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Items: 1 to 50 of 76

1.

The risk of celiac disease in 107 families with at least two affected siblings.

Gudjónsdóttir AH, Nilsson S, Ek J, Kristiansson B, Ascher H.

J Pediatr Gastroenterol Nutr. 2004 Mar;38(3):338-42.

PMID:
15076637
2.

Short-term gluten challenge in children with coeliac disease does not impair spontaneous growth hormone secretion.

Jansson UH, Kristiansson B, Albertsson-Wikland K, Bjarnason R.

J Pediatr Endocrinol Metab. 2003 Jun;16(5):771-8.

PMID:
12880127
3.

Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11.

Naluai AT, Nilsson S, Gudjónsdóttir AH, Louka AS, Ascher H, Ek J, Hallberg B, Samuelsson L, Kristiansson B, Martinsson T, Nerman O, Sollid LM, Wahlström J.

Eur J Hum Genet. 2001 Dec;9(12):938-44.

4.

Henna causes life threatening haemolysis in glucose-6-phosphate dehydrogenase deficiency.

Raupp P, Hassan JA, Varughese M, Kristiansson B.

Arch Dis Child. 2001 Nov;85(5):411-2.

5.

Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations.

Erlandson A, Bjursell C, Stibler H, Kristiansson B, Wahlström J, Martinsson T.

Hum Genet. 2001 May;108(5):359-67.

PMID:
11409861
6.
7.

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 disease.

Jansson UH, Kristiansson B, Magnusson P, Larsson L, Albertsson-Wikland K, Bjarnason R.

Eur J Endocrinol. 2001 Apr;144(4):417-23.

PMID:
11275953
8.
9.

The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders.

Naluai AT, Nilsson S, Samuelsson L, Gudjónsdóttir AH, Ascher H, Ek J, Hallberg B, Kristiansson B, Martinsson T, Nerman O, Sollid LM, Wahlström J.

Tissue Antigens. 2000 Oct;56(4):350-5.

PMID:
11098935
10.

PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families.

Bjursell C, Erlandson A, Nordling M, Nilsson S, Wahlström J, Stibler H, Kristiansson B, Martinsson T.

Hum Mutat. 2000 Nov;16(5):395-400.

PMID:
11058896
11.

Chronic hepatitis B in children in Gothenburg, Sweden.

Söderström A, Lindh M, Eriksson K, Horal P, Krantz M, Kristiansson B, Lindberg J, Norkrans G.

Scand J Infect Dis. 1999;31(2):109-14.

PMID:
10447315
12.

Thrombectomy and in situ fibrinolysis in the treatment of acute hepatic arterial thrombosis after liver transplantation in two children.

Olausson M, Bäckman L, Mjörnstedt L, Krantz M, Kristiansson B, Wiklund LM, Friman S.

Eur J Surg. 1999 Jun;165(6):618-20. No abstract available.

PMID:
10433151
13.

[CDGS-1--a recently discovered hereditary metabolic disease. Multiple organ manifestations, incidence 1/80,000, difficult to treat].

Kristiansson B, Stibler H, Hagberg B, Wahlström J.

Lakartidningen. 1998 Dec 9;95(50):5742-8. Review. Swedish.

PMID:
9889493
14.

Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families.

Bjursell C, Wahlström J, Berg K, Stibler H, Kristiansson B, Matthijs G, Martinsson T.

Eur J Hum Genet. 1998 Nov-Dec;6(6):603-11.

15.

Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A.

Kjaergaard S, Kristiansson B, Stibler H, Freeze HH, Schwartz M, Martinsson T, Skovby F.

Acta Paediatr. 1998 Aug;87(8):884-8.

PMID:
9736238
16.

Intestinal, pancreatic and hepatic involvement in carbohydrate-deficient glycoprotein syndrome type I.

Kristiansson B, Borulf S, Conradi N, Erlanson-Albertsson C, Ryd W, Stibler H.

J Pediatr Gastroenterol Nutr. 1998 Jul;27(1):23-9.

