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Saber, Siamak
34
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Online (34)
Mediatypes
Articles (Online) (19)
OpenAccess-fulltext (15)
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1
Allelic Dropout Is a Common Phenomenon That Reduces the Dia..:
Shestak, Anna G.
;
Bukaeva, Anna A.
;
Saber, Siamak
.
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
2
A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic..:
Sadeghi, Zahra
;
Chavoshi Tarzjani, Seyedeh Parisa
;
Miri Moosavi, Reyhaneh Sadat
..
International Medical Case Reports Journal. 13 (2020) - p. 291-296 , 2020
Link:
https://doi.org/10.2147/..
?
3
Mutational Spectrum of the SCN5A gene in Brugada Syndrome P..:
Shestak, Anna
;
Saber, Siamak
;
Makarov, Leonid
.
Journal of Electrocardiology. 53 (2019) - p. e5-e6 , 2019
Link:
https://doi.org/10.1016/..
?
4
Mutational Spectrum of the SCN5A gene in Brugada Syndrome P..:
Shestak, Anna
;
Saber, Siamak
;
Makarov, Leonid
.
Journal of Electrocardiology. 51 (2018) 6 - p. 1166 , 2018
Link:
https://doi.org/10.1016/..
?
5
Detection of a new KCNQ1 frameshift mutation associated wit..:
Amirian, Azam
;
Zafari, Zahra
;
Dalili, Mohammad
...
Journal of Arrhythmia. 34 (2018) 3 - p. 286-290 , 2018
Link:
https://doi.org/10.1002/..
?
6
Identification and characterization of a novel recessive KC..:
Zafari, Zahra
;
Dalili, Mohammad
;
Zeinali, Sirus
...
Journal of Electrocardiology. 50 (2017) 6 - p. 912-918 , 2017
Link:
https://doi.org/10.1016/..
?
7
Identification of a new mutation in an Iranian family with ..:
Akbaroghli, Susan
;
Balali, Maryam
;
Kamalidehghan, Behnam
...
Therapeutics and Clinical Risk Management. 13 (2016) - p. 15-19 , 2016
Link:
https://doi.org/10.2147/..
?
8
Complex genetic background in a large family with Brugada s..:
Saber, Siamak
;
Amarouch, Mohamed-Yassine
;
Fazelifar, Amir-Farjam
...
Physiological Reports. 3 (2015) 1 - p. e12256 , 2015
Link:
https://doi.org/10.14814..
?
9
Positive Brugada Challenge Test in V1R–V3R as a Predictor o..:
Hashemi, Arash
;
Shahrzad, Shahab
;
Shahrzad, Sorayya
...
Annals of Noninvasive Electrocardiology. 18 (2013) 5 - p. 421-426 , 2013
Link:
https://doi.org/10.1111/..
?
10
Sodium Current and Potassium Transient Outward Current Gene..:
Holst, Anders G.
;
Saber, Siamak
;
Houshmand, Massoud
...
Canadian Journal of Cardiology. 28 (2012) 2 - p. 196-200 , 2012
Link:
https://doi.org/10.1016/..
?
11
Accumulation of mitochondrial genome variations in Persian ..:
Khatami, Mehri
;
Houshmand, Massoud
;
Sadeghizadeh, Majid
...
Cardiovascular Pathology. 19 (2010) 2 - p. e21-e27 , 2010
Link:
https://doi.org/10.1016/..
?
12
A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic..:
Sadeghi, Zahra
;
Chavoshi Tarzjani, Seyedeh Parisa
;
Miri Moosavi, Reyhaneh Sadat
..
info:eu-repo/semantics/altIdentifier/doi/10.2147/IMCRJ.S257654. , 2020
Link:
https://www.dovepress.co..
?
13
Identification of a new mutation in an Iranian family with ..:
Akbaroghli, Susan
;
Balali, Maryam
;
Kamalidehghan, Behnam
...
info:eu-repo/semantics/altIdentifier/doi/10.2147/TCRM.S111717. , 2016
Link:
https://www.dovepress.co..
?
14
Complex genetic background in a large family with Brugada s..:
Saber, Siamak
;
Amarouch, Mohamed Yassine
;
Fazelifar, Amir-Farjam
...
https://boris.unibe.ch/80625/. , 2015
Link:
https://boris.unibe.ch/8..
?
15
Table_2_Allelic Dropout Is a Common Phenomenon That Reduces..:
Anna G. Shestak
;
Anna A. Bukaeva
;
Siamak Saber
.
doi:10.3389/fgene.2021.620337.s003. , 2021
Link:
https://doi.org/10.3389/..
1-15