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Compound heterozygous mutations of the TNXB gene cause primary myopathy.
Pénisson-Besnier I, Allamand V, Beurrier P, Martin L, Schalkwijk J, van Vlijmen-Willems I, Gartioux C, Malfait F, Syx D, Macchi L, Marcorelles P, Arbeille B, Croué A, De Paepe A, Dubas F. Pénisson-Besnier I, et al. Among authors: croue a. Neuromuscul Disord. 2013 Aug;23(8):664-9. doi: 10.1016/j.nmd.2013.04.009. Epub 2013 Jun 12. Neuromuscul Disord. 2013. PMID: 23768946
[Papular mucinosis associated with myopathy].
Marteau N, Croue A, Dubas F, Maillard H, Verret JL. Marteau N, et al. Among authors: croue a. Ann Dermatol Venereol. 2000 Mar;127(3):289-91. Ann Dermatol Venereol. 2000. PMID: 10804304 French.
Myopathy caused by anoctamin 5 mutations and necrotizing vasculitis.
Pénisson-Besnier I, Saint-André JP, Hicks D, Sarkozy A, Croué A, Hudson J, Lochmüller H, Dubas F. Pénisson-Besnier I, et al. Among authors: croue a. J Neurol. 2012 Sep;259(9):1988-90. doi: 10.1007/s00415-012-6502-x. Epub 2012 Apr 19. J Neurol. 2012. PMID: 22527239 No abstract available.
Late diagnosis of neurofibromatosis type 1 in an 81-year-old patient.
Marchand A, Rousseau P, Croue A, Vidaud D, Wolkenstein P, Martin L. Marchand A, et al. Among authors: croue a. Clin Exp Dermatol. 2015 Mar;40(2):225-6. doi: 10.1111/ced.12403. Epub 2014 Aug 22. Clin Exp Dermatol. 2015. PMID: 25156439 No abstract available.
[An atypical case of lipoid proteinosis].
Grimaux X, Ayoubi RE, Rabin M, Martin L, Bonneau D, Bouyx F, Blanchard E, Croue A, Breton Q. Grimaux X, et al. Among authors: croue a. Ann Pathol. 2017 Oct;37(5):425-428. doi: 10.1016/j.annpat.2017.06.009. Epub 2017 Sep 19. Ann Pathol. 2017. PMID: 28935411 French.
130 results