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Bendt Brock Jacobsen

Showing results (1-10 of 11) with videos related to

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Ugeskrift for Laeger|February 24, 2006
[Vitamin D1alpha-hydroxylase deficiency as the cause of severe rickets in a 1-year-old-old boy]Signe Sparre Beck-Nielsen, Niels Thomas Hertel, Bendt Brock-Jacobsen
Immunogenetics|August 17, 2004
No allelic variation in genes with high gliadin homology in patients with celiac disease and type 1 diabetesChristian Nielsen, Dorte Hansen, Steffen Husby, et al.
European Journal of Endocrinology|December 20, 2008
Incidence and prevalence of nutritional and hereditary rickets in southern DenmarkSigne Sparre Beck-Nielsen, Bendt Brock-Jacobsen, Jeppe Gram, et al.
European Journal of Pediatrics|November 6, 2008
Nutritional rickets in Denmark: a retrospective review of children's medical records from 1985 to 2005Signe Sparre Beck-Nielsen, Tina Kold Jensen, Jeppe Gram, et al.
Ugeskrift for Laeger|September 15, 2005
[Primary hyperparathyroidism in pregnancy]Morten Munk Frost Nielsen, Jan Stener Jørgensen, Bendt Brock Jacobsen, et al.
Diabetes Care|October 27, 2006
Clinical benefit of a gluten-free diet in type 1 diabetic children with screening-detected celiac disease: a population-based screening study with 2 years' follow-upDorte Hansen, Bendt Brock-Jacobsen, Elisabeth Lund, et al.
Ugeskrift for Laeger|June 8, 2007
[Prevalence of coeliac disease (CD) in children with type 1 diabetes (T1D)]Dorte Hansen, Bendt Brock-Jacobsen, Elisabeth Lund, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 17, 2002
Recombinant human growth hormone treatment, using two dose regimens in children with chronic renal failure--a report on linear growth and adverse effectsNiels Thomas Hertel, Christer Holmberg, Kai A R Rönnholm, et al.
Hormone Research|November 23, 2006
Rapid genetic analysis in congenital hyperinsulinismHenrik B T Christesen, Klaus Brusgaard, Jan Alm, et al.
European Journal of Endocrinology|May 3, 2008
Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutationHenrik B T Christesen, Nicholas D Tribble, Anders Molven, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Ugeskrift for Laeger|February 24, 2006
[Vitamin D1alpha-hydroxylase deficiency as the cause of severe rickets in a 1-year-old-old boy]Signe Sparre Beck-Nielsen, Niels Thomas Hertel, Bendt Brock-Jacobsen
Immunogenetics|August 17, 2004
No allelic variation in genes with high gliadin homology in patients with celiac disease and type 1 diabetesChristian Nielsen, Dorte Hansen, Steffen Husby, et al.
European Journal of Endocrinology|December 20, 2008
Incidence and prevalence of nutritional and hereditary rickets in southern DenmarkSigne Sparre Beck-Nielsen, Bendt Brock-Jacobsen, Jeppe Gram, et al.
European Journal of Pediatrics|November 6, 2008
Nutritional rickets in Denmark: a retrospective review of children's medical records from 1985 to 2005Signe Sparre Beck-Nielsen, Tina Kold Jensen, Jeppe Gram, et al.
Ugeskrift for Laeger|September 15, 2005
[Primary hyperparathyroidism in pregnancy]Morten Munk Frost Nielsen, Jan Stener Jørgensen, Bendt Brock Jacobsen, et al.
Diabetes Care|October 27, 2006
Clinical benefit of a gluten-free diet in type 1 diabetic children with screening-detected celiac disease: a population-based screening study with 2 years' follow-upDorte Hansen, Bendt Brock-Jacobsen, Elisabeth Lund, et al.
Ugeskrift for Laeger|June 8, 2007
[Prevalence of coeliac disease (CD) in children with type 1 diabetes (T1D)]Dorte Hansen, Bendt Brock-Jacobsen, Elisabeth Lund, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 17, 2002
Recombinant human growth hormone treatment, using two dose regimens in children with chronic renal failure--a report on linear growth and adverse effectsNiels Thomas Hertel, Christer Holmberg, Kai A R Rönnholm, et al.
Hormone Research|November 23, 2006
Rapid genetic analysis in congenital hyperinsulinismHenrik B T Christesen, Klaus Brusgaard, Jan Alm, et al.
European Journal of Endocrinology|May 3, 2008
Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutationHenrik B T Christesen, Nicholas D Tribble, Anders Molven, et al.
Pageof 2