S. Tulbah

发表

Polymorphisms in RAD51 and their relation with breast cancer in Saudi females

A. Al-amri, W. Khan, A. Warsy, 2016, OncoTargets and therapy.

Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications

A. Al-Hazzani, N. Dzimiri, Y. Mallawi, 2013, Clinical genetics.

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

Olfat Al-Harazi, N. Kaya, D. Çolak, 2014, Journal of Medical Genetics.

Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.

N. Dzimiri, Z. Al-Hassnan, B. Meyer, 2017, Heart rhythm.

Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia.

N. Kaya, D. Çolak, M. Daghestani, 2013, Gene.

The Phenotype of a CASQ2 Mutation in a Saudi Family with Catecholaminergic Polymorphic Ventricular Tachycardia

Z. Al-Hassnan, M. Al-Fayyadh, S. Tulbah, 2013, Pacing and clinical electrophysiology : PACE.

Recessively inherited severe aortic aneurysm caused by mutated EFEMP2.

Z. Al-Hassnan, B. Meyer, M. Al-Fayyadh, 2012, The American journal of cardiology.

Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy

E. Faqeih, Z. Al-Hassnan, A. Almesned, 2020, Circulation. Genomic and precision medicine.

The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients

Z. Al-Hassnan, O. Khalifa, M. Alkorashy, 2018, Molecular genetics and metabolism reports.

Phenotypic variability in a series of four pediatric patients with Andersen-Tawil syndrome: A Saudi experience

Z. Al-Hassnan, S. Tulbah, Waleed Al-Manea, 2019, International journal of pediatrics & adolescent medicine.

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

N. Kaya, D. Çolak, Z. Al-Hassnan, 2016, BMC Medical Genetics.

A novel homozygous SCN5A variant detected in sick sinus syndrome

Z. Al-Hassnan, N. Al-Numair, M. Alkorashy, 2020, Pacing and clinical electrophysiology : PACE.

Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications

A. Al-Hazzani, N. Dzimiri, Z. Al-Hassnan, 2013, Clinical genetics.

Identification of a novel homozygous NEXN gene mutation in recessively inherited dilated cardiomyopathy

Z. Al-Hassnan, A. Almesned, S. Tulbah, 2013 .