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Lars Hansen

Showing results (141-150 of 178) with videos related to

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Pediatric Diabetes|October 8, 2014
Partial remission definition: validation based on the insulin dose-adjusted HbA1c (IDAA1C) in 129 Danish children with new-onset type 1 diabetesMarie Louise C Max Andersen, Philip Hougaard, Sven Pörksen, et al.
Autoimmunity|May 25, 2011
Relationship between ZnT8Ab, the SLC30A8 gene and disease progression in children with newly diagnosed type 1 diabetesLotte B Nielsen, Fariba Vaziri-Sani, Sven Pörksen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 5, 2017
Discovery of an O-mannosylation pathway selectively serving cadherins and protocadherinsIda Signe Bohse Larsen, Yoshiki Narimatsu, Hiren Jitendra Joshi, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRSMuhammad Farooq, Jesper T Troelsen, Mette Boyd, et al.
BMJ Open|December 23, 2016
Protocol for a multicentre study to assess feasibility, acceptability, effectiveness and direct costs of TRIumPH (Treatment and Recovery In PsycHosis): integrated care pathway for psychosisShanaya Rathod, Christie Garner, Alison Griffiths, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Compound heterozygous ASPM mutations in Pakistani MCPH familiesFarooq Muhammad, Shahid Mahmood Baig, Lars Hansen, et al.
Plos One|June 12, 2013
Complex multi-block analysis identifies new immunologic and genetic disease progression patterns associated with the residual β-cell function 1 year after diagnosis of type 1 diabetesMarie Louise Max Andersen, Morten Arendt Rasmussen, Sven Pörksen, et al.
Diabetes|November 28, 2002
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian CaucasiansSøren K Rasmussen, Søren A Urhammer, Lars Berglund, et al.
European Journal of Endocrinology|May 31, 2007
Co-localisation of the Kir6.2/SUR1 channel complex with glucagon-like peptide-1 and glucose-dependent insulinotrophic polypeptide expression in human ileal cells and implications for glycaemic control in new onset type 1 diabetesLotte B Nielsen, Kenneth B Ploug, Peter Swift, et al.
Diabetes, Obesity & Metabolism|April 11, 2022
Efficacy and safety of cotadutide, a dual glucagon-like peptide-1 and glucagon receptor agonist, in a randomized phase 2a study of patients with type 2 diabetes and chronic kidney diseaseVictoria E R Parker, Thuong Hoang, Heike Schlichthaar, et al.
Pageof 18

Showing results (141-150 of 178) with videos related to

Sort By:
Pageof 18
Pediatric Diabetes|October 8, 2014
Partial remission definition: validation based on the insulin dose-adjusted HbA1c (IDAA1C) in 129 Danish children with new-onset type 1 diabetesMarie Louise C Max Andersen, Philip Hougaard, Sven Pörksen, et al.
Autoimmunity|May 25, 2011
Relationship between ZnT8Ab, the SLC30A8 gene and disease progression in children with newly diagnosed type 1 diabetesLotte B Nielsen, Fariba Vaziri-Sani, Sven Pörksen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 5, 2017
Discovery of an O-mannosylation pathway selectively serving cadherins and protocadherinsIda Signe Bohse Larsen, Yoshiki Narimatsu, Hiren Jitendra Joshi, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRSMuhammad Farooq, Jesper T Troelsen, Mette Boyd, et al.
BMJ Open|December 23, 2016
Protocol for a multicentre study to assess feasibility, acceptability, effectiveness and direct costs of TRIumPH (Treatment and Recovery In PsycHosis): integrated care pathway for psychosisShanaya Rathod, Christie Garner, Alison Griffiths, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Compound heterozygous ASPM mutations in Pakistani MCPH familiesFarooq Muhammad, Shahid Mahmood Baig, Lars Hansen, et al.
Plos One|June 12, 2013
Complex multi-block analysis identifies new immunologic and genetic disease progression patterns associated with the residual β-cell function 1 year after diagnosis of type 1 diabetesMarie Louise Max Andersen, Morten Arendt Rasmussen, Sven Pörksen, et al.
Diabetes|November 28, 2002
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian CaucasiansSøren K Rasmussen, Søren A Urhammer, Lars Berglund, et al.
European Journal of Endocrinology|May 31, 2007
Co-localisation of the Kir6.2/SUR1 channel complex with glucagon-like peptide-1 and glucose-dependent insulinotrophic polypeptide expression in human ileal cells and implications for glycaemic control in new onset type 1 diabetesLotte B Nielsen, Kenneth B Ploug, Peter Swift, et al.
Diabetes, Obesity & Metabolism|April 11, 2022
Efficacy and safety of cotadutide, a dual glucagon-like peptide-1 and glucagon receptor agonist, in a randomized phase 2a study of patients with type 2 diabetes and chronic kidney diseaseVictoria E R Parker, Thuong Hoang, Heike Schlichthaar, et al.
Pageof 18