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Page 1
Rituximab therapy in ROHHAD(NET) syndrome.
Hawton KAC, Doffinger R, Ramanan AV, Langton Hewer SC, Evans HJ, Giri D, Hamilton Shield JP. Hawton KAC, et al. Among authors: giri d. J Pediatr Endocrinol Metab. 2022 Apr 26;35(8):1102-1106. doi: 10.1515/jpem-2022-0085. Print 2022 Aug 26. J Pediatr Endocrinol Metab. 2022. PMID: 35470643
Acanthosis Nigricans and Its Response to Metformin.
Giri D, Alsaffar H, Ramakrishnan R. Giri D, et al. Pediatr Dermatol. 2017 Sep;34(5):e281-e282. doi: 10.1111/pde.13206. Epub 2017 Jul 30. Pediatr Dermatol. 2017. PMID: 28758315
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements.
Laver TW, Wakeling MN, Caswell RC, Bunce B, Yau D, Männistö JME, Houghton JAL, Hopkins JJ, Weedon MN, Saraff V, Kershaw M, Honey EM, Murphy N, Giri D, Nath S, Tangari Saredo A, Banerjee I, Hussain K, Owens NDL, Flanagan SE. Laver TW, et al. Among authors: giri d. Eur J Hum Genet. 2024 Jul;32(7):813-818. doi: 10.1038/s41431-024-01593-z. Epub 2024 Apr 11. Eur J Hum Genet. 2024. PMID: 38605124 Free PMC article.
36 results