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E. V. Shreder

Observed names: Ekaterina Shreder, Ekaterina V. Shreder
ORCID: 0000-0003-0031-1389
Observed ORCID: 0000-0003-0031-1389
OpenAlex ID: A5047823419
Clinical guideline of «congenital hypothyroidism»
2022 · V. A. Peterkova, O. B. Bezlepkina, et al. · Problems of Endocrinology · 21
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Ectopic thyroid gland: clinical features and diagnostics in children
2022 · E. V. Shreder, T. A. Vadina, et al. · Problems of Endocrinology · 12
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Clinical guidelines «Thyroiditis in children»
2021 · V. A. Peterkova, O. B. Bezlepkina, et al. · Clinical and experimental thyroidology · 10
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Duchenne Muscular Dystrophy: Modern Approaches in Patient Management
2023 · Inga V. Anisimova, Svetlana B. Artemyeva, et al. · Педиатрическая фармакология · 7
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Pathogenic TSHR variants in children with thyroid dysgenesis
2023 · E. V. Shreder, T. A. Vadina, et al. · Problems of Endocrinology · 3
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Clinical, hormonal and molecular-genetic characteristics of monogenic diabetes mellitus associated with the mutations in the INS gene
2022 · Yu. V. Tikhonovich, E. E. Petryaykina, et al. · Diabetes Mellitus · 3
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Consensus guidelines of congenital hypothyroidism by the European Society for pediatric endocrinology and the European Society for Endocrinology: key points and comments
2021 · E. V. Shreder, T. Y. Shiryaeva, et al. · Clinical and experimental thyroidology · 2
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Results of a study on the clinical efficacy of viltolarsen in patients with Duchenne muscular dystrophy in real-world clinical practice in the Russian Federation
2026 · T. A. Gremyakova, O. I. Gremyakova, et al. · Neuromuscular Diseases
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Clinical guidelines “Congenital hypothyroidism”
2024 · V. A. Peterkova, O. B. Bezlepkina, et al. · Clinical and experimental thyroidology
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Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome)
2022 · Yu. V. Tikhonovich, L. G. Chernich, et al. · Diabetes Mellitus
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Retrospective trial of long acting analogues detemir and degludec usage in children and adolescents to overcome glucose variability caused by dawn phenomenon and reverse dawn phenomenon
2021 · A. V. Vitebskaya, E. V. Shreder, et al. · Diabetes Mellitus
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A novel DUOXA2 mutation in russian family with thyroid dysgenesis
2021 · Ekaterina Shreder, Tatiana Vadina, et al. · Endocrine Abstracts
Thyroid dyshormonogenesis: a case report of two siblings with a heterozygous variant in the TPO gene.
2021 · Т. A. Вадина, Marina Konushova, et al. · 59th ESPE Annual Meeting (ESPE 2021 Online)
Works count: 13
Citation count: 58
H-index: 4
I10-index: 3
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