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Sian Ellard

Showing results (31-40 of 439) with videos related to

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Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.
BMJ (Clinical Research Ed.)|December 5, 2012
Many patients have an identifiable genetic cause of Hirschsprung's diseaseFrancis H Sansbury, Sian Ellard, Charles Shaw-Smith, et al.
Clinical Endocrinology|August 20, 2011
Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 geneRitika R Kapoor, Sarah E Flanagan, Sian Ellard, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 19, 2015
Anemia in a Child with Deafness: Be Vigilant for a Rare Cause!Mohammed Ramzan, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital HyperinsulinismAyla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.
Annals of the Academy of Medicine, Singapore|July 17, 2014
Neonatal Diabetes in a Singapore Children's Hospital: Molecular Diagnoses of Four CasesRashida F Vasanwala, Song Hai Lim, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 geneErcan Mihci, Doğa Türkkahraman, Sian Ellard, 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.
The Journal of Molecular Diagnostics : JMD|August 1, 2009
Evaluation of 13q14 status in multiple myeloma by digital single nucleotide polymorphism technologyKaty Hanlon, Lorna W Harries, Sian Ellard, et al.
Diabetes Research and Clinical Practice|July 4, 2012
Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian childrenCresio Alves, Sarah E Flanagan, Sian Ellard, et al.
Pageof 44

Showing results (31-40 of 439) with videos related to

Sort By:
Pageof 44
Indian Pediatrics|October 14, 2011
Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) geneSeema Thakur, Sarah E Flanagan, Sian Ellard, et al.
BMJ (Clinical Research Ed.)|December 5, 2012
Many patients have an identifiable genetic cause of Hirschsprung's diseaseFrancis H Sansbury, Sian Ellard, Charles Shaw-Smith, et al.
Clinical Endocrinology|August 20, 2011
Congenital hyperinsulinism: marked clinical heterogeneity in siblings with identical mutations in the ABCC8 geneRitika R Kapoor, Sarah E Flanagan, Sian Ellard, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|June 19, 2015
Anemia in a Child with Deafness: Be Vigilant for a Rare Cause!Mohammed Ramzan, Sarah E Flanagan, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital HyperinsulinismAyla Güven, Ayşe Nurcan Cebeci, Sian Ellard, et al.
Annals of the Academy of Medicine, Singapore|July 17, 2014
Neonatal Diabetes in a Singapore Children's Hospital: Molecular Diagnoses of Four CasesRashida F Vasanwala, Song Hai Lim, Sian Ellard, et al.
Journal of Clinical Research in Pediatric Endocrinology|June 8, 2012
Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 geneErcan Mihci, Doğa Türkkahraman, Sian Ellard, 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.
The Journal of Molecular Diagnostics : JMD|August 1, 2009
Evaluation of 13q14 status in multiple myeloma by digital single nucleotide polymorphism technologyKaty Hanlon, Lorna W Harries, Sian Ellard, et al.
Diabetes Research and Clinical Practice|July 4, 2012
Clinical and molecular basis of transient neonatal diabetes mellitus in Brazilian childrenCresio Alves, Sarah E Flanagan, Sian Ellard, et al.
Pageof 44