Search Results - "Ryznychuk, M.O."
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Growth indices and vitamin D content in children with idiopathic short stature depending on the variants of the Taql polymorphism genotype of the VDR gene
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (03-03-2024)“…Background. The vitamin D receptor (VDR) gene is a key regulator of biological processes, including tissue and cell growth and differentiation, bone…”
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Involvement of the vitamin D receptor gene in the development of idiopathic short stature
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (20-03-2023)“…Background. The vitamin D receptor (VDR) gene is localized in the chromosome 12 (region 12q13). Its polymorphic variants BsmI and FokI are the most promising…”
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3
Vitamin D content in children with short stature due to intrauterine growth restriction against normosomatotropinemia
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (01-09-2021)“…Background. There are no data about the status of vitamin D and its effect on the growth hormone/growth factors axis in prepubertal children with intrauterine…”
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TaqI polymorphism of the vitamin D receptor gene in children with growth hormone deficiency
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (18-07-2023)“…Background. The nuclear receptor for vitamin D mediates most of the biological functions of this vitamin. It belongs to the steroid hormone receptor family,…”
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Osteoporosis in Сhildren with Itsenko — Cushing Disease: Etiology, Pathogenesis, Diagnosis
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (03-09-2021)“…The review describes the etiology, pathogenetic mechanisms of osteoporosis in children with Itsenko — Cushing syndrome. The new methods for the diagnosis of…”
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An interaction between growth hormone/insulin-like growth factor-1 and vitamin D in children with short stature
Published in Reproduktivnaâ èndokrinologiâ (27-05-2022)“…There are disorders in the growth hormone (GH)/growth factors system in a significant part of patients with short stature; first of all, this concerns such…”
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Vitamin D status in children with idiopathic stunting
Published in Suchasna pediatrii︠a︡. Ukraïna (28-09-2024)“…Short stature is considered idiopathic in the absence of systemic, endocrine, nutritional, or genetic abnormalities and is defined as growth below two standard…”
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Idiopathic short stature: characteristics of polymorphism of the Taql gene of vitamin D receptor
Published in Suchasna pediatrii︠a︡. Ukraïna (28-12-2023)“…The causes of idiopathic short stature (IS) are diverse and not well understood, including polymorphisms of the vitamin D receptor (VDR) gene, dysfunction of…”
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9
Adrenogenital syndrome: molecular mechanisms of development
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (01-03-2017)“…On the long multistage pathway of biosynthesis of steroid hormones from cholesterol to cortisol, testosterone and estradiol, due to mutations in genes, there…”
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Синдром Шерешевського — Тернера: фенотипова варіабельність хромосомного поліморфізму
Published in Zdorovʹe rebenka (19-01-2022)“…Синдром Шерешевського — Тернера вперше описаний Н. Шерешевським в 1925 р., а потім Г. Тернером у 1938 р. У 1959 р. Форд встановив, що у хворих на цей синдром…”
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Орфанні спадкові синдроми у практиці педіатра-ендокринолога
Published in Zdorovʹe rebenka (19-01-2022)“…Орфанні синдроми — це група захворювань, що трапляються вкрай рідко, із частотою 10 випадків на 100 000 населення. Суттєвої уваги лікарів різного профілю…”
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Орфанні спадкові синдроми у практиці педіатра-ендокринолога
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (02-12-2021)“…У лекції подано коротку фенотипово-генетичну характеристику орфанних ендокринних синдромів, що супроводжуються гігантизмом…”
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Адреногенітальний синдром: молекулярні механізми розвитку
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (02-09-2021)“…На довгому, багатоступінчастому шляху біосинтезу стероїдних гормонів від холестеролу до кортизолу, тестостерону й естрадіолу внаслідок мутацій генів виникає…”
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Orphan Hereditary Syndromes in the Practice of Pediatric Endocrinologist
Published in Zdorovʹe rebenka (01-05-2015)“…Orphan syndromes — a group of diseases that are extremely rare, with an incidence of 10 cases per 100,000 people. Doctors in different fields should pay…”
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15
Turner Syndrome: Phenotypic Variability of Chromosomal Polymorphism
Published in Zdorovʹe rebenka (01-04-2015)“…Turner syndrome was firstly described by N. Shereshevskyi in 1925, and then by H. Turner in 1938. In 1959, Ch. Ford found that in patients with this syndrome…”
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Orphan Hereditary Syndromes in the Practice of Pediatric Endocrinologist
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (01-03-2015)“…The lecture presents short phenotypic and genetic characteristics of orphan endocrine syndromes associated with gigantism…”
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The Syndromic Characteristic of Hereditary Endocrine Pathology
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (01-02-2014)“…The review considers the brief clinical characteristic of separate syndromes of endocrine pathology, which are based on hereditary factors. Ro define…”
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Синдромна характеристика спадкової ендокринної патології
Published in Miz︠h︡narodnyĭ endokrynolohichnyĭ z︠h︡urnal (18-03-2014)“…В огляді наведено коротку клінічну характеристику деяких синдромів ендокринної патології, основу яких складають спадкові чинники. Для позначення нозологічних…”
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