Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mirta Gryngarten"'
Autor:
Rodolfo Rey, Kenny Y Del Toro Camargo, Ignacio Bergadá, Mariana Gutierrez, Mirta Gryngarten, Paula Scaglia, Andrea Arcari, Laura E. Valinotto, Analia Freire, Laura Suarez, María Gabriela Ballerini, Mónica I Natale, María Gabriela Ropelato
Publikováno v:
International Journal of Clinical Endocrinology and Metabolism. 5:020-023
Type A Insulin Resistance Syndrome is due to heterozygous mutations in the insulin receptor (INSR) gene or its signaling pathway. We present a premenarcheal 14 year-old girl with normal BMI, severe hirsutism, acanthosis nigricans, clitoral hypertroph
Autor:
Berenice B. Mendonca, José I Labarta, Leandro Soriano-Guillén, Anna Flavia Figueiredo Benedetti, Lourdes Travieso-Suárez, Sonir Roberto Rauber Antonini, Ana Paula Abreu, Andrea de Castro Leal, Raquel Corripio, Priscila Gagliardi, Ana Claudia Latronico, Mirta Gryngarten, Maiara Ribeiro Piovesan, Luciana Ribeiro Montenegro, Andrea Arcari, Vinicius Nahime Brito, Jesús Argente, Ana Pinheiro Machado Canton, Nelmar Valentina Ortiz-Cabrera, Marina Cunha, Ursula B. Kaiser, Delanie B Macedo, Carolina Ramos, Arancha Escribano-Muñoz, Aline Guimaraes, Carlos Eduardo Seraphim
Publikováno v:
J Clin Endocrinol Metab
Context Loss-of-function mutations of makorin RING finger protein 3 (MKRN3) are the most common monogenic cause of familial central precocious puberty (CPP). Objective To describe the clinical and hormonal features of a large cohort of patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc2ac84958412f0da28ca2f0025f8938
https://europepmc.org/articles/PMC7993586/
https://europepmc.org/articles/PMC7993586/
Autor:
Andrea Arcari, E Boulgourdjian, Mirta Gryngarten, M E Escobar, Haydeé Comar, Horacio M. Domené
Publikováno v:
Archivos argentinos de pediatria. 119(5)
McCune-Albright syndrome (MAS) is a genetic disorder defined by fibrous dysplasia of bone, café-au-lait skin spots, and autonomous hyperfunction of one or more endocrine organs. MAS is caused by activating mutations of the GNAS1 gene. The most frequ
Autor:
Mirta Gryngarten, Erica A. Eugster, Karen O Klein, Bradley S. Miller, Matthew Benson, Gad B. Kletter, Nelly Mauras, Tala Dajani, Analia Freire
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Context Gonadotropin-releasing hormone agonists (GnRHas) are standard of care for central precocious puberty (CPP). A 6-month subcutaneous injection has recently been approved by the Food and Drug Administration. Objective Determine efficacy, pharmac
Autor:
M E Escobar, Mirta Gryngarten, Ignacio Bergadá, María Gabriela Ropelato, Analia Freire, María Gabriela Ballerini, Andrea Arcari
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 32(2)
Background Puberty is associated with a physiological decline in insulin sensitivity (IS). Overweight (OW) and obesity (OB) are common among girls with central precocious puberty (CPP). CPP is considered a risk factor for metabolic diseases. The aim
Autor:
M E Escobar, Mirta Gryngarten, Analia Freire, María Gabriela Ballerini, Andrea Arcari, Ignacio Bergadá, María Gabriela Ropelato
Publikováno v:
International Journal of Pediatric Endocrinology
Background In girls with Idiopathic Central Precocious Puberty (ICPP) concern has been raised by the potential impact of GnRH-analogues (GnRHa) treatment on body weight. We evaluated the effect of GnRHa on Body Mass Index (BMI) in girls with ICPP acc
Autor:
Ana Claudia Latronico, Berenice B. Mendonca, Ivo J.P. Arnhold, Sekoni D. Noel, Mario G. Santos, Shuyun Xu, Wendy Kuohung, A. P. Silveira-Neto, Mirta Gryngarten, Vinicius Nahime Brito, Suzy D.C. Bianco, Ana Paula Abreu, Ursula B. Kaiser, Leticia Ferreira Gontijo Silveira, M. E. Escobar
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 95:2276-2280
Context: Kisspeptin, encoded by the KISS1 gene, is a key stimulatory factor of GnRH secretion and puberty onset. Inactivating mutations of its receptor (KISS1R) cause isolated hypogonadotropic hypogonadism (IHH). A unique KISS1R-activating mutation w
Autor:
Andrea Arcari, M E Escobar, Ignacio Bergadá, Mirta Gryngarten, María Gabriela Ballerini, María Gabriela Ropelato, Analia Freire
Publikováno v:
Hormone research in paediatrics. 85(1)
Background: Estradiol at baseline or after a classical gonadotropin-releasing hormone test did not reflect ovarian steroidogenesis in central precocious puberty (CPP) girls. Aims: To evaluate estradiol response to depot triptorelin, both at start and
Autor:
Johannes D. Veldhuis, Valentina Alexandrovna Peterkova, Paul Saenger, Marta Barontini, Ilknur Arslanoglu, Martijn H. Breuning, María Cecilia García Rudaz, W. Oostdijk, Delphine Mitanchez, Tomasz Romer, Pierre Chatelain, Marwa E. Fahmi, Hyi-Jeong Ji, Peter J Simm, Robert L. Rosenfield, María Gabriela Ropelato, Pinchas Cohen, Conrad Savoy, Guy Van Vliet, María Gabriela Ballerini, M.H. de Ru, Mirta Gryngarten, Jürgen Kratzsch, G Bona, Mohamed El Kholy, Eileen Fowler, Samia Selim, Margaret Zacharin, Wolfgang G. Sippell, Melanie Shim, J.M. Wit, Heba Elsedfy, Elena Bolshova-Zubkovskaya, William L. Oppenheim, A. Ferrandez-Longas, Ayman E. Nassar, A. Carrascosa, Claude J. Migeon, M E Escobar, F K Grote, H.M. Zonderland, Dragan Zdravkovic, Omar Ali, S.G. Kant
Publikováno v:
Hormone Research in Paediatrics. 68:327-329
Autor:
M E Escobar, Andrea Arcari, María Gabriela Ropelato, Mirta Gryngarten, Ignacio Bergadá, Analia Freire, María Gabriela Ballerini
Publikováno v:
Clinical endocrinology. 78(3)
SummaryContext The GnRH test is the gold standard to confirm the diagnosis of central precocious puberty (CPP); however, this compound is not always readily available. Diagnostic accuracy of subcutaneous GnRH analogues tests compared to classical GnR