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The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline

The journal of clinical endocrinology and metabolism, 2016-12, Vol.101 (12), p.4500-4511

2016

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The Effects of Glucagon-Like Peptide Type 1 (GLP-1) and its Analogues in Adipose Tissue: Is there a way to Thermogenesis?

Current molecular medicine, 2021-01, Vol.21 (7), p.527-538

2021

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A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

The journal of clinical endocrinology and metabolism, 2018-03, Vol.103 (3), p.1005-1014

2018

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Direct Effect of the Synthetic Analogue of Glucagon-Like Peptide Type 1, Liraglutide, on Mature Adipocytes Is Realized through Adenylate-Cyclase-Dependent Enhancing of Insulin Sensitivity

Biochemistry (Moscow), 2021-03, Vol.86 (3), p.350-360

2021

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Atypical progeroid syndrome (p.E262K LMNA mutation): a rare cause of short stature and osteoporosis

Endocrinology, diabetes & metabolism case reports, 2021-04, Vol.2021 (1), p.1-9

2021

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European lipodystrophy registry: background and structure

Orphanet journal of rare diseases, 2020-01, Vol.15 (1), p.17-17, Article 17

2020

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Unusual clinical features associated with congenital generalized lipodystrophy type 4 in a patient with a novel E211X CAVIN1 gene variant

Clinical diabetes and endocrinology, 2020-05, Vol.6 (1), p.7-9, Article 7

2020

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Generalized lipoatrophy syndromes

La Presse médicale (1983), 2021-11, Vol.50 (3), p.104075-104075, Article 104075

2021

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Inherited and acquired lipodystrophies: molecular-genetic and autoimmune mechanisms

Ozhirenie i metabolizm, 2018-04, Vol.15 (1), p.39-42

2018

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Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients

Endocrine-related cancer, 2015-10, Vol.22 (5), p.745-757

2015

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Progressive Generalized Lipodystrophy as a Manifestation of Autoimmune Polyglandular Syndrome Type 1

The journal of clinical endocrinology and metabolism, 2016-04, Vol.101 (4), p.1344-1347

2016

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Development of metabolic syndrome at a young age as a manifestation of familial partial lipodystrophy type 3 (PPARG mutation): the first description of its clinical case in Russia

Sakharnyĭ diabet, 2015-01, Vol.18 (3), p.99-105

2015

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High frequency of pathogenic and rare sequence variants in diabetes-related genes among Russian patients with diabetes in pregnancy

Acta diabetologica, 2019-04, Vol.56 (4), p.413-420

2019

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Metabolic and other morbid complications in congenital generalized lipodystrophy type 4

American journal of medical genetics. Part A, 2024-06, Vol.194 (6), p.e63533-n/a

2024

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FRI058 Treatment With Mibavademab, A Novel Leptin Receptor Agonist, Is Associated With Improvement In Metabolic Parameters In Individuals With Generalized Lipodystrophy

Journal of the Endocrine Society, 2023-10, Vol.7 (Supplement_1)

2023

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The role of glucose and insulin in the metabolic regulation of growth hormone secretion

Problemy ėndokrinologii, 2021-01, Vol.67 (1), p.52-59

2021

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A rare case of hypoparathyroidism due to MELAS syndrome

Endocrine Abstracts, 2019-05

2019

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Gynaecomastia in a patient with von Recklinghausen's disease (neurofibromatosis type 1)

Endocrine Abstracts, 2015-05

2015

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An unusual case of diabetes mellitus as a result of heterozygous missense mutation R482W in LMNA gene (familial partial lipodystrophy type 2), described for the first time in Russian population

Endocrine Abstracts, 2014-04

2014

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Multiple endocrine disorders in Werner syndrome

Endocrine Abstracts, 2016-05

2016

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Unusual clinical features associated with congenital generalized lipodystrophy type 4 in a patient with a novel E211X CAVIN1 gene variant

Clinical diabetes and endocrinology, 2020, Vol.6, p.7-7

2020

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Cardiovascular complications in pituitary gigantism (results of an international study)

Endocrine Abstracts, 2018-10

2018

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The survival and sequestration of transfused donor platelets in cytostatic cytopenias

Terapevtic̆eskii arhiv, 2010-01, Vol.82 (12), p.51

2010

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The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline

The Effects of Glucagon-Like Peptide Type 1 (GLP-1) and its Analogues in Adipose Tissue: Is there a way to Thermogenesis?

A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation

Direct Effect of the Synthetic Analogue of Glucagon-Like Peptide Type 1, Liraglutide, on Mature Adipocytes Is Realized through Adenylate-Cyclase-Dependent Enhancing of Insulin Sensitivity

Atypical progeroid syndrome (p.E262K LMNA mutation): a rare cause of short stature and osteoporosis

European lipodystrophy registry: background and structure

Unusual clinical features associated with congenital generalized lipodystrophy type 4 in a patient with a novel E211X CAVIN1 gene variant

Generalized lipoatrophy syndromes

Inherited and acquired lipodystrophies: molecular-genetic and autoimmune mechanisms

Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients

Progressive Generalized Lipodystrophy as a Manifestation of Autoimmune Polyglandular Syndrome Type 1

Development of metabolic syndrome at a young age as a manifestation of familial partial lipodystrophy type 3 (PPARG mutation): the first description of its clinical case in Russia

High frequency of pathogenic and rare sequence variants in diabetes-related genes among Russian patients with diabetes in pregnancy

Metabolic and other morbid complications in congenital generalized lipodystrophy type 4

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip) Cambridge

Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip) Cambridge, UK, 7–8 April 2022

FRI058 Treatment With Mibavademab, A Novel Leptin Receptor Agonist, Is Associated With Improvement In Metabolic Parameters In Individuals With Generalized Lipodystrophy

The role of glucose and insulin in the metabolic regulation of growth hormone secretion

A rare case of hypoparathyroidism due to MELAS syndrome

Gynaecomastia in a patient with von Recklinghausen's disease (neurofibromatosis type 1)

An unusual case of diabetes mellitus as a result of heterozygous missense mutation R482W in LMNA gene (familial partial lipodystrophy type 2), described for the first time in Russian population

Multiple endocrine disorders in Werner syndrome

Unusual clinical features associated with congenital generalized lipodystrophy type 4 in a patient with a novel E211X CAVIN1 gene variant

Cardiovascular complications in pituitary gigantism (results of an international study)

The survival and sequestration of transfused donor platelets in cytostatic cytopenias

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