Rym Dabboubi Selected Research

Congenital atransferrinemia

5/2020

A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del.

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Rym Dabboubi Research Topics

Disease

2	Thalassemia 09/2016 - 05/2015
1	Asthma (Bronchial Asthma) 01/2022
1	Cystic Fibrosis (Mucoviscidosis) 02/2021
1	Glucosephosphate Dehydrogenase Deficiency 08/2020
1	Kernicterus 08/2020
1	Neonatal Jaundice 08/2020
1	Hemolysis 08/2020
1	Congenital atransferrinemia 05/2020
1	Diabetes Mellitus 12/2018
1	Coronary Artery Disease (Coronary Atherosclerosis) 12/2018
1	Thrombosis (Thrombus) 09/2016
1	Afibrinogenemia (Fibrinogen Deficiency) 09/2016
1	Rare Diseases (Rare Disease) 09/2016
1	Hemorrhage 09/2016
1	Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders) 09/2016
1	Sickle Cell Anemia (Hemoglobin S Disease) 05/2015

Drug/Important Bio-Agent (IBA)

1	Protein CIBA 01/2022
1	Surface-Active Agents (Surfactants)IBA 01/2022
1	Chloride Channels (Chloride Channel)IBA 02/2021
1	Cystic Fibrosis Transmembrane Conductance Regulator (Protein, CFTR)IBA 02/2021
1	Hemolytic AgentsIBA 08/2020
1	Glucosephosphate Dehydrogenase (Glucose 6 Phosphate Dehydrogenase)IBA 08/2020
1	Transferrin (beta 2 Transferrin)IBA 05/2020
1	Cytochrome P-450 CYP2C19IBA 12/2018
1	Clopidogrel (Plavix)FDA Link 12/2018
1	Cytochrome P-450 Enzyme System (Cytochrome P450)IBA 12/2018
1	Hemoglobins (Hemoglobin)IBA 09/2016
1	Fibrinogen (Factor I)FDA Link 09/2016
1	FibrinIBA 09/2016
1	DNA (Deoxyribonucleic Acid)IBA 09/2016
1	GlobinsIBA 05/2015

Therapy/Procedure

1	Therapeutics 12/2018