Haldorsen IS

References (5)

Title : Two new mutations in the CEL gene causing diabetes and hereditary pancreatitis: How to correctly identify MODY8 cases - El Jellas_2021_J.Clin.Endocrinol.Metab__
Author(s) : El Jellas K , Dusatkova P , Haldorsen IS , Molnes J , Tjora E , Johansson BB , Fjeld K , Johansson S , Pruhova S , Groop L , Lohr JM , Njolstad PR , Molven A
Ref : J Clinical Endocrinology Metab , : , 2021
PubMedID: 34850019
Gene_locus related to this paper: human-CEL

Title : Lack of pancreatic body and tail in HNF1B mutation carriers - Haldorsen_2008_Diabet.Med_25_782
Author(s) : Haldorsen IS , Vesterhus M , Raeder H , Jensen DK , Sovik O , Molven A , Njolstad PR
Ref : Diabet Med , 25 :782 , 2008
PubMedID: 18644064

Title : Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young - Vesterhus_2008_J.Clin.Endocrinol.Metab_93_3505
Author(s) : Vesterhus M , Haldorsen IS , Raeder H , Molven A , Njolstad PR
Ref : J Clinical Endocrinology Metab , 93 :3505 , 2008
PubMedID: 18593771

Title : Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase - Raeder_2007_Diabetes_56_444
Author(s) : Raeder H , Haldorsen IS , Ersland L , Gruner R , Taxt T , Sovik O , Molven A , Njolstad PR
Ref : Diabetes , 56 :444 , 2007
PubMedID: 17259390

Title : Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. - Raeder_2006_Nat.Genet_38_54
Author(s) : Raeder H , Johansson S , Holm PI , Haldorsen IS , Mas E , Sbarra V , Nermoen I , Eide SA , Grevle L , Bjorkhaug L , Sagen JV , Aksnes L , Svik O , Lombardo D , Molven A , Njolstad PR
Ref : Nat Genet , 38 :54 , 2006
PubMedID: 16369531
Gene_locus related to this paper: human-CEL