Search Results - "Bessonova L"

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Population genetics of hereditary diseases in the child population of the Republic of Bashkortostan, Chuvashia, and Udmurtia.

Authors: Bessonova, L. El'chinova, G. Zinchenko, R.

Source: Russian Journal of Genetics. May2012, Vol. 48 Issue 5, p548-557. 10p.

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EPS5.10 Real-world outcomes in patients (pts) with cystic fibrosis (CF) treated with ivacaftor (IVA): analysis of 2015 US and UK CF registry data.

Authors: Bessonova, L. Volkova, N. Higgins, M. et al.

Source: Journal of Cystic Fibrosis. Jun2017 Supplement 1, Vol. 16, pS49-S50. 1p.

411 Disease progression in patients (pts) with cystic fibrosis (CF) treated with ivacaftor (IVA): analysis of real-world data from the UK CF Registry.

Authors: Bessonova, L. Volkova, N. Higgins, M. et al.

Source: Journal of Cystic Fibrosis. Jun2017 Supplement 1, Vol. 16, pS167-S167. 1p.

158 Background incidence of liver function test (LFT) abnormalities in patients (pts) with cystic fibrosis (CF).

Authors: Seliger, V. Bessonova, L. Volkova, N. et al.

Source: Journal of Cystic Fibrosis. Jun2016 Supplement 1, Vol. 15, pS91-S91. 1p.

Beta blocker use and ovarian cancer survival: A retrospective cohort study

Authors: Eskander, R. Bessonova, L. Chiu, C. et al.

Source: Gynecologic Oncology. Oct2012, Vol. 127 Issue 1, pS21-S21. 1p.

Abstract: P1238 EVALUATION OF PARAMETERS OF GLUTATIONE SYSTEM IN PATIENTS WITH CHRONIC OBSTRUKTIVE PULMONARY DISEASE IN PHARMACOLOGICAL CORRECTION

Authors: Bessonova, L Verlan, N Kolesnichenko et al.

Source: Atherosclerosis (Supplements). Jun2009, Vol. 10 Issue 2, pe1293-e1293. 1p.

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families.

Authors: Rudenskaya, G. E. Kadnikova, V. A. Ryzhkova, O. P. et al.

Source: BMC Neurology. 8/3/2020, Vol. 20 Issue 1, p1-14. 14p. 1 Black and White Photograph, 6 Charts.

RWD140 Obeticholic Acid for Primary Biliary Cholangitis: Modeling Prevention of Clinical Events Using Real-World Data.

Authors: Younossi, ZM Ellis, A Lee, J et al.

Source: Value in Health. 2024 Supplement, Vol. 27 Issue 6, pS385-S385. 1p.

Genetic epidemiological study of monogenic hereditary diseases in the Republic of Tatarstan: Population dynamic factors determining the differentiation of the load of hereditary diseases in five districts.

Authors: Ginter, E. El'chinova, G. Petrin, A. et al.

Source: Russian Journal of Genetics. Sep2012, Vol. 48 Issue 9, p945-951. 7p.

Rare Cause 5q SMA: Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus.

Authors: Mikhalchuk K Zabnenkova V Braslavskaya S et al.

Source: Clinical genetics [Clin Genet] 2025 Jul; Vol. 108 (1), pp. 58-68. Date of Electronic Publication: 2025 Feb 04.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE

Longitudinal Relationship Between Elevated Liver Biochemical Tests and Negative Clinical Outcomes in Primary Biliary Cholangitis: A Population-Based Study.

Authors: Kowdley KV Victor DW 3rd MacEwan JP et al.

Source: Alimentary pharmacology & therapeutics [Aliment Pharmacol Ther] 2025 Jun; Vol. 61 (11), pp. 1775-1784. Date of Electronic Publication: 2025 Apr 02.

Publication Type: Journal Article

Journal Info: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 8707234 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2036 (Electronic) Linking ISSN: 02692813 NLM ISO Abbreviation: Aliment Pharmacol Ther Subsets: MEDLINE

Cost of hepatic decompensation and liver transplantation events in primary biliary cholangitis: a retrospective observational study.

Authors: Gish RG MacEwan JP Liu Y et al.

