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A rare cause of midbrain haemorrhage.
Lange KS, Taieb G, Lepretre P, De La Cruz E, Arquizan C, Gaillard N. Lange KS, et al. Among authors: de la cruz e. Eur J Neurol. 2021 Mar;28(3):e22-e24. doi: 10.1111/ene.14688. Epub 2020 Dec 30. Eur J Neurol. 2021. PMID: 33332693 No abstract available.
Post viral upper and lower motor neuron injuries.
De La Cruz E, Metzger A, Braquet P, Gaillard N, Taieb G. De La Cruz E, et al. Neurology. 2017 Oct 31;89(18):1928-1929. doi: 10.1212/WNL.0000000000004601. Neurology. 2017. PMID: 29084922 No abstract available.
Heterozygous SPTLC1 p.Leu39del is a major cause of slow-progressing juvenile ALS.
Guissart C, De la Cruz E, Flabeau O, Grapperon AM, Corazza G, Junilhon L, Delmas JC, Millecamps S, Polge A, Amador MDM, Salachas F, Rochat J, Goizet C, Juntas Morales R, Lumbroso S, Philibert P, Cheillan D, Mouzat K. Guissart C, et al. Among authors: de la cruz e. J Neurol Neurosurg Psychiatry. 2024 Feb 14;95(3):288-290. doi: 10.1136/jnnp-2023-331753. J Neurol Neurosurg Psychiatry. 2024. PMID: 38041669 No abstract available.
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy.
Sanson B, Stalens C, Guien C, Villa L, Eng C, Rabarimeriarijaona S, Bernard R, Cintas P, Solé G, Tiffreau V, Echaniz-Laguna A, Magot A, Juntas Morales R, Boyer FC, Nadaj-Pakleza A, Jacquin-Piques A, Béroud C, Sacconi S; French FSHD registry collaboration group. Sanson B, et al. Orphanet J Rare Dis. 2022 Mar 2;17(1):96. doi: 10.1186/s13023-021-01793-6. Orphanet J Rare Dis. 2022. PMID: 35236385 Free PMC article.
244 results