Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Nikolinka Yordanova"'
Autor:
Nikolinka Yordanova, Violeta Iotova, Deborah J. G. Mackay, I. Karen Temple, Sara Stoyanova, Mari Hachmeriyan
Publikováno v:
JCRPE, Vol 16, Iss 4, Pp 475-480 (2024)
Temple syndrome is a rare imprinting disorder, caused by alterations in the critical imprinted region 14q32 of chromosome 14. It is characterized by pre- and postnatal growth retardation, truncal hypotonia and facial dysmorphism in the neonatal perio
Externí odkaz:
https://doaj.org/article/84082f8e1c2148059da009bfc3b43e35
Autor:
Kamelia Rankova, Teodora Karamfilova, Violeta Iotova, Sonya Galcheva, Yana Bocheva, Nikolinka Yordanova, Mari Hachmeriyan, Veselin Boyadzhiev, Vilchelm Mladenov, Yuliya Bazdarska, Irina Halvadjian
Introduction : Turner syndrome (TS) is a rare disease with typical phenotype manifestations and short stature. Part of the therapy in TS patients is the recombinant human growth hormone (rhGH) that leads to improved height velocity and final height.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea8fc94eee4cecfb196dc3eaaf611f26
Autor:
Yana Deyanova, Violeta Iotova, Milena Stoyanova, Irina Halvadzhiyan, Rositsa Stoicheva, Kaloyan Tsochev, Vilhelm Mladenov, Yuliya Bazdarska, Nikolinka Yordanova, Sonya Galcheva, Vesselin Boyadzhiev, Martin Zenker
Publikováno v:
Scripta Scientifica Medica. 54:21