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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 7
2003 5
2004 6
2005 5
2006 6
2007 9
2008 7
2009 9
2010 12
2011 6
2012 1
2013 4
2014 2
2015 1
2016 3
2017 3
2018 1
2019 2
2021 5
2022 1
2023 1
2025 0

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82 results

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Page 1
HESX1 and Septo-Optic Dysplasia.
Dattani MT, Robinson IC. Dattani MT, et al. Among authors: robinson ic. Rev Endocr Metab Disord. 2002 Dec;3(4):289-300. doi: 10.1023/a:1020945406356. Rev Endocr Metab Disord. 2002. PMID: 12424431 Review. No abstract available.
Growth hormone replacement therapy for adults: into the new millennium.
Simpson H, Savine R, Sönksen P, Bengtsson BA, Carlsson L, Christiansen JS, Clemmons D, Cohen P, Hintz R, Ho K, Mullis P, Robinson I, Strasburger C, Tanaka T, Thorner M; GRS Council. Simpson H, et al. Among authors: robinson i. Growth Horm IGF Res. 2002 Feb;12(1):1-33. doi: 10.1054/ghir.2001.0263. Growth Horm IGF Res. 2002. PMID: 12127299 Review. No abstract available.
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.
Akin L, Rizzoti K, Gregory LC, Corredor B, Le Quesne Stabej P, Williams H, Buonocore F, Mouilleron S, Capra V, McGlacken-Byrne SM, Martos-Moreno GÁ, Azmanov DN, Kendirci M, Kurtoglu S, Suntharalingham JP, Galichet C, Gustincich S, Tasic V, Achermann JC, Accogli A, Filipovska A, Tuilpakov A, Maghnie M, Gucev Z, Gonen ZB, Pérez-Jurado LA, Robinson I, Lovell-Badge R, Argente J, Dattani MT. Akin L, et al. Among authors: robinson i. Genet Med. 2022 Feb;24(2):384-397. doi: 10.1016/j.gim.2021.09.019. Epub 2021 Nov 30. Genet Med. 2022. PMID: 34906446 Free PMC article.
Somatostatin triggers rhythmic electrical firing in hypothalamic GHRH neurons.
Osterstock G, Mitutsova V, Barre A, Granier M, Fontanaud P, Chazalon M, Carmignac D, Robinson IC, Low MJ, Plesnila N, Hodson DJ, Mollard P, Méry PF. Osterstock G, et al. Among authors: robinson ic. Sci Rep. 2016 Apr 13;6:24394. doi: 10.1038/srep24394. Sci Rep. 2016. PMID: 27072430 Free PMC article.
Angoff anchor statements: setting a flawed gold standard?
Burr SA, Zahra D, Cookson J, Salih VM, Gabe-Thomas E, Robinson IM. Burr SA, et al. Among authors: robinson im. MedEdPublish (2016). 2017 Sep 21;6:167. doi: 10.15694/mep.2017.000167. eCollection 2017. MedEdPublish (2016). 2017. PMID: 38406395 Free PMC article.
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia.
Whittaker DE, Oleari R, Gregory LC, Le Quesne-Stabej P, Williams HJ; GOSgene; Torpiano JG, Formosa N, Cachia MJ, Field D, Lettieri A, Ocaka LA, Paganoni AJ, Rajabali SH, Riegman KL, De Martini LB, Chaya T, Robinson IC, Furukawa T, Cariboni A, Basson MA, Dattani MT. Whittaker DE, et al. Among authors: robinson ic. J Clin Invest. 2021 Dec 15;131(24):e141587. doi: 10.1172/JCI141587. J Clin Invest. 2021. PMID: 34730112 Free PMC article.
82 results