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

Year Number of Results
1984 1
1986 1
1987 1
1988 1
1989 3
1990 4
1991 2
1992 3
1993 3
1994 3
1995 1
1996 2
1998 1
1999 5
2000 3
2001 2
2002 2
2003 2
2004 4
2005 3
2006 1
2007 3
2008 2
2009 8
2010 9
2011 10
2012 11
2013 7
2014 8
2015 6
2016 7
2017 6
2018 6
2019 3
2020 2
2021 3
2022 3
2024 1

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131 results

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Page 1
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: guiochon mantel a. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
Hypertension and aortorenal disease in Alagille syndrome.
Salem JE, Bruguiere E, Iserin L, Guiochon-Mantel A, Plouin PF. Salem JE, et al. Among authors: guiochon mantel a. J Hypertens. 2012 Jul;30(7):1300-6. doi: 10.1097/HJH.0b013e3283531e1f. J Hypertens. 2012. PMID: 22525199 Review.
Genetic mutations in sporadic pituitary adenomas--what to screen for?
Lecoq AL, Kamenický P, Guiochon-Mantel A, Chanson P. Lecoq AL, et al. Among authors: guiochon mantel a. Nat Rev Endocrinol. 2015 Jan;11(1):43-54. doi: 10.1038/nrendo.2014.181. Epub 2014 Oct 28. Nat Rev Endocrinol. 2015. PMID: 25350067 Review.
Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009-2019).
Adams D, Cintas P, Solé G, Tard C, Labeyrie C, Echaniz-Laguna A, Cauquil C, Pereon Y, Magy L, Morales RJ, Antoine JC, Lagrange E, Petiot P, Mallaret M, Francou B, Guiochon-Mantel A, Coste A, Demarcq O, Geffroy C, Famelart V, Rudant J, Bartoli M, Donal E, Lairez O, Eicher JC, Kharoubi M, Oghina S, Trochu JN, Inamo J, Habib G, Roubille F, Hagège A, Morio F, Cariou E, Adda J, Slama MS, Charron P, Algalarrondo V, Damy T, Attarian S. Adams D, et al. Among authors: guiochon mantel a. Rev Neurol (Paris). 2024 Sep;180(7):661-672. doi: 10.1016/j.neurol.2024.02.393. Epub 2024 Apr 19. Rev Neurol (Paris). 2024. PMID: 38643028
R31C GNRH1 mutation and congenital hypogonadotropic hypogonadism.
Maione L, Albarel F, Bouchard P, Gallant M, Flanagan CA, Bobe R, Cohen-Tannoudji J, Pivonello R, Colao A, Brue T, Millar RP, Lombes M, Young J, Guiochon-Mantel A, Bouligand J. Maione L, et al. Among authors: guiochon mantel a. PLoS One. 2013 Jul 25;8(7):e69616. doi: 10.1371/journal.pone.0069616. Print 2013. PLoS One. 2013. PMID: 23936060 Free PMC article.
131 results