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Percutaneous aspiration of the gall bladder for the treatment of acute cholecystitis: a prospective study

Surgical endoscopy, 2016-05, Vol.30 (5), p.1948-1951

2016

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A Novel Titin Mutation in Adult-Onset Familial Dilated Cardiomyopathy

The American journal of cardiology, 2012-06, Vol.109 (11), p.1644-1650

2012

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Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia

Circulation (New York, N.Y.), 2007-07, Vol.116 (5), p.463-470

2007

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Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: Clinical features and assignment of the disease gene to chromosome 1p13-21

Circulation (New York, N.Y.), 2001-06, Vol.103 (23), p.2822-2827

2001

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Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

Nature genetics, 2003-06, Vol.34 (2), p.151-153

2003

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A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family

American journal of human genetics, 2002-05, Vol.70 (5), p.1363-1367

2002

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A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

Trends in Cardiovascular Medicine, 2003-05, Vol.13 (4), p.148-151

2003

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Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing

BMC medical genomics, 2016-05, Vol.9 (1), p.24-24, Article 24

2016

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RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardia

Circulation (New York, N.Y.), 2003-01, Vol.107 (3), p.e29; author reply e29-e29; author reply e29

2003

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A novel form of familial bidirectional ventricular tachycardia

The American journal of cardiology, 2004-01, Vol.93 (2), p.231-234

2004

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Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan jews

Human genetics, 2002-08, Vol.111 (2), p.214-218

2002

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A novel form of familial bidirectional ventricular tachycardia

Journal of the American College of Cardiology, 2003-03, Vol.41 (6), p.133-133

2003

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Autosomal recessive catecholamine-induced polymorphic ventricular tachycardia

Experimental and clinical cardiology, 2002-01, Vol.7 (2-3), p.128-130

2002

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A new gene causing sudden cardiac death in children from a Bedouin tribe in North Israel

Journal of molecular and cellular cardiology, 2002-06, Vol.34 (6), p.A37-A37

2002

Volltextzugriff (PDF)

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity

Genetic testing, 2001, Vol.5 (4), p.331-334

2001

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Percutaneous aspiration of the gall bladder for the treatment of acute cholecystitis: a prospective study

A Novel Titin Mutation in Adult-Onset Familial Dilated Cardiomyopathy

Point mutation in the HCN4 cardiac ion channel pore affecting synthesis, trafficking, and functional expression is associated with familial asymptomatic sinus bradycardia

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: Clinical features and assignment of the disease gene to chromosome 1p13-21

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family

A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing

RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardia

A novel form of familial bidirectional ventricular tachycardia

Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan jews

A novel form of familial bidirectional ventricular tachycardia

Autosomal recessive catecholamine-induced polymorphic ventricular tachycardia

A new gene causing sudden cardiac death in children from a Bedouin tribe in North Israel

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity

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