Zobrazeno 1 - 10
of 81
pro vyhledávání: '"Lecka-Ambroziak A"'
Autor:
Anna Maria Wędrychowicz, Katarzyna Doleżal-Ołtarzewska, Agata Zygmunt-Górska, Anna Urszula Kalicka-Kasperczyk, Katarzyna Tyrawa, Malgorzata Wojcik, Dominika Janus, Adrianna Kot, Agnieszka Lecka-Ambroziak, Elzbieta Petriczko, Joanna Wielopolska, Jerzy Starzyk
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
BackgroundIt has been reported that central adrenal insufficiency (CAI) in pediatric patients (pts) with Prader–Willi syndrome (PWS) may be a potential cause of their sudden death. In addition, the risk of CAI may increase during treatment with rec
Externí odkaz:
https://doaj.org/article/d15855422b134a6b94411757689fac1e
Autor:
Lecka-Ambroziak, Agnieszka1 (AUTHOR) aleckaambroziak@gmail.com, Kot, Karolina2 (AUTHOR) k.kot@ipczd.pl
Publikováno v:
Life (2075-1729). Mar2024, Vol. 14 Issue 3, p302. 10p.
Publikováno v:
Life, Vol 14, Iss 3, p 302 (2024)
There is limited data on hypotheses linking autoimmune thyroid diseases (AITD) and hypothyroidism with pulmonary hypertension (PH). Moreover, the prevalence of this coincidence, as well as the possible common pathogenic mechanisms, are even less expl
Externí odkaz:
https://doaj.org/article/448c188642f746a0bf702baad993c4f5
Autor:
Lecka-Ambroziak, Agnieszka1,2 (AUTHOR) a.lecka-ambroziak@ipczd.pl, Skobejko-Włodarska, Lidia3 (AUTHOR) l.skobejko-wlodarska@ipczd.pl, Ruta, Hanna4 (AUTHOR) hania.ruta@gmail.com
Publikováno v:
Journal of Clinical Medicine. Dec2023, Vol. 12 Issue 23, p7284. 10p.
Akademický článek
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Autor:
Elżbieta Lipska, Agnieszka Lecka-Ambroziak, Daniel Witkowski, Katarzyna Szamotulska, Ewa Mierzejewska, Mariusz Ołtarzewski
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Worldwide neonatal screening for congenital hypothyroidism (CH) is a gold standard of active surveillance in newborns. Prompt diagnosis, subsequent timely treatment implementation, and proper dosage of levothyroxine (L-T4) are crucial for normal grow
Externí odkaz:
https://doaj.org/article/fbc3a2d2b4b14ffc93be55aeeaf96c48
Autor:
Agnieszka Lecka-Ambroziak, Marta Wysocka-Mincewicz, Katarzyna Doleżal-Ołtarzewska, Agata Zygmunt-Górska, Teresa Żak, Anna Noczyńska, Dorota Birkholz-Walerzak, Renata Stawerska, Maciej Hilczer, Monika Obara-Moszyńska, Barbara Rabska-Pietrzak, Elżbieta Gołębiowska, Adam Dudek, Elżbieta Petriczko, Mieczysław Szalecki, on behalf of the Polish Coordination Group for rhGH Treatment
Publikováno v:
Diagnostics, Vol 11, Iss 5, p 798 (2021)
Genotype–phenotype correlation in patients with Prader–Willi syndrome (PWS) has still not been fully described. We retrospectively analysed data of 147 patients and compared groups according to genetic diagnosis: paternal deletion of chromosome 1
Externí odkaz:
https://doaj.org/article/1b4e6c7c88e8489294f0bdb9a0cb38d0
Autor:
Agnieszka Lecka-Ambroziak, Marta Wysocka-Mincewicz, Kamila Marszałek-Dziuba, Agnieszka Rudzka-Kocjan, Mieczysław Szalecki
Publikováno v:
Life, Vol 10, Iss 10, p 237 (2020)
Puberty in children with Prader-Willi syndrome (PWS) is usually delayed and/or incomplete but in some patients premature/early adrenarche is observed. We assessed the premature adrenarche (PA) in PWS patients during the recombinant human growth hormo
Externí odkaz:
https://doaj.org/article/a981bc168b424010956671fe808f5cea
Autor:
Lipska, Elżbieta, Lecka-Ambroziak, Agnieszka, Witkowski, Daniel, Szamotulska, Katarzyna, Mierzejewska, Ewa, Ołtarzewski, Mariusz
Publikováno v:
Frontiers in Endocrinology. 13
Worldwide neonatal screening for congenital hypothyroidism (CH) is a gold standard of active surveillance in newborns. Prompt diagnosis, subsequent timely treatment implementation, and proper dosage of levothyroxine (L-T4) are crucial for normal grow
Autor:
Klecz, Zofia1,2 zakklecz@gmail.com, Lecka-Ambroziak, Agnieszka1, Szarras-Czapnik, Maria1, Skórka, Agata3, Walewska-Wolf, Małgorzata4, Moszczyńska, Elżbieta1, Szalecki, Mieczysław1,5
Publikováno v:
Pediatric Endocrinology / Endokrynologia Pediatryczna. 2019, Vol. 18 Issue 1, p29-36. 8p.