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52. Placement of Labcor Pulmonary Conduit Results in a High Incidence of Postoperative Fever

55. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy

56. Establishing a High-Quality Congenital Cardiac Surgery Program in a Developing Country: Lessons Learned

62. QTc interval on 24‐hour holter monitor: To trust or not to trust?

64. Additional file 1: of Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases

65. Pre-operative assessment of pediatric congenital heart disease patients in the COVID-19 era: lessons learned

66. Abstract 202: The R21C Mutation in Troponin I Has a Founder Effect in South Lebanon and Causes Malignant Hypertrophic Cardiomyopathy

72. Sotalol as an effective adjunct therapy in the management of supraventricular tachycardia induced fetal hydrops fetalis.

74. A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

77. TARGETED AND EXOME SEQUENCING OF 27 LEBANESE PATIENTS WITH CARDIOMYOPATHIES: NOVEL VARIANTS IN KNOWN GENES, AND POTENTIAL NOVEL GENES

79. Aortopulmonary window in adults: A rare entity leading to Eisenmenger syndrome.

81. THE R21C MUTATION IN TROPONIN I HAS A FOUNDER EFFECT IN SOUTH LEBANON AND CAUSES MALIGNANT HYPERTROPHIC CARDIOMYOPATHY

87. Elevated Tricuspid Regurgitant Jet Velocity In Lebanese Patients With Sickle Cell Disease Is Associated With Severe Disease and Is Clustered In Families

93. Pulmonary hypertension in children and young adults with sickle cell disease: Evidence for familial clustering

94. A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

95. COVID-19 in Cyanotic Congenital Heart Disease

99. Cardiac Ablation in the Pediatric Population at a Tertiary Care Center in a Developing Country.

100. Endovascular Stent Repair of Aortic Coarctation in a Developing Country: A Single-Center Experience.

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