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

Year Number of Results
1983 3
1984 1
1990 3
1991 3
1993 1
1994 1
1997 1
2000 1
2001 2
2002 3
2003 2
2004 3
2006 1
2007 1
2008 1
2009 1
2010 2
2011 3
2013 2
2014 3
2015 5
2016 9
2017 7
2018 4
2019 8
2020 5
2021 10
2022 8
2023 9
2024 5

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97 results

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Page 1
[Telomeres and lung].
Guérin C, Crestani B, Dupin C, Kawano-Dourado L, Ba I, Kannengiesser C, Borie R. Guérin C, et al. Among authors: ba i. Rev Mal Respir. 2022 Sep;39(7):595-606. doi: 10.1016/j.rmr.2022.03.011. Epub 2022 Jun 14. Rev Mal Respir. 2022. PMID: 35715316 Review. French.
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective.
Papiris SA, Kannengiesser C, Borie R, Kolilekas L, Kallieri M, Apollonatou V, Ba I, Nathan N, Bush A, Griese M, Dieude P, Crestani B, Manali ED. Papiris SA, et al. Among authors: ba i. Diagnostics (Basel). 2022 Nov 23;12(12):2928. doi: 10.3390/diagnostics12122928. Diagnostics (Basel). 2022. PMID: 36552935 Free PMC article. Review.
[Rituals of birth in Senegal].
Ba I, Diodo Ly O, Rizzi AT, Sandri R, Thiam MH. Ba I, et al. Soins Pediatr Pueric. 2017 Sep-Oct;38(298):20-22. doi: 10.1016/j.spp.2017.06.007. Soins Pediatr Pueric. 2017. PMID: 28890098 French.
High risk of lung cancer in surfactant-related gene variant carriers.
Brudon A, Legendre M, Mageau A, Bermudez J, Bonniaud P, Bouvry D, Cadranel J, Cazes A, Crestani B, Dégot T, Delestrain C, Diesler R, Epaud R, Philippot Q, Théou-Anton N, Kannengiesser C, Ba I, Debray MP, Fanen P, Manali E, Papiris S, Nathan N, Amselem S, Gondouin A, Guillaumot A, Andréjak C, Jouneau S, Beltramo G, Uzunhan Y, Galodé F, Westeel V, Mehdaoui A, Hirschi S, Leroy S, Marchand-Adam S, Nunes H, Picard C, Prévot G, Reynaud-Gaubert M, De Vuyst P, Wemeau L, Defossez G, Zalcman G, Cottin V, Borie R; OrphaLung network. Brudon A, et al. Among authors: ba i. Eur Respir J. 2024 May 2;63(5):2301809. doi: 10.1183/13993003.01809-2023. Print 2024 May. Eur Respir J. 2024. PMID: 38575158 Free PMC article.
Hunting for the genetic basis of Susac syndrome.
David C, Papo T, Ba I, Ollivier E, Boileau C, Dieudé P, Keren B, Kannengiesser C, Sacre K. David C, et al. Among authors: ba i. Eur J Neurol. 2021 Jul;28(7):e57-e59. doi: 10.1111/ene.14836. Epub 2021 Apr 7. Eur J Neurol. 2021. PMID: 33773011 No abstract available.
[Tuberculous meningitis in children in Dakar].
Thiongane A, Ba ID, Faye PM, Sylla A. Thiongane A, et al. Among authors: ba id. Arch Pediatr. 2016 Apr;23(4):414-5. doi: 10.1016/j.arcped.2016.01.001. Epub 2016 Mar 9. Arch Pediatr. 2016. PMID: 26971138 French. No abstract available.
First heterozygous NOP10 mutation in familial pulmonary fibrosis.
Kannengiesser C, Manali ED, Revy P, Callebaut I, Ba I, Borgel A, Oudin C, Haritou A, Kolilekas L, Malagari K, Borie R, Lainey E, Boileau C, Crestani B, Papiris SA. Kannengiesser C, et al. Among authors: ba i. Eur Respir J. 2020 Jun 11;55(6):1902465. doi: 10.1183/13993003.02465-2019. Print 2020 Jun. Eur Respir J. 2020. PMID: 32139460 Free article. No abstract available.
Liver disease in germline mutations of telomere-related genes: Prevalence, clinical, radiological, pathological features, outcome, and risk factors.
Sidali S, Borie R, Sicre de Fontbrune F, El Husseini K, Rautou PE, Lainey E, Goria O, Crestani B, Cadranel J, Cottin V, Bunel V, Dumortier J, Jacquemin E, Reboux N, Hirschi S, Bourdin A, Meszaros M, Dharancy S, Hilaire S, Mallet V, Reynaud-Gaubert M, Terriou L, Gottrand F, Abou Chahla W, Khan JE, Carrier P, Saliba F, Rubbia-Brandt L, Aubert JD, Elkrief L, de Lédinghen V, Abergel A, Olivier T, Houssel P, Jouneau S, Wemeau L, Bergeron A, Leblanc T, Ollivier-Hourmand I, Nguyen Khac E, Morisse-Pradier H, Ba I, Boileau C, Roudot-Thoraval F, Vilgrain V, Bureau C, Nunes H, Naccache JM, Durand F, Francoz C, Roulot D, Valla D, Paradis V, Kannengiesser C, Plessier A. Sidali S, et al. Among authors: ba i. Hepatology. 2024 Jun 1;79(6):1365-1380. doi: 10.1097/HEP.0000000000000667. Epub 2023 Nov 6. Hepatology. 2024. PMID: 37934624
97 results