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Andrew Hattersley

Showing results (21-30 of 51) with videos related to

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Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|May 25, 2020
Phantasia-The psychological significance of lifelong visual imagery vividness extremesAdam Zeman, Fraser Milton, Sergio Della Sala, et al.
Human Genetics|September 18, 2009
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesJanniche Torsvik, Stefan Johansson, Anders Johansen, et al.
The Pan African Medical Journal|July 1, 2024
Impact of haemoglobin variants on the diagnostic sensitivity of glycated haemoglobin (HbA1c) assay methodologies in sub-Saharan Africa: a laboratory-based method validation studyPriscilla Agatha Balungi, Anxious Jackson Niwaha, Rachel Nice, et al.
Journal of Hypertension|April 26, 2003
Ethnic subgroup differences in hypertension in PakistanTazeen H Jafar, Andrew S Levey, Fahim H Jafary, et al.
Scientific Reports|May 8, 2024
Development of a clinical calculator to aid the identification of MODY in pediatric patients at the time of diabetes diagnosisBeverley M Shields, Annelie Carlsson, Kashyap Patel, et al.
Pediatric Diabetes|October 12, 2012
Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth StudyRoopa Kanakatti Shankar, Catherine Pihoker, Lawrence M Dolan, et al.
Human Molecular Genetics|July 23, 2003
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetesFlorence Demenais, Timo Kanninen, Cecilia M Lindgren, et al.
European Journal of Human Genetics : EJHG|May 19, 2022
Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1Maya Chopra, Richard Caswell, Giulia Barcia, et al.
EMBO Molecular Medicine|January 6, 2010
Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinismKenju Shimomura, Sarah E Flanagan, Brittany Zadek, et al.
American Journal of Medical Genetics. Part A|May 15, 2008
Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644CJulia Rankin, Michaela Auer-Grumbach, Warwick Bagg, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|May 25, 2020
Phantasia-The psychological significance of lifelong visual imagery vividness extremesAdam Zeman, Fraser Milton, Sergio Della Sala, et al.
Human Genetics|September 18, 2009
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesJanniche Torsvik, Stefan Johansson, Anders Johansen, et al.
The Pan African Medical Journal|July 1, 2024
Impact of haemoglobin variants on the diagnostic sensitivity of glycated haemoglobin (HbA1c) assay methodologies in sub-Saharan Africa: a laboratory-based method validation studyPriscilla Agatha Balungi, Anxious Jackson Niwaha, Rachel Nice, et al.
Journal of Hypertension|April 26, 2003
Ethnic subgroup differences in hypertension in PakistanTazeen H Jafar, Andrew S Levey, Fahim H Jafary, et al.
Scientific Reports|May 8, 2024
Development of a clinical calculator to aid the identification of MODY in pediatric patients at the time of diabetes diagnosisBeverley M Shields, Annelie Carlsson, Kashyap Patel, et al.
Pediatric Diabetes|October 12, 2012
Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth StudyRoopa Kanakatti Shankar, Catherine Pihoker, Lawrence M Dolan, et al.
Human Molecular Genetics|July 23, 2003
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetesFlorence Demenais, Timo Kanninen, Cecilia M Lindgren, et al.
European Journal of Human Genetics : EJHG|May 19, 2022
Mild MDPL in a patient with a novel de novo missense variant in the Cys-B region of POLD1Maya Chopra, Richard Caswell, Giulia Barcia, et al.
EMBO Molecular Medicine|January 6, 2010
Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinismKenju Shimomura, Sarah E Flanagan, Brittany Zadek, et al.
American Journal of Medical Genetics. Part A|May 15, 2008
Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644CJulia Rankin, Michaela Auer-Grumbach, Warwick Bagg, et al.
Pageof 6