A comprehensive integrated disease management program for phenylketonuria (IDMP-PKU) from Türkiye: rationale, design and patient characteristics by Mehmet Cihan Balci, Deniz Kor, Yilmaz Yildiz, Meryem Karaca, Fatma Derya Bulut, Ayca Burcu Kahraman, Alihan Yesil, Ezgi Burgac, Kismet Ciki, Arzu Selamioglu, Burcu Koseci, Asli Durmus, Irem Kaplan, Esra Kara, Halise Neslihan Mungan, Serap Sivri, Gulden Fatma Gokcay, Aysegul Tokatli, Mubeccel Demirkol, Turgay Coskun, Imran Ozalp

Subjects: Get full text

Vaccine antigen-based genotyping of Bordetella pertussis by direct Sanger sequencing of clinical samples in Peru from 2018 to 2019 by Eduardo Juscamayta-López, Betsabé Vega-Abad, Faviola Valdivia, María Pía Soto, Helen Horna, Ruth García-de-la-Guarda

Subjects: Get full text

Molecular genetic indicators of the probability of early myocardial systolic dysfunction signs in doxorubicin chemotherapy in patients with breast cancer of moderate and low HFA-IC... by I. A. Karput, V. A. Snezhitsky, M. N. Kurbat, O. A. Gorustovich, A. V. Kopytsky, A. S. Babenko

Subjects: Get full text

Polymorphism rs3088232 in the BRDT gene is associated with idiopathic male infertility in the West Siberian Region of Russia by A. S. Wainer, V. M. Nagaitsev, O. V. Korolkova, V. V. Vostrikov, L. V. Osadchuk, Ye. V. Pechkovsky, I. S. Malinovskaya, M. L. Filipenko

Subjects: Get full text

REGIONAL ASPECTS OF THE GENE POLYMORPHISM VЕGFR2 WITH CORONARY ATHEROSCLEROSIS IN ACUTE CORONARY SYNDROME by K. Yu. Nikolaev, I. A. Urvantseva, К. Yu. Batueva, К. A. Apartsin, А. V. Gorokhova, V. I. Ganyukov, N. А. Kochergin, Е. M. Zelenskaya, G. I. Lifshits

Subjects: Get full text

Principal results of Borrelia genotyping in Russia by E. I. Korenberg, V. V. Nefedova, I. A. Fadeyeva, N. B. Gorelova

Subjects: Get full text

GENOMIC FACTORS (TOLL-LIKE RECEPTORS GENES) IN DEVELOPMENT OF ATHEROSCLEROSIS AND ITS CLINICAL MANIFESTATIONS by I. I. Zhidkova, A. V. Ponasenko, M. V. Khutornaya, A. G. Kutikhin, O. L. Barbarash

Subjects: Get full text

Regional aspects of associations of the CYP2C19 gene polymorphism with coronary atherosclerosis in acute coronary syndrome by K. Yu. Nikolaev, I. A. Urvantseva, K. Yu. Batueva, K. A. Apartsin, A. V. Gorokhova, V. I. Ganyukov, N. A. Kochergin, E. M. Zelenskaya, G. I. Lifshitz

Subjects: Get full text

Genetic Heterogeneity in Four Probands Reveals <i>HGSNAT</i>, <i>KDM6B</i>, <i>LMNA</i> and <i>WFS1</i> Related Neurodevelopmental Disorders by Behjat Ul Mudassir, Mujaddid Mudassir, Jamal B. Williams, Zehra Agha

Subjects: “…mono-allelic and bi-allelic variants causing NDDs…”
Get full text

Role of Pharmacogenetic Testing in the Risk and Safety Assessment of Valproates: The Ethnic Aspect (Review) by N. A. Shnayder, V. V. Grechkina, V. V. Arkhipov, R. F. Nasyrova

Subjects: Get full text

Efficacy of P2Y₁₂ receptor inhibitors in myocardial infarction in individuals carrying different <i>CYP2C19</i> genotypes living in the northern region of Russia by A. S. Vorobyov, G. I. Lifshits, E. M. Zelenskaya, K. Yu. Batueva, L. V. Kovalenko, I. A. Urvantseva, M. Yu. Donnikov, M. S. Poptsova, E. P. Zbirovskaya, K. Yu. Nikolaev

Subjects: Get full text