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

Year Number of Results
1985 1
1987 1
1988 1
1989 1
1993 2
1994 1
1996 1
1997 3
1998 3
1999 2
2000 4
2001 1
2002 2
2003 7
2004 4
2005 5
2006 6
2007 4
2008 7
2009 9
2010 9
2011 8
2012 5
2013 6
2014 3
2015 2
2016 5
2017 5
2018 3
2019 3
2020 2
2021 1
2022 2
2023 4
2024 1

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Page 1
Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I Deficiency.
Grimberg A, DiVall SA, Polychronakos C, Allen DB, Cohen LE, Quintos JB, Rossi WC, Feudtner C, Murad MH; Drug and Therapeutics Committee and Ethics Committee of the Pediatric Endocrine Society. Grimberg A, et al. Horm Res Paediatr. 2016;86(6):361-397. doi: 10.1159/000452150. Epub 2016 Nov 25. Horm Res Paediatr. 2016. PMID: 27884013 Free article.
IGF1 deficiency integrates stunted growth and neurodegeneration in Down syndrome.
Araya P, Kinning KT, Coughlan C, Smith KP, Granrath RE, Enriquez-Estrada BA, Worek K, Sullivan KD, Rachubinski AL, Wolter-Warmerdam K, Hickey F, Galbraith MD, Potter H, Espinosa JM. Araya P, et al. Cell Rep. 2022 Dec 27;41(13):111883. doi: 10.1016/j.celrep.2022.111883. Cell Rep. 2022. PMID: 36577365 Free PMC article.
Partial growth hormone insensitivity.
Johnston LB, Savage MO. Johnston LB, et al. J Pediatr Endocrinol Metab. 1999 Apr;12 Suppl 1:251-7. J Pediatr Endocrinol Metab. 1999. PMID: 10698589 Review.
Molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uraemic syndrome patients.
Jlajla H, Dehman F, Jallouli M, Khedher R, Ayadi I, Zerzeri Y, Laadhar L, Sfar I, Mahfoudh A, Gorgi Y, Cheour E, Zouaghi K, Gargah T, Kallel Sellami M. Jlajla H, et al. Nephrology (Carlton). 2019 Mar;24(3):357-364. doi: 10.1111/nep.13217. Nephrology (Carlton). 2019. PMID: 29292855
AIM: The aim of the present study was to characterize the molecular basis of complement factor I deficiency in Tunisian atypical haemolytic and uremic syndrome patients with low factor I levels. ...
AIM: The aim of the present study was to characterize the molecular basis of complement factor I deficiency in Tunisian …
111 results