Source: Journal of comparative effectiveness research [J Comp Eff Res] 2026 Mar; Vol. 15 (3), pp. e250110. Date of Electronic Publication: 2026 Feb 16.

Publication Type: Journal Article; Observational Study

Journal Info: Publisher: Becaris Publishing Country of Publication: England NLM ID: 101577308 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2042-6313 (Electronic) Linking ISSN: 20426305 NLM ISO Abbreviation: J Comp Eff Res Subsets: MEDLINE

Common Variants in the TYR Gene with Unclear Pathogenicity as the Cause of Oculocutaneous Albinism in a Cohort of Russian Patients.

Authors: Shchagina O Stepanova A Mishakova P et al.

Source: Biomedicines [Biomedicines] 2024 Oct 01; Vol. 12 (10). Date of Electronic Publication: 2024 Oct 01.

Publication Type: Journal Article

Journal Info: Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101691304 Publication Model: Electronic Cited Medium: Print ISSN: 2227-9059 (Print) Linking ISSN: 22279059 NLM ISO Abbreviation: Biomedicines Subsets: PubMed not MEDLINE

A rare case of uniparental disomy 9 concomitant with low-level mosaicism for trisomy 9.

Authors: Iakovleva AS Markova ZG Bessonova LA et al.

Source: Vavilovskii zhurnal genetiki i selektsii [Vavilovskii Zhurnal Genet Selektsii] 2025 Sep; Vol. 29 (5), pp. 629-635.

Publication Type: Journal Article

Journal Info: Publisher: Institut t︠s︡itologii i genetiki Sibirskogo otdelenii︠a︡ Rossiĭskoi akademii nauk Country of Publication: Russia (Federation) NLM ID: 101583566 Publication Model: Print Cited Medium: Print ISSN: 2500-0462 (Print) Linking ISSN: 25003259 NLM ISO Abbreviation: Vavilovskii Zhurnal Genet Selektsii Subsets: PubMed not MEDLINE

Hepatic real-world outcomes with obeticholic acid in primary biliary cholangitis (HEROES): A trial emulation study design.

Authors: Brookhart MA Mayne TJ Coombs C et al.

Source: Hepatology (Baltimore, Md.) [Hepatology] 2025 Jun 01; Vol. 81 (6), pp. 1647-1659. Date of Electronic Publication: 2025 Jan 03.

Publication Type: Journal Article; Pragmatic Clinical Trial

Journal Info: Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 8302946 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1527-3350 (Electronic) Linking ISSN: 02709139 NLM ISO Abbreviation: Hepatology Subsets: MEDLINE

Four Novel Disease-Causing Variants in the NOTCH3 Gene in Russian Patients with CADASIL.

Authors: Bostanova F Tsygankova P Nagornov I et al.

Source: Genes [Genes (Basel)] 2023 Aug 28; Vol. 14 (9). Date of Electronic Publication: 2023 Aug 28.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

A nationwide study of primary biliary cholangitis prevalence, geographic distribution, and health care providers.

Authors: Levy C Buchanan-Peart KA MacEwan JP et al.

Source: Hepatology communications [Hepatol Commun] 2025 Apr 14; Vol. 9 (5). Date of Electronic Publication: 2025 Apr 14 (Print Publication: 2025).

Publication Type: Journal Article

Journal Info: Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 101695860 Publication Model: eCollection Cited Medium: Internet ISSN: 2471-254X (Electronic) Linking ISSN: 2471254X NLM ISO Abbreviation: Hepatol Commun Subsets: MEDLINE

Burden of illness for patients with primary biliary cholangitis: an observational study of clinical characteristics and healthcare resource utilization.

Authors: Gish RG MacEwan JP Levine A et al.

Source: Journal of comparative effectiveness research [J Comp Eff Res] 2025 Apr; Vol. 14 (4), pp. e240174. Date of Electronic Publication: 2025 Mar 06.

Publication Type: Journal Article; Observational Study; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Becaris Publishing Country of Publication: England NLM ID: 101577308 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2042-6313 (Electronic) Linking ISSN: 20426305 NLM ISO Abbreviation: J Comp Eff Res Subsets: MEDLINE