PMID:
9669722
17.

[Different policy on gluten-free food in child day care centers. Unified national guidelines are needed].

Mikkelsen A, Borres M, Kristiansson B, Odenman I.

Lakartidningen. 1998 Apr 15;95(16):1820-2, 1824. Swedish. No abstract available.

PMID:
9599489
18.

The heart and pericardial effusions in CDGS-I (carbohydrate-deficient glycoprotein syndrome type I).

Kristiansson B, Stibler H, Conradi N, Eriksson BO, Ryd W.

J Inherit Metab Dis. 1998 Apr;21(2):112-24.

PMID:
9584262
20.

Carbohydrate-deficient transferrin in galactosaemia.

Stibler H, von Döbeln U, Kristiansson B, Guthenberg C.

Acta Paediatr. 1997 Dec;86(12):1377-8.

PMID:
9475320
21.

Immunoglobulin levels in patients with carbohydrate-deficient glycoprotein syndrome type I.

Björklund JE, Stibler H, Kristiansson B, Johansson SG, Magnusson CG.

Int Arch Allergy Immunol. 1997 Oct;114(2):116-9.

PMID:
9338604
22.

The highest incidence of celiac disease in Europe: the Swedish experience.

Ascher H, Kristiansson B.

J Pediatr Gastroenterol Nutr. 1997 May;24(5):S3-6. Review. No abstract available.

PMID:
9161966
23.

Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian families.

Bjursell C, Stibler H, Wahlström J, Kristiansson B, Skovby F, Strömme P, Blennow G, Martinsson T.

Genomics. 1997 Feb 1;39(3):247-53.

PMID:
9119361
24.

Influence of infant feeding and gluten intake on coeliac disease.

Ascher H, Krantz I, Rydberg L, Nordin P, Kristiansson B.

Arch Dis Child. 1997 Feb;76(2):113-7.

25.

[Phytosterolemia is an uknown but serious disease. Xanthomatosis in childhood is a warning signal].

Hallböök T, Kristiansson B, Hildebrand H, Nordin G, Lutjohann D, Björkhem I.

Lakartidningen. 1996 Nov 20;93(47):4275-7. Swedish. No abstract available.

PMID:
8984295
26.

Complex functional and structural coagulation abnormalities in the carbohydrate-deficient glycoprotein syndrome type I.

Stibler H, Holzbach U, Tengborn L, Kristiansson B.

Blood Coagul Fibrinolysis. 1996 Mar;7(2):118-26.

PMID:
8735800
27.

[Take neonatal jaundice seriously!].

Krantz M, Rubenson A, Kristiansson B.

Lakartidningen. 1996 Feb 7;93(6):461-4, 467. Swedish. No abstract available.

PMID:
8637323
28.

Gonadal function and glycoprotein hormones in the carbohydrate-deficient glycoprotein (CDG) syndrome.

Kristiansson B, Stibler H, Wide L.

Acta Paediatr. 1995 Jun;84(6):655-9.

PMID:
7670249
29.

Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions.

Tulinius MH, Oldfors A, Holme E, Larsson NG, Houshmand M, Fahleson P, Sigström L, Kristiansson B.

Eur J Pediatr. 1995 Jan;154(1):35-42.

PMID:
7895754
30.

[Infant food and celiac disease. Risk of increase when changing the diet].

Ascher H, Hernell O, Ivarsson A, Kristiansson B, Lindberg T, Stenhammar L.

Lakartidningen. 1994 Dec 7;91(49):4641-3. Swedish. No abstract available.

PMID:
7808180
31.

Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406.

Martinsson T, Bjursell C, Stibler H, Kristiansson B, Skovby F, Jaeken J, Blennow G, Strömme P, Hanefeld F, Wahlström J.

Hum Mol Genet. 1994 Nov;3(11):2037-42.

PMID:
7874123
32.

Childhood coeliac disease in Sweden.

Ascher H, Kristiansson B.

Lancet. 1994 Jul 30;344(8918):340-1. No abstract available.

