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Hormone Research in Paediatrics|January 31, 2024
Congenital Central Hypothyroidism Caused by Novel Variants in IGSF1 Gene: Case Series of 3 PatientsHelen MacGloin, Nadia Schoenmakers, Catherine Moorwood, et al.
Endocrinology, Diabetes & Metabolism Case Reports|May 17, 2019
Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutationVed Bhushan Arya, Jennifer Kalitsi, Ann Hickey, et al.
Endocrine|June 29, 2022
Endocrine manifestations of paediatric intracranial germ cell tumours: from diagnosis to long-term follow-upCristina Partenope, Gabriella Pozzobon, Giovanna Weber, et al.
The Journal of Clinical Endocrinology and Metabolism|November 29, 2013
Activating AKT2 mutation: hypoinsulinemic hypoketotic hypoglycemiaVed Bhushan Arya, Sarah E Flanagan, Edith Schober, et al.
Archives of Disease in Childhood. Education and Practice Edition|November 20, 2023
A well child with prolonged oral thrush: an unexpected diagnostic journeyEleni Gounari, Reem Elfeky, Lea Ghataore, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 18, 2014
Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutationPratik Shah, Ved Bhushan Arya, Sarah E Flanagan, et al.
European Journal of Endocrinology|January 25, 2013
Clinical and molecular characterisation of 300 patients with congenital hyperinsulinismRitika R Kapoor, Sarah E Flanagan, Ved Bhushan Arya, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2014
Long-term follow-up of children with congenital hyperinsulinism on octreotide therapyHuseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, et al.
International Journal of Endocrinology|March 21, 2022
Central Diabetes Insipidus in Children and Adolescents: Twenty-Six Year Experience from a Single CentreHüseyin Anil Korkmaz, Ritika R Kapoor, Jennifer Kalitsi, et al.
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