289 results on '"Arabi, Mariam"'
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52. Placement of Labcor Pulmonary Conduit Results in a High Incidence of Postoperative Fever
53. COVID-19 in Pediatric Patients: A Focus on CHD Patients
54. Hydroxychloroquine in COVID-19 Patients: Pros and Cons
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
57. Cardiac Tamponade Caused by Cutibacterium acnes: An Updated and Comprehensive Review of the Literature
58. Sotalol as an effective adjunct therapy in the management of supraventricular tachycardia induced fetal hydrops fetalis
59. Large congenital left atrial wall aneurysm: An updated and comprehensive review of the literature
60. Steroids as a possible effective therapy in the management of large isolated chylopericardium following open heart surgery
61. Pulmonary hypertension in children and young adults with sickle cell disease: Evidence for familial clustering
62. QTc interval on 24‐hour holter monitor: To trust or not to trust?
63. MOESM2 of Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension
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
67. The first Fetal Echocardiography experience for Prenatal diagnosis of Congenital Heart Disease in Lebanon: Successes and challenges
68. Atrial septal defect closure complicated by anomalous inferior vena cava return to the left atrium: a case report of a 5-year-old child
69. Fetal Intra‐pericardial Morgagni Hernia with effusion affecting one member of a twin gestation
70. ECMO is in the air: Long distance air/ground transport of a child on extra corporeal membrane oxygenation
71. Port-a-Cath fracture and migration in paediatric cancer patients: incidence and management at a tertiary care centre - a 15-year experience.
72. Sotalol as an effective adjunct therapy in the management of supraventricular tachycardia induced fetal hydrops fetalis.
73. Lower extremity thrombosis and myocarditis due to Human PVB19 infection
74. A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects
75. A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
76. Premature Valvular Heart Disease in Homozygous Familial Hypercholesterolemia
77. TARGETED AND EXOME SEQUENCING OF 27 LEBANESE PATIENTS WITH CARDIOMYOPATHIES: NOVEL VARIANTS IN KNOWN GENES, AND POTENTIAL NOVEL GENES
78. Founder Mutation in N Terminus of Cardiac Troponin I Causes Malignant Hypertrophic Cardiomyopathy
79. Aortopulmonary window in adults: A rare entity leading to Eisenmenger syndrome.
80. NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity
81. THE R21C MUTATION IN TROPONIN I HAS A FOUNDER EFFECT IN SOUTH LEBANON AND CAUSES MALIGNANT HYPERTROPHIC CARDIOMYOPATHY
82. Surgical repair of partial atrioventricular defect
83. Surgical repair of complete atrioventricular defect (Nunn technique)
84. Lack of Cardiac Iron in SCD Patients Despite Severe Iron Overload
85. Noninvasive Nitric Oxide Therapy in Right Ventricular Systolic Dysfunction Following Arterial Switch Procedure
86. Low-Density Lipoprotein Levels and Not Mutation Status Predict Intima-Media Thickness in Familial Hypercholesterolemia
87. Elevated Tricuspid Regurgitant Jet Velocity In Lebanese Patients With Sickle Cell Disease Is Associated With Severe Disease and Is Clustered In Families
88. Rupture of Sinus of Valsalva Aneurysm With Aorto-Biventricular Fistulas and Right-Ventricular Outflow Tract Obstruction: A Unique Association
89. Research in Congenital Heart Disease: A Comparative Bibliometric Analysis Between Developing and Developed Countries
90. Cardiac Involvement in Nonketotic Hyperglycinemia
91. Homozygous familial hypercholesterolemia in Lebanon: A genotype/phenotype correlation
92. Prolonged Fever With Pulmonary Nodules in a 4-Month-Old Baby
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
96. Cardiac tamponade as the first manifestation of systemic lupus erythematosus in children.
97. THE STATUS OF PEDIATRIC CARDIOLOGY AT A TERTIARY CENTER IN LEBANON.
98. ABSENCE OF GJA1 GENE MUTATIONS IN FOUR PATIENTS WITH ANOMALOUS LEFT CORONARY ARTERY FROM THE PULMONARY ARTERY (ALCAPA).
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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