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

Year Number of Results
1950 1
1951 1
1952 2
1953 1
1954 1
1958 1
1960 1
1963 1
1967 1
1975 2
1976 1
1984 2
1997 2
1998 1
1999 1
2000 2
2001 3
2002 1
2003 7
2004 7
2005 9
2006 7
2007 5
2008 3
2009 2
2010 5
2011 5
2012 5
2013 11
2014 11
2015 9
2016 11
2017 9
2018 12
2019 15
2020 14
2021 13
2022 16
2023 25
2024 10

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205 results

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Page 1
Hirschsprung disease.
Montalva L, Cheng LS, Kapur R, Langer JC, Berrebi D, Kyrklund K, Pakarinen M, de Blaauw I, Bonnard A, Gosain A. Montalva L, et al. Among authors: bonnard a. Nat Rev Dis Primers. 2023 Oct 12;9(1):54. doi: 10.1038/s41572-023-00465-y. Nat Rev Dis Primers. 2023. PMID: 37828049 Review.
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Motta M, Fasano G, Gredy S, Brinkmann J, Bonnard AA, Simsek-Kiper PO, Gulec EY, Essaddam L, Utine GE, Guarnetti Prandi I, Venditti M, Pantaleoni F, Radio FC, Ciolfi A, Petrini S, Consoli F, Vignal C, Hepbasli D, Ullrich M, de Boer E, Vissers LELM, Gritli S, Rossi C, De Luca A, Ben Becher S, Gelb BD, Dallapiccola B, Lauri A, Chillemi G, Schuh K, Cavé H, Zenker M, Tartaglia M. Motta M, et al. Among authors: bonnard aa. Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8. Am J Hum Genet. 2021. PMID: 34626534 Free PMC article.
1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients.
Jacquin C, Landais E, Poirsier C, Afenjar A, Akhavi A, Bednarek N, Bénech C, Bonnard A, Bosquet D, Burglen L, Callier P, Chantot-Bastaraud S, Coubes C, Coutton C, Delobel B, Descharmes M, Dupont JM, Gatinois V, Gruchy N, Guterman S, Heddar A, Herissant L, Heron D, Isidor B, Jaeger P, Jouret G, Keren B, Kuentz P, Le Caignec C, Levy J, Lopez N, Manssens Z, Martin-Coignard D, Marey I, Mignot C, Missirian C, Pebrel-Richard C, Pinson L, Puechberty J, Redon S, Sanlaville D, Spodenkiewicz M, Tabet AC, Verloes A, Vieville G, Yardin C, Vialard F, Doco-Fenzy M. Jacquin C, et al. Among authors: bonnard a. Am J Med Genet A. 2023 Feb;191(2):445-458. doi: 10.1002/ajmg.a.63041. Epub 2022 Nov 11. Am J Med Genet A. 2023. PMID: 36369750 Free PMC article.
Germline bi-allelic SH2B3/LNK alteration predisposes to a neonatal juvenile myelomonocytic leukemia-like disorder.
Arfeuille C, Vial Y, Cadenet M, Caye-Eude A, Fenneteau O, Neven Q, Bonnard AA, Pizzi S, Carpentieri G, Capri Y, Girardi K, Pedace L, Macchiaiolo M, Boudhar K, Khaled MB, Chahla WA, Lutun A, Fahd M, Drunat S, Flex E, Dalle JH, Strullu M, Locatelli F, Tartaglia M, Cavé H. Arfeuille C, et al. Among authors: bonnard aa. Haematologica. 2023 Nov 16. doi: 10.3324/haematol.2023.283917. Online ahead of print. Haematologica. 2023. PMID: 37981895 Free article.
Global economic burden of unmet surgical need for appendicitis.
Reuter A, Rogge L, Monahan M, Kachapila M, Morton DG, Davies J, Vollmer S; NIHR Global Surgery Collaboration. Reuter A, et al. Br J Surg. 2022 Sep 9;109(10):995-1003. doi: 10.1093/bjs/znac195. Br J Surg. 2022. PMID: 35881506 Free PMC article.
Feeding disorders in children with oesophageal atresia: a cross-sectional study.
Pham A, Ecochard-Dugelay E, Bonnard A, Le Roux E, Gelas T, Rousseau V, Thomassin N, Cabon-Boudard I, Nicolas A, Guinot A, Rebeuh J, Le Mandat A, Djeddi DD, Fouquet V, Boucharny A, Irtan S, Lemale J, Comte A, Bridoux-Henno L, Dupont-Lucas C, Dimitrov G, Turquet A, Borderon C, Pelatan C, Chaillou Legault E, Jung C, Willot S, Montalva L, Mitanchez D, Gottrand F, Bellaiche M. Pham A, et al. Among authors: bonnard a. Arch Dis Child. 2022 Jan;107(1):52-58. doi: 10.1136/archdischild-2020-320609. Epub 2021 Apr 16. Arch Dis Child. 2022. PMID: 33863700
Reply to letter to the editor concerning: a variant pattern of Calretinin immunohistochemistry on rectal suction-biopsies is fully specific of short-segment Hirschsprung's disease. Vincent Guinard-Samuel, Arnaud Bonnard, Michel Peuchmaur and Dominique Berrebi. Pediatr Surg Int (2014) 30: 803-808.
Bonnard A, Berrebi D, Guinard-Samuel V. Bonnard A, et al. Pediatr Surg Int. 2015 Jan;31(1):109. doi: 10.1007/s00383-014-3631-6. Epub 2014 Nov 7. Pediatr Surg Int. 2015. PMID: 25376166 No abstract available.
205 results