Search Results - "Bessonova, L. A."

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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.

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

[Autosomal dominant spastic paraplegias].

Transliterated Title: Autosomno-dominantnye spasticheskie paraplegii.

Authors: Rudenskaya GE Kadnikova VA Bessonova LA et al.

Source: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova [Zh Nevrol Psikhiatr Im S S Korsakova] 2021; Vol. 121 (5), pp. 75-87.

Publication Type: Journal Article

Journal Info: Publisher: Media Sfera Country of Publication: Russia (Federation) NLM ID: 9712194 Publication Model: Print Cited Medium: Print ISSN: 1997-7298 (Print) Linking ISSN: 19977298 NLM ISO Abbreviation: Zh Nevrol Psikhiatr Im S S Korsakova Subsets: MEDLINE

[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 EK El'chinova GI Petrin AN et al.

Source: Genetika [Genetika] 2012 Sep; Vol. 48 (9), pp. 1105-12.

Publication Type: English Abstract; Journal Article

Journal Info: Publisher: Izdatelstvo Nauka Country of Publication: Russia (Federation) NLM ID: 0047354 Publication Model: Print Cited Medium: Print ISSN: 0016-6758 (Print) Linking ISSN: 00166758 NLM ISO Abbreviation: Genetika Subsets: MEDLINE

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

Authors: Bessonova LA El'chinova GI Zinchenko RA

Source: Genetika [Genetika] 2012 May; Vol. 48 (5), pp. 644-54.

Publication Type: English Abstract; Journal Article

Journal Info: Publisher: Izdatelstvo Nauka Country of Publication: Russia (Federation) NLM ID: 0047354 Publication Model: Print Cited Medium: Print ISSN: 0016-6758 (Print) Linking ISSN: 00166758 NLM ISO Abbreviation: Genetika Subsets: MEDLINE