Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution
Brandt, Agnieszka, Agarwal, Neha, Giri, Dinesh, Yung, Zoe, Didi, Mohammad, Senniappan, Senthil
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2020)
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2020)
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Journal Article
Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy
Taylor-Miller, Tashunka, Houghton, Jayne, Munyard, Paul, Kumar, Yadlapalli, Puvirajasinghe, Clinda, Giri, Dinesh
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2020)
Published in Journal of Pediatric Endocrinology & Metabolism (26.05.2020)
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Journal Article
Insights from the ACTION Teens Study: a survey of adolescents living with obesity, their caregivers and healthcare professionals in the UK
Halford, Jason C G, Brown, Adrian, Clare, Kenneth, Ells, Louisa J, Ghosh, Anngona, Giri, Dinesh, Hughes, Carly, Senniappan, Senthil
Published in BMJ open (23.07.2024)
Published in BMJ open (23.07.2024)
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Journal Article
Case report: Molecular characterisation of adipose-tissue derived cells from a patient with ROHHAD syndrome
Biernacka, Kalina M, Giri, Dinesh, Hawton, Katherine, Segers, Francisca, Perks, Claire M, Hamilton-Shield, Julian P
Published in Frontiers in pediatrics (30.06.2023)
Published in Frontiers in pediatrics (30.06.2023)
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Journal Article
Qualitative Parental Perceptions of a Paediatric Multidisciplinary Team Clinic for Prader-Willi Syndrome
Cox, Jennifer S., Semple, Claire, Augustus, Rhian, Wenn, Melanie, Easter, Shelley, Broadbent, Rebecca, Giri, Dinesh, Hinton, Elanor C.
Published in Journal of clinical research in pediatric endocrinology (01.12.2021)
Published in Journal of clinical research in pediatric endocrinology (01.12.2021)
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Journal Article
A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular Carcinoma
Senniappan, Senthil, Jones, Matthew, Kokai, George, Didi, Mohammad, Gossan, Nicole, Ciolka, Barbara, Giri, Dinesh, Blackburn, James, Waghorn, Alison
Published in Case reports in genetics (2018)
Published in Case reports in genetics (2018)
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Journal Article
Phosgene oxime: Injury and associated mechanisms compared to vesicating agents sulfur mustard and lewisite
Goswami, Dinesh Giri, Agarwal, Rajesh, Tewari-Singh, Neera
Published in Toxicology letters (01.09.2018)
Published in Toxicology letters (01.09.2018)
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Journal Article
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities
Giri, Dinesh, Vignola, Maria Lillina, Gualtieri, Angelica, Scagliotti, Valeria, McNamara, Paul, Peak, Matthew, Didi, Mohammed, Gaston-Massuet, Carles, Senniappan, Senthil
Published in Human molecular genetics (15.11.2017)
Published in Human molecular genetics (15.11.2017)
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Journal Article
Acanthosis Nigricans and Its Response to Metformin
Giri, Dinesh, Alsaffar, Hussain, Ramakrishnan, Renuka
Published in Pediatric dermatology (01.09.2017)
Published in Pediatric dermatology (01.09.2017)
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Journal Article
Current understanding and management of paediatric diabetic ketoacidosis
Leach, Daniel, Chatterjee, Sumana, Sen, Proteek, Shirodkar, Diksha, Giri, Dinesh
Published in Paediatrics and child health (01.07.2023)
Published in Paediatrics and child health (01.07.2023)
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Journal Article
Perceptions of non-successful families attending a weight-management clinic
Cox, Jennifer S, Searle, Aidan J, Hinton, Elanor C, Giri, Dinesh, Shield, Julian P H
Published in Archives of disease in childhood (01.04.2021)
Published in Archives of disease in childhood (01.04.2021)
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