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Cor Triatriatum Sinistrum: A Rare Disease with a Common Presentation

Sultan Qaboos University medical journal, 2021-06, Vol.21 (2), p.324-326

2021

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Transcatheter Closure of Ruptured Sinus of Valsalva Aneurysm: Report of two cases

Sultan Qaboos University medical journal, 2016-11, Vol.16 (4), p.e511-515

2016

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Successful Treatment of Cardiomyopathy due to Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: First Case Report from Oman with Literature Review

Oman medical journal, 2013-09, Vol.28 (5), p.354-356

2013

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Echocardiographic Evidence of Early Diastolic Dysfunction in Asymptomatic Children with Osteogenesis Imperfecta

Sultan Qaboos University medical journal, 2015-11, Vol.15 (4), p.456-462

2015

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Congenital Giant Left Atrium with Severe Mitral Valve Regurgitation

Sultan Qaboos University medical journal, 2016-05, Vol.16 (2), p.254-256

2016

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Comparison of Two Surgical Techniques for Complete Atrioventricular Septal Defect Repair Using Two- and Three-Dimensional Echocardiography

Pediatric cardiology, 2014-03, Vol.35 (3), p.393-398

2014

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Phenotypic spectrum of ALPK3‐related cardiomyopathy

American journal of medical genetics. Part A, 2019-07, Vol.179 (7), p.1235-1240

2019

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Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive

Human mutation, 2017-06, Vol.38 (6), p.692-703

2017

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Complicated Subacute Bacterial Endocarditis in a Patient with Ventricular Septal Defect

Sultan Qaboos University medical journal, 2014-02, Vol.14 (1), p.130-133

2014

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Pulmonary Artery Pseudoaneurysm in a Child With β-Thalassemia Major

Journal of pediatric hematology/oncology, 2020-08, Vol.42 (6), p.e503

2020

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Coarctation of the Aorta , Known Yet Can Be Missed

Oman medical journal, 2013-05, Vol.28 (3), p.204-206

2013

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Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study

Acta bio-medica : Atenei Parmensis, 2022-05, Vol.93 (2), p.e2022022

2022

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Percutaneous Closure of Ventricular Septal Defects in 116 Patients: Experience with different devices

Sultan Qaboos University medical journal, 2020-11, Vol.20 (4), p.e352-359

2020

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Kawarabi: Administrative Structuring of a Multicenter Research Collaborative to Study Kawasaki Disease in the Arab Countries

World journal for pediatric & congenital heart surgery, 2024-03, Vol.15 (2), p.177-183

2024

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Echocardiography in PICU: when the heart sees what is invisible to the eye

Jornal de pediatria, 2016-01, Vol.92 (1), p.96-100

2016

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Changing Survival Rate of Infants Born Before 26 Gestational Weeks: Single-centre study

Sultan Qaboos University medical journal, 2015-08, Vol.15 (3), p.e351-356

2015

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Echocardiographic Detection of Early Myocardial Calcification in Acute Neonatal Myocarditis Due to Coxsackie Virus Type B

Pediatric cardiology, 2009-08, Vol.30 (6), p.862-863

2009

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PM025 A Severe Type of Long QT Syndrome and Cardiovascular Anomaly in a Homozygous Carrier of a Novel KCNH2 Mutation and Findings in Family Screening

Global heart, 2014-03, Vol.9 (1), p.e66-e67

2014

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Paediatric Restrictive Cardiomyopathy - Diagnosis and Challenges: A report of two cases

Sultan Qaboos University medical journal, 2023-09

2023

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Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey

Pediatric cardiology, 2023-08, Vol.44 (6), p.1277-1284

2023

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Re: Maxillary Artery Pseudoaneurysm as a Complication of Maxillofacial Injuries : Report of Three Cases and Literature Review = رد : تمدد كاذب للشريان الفكي العلوي كإحدى مضاعفات إصابات الوجه والفكين : تقرير ثلاث حالات مع مراجعة أدبية

Sultan Qaboos University medical journal, 2020-01, Vol.20 (4), p.401-403

2020

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Kawasaki Disease Arab Initiative [Kawarabi]: Establishment and Results of a Multicenter Survey

Pediatric cardiology, 2022-08, Vol.43 (6), p.1239-1246

2022

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Percutaneous transhepatic stenting of a restrictive atrial septal communication in hypoplastic left heart syndrome

Catheterization and cardiovascular interventions, 2014-06, Vol.83 (7), p.E269-E271

2014

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Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive: BAERTLING et al

Human mutation, 2017-06, Vol.38 (6), p.692-703

2017

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Hypertrophic Obstructive Cardiomyopathy in An Infant With Hemophagocytic Lymphohistiocytosis; Answer to a Riddle

Journal of pediatric hematology/oncology, 2015-08, Vol.37 (6), p.459-461

2015

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Cor Triatriatum Sinistrum: A Rare Disease with a Common Presentation

Transcatheter Closure of Ruptured Sinus of Valsalva Aneurysm: Report of two cases

Successful Treatment of Cardiomyopathy due to Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: First Case Report from Oman with Literature Review

Echocardiographic Evidence of Early Diastolic Dysfunction in Asymptomatic Children with Osteogenesis Imperfecta

Congenital Giant Left Atrium with Severe Mitral Valve Regurgitation

Comparison of Two Surgical Techniques for Complete Atrioventricular Septal Defect Repair Using Two- and Three-Dimensional Echocardiography

Phenotypic spectrum of ALPK3‐related cardiomyopathy

Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive

Complicated Subacute Bacterial Endocarditis in a Patient with Ventricular Septal Defect

Pulmonary Artery Pseudoaneurysm in a Child With β-Thalassemia Major

Coarctation of the Aorta , Known Yet Can Be Missed

Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort study

Percutaneous Closure of Ventricular Septal Defects in 116 Patients: Experience with different devices

Kawarabi: Administrative Structuring of a Multicenter Research Collaborative to Study Kawasaki Disease in the Arab Countries

Echocardiography in PICU: when the heart sees what is invisible to the eye

Changing Survival Rate of Infants Born Before 26 Gestational Weeks: Single-centre study

Echocardiographic Detection of Early Myocardial Calcification in Acute Neonatal Myocarditis Due to Coxsackie Virus Type B

PM025 A Severe Type of Long QT Syndrome and Cardiovascular Anomaly in a Homozygous Carrier of a Novel KCNH2 Mutation and Findings in Family Screening

Paediatric Restrictive Cardiomyopathy - Diagnosis and Challenges: A report of two cases

Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey

Kawasaki Disease Arab Initiative [Kawarabi]: Establishment and Results of a Multicenter Survey

Percutaneous transhepatic stenting of a restrictive atrial septal communication in hypoplastic left heart syndrome

Mutation in mitochondrial complex IV subunit COX5A causes pulmonary arterial hypertension, lactic acidemia, and failure to thrive: BAERTLING et al

Hypertrophic Obstructive Cardiomyopathy in An Infant With Hemophagocytic Lymphohistiocytosis; Answer to a Riddle

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