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Sivitskaya, Larysa
19  Ergebnisse:
Personensuche X
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1

Optimised, Broad NGS Panel for Inherited Eye Diseases to Di..:

Matczyńska, Ewa ; Beć-Gajowniczek, Marta ; Sivitskaya, Larysa...
Biomedicines.  12 (2024)  6 - p. 1355 , 2024
Link: https://doi.org/10.3390/..
 
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2

New deletion in LAMP2 causing familial Danon disease. Effec..:

Sivitskaya, Larysa ; Vaikhanskaya, Tatiyana ; Danilenko, Nina...
Folia Medica.  64 (2022)  5 - p. 853-862 , 2022
Link: https://doi.org/10.3897/..
 
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3

Application of NGS Technology in Understanding the Patholog..:

Wajda, Anna ; Sivitskaya, Larysa ; Paradowska-Gorycka, Agnieszka
Journal of Clinical Medicine.  10 (2021)  15 - p. 3334 , 2021
Link: https://doi.org/10.3390/..
 
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4

AHR-dependent genes and response to MTX therapy in rheumato..:

Wajda, Anna ; Walczuk, Ewa ; Stypińska, Barbara...
The Pharmacogenomics Journal.  21 (2021)  5 - p. 608-621 , 2021
Link: https://doi.org/10.1038/..
 
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5

Splicing mutation in LAMP2 gene leading to exon skipping an..:

Sivitskaya, Larysa ; Vaikhanskaya, Tatiyana ; Danilenko, Nina...
Gene Reports.  18 (2020)  - p. 100564 , 2020
Link: https://doi.org/10.1016/..
 
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6

Uniparental Genetic Heritage of Belarusians: Encounter of R..:

Kushniarevich, Alena ; Sivitskaya, Larysa ; Danilenko, Nina...
PLoS ONE.  8 (2013)  6 - p. e66499 , 2013
Link: https://doi.org/10.1371/..
 
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7

HFE Gene Mutation Associated with the Severity of Gestation..:

Sivitskaya, Larysa ; Danilenko, Nina ; Zabarouskaya, Zoya.
Open Journal of Endocrine and Metabolic Diseases.  3 (2013)  1 - p. 13-17 , 2013
Link: https://doi.org/10.4236/..
 
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8

New deletion in LAMP2 causing familial Danon disease. Effec..:

Sivitskaya, Larysa ; Vaikhanskaya2, Tatiyana ; Danilenko, Nina...
info:eu-repo/semantics/altIdentifier/eissn/1314-2143.  , 2022
Link: https://doi.org/10.3897/..
 
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9

Application of NGS Technology in Understanding the Patholog..:

Wajda, Anna ; Sivitskaya, Larysa ; Paradowska-Gorycka, Agnieszka
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8348854/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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10

AHR-dependent genes and response to MTX therapy in rheumato..:

Wajda, Anna ; Walczuk, Ewa ; Stypińska, Barbara...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455325/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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11

Splicing mutation in TAZ gene leading to exon skipping and ..:

Sivitskaya, Larysa ; Danilenko, Nina ; Motuk, Iryna.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290511/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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12

Novel desmoplakin mutations in familial Carvajal syndrome:

YERMAKOVICH, DANAT ; SIVITSKAYA, LARYSA ; VAIKHANSKAYA, TATIYANA..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416697/.  , 2018
Link: http://www.ncbi.nlm.nih...
 
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13

LMNA-related dilated cardiomyopathy:

Vaikhanskaya, Tatiyana ; Sivitskaya, Larysa ; Danilenko, Nina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4369987/.  , 2014
Link: http://www.ncbi.nlm.nih...
 
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14

Uniparental Genetic Heritage of Belarusians: Encounter of R..:

Kushniarevich, Alena ; Sivitskaya, Larysa ; Danilenko, Nina...
https://eprints.hud.ac.uk/id/eprint/25744/1/Gandinduniparental.pdf.  , 2013
Link: http://eprints.hud.ac.uk..
 
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15

New deletion in LAMP2 causing familial Danon disease. Effec..:

Larysa Sivitskaya ; Tatiyana Vaikhanskaya ; Nina Danilenko...
https://foliamedica.bg/article/66292/download/pdf/.  , 2022
Link: https://doi.org/10.3897/..
 
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