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ArticlesPeer ReviewedFull Text
β-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1α Mutation Carriers
Author / Creator:Stride, Amanda ; Ellard, Sian ; Clark, Penny ; Shakespeare, Lynette ; Salzmann, Maurice ; Shepherd, Maggie ; Hattersley, Andrew T.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2005-07, Vol.28 (7), p.1751-1756
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ArticlesPeer ReviewedFull Text
Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY)
Author / Creator:Cuesta-Muñoz, Antonio L ; Tuomi, Tiinamaija ; Cobo-Vuilleumier, Nadia ; Koskela, Hanna ; Odili, Stella ; Stride, Amanda ; Buettger, Carol ; Otonkoski, Timo ; Froguel, Philippe ; Grimsby, Joseph ; Garcia-Gimeno, Maria ; Matschinsky, Franz M
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2010-02, Vol.33 (2), p.290-292
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ArticlesPeer ReviewedFull Text
Intrauterine Hyperglycemia Is Associated With an Earlier Diagnosis of Diabetes in HNF-1α Gene Mutation Carriers
Author / Creator:Stride, Amanda ; Shepherd, Maggie ; Frayling, Timothy M. ; Bulman, Mike P. ; Ellard, Sian ; Hattersley, Andrew T.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2002-12, Vol.25 (12), p.2287-2291
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ArticlesPeer ReviewedFull Text
Etiological Investigation of Diabetes in Young Adults Presenting With Apparent Type 2 Diabetes
Author / Creator:Owen, Katharine R. ; Stride, Amanda ; Ellard, Sian ; Hattersley, Andrew T.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2003-07, Vol.26 (7), p.2088-2093
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ArticlesPeer ReviewedFull Text
Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia
Author / Creator:Stride, Amanda ; Shields, Beverley ; Gill-Carey, Olivia ; Chakera, Ali J. ; Colclough, Kevin ; Ellard, Sian ; Hattersley, Andrew T.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Diabetologia, 2014-01, Vol.57 (1), p.54-56
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ArticlesPeer ReviewedFull Text
Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutation
Author / Creator:Bingham, Coralie ; Ellard, Sian ; van't Hoff, William G. ; Simmonds, H. Anne ; Marinaki, Anthony M. ; Badman, Michael K. ; Winocour, Peter H. ; Stride, Amanda ; Lockwood, Christopher R. ; Nicholls, Anthony J. ; Owen, Katharine R. ; Spyer, Ghislaine ; Pearson, Ewan R. ; Hattersley, Andrew T.
Publisher:New York, NY: Elsevier Inc
Journal title:Kidney international, 2003-05, Vol.63 (5), p.1645-1651
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Conference ProceedingsPeer ReviewedFull Text
β-cell genes and diabetes : Quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1α and glucokinase mutations
Author / Creator:PEARSON, Ewan R ; VELHO, Gilberto ; CLARK, Penny ; STRIDE, Amanda ; SHEPHERD, Maggie ; FRAYLING, Timothy M ; BULMAN, Michael P ; ELLARD, Sian ; FROGUEL, Phillipe ; HATTERSLEY, Andrew T
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001, Vol.50, p.S101-S107
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ArticlesPeer ReviewedFull Text
Beta-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers
Author / Creator:Stride, Amanda ; Ellard, Sian ; Clark, Penny ; Shakespeare, Lynette ; Salzmann, Maurice ; Shepherd, Maggie ; Hattersley, Andrew T
Publisher:United States
Journal title:Diabetes care, 2005-07, Vol.28 (7), p.1751
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ArticlesPeer ReviewedFull Text
{szligbeta}-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1[alpha] Mutation Carriers
Author / Creator:Stride, Amanda ; Ellard, Sian ; Clark, Penny ; Shakespeare, Lynette ; Salzmann, Maurice ; Shepherd, Maggie ; Hattersley, Andrew T
Publisher:Alexandria: American Diabetes Association
Journal title:Diabetes care, 2005-07, Vol.28 (7), p.1751-1756
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ArticlesPeer ReviewedFull Text
Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1(alpha) gene mutation carriers
Author / Creator:Stride, Amanda ; Shepherd, Maggie ; Frayling, Timothy M ; Bulman, Mike P
Publisher:Alexandria: American Diabetes Association
Journal title:Diabetes care, 2002-12, Vol.25 (12), p.2287
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ArticlesPeer ReviewedFull Text
Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers
Author / Creator:Stride, Amanda ; Shepherd, Maggie ; Frayling, Timothy M ; Bulman, Mike P ; Ellard, Sian ; Hattersley, Andrew T
Publisher:United States
Journal title:Diabetes care, 2002-12, Vol.25 (12), p.2287
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ArticlesPeer ReviewedFull Text
Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1[beta] gene mutation
Author / Creator:Bingham, Coralie ; Ellard, Sian ; van't Hoff, William G ; Simmonds, H Anne ; Marinaki, Anthony M ; Badman, Michael K ; Winocour, Peter H ; Stride, Amanda ; Lockwood, Christopher R ; Nicholls, Anthony J ; Owen, Katharine R ; Spyer, Ghislaine ; Pearson, Ewan R ; Hattersley, Andrew T
Publisher:London: Elsevier Limited
Journal title:Kidney international, 2003-05, Vol.63 (5), p.1645
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ArticlesPeer ReviewedFull Text
Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation
Author / Creator:Bingham, Coralie ; Ellard, Sian ; van't Hoff, William G ; Simmonds, H Anne ; Marinaki, Anthony M ; Badman, Michael K ; Winocour, Peter H ; Stride, Amanda ; Lockwood, Christopher R ; Nicholls, Anthony J ; Owen, Katharine R ; Spyer, Ghislaine ; Pearson, Ewan R ; Hattersley, Andrew T
Publisher:United States
Journal title:Kidney international, 2003-05, Vol.63 (5), p.1645
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ArticlesPeer ReviewedFull Text
Necrobiosis Lipodica Is a Clinical Feature of Maturity-Onset Diabetes of the Young
Author / Creator:Stride, Amanda ; Lambert, Paul ; Burden, A.C. Felix ; Mansell, Peter ; Page, Simon ; Hattersley, Andrew T.
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2002-07, Vol.25 (7), p.1249-1250
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ArticlesPeer ReviewedFull Text
Β-Cell Genes and Diabetes: Quantitative and Qualitative Differences in the Pathophysiology of Hepatic Nuclear Factor-1[Alpha] and Glucokinase Mutations
Author / Creator:Pearson, Ewan R ; Velho, Gilberto ; Clark, Penny ; Stride, Amanda ; Shepherd, Maggie ; Frayling, Timothy M ; Bulman, Michael P ; Ellard, Sian ; Froguel, Phillipe ; Hattersley, Andrew T
Publisher:American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.S101
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ArticlesPeer ReviewedFull Text
[Beta]-Cell Genes and Diabetes: Quantitative and Qualitative Differences in the Pathophysiology of Hepatic Nuclear Factor-1[Alpha] and Glucokinase Mutations
Author / Creator:Pearson, Ewan R ; Velho, Gilberto ; Clark, Penny ; Stride, Amanda ; Shepherd, Maggie ; Frayling, Timothy M ; Bulman, Michael P ; Ellard, Sian ; Froguel, Phillipe ; Hattersley, Andrew T
Publisher:New York: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001-02, Vol.50 (2), p.S101
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ArticlesFull Text
Integrating genetics into diabetes care: a new role for DSNs
Author / Creator:Shepherd, Maggie ; Stride, Amanda ; Ellard, Sian ; Hattersley, Andrew T
Publisher:S.B. Communications
Journal title:Journal of diabetes nursing, 2003-09, Vol.7 (8), p.289-292
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β-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1α Mutation Carriers

