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Pacing and Clinical Electrophysiology : PACE
|
March 25, 2008
DNA analysis in inherited cardiomyopathies: current status and clinical relevance
Karin Y van Spaendonck-Zwarts, Maarten P van den Berg, J Peter van Tintelen
Cardiovascular Research
|
January 31, 2015
Genetic advances in sarcomeric cardiomyopathies: state of the art
Carolyn Y Ho, Philippe Charron, Pascale Richard, et al.
Cardiovascular Research
|
January 24, 2014
Pregnancy, cardiomyopathies, and genetics
J Peter Van Tintelen, Petronella G Pieper, Karin Y Van Spaendonck-Zwarts, et al.
Orphanet Journal of Rare Diseases
|
March 21, 2014
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 25, 2017
Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutations
Barbara W van Paassen, Marieke Bronk, Camiel Verhamme, et al.
European Journal of Heart Failure
|
April 13, 2011
Systematic review of pregnancy in women with inherited cardiomyopathies
Sébastien P J Krul, Jasper J van der Smagt, Maarten P van den Berg, et al.
Open Heart
|
October 22, 2014
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy
Marijke Wasielewski, Karin Y van Spaendonck-Zwarts, Nico-Derk L Westerink, et al.
Circulation
|
May 12, 2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy
Karin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, et al.
Familial Cancer
|
November 17, 2011
Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance
Karin Y van Spaendonck-Zwarts, Sadhanna Badeloe, Sjoukje F Oosting, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death
Najim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 42) with videos related to
Sort By:
Page
of 5
Pacing and Clinical Electrophysiology : PACE
|
March 25, 2008
DNA analysis in inherited cardiomyopathies: current status and clinical relevance
Karin Y van Spaendonck-Zwarts, Maarten P van den Berg, J Peter van Tintelen
Cardiovascular Research
|
January 31, 2015
Genetic advances in sarcomeric cardiomyopathies: state of the art
Carolyn Y Ho, Philippe Charron, Pascale Richard, et al.
Cardiovascular Research
|
January 24, 2014
Pregnancy, cardiomyopathies, and genetics
J Peter Van Tintelen, Petronella G Pieper, Karin Y Van Spaendonck-Zwarts, et al.
Orphanet Journal of Rare Diseases
|
March 21, 2014
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 25, 2017
Pseudodominant inheritance pattern in a family with CMT2 caused by GDAP1 mutations
Barbara W van Paassen, Marieke Bronk, Camiel Verhamme, et al.
European Journal of Heart Failure
|
April 13, 2011
Systematic review of pregnancy in women with inherited cardiomyopathies
Sébastien P J Krul, Jasper J van der Smagt, Maarten P van den Berg, et al.
Open Heart
|
October 22, 2014
Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy
Marijke Wasielewski, Karin Y van Spaendonck-Zwarts, Nico-Derk L Westerink, et al.
Circulation
|
May 12, 2010
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy
Karin Y van Spaendonck-Zwarts, J Peter van Tintelen, Dirk J van Veldhuisen, et al.
Familial Cancer
|
November 17, 2011
Hereditary leiomyomatosis and renal cell cancer presenting as metastatic kidney cancer at 18 years of age: implications for surveillance
Karin Y van Spaendonck-Zwarts, Sadhanna Badeloe, Sjoukje F Oosting, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death
Najim Lahrouchi, Elisabeth M Lodder, Maria Mansouri, et al.
Page
of 5