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M Sinaasappel

Boston Children's Hospital

28

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539

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Metabolism and membrane composition of essential fatty Acids in murine cystic fibrosis

2004 Pediatric Research
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P0154 PP FAT MALABSORPTION IN CYSTIC FIBROSIS MICE IS CAUSED BY DEFECTIVE LIPOLYSIS AND POST-LIPOLYTIC EVENTS

2004 Journal of Pediatric Gastroenterology and Nutrition
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Defecte enterocytaire ATP secretie in cystic fibrosis

2001
- H.R. (Hugo) de Jonge
- M Sinaasappel
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Identification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrhea.

2001 Human Mutation
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Defect enterocytic ATP secretion in cystic fibrosis

2001
- H.R. (Hugo) de Jonge
- M Sinaasappel
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Splice-Site Mutations: A Novel Genetic Mechanism of Crigler-Najjar Syndrome Type 1

1998 American Journal of Human Genetics
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Low-dose versus high-dose ursodeoxycholic acid in cystic fibrosis-related cholestatic liver disease - Results of a randomized study with 1-year follow-up

1997 Scandinavian Journal of Gastroenterology
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Benign recurrent intrahepatic cholestasis (BRIC): evidence of genetic heterogeneity and delimitation of the BRIC locus to a 7-cM interval between D18S69 and D18S64

1997 Human Genetics
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In Vivo Measurement of Chloride and Water Secretion in the Jejunum of Cystic Fibrosis Patients

1996 Pediatric Research
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Present and future treatment modalities for gastrointestinal diseases in cystic fibrosis

1995 Netherlands Journal of Medicine
- M Sinaasappel
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