Marwan Alfalah Selected Research

congenital Sucrase-isomaltase deficiency

3/2009	Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.
5/2006	Altered folding, turnover, and polarized sorting act in concert to define a novel pathomechanism of congenital sucrase-isomaltase deficiency.
1/2006	Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption.
12/2003	Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum.

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Marwan Alfalah Research Topics

Disease

4	congenital Sucrase-isomaltase deficiency 03/2009 - 12/2003
2	Carcinoma (Carcinomatosis) 01/2008 - 02/2006
1	Cystic Fibrosis (Mucoviscidosis) 10/2006
1	Asthma (Bronchial Asthma) 10/2006
1	Inflammation (Inflammations) 04/2006
1	Leukemia 04/2006
1	Gaucher Disease (Gaucher's Disease) 11/2005

Drug/Important Bio-Agent (IBA)

3	Oligo-1,6-Glucosidase (Isomaltase)IBA 03/2009 - 12/2003
3	Sucrase (Sucrose alpha-D-Glucohydrolase)IBA 03/2009 - 12/2003
3	Proteins (Proteins, Gene)FDA Link 01/2008 - 04/2006
3	EnzymesIBA 05/2006 - 12/2003
2	AntigensIBA 01/2008 - 02/2006
2	DisaccharidesIBA 05/2006 - 01/2006
1	Hormones (Hormone)IBA 01/2008
1	Detergents (Detergent)IBA 01/2008
1	Chloride Channels (Chloride Channel)IBA 10/2006
1	Sucrase-Isomaltase ComplexIBA 05/2006
1	CD13 Antigens (Alanine Aminopeptidase)IBA 04/2006
1	Membrane Glycoproteins (Membrane Glycoprotein)IBA 02/2006
1	Glucosylceramidase (Glucocerebrosidase)IBA 11/2005