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Sian Ellard

Showing results (1-10 of 439) with videos related to

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Methods in Molecular Medicine|January 22, 2004
Multiple endocrine neoplasia types 1 and 2Sian Ellard
Human Mutation|August 19, 2006
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the youngSian Ellard, Kevin Colclough
European Journal of Human Genetics : EJHG|November 8, 2021
Rapid genomic testing for critically ill children: time to become standard of care?Zornitza Stark, Sian Ellard
Expert Opinion on Pharmacotherapy|August 24, 2006
Defining the genetic aetiology of monogenic diabetes can improve treatmentAnna L Gloyn, Sian Ellard
European Journal of Human Genetics : EJHG|September 22, 2011
Alagille syndrome: pathogenesis, diagnosis and managementPeter D Turnpenny, Sian Ellard
Pediatric Clinics of North America|July 27, 2015
Genome, Exome, and Targeted Next-Generation Sequencing in Neonatal DiabetesElisa De Franco, Sian Ellard
Annals of Clinical Biochemistry|July 24, 2013
Maturity onset diabetes of the young: identification and diagnosisTim J McDonald, Sian Ellard
Methods in Molecular Biology (Clifton, N.J.)|November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channelSarah E Flanagan, Sian Ellard
Hormone Research in Paediatrics|September 21, 2013
Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic optionsOscar Rubio-Cabezas, Sian Ellard
Clinical Endocrinology|September 15, 2007
Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1Martina Owens, Sian Ellard, Bijay Vaidya
Pageof 44

Showing results (1-10 of 439) with videos related to

Sort By:
Pageof 44
Methods in Molecular Medicine|January 22, 2004
Multiple endocrine neoplasia types 1 and 2Sian Ellard
Human Mutation|August 19, 2006
Mutations in the genes encoding the transcription factors hepatocyte nuclear factor 1 alpha (HNF1A) and 4 alpha (HNF4A) in maturity-onset diabetes of the youngSian Ellard, Kevin Colclough
European Journal of Human Genetics : EJHG|November 8, 2021
Rapid genomic testing for critically ill children: time to become standard of care?Zornitza Stark, Sian Ellard
Expert Opinion on Pharmacotherapy|August 24, 2006
Defining the genetic aetiology of monogenic diabetes can improve treatmentAnna L Gloyn, Sian Ellard
European Journal of Human Genetics : EJHG|September 22, 2011
Alagille syndrome: pathogenesis, diagnosis and managementPeter D Turnpenny, Sian Ellard
Pediatric Clinics of North America|July 27, 2015
Genome, Exome, and Targeted Next-Generation Sequencing in Neonatal DiabetesElisa De Franco, Sian Ellard
Annals of Clinical Biochemistry|July 24, 2013
Maturity onset diabetes of the young: identification and diagnosisTim J McDonald, Sian Ellard
Methods in Molecular Biology (Clifton, N.J.)|November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channelSarah E Flanagan, Sian Ellard
Hormone Research in Paediatrics|September 21, 2013
Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic optionsOscar Rubio-Cabezas, Sian Ellard
Clinical Endocrinology|September 15, 2007
Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1Martina Owens, Sian Ellard, Bijay Vaidya
Pageof 44