Evgeny V. Vasilyev

Moscow, MOW 117036, Russian Federation

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 22 publications

Association of Alleles of Human Leukocyte Antigen Class II Genes and Severity of COVID-19 in Patients of the 'Red Zone' of the Endocrinology Research Center, Moscow, Russia.

Association of Alleles of Human Leukocyte Antigen Class II Genes and Severity of COVID-19 in Patients of the 'Red Zone' of the Endocrinology Research Center, Moscow, Russia.

Journal: Diseases (Basel, Switzerland)

Published: September 23, 2022

A Founder Mutation in the POMC 5'-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA.

A Founder Mutation in the POMC 5'-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA.

Journal: The Journal of clinical endocrinology and metabolism

Published: March 30, 2022

Circular RNAs and thyroid cancer: Closed molecules, open possibilities.

Circular RNAs and thyroid cancer: Closed molecules, open possibilities.

Journal: Critical reviews in oncology/hematology

Published: November 17, 2021

Morphological characteristics of pituitary adenomas in the phenocopy of multiple endocrine neoplasia type 1

Morphological characteristics of pituitary adenomas in the phenocopy of multiple endocrine neoplasia type 1

Journal: Problemy endokrinologii

Published: September 13, 2021

Kalmann syndrome in monozygous twins as an isolated manifestation of the SOX10 gene defect

Kalmann syndrome in monozygous twins as an isolated manifestation of the SOX10 gene defect

Journal: Problemy endokrinologii

Published: July 13, 2021

Familial case of hypogonadotropic hypogonadism as the CHARGE syndrome manifestation

Familial case of hypogonadotropic hypogonadism as the CHARGE syndrome manifestation

Journal: Problemy endokrinologii

Published: April 16, 2021

Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes

Clinical and molecular genetic features of cases of isolated hypogonadotropic hypogonadism, associated with defects in GNRHR genes

Journal: Problemy endokrinologii

Published: April 12, 2021

Familial Acromegaly and Bilateral Asynchronous Pheochromocytomas in a Female Patient With a MAX Mutation: A Case Report.

Familial Acromegaly and Bilateral Asynchronous Pheochromocytomas in a Female Patient With a MAX Mutation: A Case Report.

Journal: Frontiers in endocrinology

Published: March 21, 2021

Search for Genetic Predictors of Adult Autoimmune Polyendocrine Syndrome in Monozygotic Twins.

Search for Genetic Predictors of Adult Autoimmune Polyendocrine Syndrome in Monozygotic Twins.

Journal: Clinical medicine insights. Endocrinology and diabetes

Published: December 24, 2020

A series of clinical cases of familial hypocalciuric hypercalcemia syndrome

A series of clinical cases of familial hypocalciuric hypercalcemia syndrome

Journal: Problemy endokrinologii

Published: July 18, 2020

Insulin autoimmune syndrome.

Insulin autoimmune syndrome.

Journal: Endocrinology, diabetes & metabolism case reports

Published: April 14, 2020

Second-hit APC mutation in a familial adamantinomatous craniopharyngioma.

Second-hit APC mutation in a familial adamantinomatous craniopharyngioma.

Journal: Neuro-oncology

Published: March 15, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026