatric cases have not been reported. A leukemoid reaction is co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::466ac492035f5bca2990c078cf75da48
https://doi.org/10.1097/pec.0000000000000558
https://doi.org/10.1097/pec.0000000000000558
Autor:
Marc Jeanpierre, Jacques Young, Ana Paula Abreu, Magdalena Avbelj Stefanija, Ravikumar Balasubramanian, Svetlana Ten, Nelly Pitteloud, Albert Schinzel, Lacey Plummer, Margaret G. Au, Radhika Purushothaman, Ana Claudia Latronico, Andrew A. Dwyer, Elka Jacobson-Dickman, Gerasimos P. Sykiotis, Jose C. Florez, Richard Quinton, Michel Pugeat, Simon H. S. Pearce, James F. Gusella, Catherine Dodé, Tim Cheetham, William F. Crowley
Publikováno v:
Human Molecular Genetics, vol. 21, no. 19, pp. 4314-4324
Congenital gonadotropin-releasing hormone (GnRH) deficiency manifests as absent or incomplete sexual maturation and infertility. Although the disease exhibits marked locus and allelic heterogeneity, with the causal mutations being both rare and priva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cea752603930973e97e52b1d3e031a14
http://doc.rero.ch/record/295559/files/dds264.pdf
http://doc.rero.ch/record/295559/files/dds264.pdf
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 99:1132-1141
Although vitamin D toxicity is rare in children, increased use of vitamin D formulations, re-examination of optimal vitamin D levels, and use of higher doses lend potential for an increased incidence of vitamin D toxicity.A PubMed search was conducte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea820292d4e1ea5ad4a8495b4a4b3865
https://doi.org/10.1210/jc.2013-3655
https://doi.org/10.1210/jc.2013-3655
Publikováno v:
American Journal of Perinatology Reports, Vol 06, Iss 02, Pp e243-e245 (2016)
AJP Reports
AJP Reports
Introduction Neonatal thyrotoxicosis is a life-threatening condition with potentially irreversible neurologic sequelae. Most cases are seen in neonates born to mothers with Graves' disease. Topical iodine–induced hypothyroidism has been reported in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b44fe273537503e855f642cf0bbd3fe
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1584879
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1584879
Publikováno v:
Pediatrics in review. 37(3)
1. Ximena Lopez, MD* 2. Sunita Stewart, PhD† 3. Elka Jacobson-Dickman, MD‡ 1. *Department of Pediatrics, Division of Pediatric Endocrinology, University of Texas Southwestern Medical Center, Dallas TX. 2. †Department of Psychiatry, University o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e970699579ada0269d2124c7738ead1a
https://pubmed.ncbi.nlm.nih.gov/26933223
https://pubmed.ncbi.nlm.nih.gov/26933223
Publikováno v:
IBMS BoneKEy. 7:63-83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f07d3adc67a9070dfe13453410b52243
https://doi.org/10.1138/20100429
https://doi.org/10.1138/20100429
Autor:
Susan E Sparks, Frances J. Hayes, Virginia A. Hughes, Huaibin Chen, Andrew A. Dwyer, Jinghong Ma, Hélène B. Lavoie, Taneli Raivio, Abir Mukherjee, Guy Van Vliet, Nelly Pitteloud, Ursula B. Kaiser, Lacey Plummer, Richard Quinton, Shuyun Xu, Moosa Mohammadi, Elka Jacobson-Dickman, Yisrael Sidis
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 94:4380-4390
FGFR1 mutations have been identified in about 10% of patients with Kallmann syndrome. Recently cases of idiopathic hypogonadotropic hypogonadism (IHH) with a normal sense of smell (nIHH) have been reported.The objective of the study was to define the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::430feac5e085d29beca76e026fa66ef3
https://doi.org/10.1210/jc.2009-0179
https://doi.org/10.1210/jc.2009-0179
Autor:
Lacey Plummer, Lindsay W. Cole, John L. Falardeau, Richard Quinton, Andrew A. Dwyer, Céline Huot, Andrew Beenken, Anna V. Eliseenkova, Jinghong Ma, Simon H. S. Pearce, Nelly Pitteloud, Elka Jacobson-Dickman, Wilson C. J. Chung, Yisrael Sidis, Natalie Alois, Sandra Na, Janet E. Hall, Pei Tsai, Moosa Mohammadi, Taneli Raivio, Virginia A. Hughes
Publikováno v:
Journal of Clinical Investigation. 118:2822-2831
Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS) or with a normal sense of smell (normosmic IHH; nIHH) are heterogeneous genetic disorders associated with deficiency of gonadotropin-releasing hormone (GnRH). While l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::115215432b2a74ee6d5d45ff46de01a3
https://doi.org/10.1172/jci34538
https://doi.org/10.1172/jci34538