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Tim Cheetham

Showing results (61-70 of 73) with videos related to

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BMJ Open|January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trialMichael Cole, Ann Marie Hynes, Denise Howel, et al.
Plos One|February 7, 2020
Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389Daphne Yau, Thomas W Laver, Antonia Dastamani, et al.
European Journal of Human Genetics : EJHG|October 18, 2007
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGHJohn C K Barber, Viv K Maloney, Shuwen Huang, et al.
Archives of Disease in Childhood|April 12, 2023
Emergency and perioperative management of adrenal insufficiency in children and young people: British Society for Paediatric Endocrinology and Diabetes consensus guidanceTalat Mushtaq, Salma R Ali, Nabil Boulos, et al.
The Journal of Clinical Investigation|November 20, 2012
Human SH2B1 mutations are associated with maladaptive behaviors and obesityMichael E Doche, Elena G Bochukova, Hsiao-Wen Su, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2026
Efficacy of 24-Weekly Versus 12-Weekly Decapeptyl SR Treatment in Central Precocious Puberty: A UK Multicentre Retrospective Cohort StudyRachel Varughese, Lydia Lake, Bharathy Kothayan, et al.
Wellcome Open Research|August 27, 2020
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndromeIndraneel Banerjee, Senthil Senniappan, Thomas W Laver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
DLG2 variants in patients with pubertal disordersYoun Hee Jee, Sehoon Won, Julian C Lui, et al.
Journal of Clinical Immunology|November 3, 2020
Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary ImmunodeficiencySu Han Lum, Reem Elfeky, Federica R Achini, et al.
Hormone Research in Paediatrics|March 12, 2024
National Service Evaluation of the Quality of Care for Children and Young People with Congenital Adrenal Hyperplasia in the UK: Survey Responses from Patients and CliniciansNeil R Lawrence, Irina A Bacila, Gary Collins, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
BMJ Open|January 24, 2019
Adjuvant rituximab, a potential treatment for the young patient with Graves' hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trialMichael Cole, Ann Marie Hynes, Denise Howel, et al.
Plos One|February 7, 2020
Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389Daphne Yau, Thomas W Laver, Antonia Dastamani, et al.
European Journal of Human Genetics : EJHG|October 18, 2007
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGHJohn C K Barber, Viv K Maloney, Shuwen Huang, et al.
Archives of Disease in Childhood|April 12, 2023
Emergency and perioperative management of adrenal insufficiency in children and young people: British Society for Paediatric Endocrinology and Diabetes consensus guidanceTalat Mushtaq, Salma R Ali, Nabil Boulos, et al.
The Journal of Clinical Investigation|November 20, 2012
Human SH2B1 mutations are associated with maladaptive behaviors and obesityMichael E Doche, Elena G Bochukova, Hsiao-Wen Su, et al.
The Journal of Clinical Endocrinology and Metabolism|March 7, 2026
Efficacy of 24-Weekly Versus 12-Weekly Decapeptyl SR Treatment in Central Precocious Puberty: A UK Multicentre Retrospective Cohort StudyRachel Varughese, Lydia Lake, Bharathy Kothayan, et al.
Wellcome Open Research|August 27, 2020
Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndromeIndraneel Banerjee, Senthil Senniappan, Thomas W Laver, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2020
DLG2 variants in patients with pubertal disordersYoun Hee Jee, Sehoon Won, Julian C Lui, et al.
Journal of Clinical Immunology|November 3, 2020
Outcome of Non-hematological Autoimmunity After Hematopoietic Cell Transplantation in Children with Primary ImmunodeficiencySu Han Lum, Reem Elfeky, Federica R Achini, et al.
Hormone Research in Paediatrics|March 12, 2024
National Service Evaluation of the Quality of Care for Children and Young People with Congenital Adrenal Hyperplasia in the UK: Survey Responses from Patients and CliniciansNeil R Lawrence, Irina A Bacila, Gary Collins, et al.
Pageof 8