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Year Number of Results
2009 2
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2013 1
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2016 3
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52 results

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Page 1
Preventing Post-Lumbar Puncture Headache.
Cognat E, Koehl B, Lilamand M, Goutagny S, Belbachir A, de Charentenay L, Guiddir T, Zetlaoui P, Roos C, Paquet C. Cognat E, et al. Among authors: koehl b. Ann Emerg Med. 2021 Sep;78(3):443-450. doi: 10.1016/j.annemergmed.2021.02.019. Epub 2021 May 7. Ann Emerg Med. 2021. PMID: 33966935 Review.
Invasive Bacterial Infections in Children With Sickle Cell Disease: 2014-2019.
Gaschignard J, Koehl B, Rees DC, Rincón-López E, Vanderfaeillie A, Pascault A, Allali S, Cela E, Odièvre MH, Hau I, Oliveira M, Guillaumat C, Brousse V, de Montalembert M, Navarro Gómez ML, Beldjoudi N, Bardon-Cancho EJ, Epalza C; BACT-SPRING study group. Gaschignard J, et al. Among authors: koehl b. Pediatrics. 2023 Oct 1;152(4):e2022061061. doi: 10.1542/peds.2022-061061. Pediatrics. 2023. PMID: 37767606
Factor H: a novel modulator in sickle cell disease.
Nemer WE, Koehl B. Nemer WE, et al. Among authors: koehl b. Haematologica. 2019 May;104(5):857-859. doi: 10.3324/haematol.2018.214668. Haematologica. 2019. PMID: 31040228 Free PMC article. No abstract available.
Inherited glycosylphosphatidylinositol defects cause the rare Emm-negative blood phenotype and developmental disorders.
Duval R, Nicolas G, Willemetz A, Murakami Y, Mikdar M, Vrignaud C, Megahed H, Cartron JP, Masson C, Wehbi S, Koehl B, Hully M, Siquier K, Chemlay N, Rotig A, Lyonnet S, Colin Y, Barcia G, Cantagrel V, Le Van Kim C, Hermine O, Kinoshita T, Peyrard T, Azouzi S. Duval R, et al. Among authors: koehl b. Blood. 2021 Jul 1;137(26):3660-3669. doi: 10.1182/blood.2020009810. Blood. 2021. PMID: 33763700 Free article.
[Spectrum of renal manifestations in sickle cell disease].
Cazenave M, Koehl B, Nochy D, Tharaux PL, Audard V. Cazenave M, et al. Among authors: koehl b. Nephrol Ther. 2014 Feb;10(1):10-6. doi: 10.1016/j.nephro.2013.07.366. Epub 2013 Oct 7. Nephrol Ther. 2014. PMID: 24113202 Review. French.
[Nosocomial rotavirus gastroenteritis].
Marinosci A, Doit C, Koehl B, Belhacel K, Mariani Kurkdjian P, Melki I, Renaud A, Lemaitre C, Ammar Khodja N, Blachier A, Bonacorsi S, Faye A, Lorrot M. Marinosci A, et al. Among authors: koehl b. Arch Pediatr. 2016 Nov;23(11):1118-1123. doi: 10.1016/j.arcped.2016.07.006. Epub 2016 Sep 15. Arch Pediatr. 2016. PMID: 27642146 French.
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
Koehl B, Vrignaud C, Mikdar M, Nair TS, Yang L, Landry S, Laiguillon G, Giroux-Lathuile C, Anselme-Martin S, El Kenz H, Hermine O, Mohandas N, Cartron JP, Colin Y, Detante O, Marlu R, Le Van Kim C, Carey TE, Azouzi S, Peyrard T. Koehl B, et al. EMBO Mol Med. 2023 Mar 8;15(3):e16320. doi: 10.15252/emmm.202216320. Epub 2023 Jan 25. EMBO Mol Med. 2023. PMID: 36695047 Free PMC article.
[Psychological care of sickle cell patients].
Lehougre MP, Koehl B. Lehougre MP, et al. Among authors: koehl b. Rev Prat. 2023 May;73(5):530-529. Rev Prat. 2023. PMID: 37309790 French. No abstract available.
52 results