Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ruta Navardauskaite"'
Autor:
Dovile Denaite, Ruta Navardauskaite
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Aim of the studyTo evaluate the clinical characteristics and treatment efficacy of patients with severe primary IGF-1 deficiency (PSIGFD) using a recombinant IGF-1 (rhIGF-1).Objectives of the studyTo examine the clinical characteristics of patients w
Externí odkaz:
https://doaj.org/article/0d5503c468b440adabe54d4ba8dfa756
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundThe effects of long-term glucocorticoid (GC) treatment on bone mineral density (BMD) in patients with congenital adrenal hyperplasia (CAH) remain controversial.ObjectivesThis cross-sectional study aimed to evaluate BMD in relation to genoty
Externí odkaz:
https://doaj.org/article/7de6117b04e341eb95221871d04f9f31
Autor:
Ruta Navardauskaite, Kristina Semeniene, Marius Sukys, Agne Pridotkaite, Aurika Vanckaviciene, Birute Zilaitiene, Rasa Verkauskiene
Publikováno v:
Medicina, Vol 58, Iss 4, p 500 (2022)
Background and objectives: Data on long-term cardiometabolic consequences in patients with congenital adrenal hyperplasia (CAH) are controversial. The aim of our study was to evaluate body mass index (BMI), body composition, blood pressure (BP) and i
Externí odkaz:
https://doaj.org/article/ebb66cbb00c3401d950bf41a8a770482
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6628f851aa0e95993c57de420ce01bab
https://doi.org/10.1530/endoabs.90.ep928
https://doi.org/10.1530/endoabs.90.ep928
Autor:
Guftar Shaikh, Ruta Navardauskaite, Enza Mozzillo, Antonia Dastamani, Zdenek Sumnik, Klaus Mohnike, Kristina Casteels, S Faisal Ahmed, Jillian Bryce, Lukas Plachy, Hoong-Wei Gan, Klara Rozenkova, Susann Empting, Rasa Verkauskiene, Annemarie A. Verrijn Stuart, Giulio Maltoni
Publikováno v:
Hormone Research in Paediatrics. 94:1-445
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19088be5f2ef8dbff0628a53f4acaa4e
https://doi.org/10.1159/000518849
https://doi.org/10.1159/000518849
Vitamin d status and bone health in adolescents and young adults with congenital adrenal hyperplasia
Autor:
Ruta Navardauskaite, Kristina Semeniene, Neringa Umaraite, Emile Rudminaite, Aurika Vanckaviciene, Rasa Verkauskiene
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bc39307f8e038108d951d6db45741ff
https://doi.org/10.1530/endoabs.81.p291
https://doi.org/10.1530/endoabs.81.p291
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80d746ecc29e6100c69d244abb5e7842
https://doi.org/10.1530/endoabs.73.aep598
https://doi.org/10.1530/endoabs.73.aep598
Autor:
Aurika Vanckaviciene, Rasa Verkauskiene, Indre Petraitiene, Ruta Navardauskaite, Kristina Liesionyte
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::629a3bd6cc1703484664de56f1cfbc27
https://doi.org/10.1530/endoabs.70.aep95
https://doi.org/10.1530/endoabs.70.aep95
Autor:
Rasa Verkauskiene, Ruta Navardauskaite
Disturbance of sodium and water is the most common disorders in clinical practice because of high prevalence of diseases associated with dehydration. Hyponatremia (serum sodium less than 135 mmol/L) and hypernatremia (serum sodium level above 145 mmo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4543d30e3223cf168d35d82460d59de3
https://doi.org/10.1016/b978-0-12-801238-3.65418-1
https://doi.org/10.1016/b978-0-12-801238-3.65418-1
Autor:
Ondrej Cinek, Roland Pfaeffle, Jan Lebl, Barbora Obermannova, Dalia Adukauskiene, Ruta Navardauskaite, Rasa Verkauskiene, Natalija Smetanina, Werner F. Blum, Petra Dusatkova
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 99:299-306
PROP1 gene mutations cause multiple pituitary hormone deficiency (MPHD).We sought to expand experience with PROP1 mutation carriers by studying a large cohort of Lithuanian patients.Sixty-seven MPHD patients were tested for PROP1 defects. Perinatal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb68a1a6dccca84dac8a38603ff9079b
https://doi.org/10.1210/jc.2013-3090
https://doi.org/10.1210/jc.2013-3090