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S Ellard

Showing results (61-70 of 144) with videos related to

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Diabetologia|February 7, 2001
A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteriaS Ellard, F Beards, L I Allen, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|August 2, 2016
Analysis of cell-free fetal DNA for non-invasive prenatal diagnosis in a family with neonatal diabetesE De Franco, R Caswell, J A L Houghton, et al.
Diabetologia|January 6, 2012
The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetesB M Shields, T J McDonald, S Ellard, et al.
Bone Marrow Transplantation|November 9, 2004
Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reactionL W Harries, C L Wickham, J C Evans, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 17, 2013
Atypical phenotype associated with reported GCK exon 10 deletions: Clinical judgement is needed alongside appropriate genetic investigationsG Thanabalasingham, K Kaur, F Talbot, et al.
Clinical Genetics|June 25, 2010
Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemiaS E Flanagan, R R Kapoor, I Banerjee, et al.
The Journal of Pediatrics|January 13, 2005
Permanent neonatal diabetes in an Asian infantJ R Porter, N J Shaw, T G Barrett, et al.
Diabetologia|April 20, 2005
The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutationT Klupa, E L Edghill, J Nazim, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Molecular Pathology : MP|July 8, 2000
Amplification of PCR products in excess of 600 base pairs using DNA extracted from decalcified, paraffin wax embedded bone marrow trephine biopsiesC L Wickham, M Boyce, M V Joyner, et al.
Pageof 15

Showing results (61-70 of 144) with videos related to

Sort By:
Pageof 15
Diabetologia|February 7, 2001
A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteriaS Ellard, F Beards, L I Allen, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|August 2, 2016
Analysis of cell-free fetal DNA for non-invasive prenatal diagnosis in a family with neonatal diabetesE De Franco, R Caswell, J A L Houghton, et al.
Diabetologia|January 6, 2012
The development and validation of a clinical prediction model to determine the probability of MODY in patients with young-onset diabetesB M Shields, T J McDonald, S Ellard, et al.
Bone Marrow Transplantation|November 9, 2004
Analysis of haematopoietic chimaerism by quantitative real-time polymerase chain reactionL W Harries, C L Wickham, J C Evans, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 17, 2013
Atypical phenotype associated with reported GCK exon 10 deletions: Clinical judgement is needed alongside appropriate genetic investigationsG Thanabalasingham, K Kaur, F Talbot, et al.
Clinical Genetics|June 25, 2010
Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemiaS E Flanagan, R R Kapoor, I Banerjee, et al.
The Journal of Pediatrics|January 13, 2005
Permanent neonatal diabetes in an Asian infantJ R Porter, N J Shaw, T G Barrett, et al.
Diabetologia|April 20, 2005
The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes: evidence for heterogeneity of beta cell function among carriers of the R201H mutationT Klupa, E L Edghill, J Nazim, et al.
Diabetes, Obesity & Metabolism|October 9, 2007
Functional analysis of two Kir6.2 (KCNJ11) mutations, K170T and E322K, causing neonatal diabetesA I Tarasov, C A Girard, B Larkin, et al.
Molecular Pathology : MP|July 8, 2000
Amplification of PCR products in excess of 600 base pairs using DNA extracted from decalcified, paraffin wax embedded bone marrow trephine biopsiesC L Wickham, M Boyce, M V Joyner, et al.
Pageof 15