Changing lives [electronic resource] : stratified medicine in monogenic diabetes / Andrew Hattersley.

By: Hattersley, Andrew [spk]Material type: FilmFilmSeries: Henry Stewart talksBiomedical & life sciences collection. Molecular genetics of human disease: Publisher: London : Henry Stewart Talks, 2015Description: 1 online resource (1 streaming video file (41 min.) : color, sound)Subject(s): Diabetes in adolescence | Diabetes in children | Human molecular genetics | Non-insulin-dependent diabetes -- Genetic aspects | Non-insulin-dependent diabetes -- Treatment | Diabetes Mellitus, Type 2 -- classification | Diabetes Mellitus, Type 2 -- genetics | Diabetes Mellitus, Type 2 -- therapy | Glucokinase | Hepatocyte Nuclear Factor 1-alpha | Kidney Diseases, Cystic | PediatricsOnline resources: Click here to access online | Series
Contents:
Contents: Approaches to diabetes treatment -- Maturity onset diabetes of the young (MODY) in the pre-genetic era -- MODY in the pre-genetic era -- Treatment in glucokinase MODY -- Treatment in HNF1a MODY -- Renal cysts and diabetes (RCAD) syndrome and its treatment -- The diagnosis of MODY in pediatric clinics -- MODY probability calculator -- Neonatal diabetes (ND) -- The role of Kir6.2 and SUR1 mutation in ND -- Testing for ND -- Using Mice model to learn on pancreatic development and ND -- Pancreatic agenesis and patients' genetics -- Mutations in PTF1A mutations and pancreatic agenesis.
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Animated audio-visual presentation with synchronized narration.

Title from title frames.

Contents: Approaches to diabetes treatment -- Maturity onset diabetes of the young (MODY) in the pre-genetic era -- MODY in the pre-genetic era -- Treatment in glucokinase MODY -- Treatment in HNF1a MODY -- Renal cysts and diabetes (RCAD) syndrome and its treatment -- The diagnosis of MODY in pediatric clinics -- MODY probability calculator -- Neonatal diabetes (ND) -- The role of Kir6.2 and SUR1 mutation in ND -- Testing for ND -- Using Mice model to learn on pancreatic development and ND -- Pancreatic agenesis and patients' genetics -- Mutations in PTF1A mutations and pancreatic agenesis.

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