[Unusual form of obesity with an autosomal recessive type of heredity]

[Main methodological approaches to the identification and diagnosis of monogenic hereditary diseases and problems in the organization of medical care and unified preventive programs].

Problemy sotsial'noi gigieny, zdravookhraneniia i istorii meditsiny·2019

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

BMC medical genetics·2019

Expression Profiles of Genes-Potential Therapy Targets-and Their Relationship to Survival in Renal Cell Carcinoma.

Doklady. Biochemistry and biophysics·2018

Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations.

Clinical genetics·2017

[Marriage and Migratory Characteristic of Circassians (Late 20th Century)].

Genetika·2016

Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.

Scientific reports·2016

[THE HISTORY OF DEPARTMENT OF FACULTY THERAPY, AT THE VORONEZH HIGHER EDUCATION INSTITUTION (ON THE OCCASION OF THE CENTENARY ANNIVERSARY OF N.N. BURDENKO VORONEZH STATE MEDICAL UNIVERSITY)].

Klinicheskaia meditsina·2018

[KYOTO CONSENSUS - THE NEW ETIOLOGICAL CLASSIFICATION OF CHRONIC GASTRITIS AND ITS DISCUSSION].

Klinicheskaia meditsina·2018

[PITUITARY ADENOMA APOPLEXY].

Klinicheskaia meditsina·2018

[A CASE OF FAMILIAL PULMONARY AND HEPATIC ECHINOCOCCOSIS)].

Klinicheskaia meditsina·2018

[SYSTEMIC LUPUS ERYTHEMATOSUS WITH LUPUS NEPHRITIS IN THE ELDERLY (CLINICAL OBSERVATION)].

Klinicheskaia meditsina·2018

[TYPICAL ERRORS IN THERAPY OF GASTROESOPHAGEAL REFLUX DISEASE].

Klinicheskaia meditsina·2018

Clinical characteristics and genetic analysis of children with corpus callosum abnormalities.

Pediatrics and neonatology·2026

SOME HEREDITARY DISEASES PREVALENT IN THE REPUBLIC OF AZERBAIJAN.

Georgian medical news·2026

Pair-based covariance under mixed mating and its consequences for REML variance estimation.

Genetics·2026

Analysis of distribution of IL13 and ADAM33 gene haplotypes in Russians, Khakass, Tuvans in relation to the risk of developing bronchial asthma.

Vavilovskii zhurnal genetiki i selektsii·2026

Exploratory Associations Between Height-for-Age and Gut Microbiota Composition in Healthy School-Aged Children.

Current microbiology·2026

Analysis of leg bone lengths from whole-body dual-energy X-ray absorptiometry in the UK biobank.

BJR artificial intelligence·2026

Related Experiment Videos

[Unusual form of obesity with an autosomal recessive type of heredity]

Related Concept Videos

[Main methodological approaches to the identification and diagnosis of monogenic hereditary diseases and problems in the organization of medical care and unified preventive programs].

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.

Expression Profiles of Genes-Potential Therapy Targets-and Their Relationship to Survival in Renal Cell Carcinoma.

Molecular analysis of patients with aniridia in Russian Federation broadens the spectrum of PAX6 mutations.

[Marriage and Migratory Characteristic of Circassians (Late 20th Century)].

Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.

[THE HISTORY OF DEPARTMENT OF FACULTY THERAPY, AT THE VORONEZH HIGHER EDUCATION INSTITUTION (ON THE OCCASION OF THE CENTENARY ANNIVERSARY OF N.N. BURDENKO VORONEZH STATE MEDICAL UNIVERSITY)].

[KYOTO CONSENSUS - THE NEW ETIOLOGICAL CLASSIFICATION OF CHRONIC GASTRITIS AND ITS DISCUSSION].

[PITUITARY ADENOMA APOPLEXY].

[A CASE OF FAMILIAL PULMONARY AND HEPATIC ECHINOCOCCOSIS)].

[SYSTEMIC LUPUS ERYTHEMATOSUS WITH LUPUS NEPHRITIS IN THE ELDERLY (CLINICAL OBSERVATION)].

[TYPICAL ERRORS IN THERAPY OF GASTROESOPHAGEAL REFLUX DISEASE].

Clinical characteristics and genetic analysis of children with corpus callosum abnormalities.

SOME HEREDITARY DISEASES PREVALENT IN THE REPUBLIC OF AZERBAIJAN.

Pair-based covariance under mixed mating and its consequences for REML variance estimation.

Analysis of distribution of IL13 and ADAM33 gene haplotypes in Russians, Khakass, Tuvans in relation to the risk of developing bronchial asthma.

Exploratory Associations Between Height-for-Age and Gut Microbiota Composition in Healthy School-Aged Children.

Analysis of leg bone lengths from whole-body dual-energy X-ray absorptiometry in the UK biobank.

Related Experiment Videos

[Unusual form of obesity with an autosomal recessive type of heredity]

Related Concept Videos

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