检索结果 - Sarah E. Flanagan

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  1. 1
    Does integrated care reduce hospital activity for patients with chronic diseases? An umbrella review of systematic reviews

    Does integrated care reduce hospital activity for patients with chronic diseases? An umbrella review of systematic reviews 由 Sarah Damery, Sarah E. Flanagan, Gill Combes

    出版 2016
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  2. 2
    Monogenic autoimmune diseases of the endocrine system

    Monogenic autoimmune diseases of the endocrine system 由 Matthew B. Johnson, Andrew T. Hattersley, Sarah E. Flanagan

    出版 2016
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  3. 3
    Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian children

    Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian children 由 Crésio Alves, Sarah E. Flanagan, Sian Ellard, Deborah Mackay

    出版 2012
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  4. 4
    Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous Disease

    Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous Disease 由 Thomas I. Hewat, Matthew B. Johnson, Sarah E. Flanagan

    出版 2022
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  5. 5
    High-Dose Glibenclamide Can Replace Insulin Therapy Despite Transitory Diarrhea in Early-Onset Diabetes Caused by a Novel R201L Kir6.2 Mutation

    High-Dose Glibenclamide Can Replace Insulin Therapy Despite Transitory Diarrhea in Early-Onset Diabetes Caused by a Novel R201L Kir6.2 Mutation 由 Ethel Codner, Sarah E. Flanagan, Sian Ellard, H García, Andrew T. Hattersley

    出版 2005
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  6. 6
    Two decades since the fetal insulin hypothesis: what have we learned from genetics?

    Two decades since the fetal insulin hypothesis: what have we learned from genetics? 由 Alice E. Hughes, Andrew T. Hattersley, Sarah E. Flanagan, Rachel M. Freathy

    出版 2021
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  7. 7
    Mutations in the <i>ABCC8</i> gene encoding the SUR1 subunit of the K<sub>ATP</sub> channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period

    Mutations in the <i>ABCC8</i> gene encoding the SUR1 subunit of the K<sub>ATP</sub> channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes dia... 由 Ann‐Marie Patch, Sarah E. Flanagan, Chris Boustred, Andrew T. Hattersley, Sian Ellard

    出版 2007
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  8. 8
    KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life

    KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life 由 Oscar Rubio‐Cabezas, Sarah E. Flanagan, Annet Damhuis, Andrew T. Hattersley, Sian Ellard

    出版 2011
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  9. 9
    Mutations in the Genes Encoding the Transcription Factors Hepatocyte Nuclear Factor 1 Alpha and 4 Alpha in Maturity-Onset Diabetes of the Young and Hyperinsulinemic Hypoglycemia

    Mutations in the Genes Encoding the Transcription Factors Hepatocyte Nuclear Factor 1 Alpha and 4 Alpha in Maturity-Onset Diabetes of the Young and Hyperinsulinemic Hypoglycemia 由 Kevin Colclough, Christine Bellanné‐Chantelot, Cécile Saint‐Martin, Sarah E. Flanagan, Sian Ellard

    出版 2013
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  10. 10
    Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype

    Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype 由 Sarah E. Flanagan, Emma L. Edghill, Anna L. Gloyn, Sian Ellard, Andrew T. Hattersley

    出版 2006
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  11. 11
    3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinemic Hypoglycemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity

    3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency and Hyperinsulinemic Hypoglycemia: Characterization of a Novel Mutation and Severe Dietary Protein Sensitivity 由 Ritika R. Kapoor, Chela James, Sarah E. Flanagan, Sian Ellard, Simon Eaton, Khalid Hussain

    出版 2009
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  12. 12
    Effective Treatment With Oral Sulfonylureas in Patients With Diabetes Due to Sulfonylurea Receptor 1 (SUR1) Mutations

    Effective Treatment With Oral Sulfonylureas in Patients With Diabetes Due to Sulfonylurea Receptor 1 (SUR1) Mutations 由 Meena Rafiq, Sarah E. Flanagan, Ann-Marie Patch, Beverley Shields, Sian Ellard, Andrew T. Hattersley

    出版 2008
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  13. 13
    Monogenic disease analysis establishes that fetal insulin accounts for half of human fetal growth

    Monogenic disease analysis establishes that fetal insulin accounts for half of human fetal growth 由 Alice E. Hughes, Elisa De Franco, Rachel M. Freathy, Sarah E. Flanagan, Andrew T. Hattersley

    出版 2023
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  14. 14
    <i>GATA6</i> Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency

    <i>GATA6</i> Mutations Cause a Broad Phenotypic Spectrum of Diabetes From Pancreatic Agenesis to Adult-Onset Diabetes Without Exocrine Insufficiency 由 Elisa De Franco, Charles Shaw‐Smith, Sarah E. Flanagan, Maggie Shepherd, Andrew T. Hattersley, Sian Ellard

    出版 2012
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  15. 15
    An <i>ABCC8</i> Gene Mutation and Mosaic Uniparental Isodisomy Resulting in Atypical Diffuse Congenital Hyperinsulinism

    An <i>ABCC8</i> Gene Mutation and Mosaic Uniparental Isodisomy Resulting in Atypical Diffuse Congenital Hyperinsulinism 由 Khalid Hussain, Sarah E. Flanagan, Virpi V. Smith, Michael Ashworth, Michael Day, Agostino Pierro, Sian Ellard

    出版 2007
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  16. 16
    Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism

    Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism 由 Ritika R. Kapoor, Sarah E. Flanagan, Ved Bhushan Arya, Julian Hamilton‐Shield, Sian Ellard, Khalid Hussain

    出版 2013
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  17. 17
    Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy

    Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy 由 Hüseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, Louise Hinchey, Sarah E. Flanagan, Sian Ellard, Khalid Hussain

    出版 2014
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  18. 18
    Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism

    Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism 由 Ved Bhushan Arya, Senthil Senniappan, Hüseyin Demirbilek, Syeda Tabassum Alam, Sarah E. Flanagan, Sian Ellard, Khalid Hussain

    出版 2014
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  19. 19
    Heterozygous ABCC8 mutations are a cause of MODY

    Heterozygous ABCC8 mutations are a cause of MODY 由 Pamela Bowman, Sarah E. Flanagan, Emma L. Edghill, Annet Damhuis, Maggie Shepherd, Richard Paisey, Andrew T. Hattersley, Sian Ellard

    出版 2011
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  20. 20
    Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age

    Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age 由 Ved Bhushan Arya, Sarah E. Flanagan, Anitha Kumaran, Julian Hamilton‐Shield, Sian Ellard, Khalid Hussain, Ritika R. Kapoor

    出版 2013
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