Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome von Larsson, N G, Holme, E, Kristiansson, B, Oldfors, A, Tulinius, M

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings von Gudjónsdóttir, Audur H., Nilsson, Staffan, Ek, Johan, Kristiansson, Bengt, Ascher, Henry

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Longitudinal Growth in Children and Adolescents with Inflammatory Bowel Disease von Hildebrand, Hans, Karlberg, Johan, Kristiansson, Bengt

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Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11 von Naluai, A T, Nilsson, S, Gudjónsdóttir, A H, Louka, A S, Ascher, H, Ek, J, Hallberg, B, Samuelsson, L, Kristiansson, B, Martinsson, T, Nerman, O, Sollid, L M, Wahlström, J

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Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations von ERLANDSON, Anna, BJURSELL, Cecilia, STIBLER, Helena, KRISTIANSSON, Bengt, WAHLSTRÖM, Jan, MARTINSSON, Tommy

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Intestinal, Pancreatic and Hepatic Involvement in Carbohydrate-Deficient Glycoprotein Syndrome Type I von Kristianson, Bengt, Borulf, Stefan, Conradi, Nils, Erlanson-Albertsson, Charlotte, Ryd, Walter, Stibler, Helena

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The decrease of IGF-I, IGF-binding protein-3 and bone alkaline phosphatase isoforms during gluten challenge correlates with small intestinal inflammation in children with coeliac d... von JANSSON, Ulf H. G, KRISTIANSSON, Bengt, MAGNUSSON, Per, LARSSON, Lasse, ALBERTSSON-WIKLAND, Kerstin, BJARNASON, Ragnar

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Carbohydrate-deficient glycoprotein syndromes: Peculiar group of new disorders von Hagberg, Bengt A., Blennow, Gösta, Kristiansson, Bengt, Stibler, Helena

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The Highest Incidence of Celiac Disease in Europe: The Swedish Experience von Ascher, Henry, Kristiansson, Bengt

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PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families von Bjursell, Cecilia, Erlandson, Anna, Nordling, Margareta, Nilsson, Staffan, Wahlström, Jan, Stibler, Helena, Kristiansson, Bengt, Martinsson, Tommy

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The Risk of Celiac Disease in 107 Families With at Least Two Affected Siblings von Gudjónsdóttir, Audur H., Nilsson, Staffan, Ek, Johan, Kristiansson, Bengt, Ascher, Henry

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The highest incidence of celiac disease in Europe: the Swedish experience von Ascher, H, Kristiansson, B

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Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations von Tulinius, Már H., Holme, Elisabeth, Kristiansson, Bengt, Larsson, Nils-Göran, Oldfors, Anders

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Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families von Bjursell, C, Wahlström, J, Berg, K, Stibler, H, Kristiansson, B, Matthijs, G, Martinsson, T

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CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY von Holme, Elisabeth, Jacobson, Carl-Eric, Nordin, Ingalill, Greter, Joachim, Lindstedt, Sven, Kristiansson, Bengt, Jodal, Ulf

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Chronic Inflammatory Bowel Disease in Children and Adolescents in Sweden von Hildebrand, Hans, Fredrikzon, Bo, Holmquist, Lars, Kristiansson, Bengt, Lindquist, Bo

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Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406 von Martinsson, T, Bjursell, C, Stibler, H, Kristiansson, B, Skovby, F, Jaeken, J, Blennow, G, Strömme, P, Hanefeld, F, Wahlström, J

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Fine Mapping of the Gene for Carbohydrate-Deficient Glycoprotein Syndrome, Type I (CDG1): Linkage Disequilibrium and Founder Effect in Scandinavian Families von Bjursell, Cecilia, Stibler, Helena, Wahlström, Jan, Kristiansson, Bengt, Skovby, Flemming, Strömme, Petter, Blennow, Gösta, Martinsson, Tommy

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Childhood coeliac disease in Sweden von Ascher, Henry, Kristiansson, Bengt, Juto, Per, Meeuwisse, Gunnar, Stenhammar, Lars

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Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes von Tulinius, Már H., Holme, Elisabeth, Kristiansson, Bengt, Larsson, Nils-Göran, Oldfors, Anders

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