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

Year Number of Results
2002 5
2003 4
2004 3
2005 1
2006 1
2007 5
2008 1
2009 1
2011 4
2012 1
2013 2
2014 2
2016 2
2017 1
2019 2
2020 3
2023 1
2024 2

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36 results

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Page 1
New understandings of the genetic basis of isolated idiopathic central hypogonadism.
Bonomi M, Libri DV, Guizzardi F, Guarducci E, Maiolo E, Pignatti E, Asci R, Persani L; Idiopathic Central Hypogonadism Study Group of the Italian Societies of Endocrinology and Pediatric Endocrinology and Diabetes. Bonomi M, et al. Asian J Androl. 2012 Jan;14(1):49-56. doi: 10.1038/aja.2011.68. Epub 2011 Dec 5. Asian J Androl. 2012. PMID: 22138902 Free PMC article. Review.
Characterization of ANGPT2 mutations associated with primary lymphedema.
Leppänen VM, Brouillard P, Korhonen EA, Sipilä T, Jha SK, Revencu N, Labarque V, Fastré E, Schlögel M, Ravoet M, Singer A, Luzzatto C, Angelone D, Crichiutti G, D'Elia A, Kuurne J, Elamaa H, Koh GY, Saharinen P, Vikkula M, Alitalo K. Leppänen VM, et al. Among authors: d elia a. Sci Transl Med. 2020 Sep 9;12(560):eaax8013. doi: 10.1126/scitranslmed.aax8013. Sci Transl Med. 2020. PMID: 32908006
A CGH array procedure to detect PAX6 gene structural defects.
Franzoni A, Russo PD, Baldan F, D'Elia AV, Puppin C, Penco S, Damante G. Franzoni A, et al. Among authors: d elia av. Mol Cell Probes. 2017 Apr;32:65-68. doi: 10.1016/j.mcp.2016.12.001. Epub 2016 Dec 2. Mol Cell Probes. 2017. PMID: 27919838
Thyroid-specific transcription factors control Hex promoter activity.
Puppin C, D'Elia AV, Pellizzari L, Russo D, Arturi F, Presta I, Filetti S, Bogue CW, Denson LA, Damante G. Puppin C, et al. Among authors: d elia av. Nucleic Acids Res. 2003 Apr 1;31(7):1845-52. doi: 10.1093/nar/gkg295. Nucleic Acids Res. 2003. PMID: 12655000 Free PMC article.
36 results