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La ricerca find articoli where authors phrase all words 'KRISTIANSSON B' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 31 riferimenti
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    1. Jansson, UHG; Kristiansson, B; Magnusson, P; Larsson, L; Albertsson-Wikland, K; Bjarnason, R
      The decrease of IGF-I, IGF-binding protein-3 and bone alkaline phosphataseisoforms during gluten challenge correlates with small intestinal inflammation in children with coeliac disease

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    2. Jansson, UHG; Gudjonsdottir, AH; Ryd, W; Kristiansson, B
      Two different doses of gluten show a dose-dependent response of enteropathy but not of serological markers during gluten challenge in children with coeliac disease

      ACTA PAEDIATRICA
    3. Erlandson, A; Bjursell, C; Stibler, H; Kristiansson, B; Wahlstrom, J; Martinsson, T
      Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations

      HUMAN GENETICS
    4. Raupp, P; Hassan, JA; Varughese, M; Kristiansson, B
      Henna causes life threatening haemolysis in glucose-6-phosphate dehydrogenase deficiency

      ARCHIVES OF DISEASE IN CHILDHOOD
    5. Erlandson, A; Stibler, H; Kristiansson, B; Wahlstrom, J; Martinsson, T
      Denaturing high-performance liquid chromatography is a suitable method forPMM2 mutation screening in carbohydrate-deficient glycoprotein syndrome type IA patients

      GENETIC TESTING
    6. Bjursell, C; Erlandson, A; Nordling, M; Nilsson, S; Wahlstrom, J; Stibler, H; Kristiansson, B; Martinsson, T
      PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian families

      HUMAN MUTATION
    7. Naluai, AT; Nilsson, S; Samuelsson, L; Gudjonsdottir, AH; Ascher, H; Ek, J; Hallberg, B; Kristiansson, B; Martinsson, T; Nerman, O; Sollid, LM; Wahlstrom, J
      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

      TISSUE ANTIGENS
    8. Olausson, M; Backman, L; Mjornstedt, L; Krantz, M; Kristiansson, B; Wiklund, LM; Friman, S
      Thrombectomy and in situ fibrinolysis in the treatment of acute hepatic arterial thrombosis after liver transplantation in two children

      EUROPEAN JOURNAL OF SURGERY
    9. Soderstrom, A; Lindh, M; Eriksson, K; Horal, P; Krantz, M; Kristiansson, B; Lindberg, J; Norkrans, G
      Chronic hepatitis B in children in Gothenburg, Sweden

      SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES
    10. Bjursell, C; Wahlstrom, J; Berg, K; Stibler, H; Kristiansson, B; Matthijs, G; Martinsson, T
      Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I families

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. KJAERGAARD S; KRISTIANSSON B; STIBLER H; FREEZE HH; SCHWARTZ M; MARTINSSON T; SKOVBY F
      FAILURE OF SHORT-TERM MANNOSE THERAPY OF PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE 1A

      Acta paediatrica
    12. KRISTIANSSON B; BORULF S; CONRADI N; ERLANSONALBERTSSON C; RYD W; STIBLER H
      INTESTINAL, PANCREATIC AND HEPATIC INVOLVEMENT IN CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I

      Journal of pediatric gastroenterology and nutrition
    13. KRISTIANSSON B; STIBLER H; CONRADI N; ERIKSSON BO; RYD W
      THE HEART AND PERICARDIAL-EFFUSIONS IN CDGS-I (CARBOHYDRATE-DEFICIENTGLYCOPROTEIN SYNDROME TYPE-I)

      Journal of inherited metabolic disease
    14. STIBLER H; HOLZBACH U; KRISTIANSSON B
      ISOFORMS AND LEVELS OF TRANSFERRIN, ANTITHROMBIN, ALPHA(1)-ANTITRYPSIN AND THYROXINE-BINDING GLOBULIN IN 48 PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I

      Scandinavian journal of clinical & laboratory investigation
    15. BJORKLUND JEM; STIBLER H; KRISTIANSSON B; JOHANSSON SGO; MAGNUSSON CGM
      IMMUNOGLOBULIN LEVELS IN PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I

