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B Kristiansson

Showing results (61-70 of 74) with videos related to

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Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 21, 1998
Intestinal, pancreatic and hepatic involvement in carbohydrate-deficient glycoprotein syndrome type IB Kristiansson, S Borulf, N Conradi, et al.
European Journal of Endocrinology|March 29, 2001
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 diseaseU H Jansson, B Kristiansson, P Magnusson, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I familiesC Bjursell, J Wahlström, K Berg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 15, 1998
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1AS Kjaergaard, B Kristiansson, H Stibler, et al.
The European Journal of Surgery = Acta Chirurgica|August 5, 1999
Thrombectomy and in situ fibrinolysis in the treatment of acute hepatic arterial thrombosis after liver transplantation in two childrenM Olausson, L Bäckman, L Mjörnstedt, et al.
Lancet (London, England)|August 26, 1989
Carnitine deficiency induced by pivampicillin and pivmecillinam therapyE Holme, J Greter, C E Jacobson, et al.
Genomics|February 1, 1997
Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian familiesC Bjursell, H Stibler, J Wahlström, et al.
Scandinavian Journal of Infectious Diseases|August 14, 1999
Chronic hepatitis B in children in Gothenburg, SwedenA Söderström, M Lindh, K Eriksson, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Acta Neuropathologica|January 1, 1987
Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosisA Oldfors, M Tulinius, E Holme, et al.
Journal of Pediatric Gastroenterology and Nutrition|July 21, 1998
Intestinal, pancreatic and hepatic involvement in carbohydrate-deficient glycoprotein syndrome type IB Kristiansson, S Borulf, N Conradi, et al.
European Journal of Endocrinology|March 29, 2001
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 diseaseU H Jansson, B Kristiansson, P Magnusson, et al.
European Journal of Human Genetics : EJHG|January 15, 1999
Detailed mapping of the phosphomannomutase 2 (PMM2) gene and mutation detection enable improved analysis for Scandinavian CDG type I familiesC Bjursell, J Wahlström, K Berg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 15, 1998
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1AS Kjaergaard, B Kristiansson, H Stibler, et al.
The European Journal of Surgery = Acta Chirurgica|August 5, 1999
Thrombectomy and in situ fibrinolysis in the treatment of acute hepatic arterial thrombosis after liver transplantation in two childrenM Olausson, L Bäckman, L Mjörnstedt, et al.
Lancet (London, England)|August 26, 1989
Carnitine deficiency induced by pivampicillin and pivmecillinam therapyE Holme, J Greter, C E Jacobson, et al.
Genomics|February 1, 1997
Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian familiesC Bjursell, H Stibler, J Wahlström, et al.
Scandinavian Journal of Infectious Diseases|August 14, 1999
Chronic hepatitis B in children in Gothenburg, SwedenA Söderström, M Lindh, K Eriksson, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Pageof 8