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Charbit-Henrion, F.
118
results:
Search for persons
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Format
Online (118)
Mediatypes
Articles (Online) (100)
Bookchapter (Online) (1)
OpenAccess-fulltext (17)
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english (93)
french (20)
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1
P142 Inflammatory bowel diseases associated with primary im..:
Malamut, G
;
Simon, M
;
Nachury, M
...
Journal of Crohn's and Colitis. 16 (2022) Supplement_1 - p. i223-i224 , 2022
Link:
https://doi.org/10.1093/..
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2
P672 A tertiary multicenter cohort of patients with chronic..:
De castelbajac, F
;
Charbit-Henrion, F
;
Goulet, O
...
Journal of Crohn's and Colitis. 15 (2021) Supplement_1 - p. S593-S594 , 2021
Link:
https://doi.org/10.1093/..
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3
P095 Consequences of an IL2RA locus duplication in a very e..:
Joosse, M
;
Charbit-Henrion, F
;
Raatgeep, H
...
Journal of Crohn's and Colitis. 12 (2018) supplement_1 - p. S141-S142 , 2018
Link:
https://doi.org/10.1093/..
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4
Early and Late Complications After Liver Transplantation fo..:
Charbit-Henrion, F.
;
Lacaille, F.
;
McKiernan, P.
...
American Journal of Transplantation. 15 (2015) 3 - p. 786-791 , 2015
Link:
https://doi.org/10.1111/..
?
5
Prix SFP 2013 – 5 – Analyses fonctionnelle et génétique des..:
Sierra, A.
;
Cerf-Bensussan, N.
;
Ruemmele, F.
..
Archives de Pédiatrie. 22 (2015) 5 - p. 378-379 , 2015
Link:
https://doi.org/10.1016/..
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6
Caractéristiques cliniques et réponse thérapeutique de la g..:
Dumas, M.
;
Henrion-Charbit, F.
;
Rybojad, M.
...
Annales de Dermatologie et de Vénéréologie. 144 (2017) 12 - p. S128 , 2017
Link:
https://doi.org/10.1016/..
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7
Bi-allelic variants in IPO8 cause a connective tissue disor..:
Ziegler, A
;
Duclaux-Loras, R
;
Revenu, C
...
issn:0002-9297. , 2021
Link:
http://hdl.handle.net/11..
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8
Bi-allelic variants in IPO8 cause a connective tissue disor..:
Ziegler, A
;
Duclaux-Loras, R
;
Revenu, C
...
https://openaccess.sgul.ac.uk/id/eprint/113390/1/1-s2.0-S0002929721001518-main.pdf. , 2021
Link:
https://openaccess.sgul...
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9
Clinical genomics for the diagnosis of monogenic forms of i..:
Uhlig, H
;
Charbit-Henrion, F
;
Kotlarz, D
...
doi:10.1097/MPG.0000000000003017. , 2021
Link:
https://doi.org/10.1097/..
?
10
Inherited p40phox deficiency differs from classic chronic g..:
van de Geer, A
;
Nieto-Patlán, A
;
Kuhns, D
...
https://www.jci.org/articles/view/97116/pdf. , 2018
Link:
http://hdl.handle.net/10..
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11
Inherited p40^{phox} deficiency differs from classic chroni..:
van de Geer, A
;
Nieto-Patlán, A
;
Kuhns, DB
...
https://discovery.ucl.ac.uk/id/eprint/10056669/1/Burns_p40%28phox%29%20deficiency%20differs%20from%20classic%20chronic%20granulomatous%20disease_VoR.pdf. , 2018
Link:
https://discovery.ucl.ac..
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12
UNC45A deficiency causes microvillus inclusion disease–like..:
Duclaux-Loras, Rémi
;
Lebreton, Corinne
;
Berthelet, Jérémy
...
Journal of Clinical Investigation. 132 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1172/..
?
13
UNC45A deficiency causes microvillus inclusion disease-like..:
Duclaux-Loras, Rémi
;
Lebreton, Corinne
;
Berthelet, Jérémy
...
info:eu-repo/semantics/altIdentifier/doi/10.1172/JCI154997. , 2022
Link:
https://hal.science/hal-..
?
14
UNC45A deficiency causes microvillus inclusion disease-like..:
Duclaux-Loras, Rémi
;
Lebreton, Corinne
;
Berthelet, Jérémy
...
info:eu-repo/semantics/altIdentifier/doi/10.1172/JCI154997. , 2022
Link:
https://hal.science/hal-..
?
15
UNC45A deficiency causes microvillus inclusion disease-like..:
Duclaux-Loras, Rémi
;
Lebreton, Corinne
;
Berthelet, Jérémy
...
info:eu-repo/semantics/altIdentifier/doi/10.1172/JCI154997. , 2022
Link:
https://hal.science/hal-..
1-15