Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Moris Angulo"'
Autor:
Jennifer Abuzzahab, Moris Angulo, Lynne Bird, Merlin Butler, Neil Cowen, Evelien Gevers, Anthony Goldstone, Patricia Hirano, Laura Konczal, Melissa Lah, Verghese Mathew, Jorge Mejia Corletto, Jennifer Miller, Kathryn Obrynba, Parisa Salehi, M Guftar Shaikh, Ashley Shoemaker, David Stevenson, David Viskochil, John Wilding, Michael Woloschak, Jack Yanovski, Eric Felner
Publikováno v:
Journal of the Endocrine Society. 6:A15-A16
Background Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental condition, characterized by hyperphagia, obesity, hormone deficiencies and behavioral/psychological manifestations. DCCR is under investigation as a treatment for hyperphagia
Autor:
Michael Woloschak, Jennifer Miller, Eric Felner, Lynne Bird, Moris Angulo, Jorge Mejia-Corletto, Evelien Gevers, Ashley Shoemaker, Jack Yanovski, Merlin Butler, Parisa Salehi, David Stevenson, John Wilding, Jennifer Abuzzahab, Laura Konczal, M Guftar Shaikh, David Viskochil, Melissa Lah, Verghese Mathew, Kristen Yen, Anish Bhatnagar, Kathryn Obrynba
Publikováno v:
Journal of the Endocrine Society. 6:A35-A36
Background Prader-Willi syndrome (PWS), a rare genetic neurobehavioral-metabolic condition, is characterized by hyperphagia, accumulation of excess fat, hypotonia, and behavioral/psychological complications. There are no currently approved medication
Autor:
Evelien Gevers, Jennifer Miller, Merlin Butler, Nicola Bridges, Tony Goldstone, Kathryn Obrynba, Parisa Salehi, Eric Felner, Lynne Bird, Ashley Shoemaker, Laura Konczal, Melissa Lah, Jack Yanovski, Moris Angulo, Jorge Mejia-Corletto, David Stevenson, John Wilding, Jennifer Abuzzahab, Guftar Shaikh, David Viskochil, Verghese Mathew, Kristen Yen, Michael Woloschak, Anish Bhatnagar
Publikováno v:
Endocrine Abstracts.
Autor:
Alberto Pietropoli, Nicky Kelepouris, Vlady Ostrow, Moris Angulo, Maithé Tauber, M. Jennifer Abuzzahab
Publikováno v:
International Journal of Pediatric Endocrinology, Vol 2020, Iss 1, Pp 1-8 (2020)
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology, BioMed Central, 2020, 2020 (1), pp.20. ⟨10.1186/s13633-020-00090-6⟩
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology, BioMed Central, 2020, 2020 (1), pp.20. ⟨10.1186/s13633-020-00090-6⟩
BackgroundGrowth hormone (GH) deficiency is common in patients with Prader-Willi syndrome (PWS) and leads to short adult stature. The current study assessed clinical outcomes based on real-world observational data in pediatric patients with PWS who w
Publikováno v:
Journal of the Endocrine Society
Polyorchidism is defined as the presence of two or more testis. We report an interesting case of Tetraorchidism an extremely rare type of Polyorchidism in a 14-year-old boy with short stature due to Growth hormone deficiency. An extensive review of l
Publikováno v:
American Journal of Medical Genetics Part A.
Psychosis is a relatively common psychiatric phenomenon seen in patients with Prader-Willi Syndrome (PWS). However, the presentation is atypical and difficult to classify within currently defined affective or psychotic disorders. This distinct presen
Publikováno v:
Journal of the Endocrine Society
Background: The American Norditropin® Studies: Web-Enabled Research (ANSWER) Program and the NordiNet® International Outcome Study (NordiNet® IOS) are complementary, large-scale, non-interventional studies designed to gather long-term data on the
Autor:
Moris Angulo, Mariano Castro-Magana
Publikováno v:
Journal of the Endocrine Society
Baseline a.m ACTH and Cortisol levels in Children with Prader-Willi-syndrome are no different from general population. Moris Angulo, MD1 & Mariano Castro-Magaña, MD1 1Dept of Peds, NYU-Winthrop Hospital, New York, NY Background Prader-Willi syndrome
Publikováno v:
Journal of child and adolescent psychopharmacology. 29(4)
Objective: To examine the role of Guanfacine Extended Release (GXR) in the management of behavioral disturbances in patients with Prader-Willi Syndrome (PWS). Methods: Twenty from a total of 27 individuals with genetically confirmed PWS, 6-26 years o
Autor:
Moris Angulo
Publikováno v:
Common Problems in the Newborn Nursery ISBN: 9783319956718
Ambiguity of a newborn’s genitalia or clinical situations in which determining the sex of a newborn is not clear represent a true dilemma in the nursery. Ambiguous genitalia are due to under-masculinization of genetic males or virilization of genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c33d846b36a760b1f2ede2dfcd9ac9a8
https://doi.org/10.1007/978-3-319-95672-5_19
https://doi.org/10.1007/978-3-319-95672-5_19