Case Report: Novel likely pathogenic MEN1 mosaic mutation in the family with MEN-1 syndrome
Rustam Salimkhanov, Marina Utkina, H. V. Bagirova, Anna Eremkina et autres
0 citationsFrontiers in Endocrinology
В. М. Петров
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74Publications signalées
633Citations signalées
2Affiliations récentes
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Domaines associés
Solar and Space Plasma DynamicsBacteriophages and microbial interactionsRNA and protein synthesis mechanismsSexual Differentiation and DisordersBacterial Genetics and Biotechnology
Publications récentes
Association between Human Leukocyte Antigen Alleles and Endocrine Disorders in a Cohort of 895 Patients from Russian Clinical Population
Anton Buzdin, Polina Pugacheva, Daniil Luppov, Marianna Zolotovskaia et autres
0 citationsBiochemistry (Moscow)
EndoGene database: reported genetic variants for 5,926 Russian patients diagnosed with endocrine disorders
Anton Buzdin, Marianna Zolotovskaia, S. A. Roumiantsev, Aleksandra G. Emelyanova et autres
1 citationFrontiers in Endocrinology
Clinical, hormonal and molecular genetic characteristics of patients with 46,XY disorders of sex development associated with variants in the HSD17B3 gene
Natalia Kalinchenko, Nina Makretskaya, А. А. Колодкина, В. А. Иоутси et autres
0 citationsProblems of Endocrinology
Clinical Case Report of Non-Diabetic Hypoglycemia Due to a Combination of Germline Mutations in the MEN1 and ABCC8 Genes
M. Yu. Yukina, Ekaterina Solodovnikova, Sergey Popov, В. В. Захарова et autres
4 citationsGenes
Novel GLIS3 mutation in patient with neonatal diabetes mellitus and congenital hypothyroidism (NDH-syndrome)
Yu. V. Tikhonovich, Lyudmila G. Chernich, I. N. Velikanov, V.M. Polyakova et autres
0 citationsDiabetes Mellitus
Clinical, hormonal and molecular-genetic characteristics of monogenic diabetes mellitus associated with the mutations in the INS gene
Yu. V. Tikhonovich, E. E. Petryaykina, A. Timofeev, Natalia V. Zubkova et autres
3 citationsDiabetes Mellitus
Kalmann syndrome in monozygous twins as an isolated manifestation of the SOX10 gene defect
Elena Frolova, В. М. Петров, Evgeny Vasilyev, Nina Makretskaya et autres
0 citationsProblems of Endocrinology
A deep intronic mutation in AR gene causing androgen insensitivity syndrome: difficulties of diagnostics
Natalia Kalinchenko, В. М. Петров, Alexandra V. Panova, Anatoly Tiulpakov
1 citationProblems of Endocrinology
Глубокая интронная мутация в гене AR как причина синдрома резистентности к андрогенам: сложности диагностики
Н. Ю. Калинченко, В. М. Петров, Alexandra V. Panova, Anatoly Tiulpakov
0 citations
Синдром Кальмана у монозиготных близнецов как изолированное проявление дефекта гена SOX10
Elena Frolova, В. М. Петров, Е. В. Васильев, Н. А. Макрецкая et autres
0 citations
Serum circulating miRNA‐342‐3p as a potential diagnostic biomarker in parathyroid carcinomas: A pilot study
Julia Krupinova, Natalia Mokrysheva, В. М. Петров, Ekaterina Pigarova et autres
17 citationsEndocrinology Diabetes & Metabolism
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