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Ugeskrift for Laeger
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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 diabetes
Christian Nielsen, Dorte Hansen, Steffen Husby, et al.
European Journal of Endocrinology
|
December 20, 2008
Incidence and prevalence of nutritional and hereditary rickets in southern Denmark
Signe 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 2005
Signe 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-up
Dorte 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 effects
Niels Thomas Hertel, Christer Holmberg, Kai A R Rönnholm, et al.
Hormone Research
|
November 23, 2006
Rapid genetic analysis in congenital hyperinsulinism
Henrik 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 mutation
Henrik B T Christesen, Nicholas D Tribble, Anders Molven, et al.
Page
of 2
Search research articles
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Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 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 diabetes
Christian Nielsen, Dorte Hansen, Steffen Husby, et al.
European Journal of Endocrinology
|
December 20, 2008
Incidence and prevalence of nutritional and hereditary rickets in southern Denmark
Signe 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 2005
Signe 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-up
Dorte 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 effects
Niels Thomas Hertel, Christer Holmberg, Kai A R Rönnholm, et al.
Hormone Research
|
November 23, 2006
Rapid genetic analysis in congenital hyperinsulinism
Henrik 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 mutation
Henrik B T Christesen, Nicholas D Tribble, Anders Molven, et al.
Page
of 2