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Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot Study.
Dermer E, Spahr A, Tran LT, Mirchi A, Pelletier F, Guerrero K, Ahmed S, Brais B, Braverman N, Buhas D, Chandratre S, Chenier S, Chrestian N, Desmeules M, Dilenge ME, Laflamme J, Larbrisseau A, Legault G, Lim KY, Maftei C, Major P, Malvey-Dorn E, Marois P, Mitchell J, Nadeau A, Osterman B, Paradis I, Pohl D, Reggin J, Riou E, Roedde G, Rossignol E, Sébire G, Shevell M, Srour M, Sylvain M, Tarnopolsky M, Venkateswaran S, Sullivan M, Bernard G. Dermer E, et al. Among authors: larbrisseau a. J Child Neurol. 2020 Nov;35(13):901-907. doi: 10.1177/0883073820938645. Epub 2020 Jul 28. J Child Neurol. 2020. PMID: 32720856
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French Canadians.
Roddier K, Thomas T, Marleau G, Gagnon AM, Dicaire MJ, St-Denis A, Gosselin I, Sarrazin AM, Larbrisseau A, Lambert M, Vanasse M, Gaudet D, Rouleau GA, Brais B. Roddier K, et al. Among authors: larbrisseau a. Neurology. 2005 May 24;64(10):1762-7. doi: 10.1212/01.WNL.0000161849.29944.43. Neurology. 2005. PMID: 15911806
Toxic reactions with valproic acid therapy.
Vanasse M, David P, Geoffroy G, Larbrisseau A. Vanasse M, et al. Among authors: larbrisseau a. Neurology. 1981 May;31(5):644. doi: 10.1212/wnl.31.5.644-a. Neurology. 1981. PMID: 6785664 No abstract available.
Neurologic crises in hereditary tyrosinemia.
Mitchell G, Larochelle J, Lambert M, Michaud J, Grenier A, Ogier H, Gauthier M, Lacroix J, Vanasse M, Larbrisseau A, et al. Mitchell G, et al. Among authors: larbrisseau a. N Engl J Med. 1990 Feb 15;322(7):432-7. doi: 10.1056/NEJM199002153220704. N Engl J Med. 1990. PMID: 2153931 Free article.
Intermittent treatment of febrile convulsions with nitrazepam.
Vanasse M, Masson P, Geoffroy G, Larbrisseau A, David PC. Vanasse M, et al. Among authors: larbrisseau a. Can J Neurol Sci. 1984 Aug;11(3):377-9. doi: 10.1017/s0317167100045741. Can J Neurol Sci. 1984. PMID: 6467089
31 results