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Pediatric Diabetes
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January 18, 2017
Diagnostic and management challenges from childhood, puberty through to transition in severe insulin resistance due to insulin receptor mutations
Christina Wei, Christine P Burren
Diabetes Care
|
June 29, 2004
Remitting diabetes: a new genetic subgroup?
Christine P Burren, Andrew T Hattersley
Radiology Case Reports
|
February 28, 2018
Pamidronate "zebra lines": A treatment timeline
Avgi Loizidou, Savvas Andronikou, Christine P Burren
American Journal of Medical Genetics. Part A
|
May 13, 2016
Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis
Rathi Prasad, Carole Brewer, Christine P Burren
Endocrinology, Diabetes & Metabolism Case Reports
|
May 5, 2017
Gonadotrophin abnormalities in an infant with Lowe syndrome
Bronwen E Warner, Carol D Inward, Christine P Burren
JCEM Case Reports
|
November 1, 2023
Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism
Christine P Burren, Georgina Williams, Edward Coxson, et al.
Clinical Endocrinology
|
January 7, 2010
The continuum of growth hormone-IGF-I axis defects causing short stature: diagnostic and therapeutic challenges
Martin O Savage, Christine P Burren, Ron G Rosenfeld
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 25, 2020
Improvement in glycaemic parameters using SGLT-2 inhibitor and GLP-1 agonist in combination in an adolescent with diabetes mellitus and Prader-Willi syndrome: a case report
Toby Candler, David McGregor, Kruthika Narayan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 17, 2011
Evaluation and management of bone health in children with epilepsy on long-term antiepileptic drugs: United Kingdom survey of paediatric neurologists
Choong Yi Fong, Andrew A Mallick, Christine P Burren, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2018
Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype
Farah Kanani, Michael J Parker, Christine P Burren, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
Pediatric Diabetes
|
January 18, 2017
Diagnostic and management challenges from childhood, puberty through to transition in severe insulin resistance due to insulin receptor mutations
Christina Wei, Christine P Burren
Diabetes Care
|
June 29, 2004
Remitting diabetes: a new genetic subgroup?
Christine P Burren, Andrew T Hattersley
Radiology Case Reports
|
February 28, 2018
Pamidronate "zebra lines": A treatment timeline
Avgi Loizidou, Savvas Andronikou, Christine P Burren
American Journal of Medical Genetics. Part A
|
May 13, 2016
Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis
Rathi Prasad, Carole Brewer, Christine P Burren
Endocrinology, Diabetes & Metabolism Case Reports
|
May 5, 2017
Gonadotrophin abnormalities in an infant with Lowe syndrome
Bronwen E Warner, Carol D Inward, Christine P Burren
JCEM Case Reports
|
November 1, 2023
Effective Long-term Pediatric Pegvisomant Monotherapy to Final Height in X-linked Acrogigantism
Christine P Burren, Georgina Williams, Edward Coxson, et al.
Clinical Endocrinology
|
January 7, 2010
The continuum of growth hormone-IGF-I axis defects causing short stature: diagnostic and therapeutic challenges
Martin O Savage, Christine P Burren, Ron G Rosenfeld
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 25, 2020
Improvement in glycaemic parameters using SGLT-2 inhibitor and GLP-1 agonist in combination in an adolescent with diabetes mellitus and Prader-Willi syndrome: a case report
Toby Candler, David McGregor, Kruthika Narayan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 17, 2011
Evaluation and management of bone health in children with epilepsy on long-term antiepileptic drugs: United Kingdom survey of paediatric neurologists
Choong Yi Fong, Andrew A Mallick, Christine P Burren, et al.
American Journal of Medical Genetics. Part A
|
December 18, 2018
Clinical report follow up: Type 1 Collagenopathy presenting with a Russell-Silver phenotype
Farah Kanani, Michael J Parker, Christine P Burren, et al.
Page
of 3