PMID:
7914289
33.

Incidence and prevalence of inflammatory bowel disease in children in south-western Sweden.

Hildebrand H, Brydolf M, Holmquist L, Krantz I, Kristiansson B.

Acta Paediatr. 1994 Jun;83(6):640-5.

PMID:
7919763
34.

Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease.

Stibler H, Blennow G, Kristiansson B, Lindehammer H, Hagberg B.

J Neurol Neurosurg Psychiatry. 1994 May;57(5):552-6.

35.

Longitudinal growth in children and adolescents with inflammatory bowel disease.

Hildebrand H, Karlberg J, Kristiansson B.

J Pediatr Gastroenterol Nutr. 1994 Feb;18(2):165-73.

PMID:
8014763
36.

Different features of coeliac disease in two neighbouring countries.

Ascher H, Holm K, Kristiansson B, Mäki M.

Arch Dis Child. 1993 Sep;69(3):375-80.

37.

Carbohydrate-deficient glycoprotein syndromes: peculiar group of new disorders.

Hagberg BA, Blennow G, Kristiansson B, Stibler H.

Pediatr Neurol. 1993 Jul-Aug;9(4):255-62. Review.

PMID:
8216537
38.

Chronic inflammatory bowel disease in children and adolescents in Sweden.

Hildebrand H, Fredrikzon B, Holmquist L, Kristiansson B, Lindquist B.

J Pediatr Gastroenterol Nutr. 1991 Oct;13(3):293-7.

PMID:
1791507
39.

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A.

J Pediatr. 1991 Aug;119(2):251-9.

PMID:
1861210
40.

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A.

J Pediatr. 1991 Aug;119(2):242-50.

PMID:
1861209
41.

Increasing incidence of coeliac disease in Sweden.

Ascher H, Krantz I, Kristiansson B.

Arch Dis Child. 1991 May;66(5):608-11.

42.

Linear growth in children with cystic fibrosis. I. Birth to 8 years of age.

Karlberg J, Kjellmer I, Kristiansson B.

Acta Paediatr Scand. 1991 May;80(5):508-14.

PMID:
1872173
43.

Khat-chewing during pregnancy-effect upon the off-spring and some characteristics of the chewers.

Eriksson M, Ghani NA, Kristiansson B.

East Afr Med J. 1991 Feb;68(2):106-11.

PMID:
2040229
44.

Cerebral function of the guinea pig neonate after chronic intrauterine exposure to khat (Catha edulis Forsk.).

Thordstein M, Jansson T, Kristiansson B.

Biol Neonate. 1991;59(3):161-70.

PMID:
2054426
45.

Ocular pathology in disialotransferrin developmental deficiency syndrome.

Strömland K, Hagberg B, Kristiansson B.

Ophthalmic Paediatr Genet. 1990 Dec;11(4):309-13.

PMID:
1710798
46.

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.

Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M.

Pediatr Res. 1990 Aug;28(2):131-6.

PMID:
2395603
47.

Stunting and tissue depletion in Yemeni children.

Bågenholm G, Nasher AA, Kristiansson B.

Eur J Clin Nutr. 1990 Jun;44(6):425-33.

PMID:
2387278
48.

A new laboratory kit for anti-gliadin IgA at diagnosis and follow-up of childhood celiac disease.

Ascher H, Lanner A, Kristiansson B.

J Pediatr Gastroenterol Nutr. 1990 May;10(4):443-50.

PMID:
2358975
49.

Carnitine deficiency induced by pivampicillin and pivmecillinam therapy.

Holme E, Greter J, Jacobson CE, Lindstedt S, Nordin I, Kristiansson B, Jodal U.

Lancet. 1989 Aug 26;2(8661):469-73.

PMID:
2570185
50.

Cytochrome c oxidase deficiency in infancy.

Oldfors A, Sommerland H, Holme E, Tulinius M, Kristiansson B.

Acta Neuropathol. 1989;77(3):267-75.

PMID:
2538042

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