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Sondess Hadj Fredj Selected Research

Congenital atransferrinemia

5/2020A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del.

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Sondess Hadj Fredj Research Topics

Disease

1Asthma (Bronchial Asthma)
01/2022
1Congenital atransferrinemia
05/2020
1Coronary Artery Disease (Coronary Atherosclerosis)
12/2018
1Diabetes Mellitus
12/2018
1Afibrinogenemia (Fibrinogen Deficiency)
07/2016
1Cystic Fibrosis (Mucoviscidosis)
03/2016

Drug/Important Bio-Agent (IBA)

1Surface-Active Agents (Surfactants)IBA
01/2022
1Protein CIBA
01/2022
1Transferrin (beta 2 Transferrin)IBA
05/2020
1Cytochrome P-450 CYP2C19IBA
12/2018
1Clopidogrel (Plavix)FDA Link
12/2018
1Cytochrome P-450 Enzyme System (Cytochrome P450)IBA
12/2018
1Fibrinogen (Factor I)FDA Link
07/2016
1Peptidyl-Dipeptidase A (Angiotensin Converting Enzyme)IBA
03/2016

Therapy/Procedure

1Therapeutics
12/2018