      International archives of allergy and immunology
    16. BJURSELL C; STIBLER H; WAHLSTROM J; KRISTIANSSON B; SKOVBY F; STROMME P; BLENNOW G; MARTINSSON T
      FINE MAPPING OF THE GENE FOR CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I (CDG1) - LINKAGE DISEQUILIBRIUM AND FOUNDER EFFECT IN SCANDINAVIAN FAMILIES

      Genomics
    17. STIBLER H; VONDOBELN U; KRISTIANSSON B; GUTHENBERG C
      CARBOHYDRATE-DEFICIENT TRANSFERRIN IN GALACTOSEMIA

      Acta paediatrica
    18. ASCHER H; KRISTIANSSON B
      THE HIGHEST INCIDENCE OF CELIAC-DISEASE IN EUROPE - THE SWEDISH EXPERIENCE

      Journal of pediatric gastroenterology and nutrition
    19. ASCHER H; KRANTS I; NORDIN P; KRISTIANSSON B
      THE OCCURRENCE OF GLUTEN ENTEROPATHY IN SIBLINGS TO CELIAC-DISEASE CASES IS OVERESTIMATED

      Gut
    20. ASCHER H; KRANTZ I; RYDBERG L; NORDIN P; KRISTIANSSON B
      INFLUENCE OF INFANT-FEEDING AND GLUTEN INTAKE ON CELIAC-DISEASE

      Archives of Disease in Childhood
    21. BJURSELL C; WAHLSTROM J; STIBLER H; KRISTIANSSON B; MATTHIJS G; MARTINSSON T
      PRENATAL DIAGNOSTIC-TOOLS FOR ANALYSIS OF SCANDINAVIAN CDG TYPE-I PATIENTS

      American journal of human genetics
    22. STIBLER H; HOLZBACH U; TENGBORN L; KRISTIANSSON B
      COMPLEX FUNCTIONAL AND STRUCTURAL COAGULATION ABNORMALITIES IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I

      Blood coagulation & fibrinolysis
    23. KRISTIANSSON B; STIBLER H; WIDE L
      GONADAL-FUNCTION AND GLYCOPROTEIN HORMONES IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN (CDG) SYNDROME

      Acta paediatrica
    24. TULINIUS MH; OLDFORS A; HOLME E; LARSSON NG; HOUSHMAND M; FAHLESON P; SIGSTROM L; KRISTIANSSON B
      ATYPICAL PRESENTATION OF MULTISYSTEM DISORDERS IN 2 GIRLS WITH MITOCHONDRIAL-DNA DELETIONS

      European journal of pediatrics
    25. MARTINSSON T; BJURSELL C; STIBLER H; KRISTIANSSON B; SKOVBY F; JAEKEN J; BLENNOW G; STROMME P; HANEFELD F; WAHLSTROM J
      LINKAGE OF A LOCUS FOR CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1) TO CHROMOSOME 16P, AND LINKAGE DISEQUILIBRIUM TO MICROSATELLITE MARKER D16S406

      Human molecular genetics
    26. HILDEBRAND H; BRYDOLF M; HOLMQUIST L; KRANTZ I; KRISTIANSSON B
      INCIDENCE AND PREVALENCE OF INFLAMMATORY BOWEL-DISEASE IN CHILDREN INSOUTH-WESTERN SWEDEN

      Acta paediatrica
    27. HILDEBRAND H; KARLBERG J; KRISTIANSSON B
      LONGITUDINAL GROWTH IN CHILDREN AND ADOLESCENTS WITH INFLAMMATORY BOWEL-DISEASE

      Journal of pediatric gastroenterology and nutrition
    28. ASCHER H; KRISTIANSSON B
      CHILDHOOD CELIAC-DISEASE IN SWEDEN

      Lancet
    29. STIBLER H; BLENNOW G; KRISTIANSSON B; LINDEHAMMER A; HAGBERG B
      CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME - CLINICAL EXPRESSION INADULTS WITH A NEW METABOLIC DISEASE

      Journal of Neurology, Neurosurgery and Psychiatry
    30. HAGBERG BA; BLENNOW G; KRISTIANSSON B; STIBLER H
      CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROMES - PECULIAR GROUP OF NEWDISORDERS

      Pediatric neurology
    31. ASCHER H; HOLM K; KRISTIANSSON B; MAKI M
      DIFFERENT FEATURES OF CELIAC-DISEASE IN 2 NEIGHBORING COUNTRIES

      Archives of Disease in Childhood


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 06:37:38