Cuisset JM - Search Results

1

[Phenotypic aspects of FKRP-linked muscular dystrophy type 2I in a series of eleven patients].

Bourteel H, Stojkovic T, Cuisset JM, Maurage CA, Laforet P, Richard P, Vermersch P. Bourteel H, et al. Among authors: cuisset jm. Rev Neurol (Paris). 2007 Feb;163(2):189-96. doi: 10.1016/s0035-3787(07)90390-2. Rev Neurol (Paris). 2007. PMID: 17351538 French.

2

Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities.

Vantyghem MC, Pigny P, Maurage CA, Rouaix-Emery N, Stojkovic T, Cuisset JM, Millaire A, Lascols O, Vermersch P, Wemeau JL, Capeau J, Vigouroux C. Vantyghem MC, et al. Among authors: cuisset jm. J Clin Endocrinol Metab. 2004 Nov;89(11):5337-46. doi: 10.1210/jc.2003-031658. J Clin Endocrinol Metab. 2004. PMID: 15531479

3

'Cap myopathy': case report of a family.

Cuisset JM, Maurage CA, Pellissier JF, Barois A, Urtizberea JA, Laing N, Tajsharghi H, Vallée L. Cuisset JM, et al. Neuromuscul Disord. 2006 Apr;16(4):277-81. doi: 10.1016/j.nmd.2006.01.014. Epub 2006 Mar 13. Neuromuscul Disord. 2006. PMID: 16531045

4

New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.

Devos D, Vuillaume I, de Becdelievre A, de Martinville B, Dhaenens CM, Cuvellier JC, Cuisset JM, Vallée L, Lemaitre MP, Bourteel H, Hachulla E, Wallaert B, Destée A, Defebvre L, Sablonnière B. Devos D, et al. Among authors: cuisset jm. Mov Disord. 2006 Dec;21(12):2237-40. doi: 10.1002/mds.21135. Mov Disord. 2006. PMID: 17044090

5

Neuropathological and MRI findings in an acute presentation of hemiconvulsion-hemiplegia: a report with pathophysiological implications.

Auvin S, Devisme L, Maurage CA, Soto-Ares G, Cuisset JM, Leclerc F, Vallée L. Auvin S, et al. Among authors: cuisset jm. Seizure. 2007 Jun;16(4):371-6. doi: 10.1016/j.seizure.2007.01.009. Epub 2007 Mar 12. Seizure. 2007. PMID: 17350294 Free article.

6

Epilepsia partialis continua and defects in the mitochondrial respiratory chain.

Riquet A, Auvin S, Cuisset JM, Lamblin MD, Sablonnière B, Cuvellier JC, Soto-Ares G, Maurage CA, Vallée L. Riquet A, et al. Among authors: cuisset jm. Epilepsy Res. 2008 Jan;78(1):1-6. doi: 10.1016/j.eplepsyres.2007.10.001. Epub 2007 Nov 26. Epilepsy Res. 2008. PMID: 18022351

7

Childhood spinal muscular atrophy induces alterations in contractile and regulatory protein isoform expressions.

Stevens L, Bastide B, Maurage CA, Dupont E, Montel V, Cieniewski-Bernard C, Cuisset JM, Vallée L, Mounier Y. Stevens L, et al. Among authors: cuisset jm. Neuropathol Appl Neurobiol. 2008 Dec;34(6):659-70. doi: 10.1111/j.1365-2990.2008.00950.x. Epub 2008 Mar 20. Neuropathol Appl Neurobiol. 2008. PMID: 18363640

8

De novo LMNA mutations cause a new form of congenital muscular dystrophy.

Quijano-Roy S, Mbieleu B, Bönnemann CG, Jeannet PY, Colomer J, Clarke NF, Cuisset JM, Roper H, De Meirleir L, D'Amico A, Ben Yaou R, Nascimento A, Barois A, Demay L, Bertini E, Ferreiro A, Sewry CA, Romero NB, Ryan M, Muntoni F, Guicheney P, Richard P, Bonne G, Estournet B. Quijano-Roy S, et al. Among authors: cuisset jm. Ann Neurol. 2008 Aug;64(2):177-86. doi: 10.1002/ana.21417. Ann Neurol. 2008. PMID: 18551513

9

Methionine synthase deficiency: a rare cause of adult-onset leukoencephalopathy.

Outteryck O, de Sèze J, Stojkovic T, Cuisset JM, Dobbelaere D, Delalande S, Lacour A, Cabaret M, Lepoutre AC, Deramecourt V, Zéphir H, Fowler B, Vermersch P. Outteryck O, et al. Among authors: cuisset jm. Neurology. 2012 Jul 24;79(4):386-8. doi: 10.1212/WNL.0b013e318260451b. Epub 2012 Jul 11. Neurology. 2012. PMID: 22786600 No abstract available.

10

Anti-HMGCR Antibody-Related Necrotizing Autoimmune Myopathy Mimicking Muscular Dystrophy.

Tard C, Tiffreau V, Jaillette E, Jouen F, Nelson I, Bonne G, Yaou RB, Romero N, Vallée L, Vermersch P, Nguyen S, Maurage CA, Cuisset JM. Tard C, et al. Among authors: cuisset jm. Neuropediatrics. 2017 Dec;48(6):473-476. doi: 10.1055/s-0037-1604402. Epub 2017 Aug 4. Neuropediatrics. 2017. PMID: 28778101 No abstract available.

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