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Results by year

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

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

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Search Results

101 results

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Page 1
GnRH replacement rescues cognition in Down syndrome.
Manfredi-Lozano M, Leysen V, Adamo M, Paiva I, Rovera R, Pignat JM, Timzoura FE, Candlish M, Eddarkaoui S, Malone SA, Silva MSB, Trova S, Imbernon M, Decoster L, Cotellessa L, Tena-Sempere M, Claret M, Paoloni-Giacobino A, Plassard D, Paccou E, Vionnet N, Acierno J, Maceski AM, Lutti A, Pfrieger F, Rasika S, Santoni F, Boehm U, Ciofi P, Buée L, Haddjeri N, Boutillier AL, Kuhle J, Messina A, Draganski B, Giacobini P, Pitteloud N, Prevot V. Manfredi-Lozano M, et al. Among authors: paoloni giacobino a. Science. 2022 Sep 2;377(6610):eabq4515. doi: 10.1126/science.abq4515. Epub 2022 Sep 2. Science. 2022. PMID: 36048943 Free PMC article.
Glomerulocystic kidney disease.
Scheen M, Paoloni-Giacobino A, Nguyen-Tang EG, Vidal J, De Seigneux S, Haidar F. Scheen M, et al. Among authors: paoloni giacobino a. Kidney Int. 2022 Nov;102(5):1193. doi: 10.1016/j.kint.2022.05.010. Kidney Int. 2022. PMID: 36272745 No abstract available.
[Preimplantation genetic testing].
Benard J, Targa C, Murisier F, Paoloni-Giacobino A, Streuli I. Benard J, et al. Among authors: paoloni giacobino a. Rev Med Suisse. 2019 Jan 9;15(N° 632-633):53-56. Rev Med Suisse. 2019. PMID: 30629370 French.
Genetics and nutrition.
Paoloni-Giacobino A, Grimble R, Pichard C. Paoloni-Giacobino A, et al. Clin Nutr. 2003 Oct;22(5):429-35. doi: 10.1016/s0261-5614(03)00064-5. Clin Nutr. 2003. PMID: 14512029 Review.
Epigenetics in reproductive medicine.
Paoloni-Giacobino A. Paoloni-Giacobino A. Pediatr Res. 2007 May;61(5 Pt 2):51R-57R. doi: 10.1203/pdr.0b013e318039d978. Pediatr Res. 2007. PMID: 17413849 Review.
Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders.
Fokstuen S, Makrythanasis P, Hammar E, Guipponi M, Ranza E, Varvagiannis K, Santoni FA, Albarca-Aguilera M, Poleggi ME, Couchepin F, Brockmann C, Mauron A, Hurst SA, Moret C, Gehrig C, Vannier A, Bevillard J, Araud T, Gimelli S, Stathaki E, Paoloni-Giacobino A, Bottani A, Sloan-Béna F, Sizonenko LD, Mostafavi M, Hamamy H, Nouspikel T, Blouin JL, Antonarakis SE. Fokstuen S, et al. Among authors: paoloni giacobino a. Hum Genomics. 2016 Jun 28;10(1):24. doi: 10.1186/s40246-016-0080-4. Hum Genomics. 2016. PMID: 27353043 Free PMC article. Review.
101 results