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Andrew Hattersley

Showing results (1-10 of 51) with videos related to

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BMC Medical Genetics|June 1, 2012
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistanceRinki Murphy, Lourdes Ibáñez, Andrew Hattersley, et al.
Midwifery|June 18, 2003
How well do midwives estimate the date of delivery?Elizabeth Stenhouse, David Wright, Andrew Hattersley, et al.
Diabetes|November 18, 2021
Syndromic Monogenic Diabetes Genes Should Be Tested in Patients With a Clinical Suspicion of Maturity-Onset Diabetes of the YoungKevin Colclough, Sian Ellard, Andrew Hattersley, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutationRinki Singh, Sian Ellard, Andrew Hattersley, et al.
Pediatric Diabetes|March 1, 2011
KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patientsYiannis S Ioannou, Sian Ellard, Andrew Hattersley, et al.
Nephron|May 30, 2015
Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic TestingRhian Clissold, Beverley Shields, Sian Ellard, et al.
Lijecnicki Vjesnik|June 15, 2010
[Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2]Jasenka Ille, Natasa Rojnić Putarek, Ana Radica, et al.
GMS Ophthalmology Cases|December 19, 2023
Multimodal analysis in symptomatic MIDD-associated retinopathy. A case report and literature reviewKatarzyna Chwiejczak, Daniel Byles, Paul Gerry, et al.
Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Pediatric Diabetes|April 5, 2013
Digenic heterozygous HNF1A and HNF4A mutations in two siblings with childhood-onset diabetesRoopa Kanakatti Shankar, Sian Ellard, Debra Standiford, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
BMC Medical Genetics|June 1, 2012
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistanceRinki Murphy, Lourdes Ibáñez, Andrew Hattersley, et al.
Midwifery|June 18, 2003
How well do midwives estimate the date of delivery?Elizabeth Stenhouse, David Wright, Andrew Hattersley, et al.
Diabetes|November 18, 2021
Syndromic Monogenic Diabetes Genes Should Be Tested in Patients With a Clinical Suspicion of Maturity-Onset Diabetes of the YoungKevin Colclough, Sian Ellard, Andrew Hattersley, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid and sensitive real-time polymerase chain reaction method for detection and quantification of 3243A>G mitochondrial point mutationRinki Singh, Sian Ellard, Andrew Hattersley, et al.
Pediatric Diabetes|March 1, 2011
KCNJ11 activating mutations cause both transient and permanent neonatal diabetes mellitus in Cypriot patientsYiannis S Ioannou, Sian Ellard, Andrew Hattersley, et al.
Nephron|May 30, 2015
Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic TestingRhian Clissold, Beverley Shields, Sian Ellard, et al.
Lijecnicki Vjesnik|June 15, 2010
[Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2]Jasenka Ille, Natasa Rojnić Putarek, Ana Radica, et al.
GMS Ophthalmology Cases|December 19, 2023
Multimodal analysis in symptomatic MIDD-associated retinopathy. A case report and literature reviewKatarzyna Chwiejczak, Daniel Byles, Paul Gerry, et al.
Human Molecular Genetics|December 22, 2009
Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptomsRoope Männikkö, Craig Jefferies, Sarah E Flanagan, et al.
Pediatric Diabetes|April 5, 2013
Digenic heterozygous HNF1A and HNF4A mutations in two siblings with childhood-onset diabetesRoopa Kanakatti Shankar, Sian Ellard, Debra Standiford, et al.
Pageof 6