Henrik B T Christesen - JoVE Visualize

Showing results (1-10 of 6) with videos related to

Pageof 1

Sort By:

Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2007

Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemiaHaya Alkhayyat, Henrik B T Christesen, James Steer, et al.

Clinical Endocrinology|May 1, 2007

Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studiesMorris Muzyamba, Tabasum Farzaneh, Phillip Behe, et al.

Human Molecular Genetics|April 10, 2009

Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinismTarvinder K Taneja, Jamel Mankouri, Rucha Karnik, 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.

Diabetes|March 28, 2002

The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapyHenrik B T Christesen, Bendt B Jacobsen, Stella Odili, et al.

Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:

Pageof 1

Journal of Pediatric Endocrinology & Metabolism : JPEM|January 27, 2007

Mosaic Turner syndrome and hyperinsulinaemic hypoglycaemiaHaya Alkhayyat, Henrik B T Christesen, James Steer, et al.

Clinical Endocrinology|May 1, 2007

Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studiesMorris Muzyamba, Tabasum Farzaneh, Phillip Behe, et al.

Human Molecular Genetics|April 10, 2009

Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinismTarvinder K Taneja, Jamel Mankouri, Rucha Karnik, 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.

Diabetes|March 28, 2002

The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapyHenrik B T Christesen, Bendt B Jacobsen, Stella Odili, et al.

Pageof 1