Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
Irgens, H. U., Molnes, J., Johansson, B. B., Ringdal, M., Skrivarhaug, T., Undlien, D. E., Søvik, O., Joner, G., Molven, A., Njølstad, P. R.
Published in Diabetologia (01.07.2013)
Published in Diabetologia (01.07.2013)
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Independent mutational events in the hypervariable region of the carboxyl ester lipase gene: Identification of two new CEL-MODY families from Sweden and the Czech Republic
El Jellas, K., Dušátková, P., Molnes, J., Haldorsen, I., Tjora, E., Johansson, B., Fjeld, K., Johansson, S., Ů, Prúhová, Groop, L., Njølstad, P., Molven, A.
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.11.2020)
Published in Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (01.11.2020)
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Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children
Jahnavi, S, Poovazhagi, V, Mohan, V, Bodhini, D, Raghupathy, P, Amutha, A, Suresh Kumar, P, Adhikari, P, Shriraam, M, Kaur, T, Das, AK, Molnes, J, Njolstad, PR, Unnikrishnan, R, Radha, V
Published in Clinical genetics (01.05.2013)
Published in Clinical genetics (01.05.2013)
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The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes
Sagen, J.V., Bjørkhaug, L., Haukanes, B.I., Grevle, L., Molnes, J., Nedrebø, B.G., Søvik, O., Njølstad, P.R., Johansson, S., Molven, A.
Published in Diabetes research and clinical practice (01.11.2017)
Published in Diabetes research and clinical practice (01.11.2017)
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Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases
El Jellas, Khadija, Dušátková, Petra, Haldorsen, Ingfrid S, Molnes, Janne, Tjora, Erling, Johansson, Bente B, Fjeld, Karianne, Johansson, Stefan, Průhová, Štěpánka, Groop, Leif, Löhr, J Matthias, Njølstad, Pål R, Molven, Anders
Published in The journal of clinical endocrinology and metabolism (01.04.2022)
Published in The journal of clinical endocrinology and metabolism (01.04.2022)
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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes
Gloyn, Anna L, Pearson, Ewan R, Antcliff, Jennifer F, Proks, Peter, Bruining, G. Jan, Slingerland, Annabelle S, Howard, Neville, Srinivasan, Shubha, Silva, José M.C.L, Molnes, Janne, Edghill, Emma L, Frayling, Timothy M, Temple, I. Karen, Mackay, Deborah, Shield, Julian P.H, Sumnik, Zdenek, van Rhijn, Adrian, Wales, Jerry K.H, Clark, Penelope, Gorman, Shaun, Aisenberg, Javier, Ellard, Sian, Njølstad, Pål R, Ashcroft, Frances M, Hattersley, Andrew T
Published in The New England journal of medicine (29.04.2004)
Published in The New England journal of medicine (29.04.2004)
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Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy
SAGEN, Jørn V, RAEDER, Helge, GLOYN, Anna L, HATTERSLEY, Andrew T, MOLVEN, Anders, SØVIK, Oddmund, NJØLSTAD, Pal R, HATHOUT, Eba, SHEHADEH, Naim, GUDMUNDSSON, Kolbeinn, BAEVRE, Halvor, ABUELO, Dianne, PHORNPHUTKUL, Chanika, MOLNES, Janne, BELL, Graeme I
Published in Diabetes (New York, N.Y.) (01.10.2004)
Published in Diabetes (New York, N.Y.) (01.10.2004)
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Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions
Tammaro, Paolo, Girard, Christophe, Molnes, Janne, Njølstad, Pål R, Ashcroft, Frances M
Published in The EMBO journal (06.07.2005)
Published in The EMBO journal (06.07.2005)
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Epidermal Growth Factor Receptor Efficiently Activates Mitogen-Activated Protein Kinase in HeLa Cells and Hep2 Cells Conditionally Defective in Clathrin-Dependent Endocytosis
Johannessen, Lene Elisabeth, Ringerike, Tove, Molnes, Janne, Madshus, Inger Helene
Published in Experimental cell research (10.10.2000)
Published in Experimental cell research (10.10.2000)
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