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Polski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego
|
October 12, 2010
[Comparison of treatment effectiveness of implantable cardioverter defibrillator in patients undergoing defibrillation threshold testing at the time of implantation versus no defibrillation threshold testing]
Jacek Lelakowski, Igor Tomala, Anna Rydlewska, et al.
Journal of Medical Genetics
|
May 22, 2021
A protein-truncating mutation in <i>CCNB3</i> in a patient with recurrent miscarriages and failure of meiosis I
Maryam Rezaei, William Buckett, Eric Bareke, et al.
BMC Genomics
|
August 19, 2006
Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphisms
Hui-Qi Qu, Steve G Lawrence, Fan Guo, et al.
Kardiologia Polska
|
October 20, 2009
[Thoracoscopic Ex-Maze III procedure and radiofrequency catheter ablation - a hybrid therapy for permanent atrial fibrillation. A case report]
Jacek Majewski, Krzysztof Bartuś, Bogusław Kapelak, et al.
BMC Genomics
|
June 25, 2010
Alternative splicing is frequent during early embryonic development in mouse
Timothée Revil, Daniel Gaffney, Christel Dias, et al.
Kardiologia Polska
|
May 20, 2011
[Electrocardiogram of the patient after Fontan operation]
Jacek Majewski, Lidia Tomkiewicz Pająk, Maria Olszowska, et al.
Journal of Medical Genetics
|
February 26, 2013
Mutations in WNT1 are a cause of osteogenesis imperfecta
Somayyeh Fahiminiya, Jacek Majewski, John Mort, et al.
Kardiologia Polska
|
July 9, 2014
Effectiveness of atrial versus atrioventricular pacing for sick sinus syndrome during long-term follow-up
Marcin Kuniewicz, Anna Rydlewska, Grzegorz Karkowski, et al.
Kardiologia Polska
|
October 17, 2008
Efficacy of intra-operative radiofrequency ablation in patients with permanent atrial fibrillation undergoing concomitant mitral valve replacement
Tomasz Myrdko, Maria Sniezek-Maciejewska, Paweł Rudziński, et al.
Ophthalmic Genetics
|
June 17, 2011
A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome
Elie Akoury, Elie El Zir, Ahmad Mansour, et al.
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of 34
Search research articles
Search
Showing results (71-80 of 333) with videos related to
Sort By:
Page
of 34
Polski Merkuriusz Lekarski : Organ Polskiego Towarzystwa Lekarskiego
|
October 12, 2010
[Comparison of treatment effectiveness of implantable cardioverter defibrillator in patients undergoing defibrillation threshold testing at the time of implantation versus no defibrillation threshold testing]
Jacek Lelakowski, Igor Tomala, Anna Rydlewska, et al.
Journal of Medical Genetics
|
May 22, 2021
A protein-truncating mutation in <i>CCNB3</i> in a patient with recurrent miscarriages and failure of meiosis I
Maryam Rezaei, William Buckett, Eric Bareke, et al.
BMC Genomics
|
August 19, 2006
Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphisms
Hui-Qi Qu, Steve G Lawrence, Fan Guo, et al.
Kardiologia Polska
|
October 20, 2009
[Thoracoscopic Ex-Maze III procedure and radiofrequency catheter ablation - a hybrid therapy for permanent atrial fibrillation. A case report]
Jacek Majewski, Krzysztof Bartuś, Bogusław Kapelak, et al.
BMC Genomics
|
June 25, 2010
Alternative splicing is frequent during early embryonic development in mouse
Timothée Revil, Daniel Gaffney, Christel Dias, et al.
Kardiologia Polska
|
May 20, 2011
[Electrocardiogram of the patient after Fontan operation]
Jacek Majewski, Lidia Tomkiewicz Pająk, Maria Olszowska, et al.
Journal of Medical Genetics
|
February 26, 2013
Mutations in WNT1 are a cause of osteogenesis imperfecta
Somayyeh Fahiminiya, Jacek Majewski, John Mort, et al.
Kardiologia Polska
|
July 9, 2014
Effectiveness of atrial versus atrioventricular pacing for sick sinus syndrome during long-term follow-up
Marcin Kuniewicz, Anna Rydlewska, Grzegorz Karkowski, et al.
Kardiologia Polska
|
October 17, 2008
Efficacy of intra-operative radiofrequency ablation in patients with permanent atrial fibrillation undergoing concomitant mitral valve replacement
Tomasz Myrdko, Maria Sniezek-Maciejewska, Paweł Rudziński, et al.
Ophthalmic Genetics
|
June 17, 2011
A novel 5-bp deletion in Clarin 1 in a family with Usher syndrome
Elie Akoury, Elie El Zir, Ahmad Mansour, et al.
Page
of 34