Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Mirjana Kočova"'
Autor:
Marija Gjorgjievska, Gjorgji Bozhinovski, Elena Sukarova-Angelovska, Mirjana Kocova, Lejla Muaremoska Kanzoska, Dijana Plaseska-Karanfilska
Publikováno v:
Balkan Medical Journal, Vol 40, Iss 4, Pp 252-261 (2023)
Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant neurocutaneous disorder, characterized by multiple café-au-lait macules, axillary and inguinal freckling, tumors of the nervous system, and iris hamartomas. More than 3,100 differen
Externí odkaz:
https://doaj.org/article/641db54125e7403187bdbc40eb21d436
Autor:
Cvetanka Bajraktarova Miševska, Mirjana Kočova, Lidija Kanurkova, Gabriela Curcieva, Cuckova, Marija Maneva, Emilija Valjakova
Publikováno v:
South European Journal of Orthodontics and Dentofacial Research, Vol 2, Iss 1, Pp 3-6 (2015)
Introduction: A complete or partial absence of an X chromosome in girls with Turner Syndrome (TS) has an impact on dental arch morphology. The aim of this study was to analyze the sizes of dental arches as well as the height of the palatal vault in p
Externí odkaz:
https://doaj.org/article/e3aa49353776436b9370b98f0bf237ac
Autor:
Cvetanka Bajraktarova Miševska, Mirjana Kočova, Lidija Kanurkova, Gabriela Curcieva, Cuckova, Bona Bajraktarova, Marija Maneva, Emilija Valjakova
Publikováno v:
South European Journal of Orthodontics and Dentofacial Research, Vol 2, Iss 1, Pp 7-13 (2015)
ABSTRACT Introduction: A complete or partial absence of an X chromosome in the karyotype of phenotypic females has an impact on craniofacial morphology. The aim of this study was to determine the characteristics of the craniofacial complex in patien
Externí odkaz:
https://doaj.org/article/dbdfe9227145498ba3b76ed4145b6e5c
Autor:
Curcieva, Cuckova, Gabriela, Lidija Kanurkova, Emilija Valjakova, Marija Maneva, Cvetanka Bajraktarova Miševska, Mirjana Kočova
Publikováno v:
South European Journal of Orthodontics and Dentofacial Research, Vol 2, Iss 1, Pp 3-6 (2015)
South European Journal of Orthodontics and Dentofacial Research
Volume 2
Issue 1
South European Journal of Orthodontics and Dentofacial Research
Volume 2
Issue 1
Introduction: A complete or partial absence of an X chromosome in girls with Turner Syndrome (TS) has an impact on dental arch morphology. The aim of this study was to analyze the sizes of dental arches as well as the height of the palatal vault in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90bd9dbec6ebdd561ce52db44571e240
http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=229377&lang=en
http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=229377&lang=en
Autor:
Marija Maneva, Cvetanka Bajraktarova Miševska, Lidija Kanurkova, Curcieva, Cuckova, Gabriela, Bona Bajraktarova, Emilija Valjakova, Mirjana Kočova
Publikováno v:
South European Journal of Orthodontics and Dentofacial Research
Volume 2
Issue 1
South European Journal of Orthodontics and Dentofacial Research, Vol 2, Iss 1, Pp 7-13 (2015)
Volume 2
Issue 1
South European Journal of Orthodontics and Dentofacial Research, Vol 2, Iss 1, Pp 7-13 (2015)
Introduction: A complete or partial absence of an X chromosome in the karyotype of phenotypic females has an impact on craniofacial morphology. The aim of this study was to determine the characteristics of the craniofacial complex in patients with Tu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fe813f64f935ed1e04cfc0dd2da74e0
https://hrcak.srce.hr/file/229378
https://hrcak.srce.hr/file/229378
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2022)
Substantial research has been performed during the last decades on the clinical and genetic variability of congenital adrenal hyperplasia (CAH) and its most common form, 21-hydroxylase deficiency (21OHD). CAH is one of the most prevalent autosomal re
Externí odkaz:
https://doaj.org/article/ca127722c3c046ccad75688f71dfcc6e
Publikováno v:
European Journal of Medical Research, Vol 24, Iss 1, Pp 1-6 (2019)
Abstract Background The simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder usually caused by steroid 21-hydroxylase deficiency due to I172N missense mutation at the CYP21A2 gene. Clinical presentati
Externí odkaz:
https://doaj.org/article/5c2cb10ccda84ab99fa8329b2dbeb45b
Autor:
Vanesa Koracin, Matej Mlinaric, Ivo Baric, Ian Brincat, Maja Djordjevic, Ana Drole Torkar, Ksenija Fumic, Mirjana Kocova, Tatjana Milenkovic, Florentina Moldovanu, Vjosa Mulliqi Kotori, Michaela Iuliana Nanu, Ziga Iztok Remec, Barbka Repic Lampret, Dimitrios Platis, Alexey Savov, Mira Samardzic, Biljana Suzic, Ildiko Szatmari, Alma Toromanovic, Mojca Zerjav Tansek, Tadej Battelino, Urh Groselj
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Significant part of Southeastern Europe (with a population of 76 million) has newborn screening (NBS) programs non-harmonized with developed European countries. Initial survey was conducted in 2013/2014 among 11 countries from the region (Albania, Bu
Externí odkaz:
https://doaj.org/article/ec423af9e8d3444db4d23e83a269945c
Autor:
Nikolina Zdraveska, Mirjana Kocova, Adeline K. Nicholas, Violeta Anastasovska, Nadia Schoenmakers
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Neonatal screening in Macedonia detects congenital hypothyroidism (CH) with an incidence of 1 in 1,585, and more than 50% of cases exhibit a normally located gland-in-situ (GIS). Monogenic mutations causing dyshormonogenesis may underlie GIS CH; addi
Externí odkaz:
https://doaj.org/article/39695879f4994480b45cb39e822b7ee6
Publikováno v:
Endocrine Connections, Vol 7, Iss 4, Pp 544-552 (2018)
Background: Testicular adrenal rest tumors (TARTs) are found in 30–94% of adult males with congenital adrenal hyperplasia (CAH). We sought to explore TART appearance through yearly ultrasound examination of testes in young boys with CAH, and its as
Externí odkaz:
https://doaj.org/article/3998e4d1d3ec49f887448891444518e6