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Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY)

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Intrauterine Hyperglycemia Is Associated With an Earlier Diagnosis of Diabetes in HNF-1α Gene Mutation Carriers

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Etiological Investigation of Diabetes in Young Adults Presenting With Apparent Type 2 Diabetes

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Cross-sectional and longitudinal studies suggest pharmacological treatment used in patients with glucokinase mutations does not alter glycaemia

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Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1β gene mutation

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β-cell genes and diabetes : Quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1α and glucokinase mutations

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Beta-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers

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{szligbeta}-Cell Dysfunction, Insulin Sensitivity, and Glycosuria Precede Diabetes in Hepatocyte Nuclear Factor-1[alpha] Mutation Carriers

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Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1(alpha) gene mutation carriers

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Intrauterine hyperglycemia is associated with an earlier diagnosis of diabetes in HNF-1alpha gene mutation carriers

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Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1[beta] gene mutation

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Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation

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Necrobiosis Lipodica Is a Clinical Feature of Maturity-Onset Diabetes of the Young

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Β-Cell Genes and Diabetes: Quantitative and Qualitative Differences in the Pathophysiology of Hepatic Nuclear Factor-1[Alpha] and Glucokinase Mutations

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[Beta]-Cell Genes and Diabetes: Quantitative and Qualitative Differences in the Pathophysiology of Hepatic Nuclear Factor-1[Alpha] and Glucokinase Mutations

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Integrating genetics into diabetes care: a new role for DSNs

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