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pro vyhledávání: '"Deschênes G"'
Autor:
Macher, M.A., Baudouin, V., Maisin, A., Kwon, T., Peycelon, M., Dahmani, S., Naudin, J., Hogan, J., Deschênes, G.
Publikováno v:
In EMC – Pediatría March 2022 57(1):1-17
Autor:
Bertholet-Thomas, A., Servais, A., Liang, H., Acquaviva, C., Vianey-Saban, C., Deschênes, G., Cochat, P., Labbé, A., Bacchetta, J., Lemoine, S.
Publikováno v:
In EMC – Pediatría June 2018 53(3):1-12
Autor:
Houdouin, V., Lavis, N., Meyzer, C., Jeziorski, E., Merlin, E., Pinquier, D., Deschenes, G., Mothe, E., Petit, C., Plantaz, D., Stoller, J., El Qomri, M.-P., Dubos, F., Reix, P.
Publikováno v:
In Vaccine Reports December 2016 6:1-7
Autor:
Pietrement, C., Allain-Launay, E., Bacchetta, J., Bertholet-Thomas, A., Dubourg, L., Harambat, J., Vieux, R., Deschênes, G.
Publikováno v:
In Archives de pédiatrie November 2016 23(11):1191-1200
Autor:
Deschênes, G., Hogan, J.
Publikováno v:
In Urgences pédiatriques Edition: Sixth Edition. 2023:690-696
Autor:
Deschênes, G., Hogan, J.
Publikováno v:
In Urgences pédiatriques Edition: Sixth Edition. 2023:687-689
Autor:
Deschênes, G., Hogan, J.
Publikováno v:
In Urgences pédiatriques Edition: Sixth Edition. 2023:704-708
Publikováno v:
In EMC – Pediatría March 2013 48(1):1-6
Autor:
Curie, A., Touil, N., Gaillard, S., Galanaud, D., Leboucq, N., Deschênes, G., Morin, D., Abad, F., Luauté, J., Bodenan, E., Roche, L., Acquaviva, C., Vianey-Saban, C., Cochat, P., Cotton, F., Bertholet-Thomas, A.
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-22 (2020)
Orphanet journal of rare diseases
Orphanet journal of rare diseases, 2020, 15 (1), pp.59. ⟨10.1186/s13023-019-1271-6⟩
Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases
Orphanet journal of rare diseases, 2020, 15 (1), pp.59. ⟨10.1186/s13023-019-1271-6⟩
Orphanet Journal of Rare Diseases
Background Cystinosis is a rare autosomal recessive disorder caused by intracellular cystine accumulation. Proximal tubulopathy (Fanconi syndrome) is one of the first signs, leading to end-stage renal disease between the age of 12 and 16. Other sympt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6c135914d6d65bad172186471d4d039e
http://link.springer.com/article/10.1186/s13023-019-1271-6
http://link.springer.com/article/10.1186/s13023-019-1271-6
Publikováno v:
In Journal of Pediatric Urology 2011 7(6):638-643