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Items: 1 to 20 of 31

1.

Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study.

Dogan C, De Antonio M, Hamroun D, Varet H, Fabbro M, Rougier F, Amarof K, Arne Bes MC, Bedat-Millet AL, Behin A, Bellance R, Bouhour F, Boutte C, Boyer F, Campana-Salort E, Chapon F, Cintas P, Desnuelle C, Deschamps R, Drouin-Garraud V, Ferrer X, Gervais-Bernard H, Ghorab K, Laforet P, Magot A, Magy L, Menard D, Minot MC, Nadaj-Pakleza A, Pellieux S, Pereon Y, Preudhomme M, Pouget J, Sacconi S, Sole G, Stojkovich T, Tiffreau V, Urtizberea A, Vial C, Zagnoli F, Caranhac G, Bourlier C, Riviere G, Geille A, Gherardi RK, Eymard B, Puymirat J, Katsahian S, Bassez G.

PLoS One. 2016 Feb 5;11(2):e0148264. doi: 10.1371/journal.pone.0148264. eCollection 2016.

2.

[Specific features of Becker Muscular Dystrophy patients and female carriers of Duchenne Muscular Dystrophy].

Magot A, Mercier S, Péréon Y.

Arch Pediatr. 2015 Dec;22(12 Suppl 1):12S31-6. doi: 10.1016/S0929-693X(16)30006-9. French.

PMID:
26773584
3.

[Duchenne muscular dystrophy pathophysiology].

Péréon Y, Mercier S, Magot A.

Arch Pediatr. 2015 Dec;22(12 Suppl 1):12S18-23. doi: 10.1016/S0929-693X(16)30004-5. French.

PMID:
26773581
4.

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations.

Mercier S, Küry S, Salort-Campana E, Magot A, Agbim U, Besnard T, Bodak N, Bou-Hanna C, Bréhéret F, Brunelle P, Caillon F, Chabrol B, Cormier-Daire V, David A, Eymard B, Faivre L, Figarella-Branger D, Fleurence E, Ganapathi M, Gherardi R, Goldenberg A, Hamel A, Igual J, Irvine AD, Israël-Biet D, Kannengiesser C, Laboisse C, Le Caignec C, Mahé JY, Mallet S, MacGowan S, McAleer MA, McLean I, Méni C, Munnich A, Mussini JM, Nagy PL, Odel J, O'Regan GM, Péréon Y, Perrier J, Piard J, Puzenat E, Sampson JB, Smith F, Soufir N, Tanji K, Thauvin C, Ulane C, Watson RM, Khumalo NP, Mayosi BM, Barbarot S, Bézieau S.

Orphanet J Rare Dis. 2015 Oct 15;10:135. doi: 10.1186/s13023-015-0352-4.

5.

[Persistent myalgia in a 58-year-old man].

Perrin F, Néel A, Magot A, Darrieutort C, Agard C, Mussini JM, Hamidou M, Ackermann F.

Rev Med Interne. 2015 Nov;36(11):780-2. doi: 10.1016/j.revmed.2015.05.015. Epub 2015 Sep 14. French. No abstract available.

PMID:
26383766
6.

Atypical nuclear abnormalities in a patient with Brody disease.

Mussini JM, Magot A, Hantaï D, Sternberg D, Chevessier F, Péréon Y.

Neuromuscul Disord. 2015 Oct;25(10):773-9. doi: 10.1016/j.nmd.2015.07.005. Epub 2015 Jul 13.

PMID:
26248958
7.

Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagy.

Mercier S, Magot A, Caillon F, Isidor B, David A, Ferrer X, Vital A, Coquet M, Penttilä S, Udd B, Mussini JM, Pereon Y.

Muscle Nerve. 2015 Oct;52(4):673-80. doi: 10.1002/mus.24664. Epub 2015 Jun 3.

PMID:
25809233
8.

Vincristine-induced neuropathy: Atypical electrophysiological patterns in children.

Courtemanche H, Magot A, Ollivier Y, Rialland F, Leclair-Visonneau L, Fayet G, Camdessanché JP, Péréon Y.

Muscle Nerve. 2015 Dec;52(6):981-5. doi: 10.1002/mus.24647. Epub 2015 Sep 12.

PMID:
25758843
9.

An exploratory randomised double-blind and placebo-controlled phase 2 study of a combination of baclofen, naltrexone and sorbitol (PXT3003) in patients with Charcot-Marie-Tooth disease type 1A.

Attarian S, Vallat JM, Magy L, Funalot B, Gonnaud PM, Lacour A, Péréon Y, Dubourg O, Pouget J, Micallef J, Franques J, Lefebvre MN, Ghorab K, Al-Moussawi M, Tiffreau V, Preudhomme M, Magot A, Leclair-Visonneau L, Stojkovic T, Bossi L, Lehert P, Gilbert W, Bertrand V, Mandel J, Milet A, Hajj R, Boudiaf L, Scart-Grès C, Nabirotchkin S, Guedj M, Chumakov I, Cohen D.

Orphanet J Rare Dis. 2014 Dec 18;9:199. doi: 10.1186/s13023-014-0199-0.

10.

Clinical and electrophysiological features in a French family presenting with seipinopathy.

Ollivier Y, Magot A, Latour P, Perrier J, Mercier S, Maisonobe T, Péréon Y.

Neuromuscul Disord. 2015 Feb;25(2):161-4. doi: 10.1016/j.nmd.2014.10.006. Epub 2014 Oct 22.

PMID:
25454168
11.

Non-invasive assessment of muscle stiffness in patients with Duchenne muscular dystrophy.

Lacourpaille L, Hug F, Guével A, Péréon Y, Magot A, Hogrel JY, Nordez A.

Muscle Nerve. 2015 Feb;51(2):284-6. doi: 10.1002/mus.24445. Epub 2014 Dec 23.

PMID:
25187068
12.

New insights on contraction efficiency in patients with Duchenne muscular dystrophy.

Lacourpaille L, Hug F, Guével A, Péréon Y, Magot A, Hogrel JY, Nordez A.

J Appl Physiol (1985). 2014 Sep 15;117(6):658-62. doi: 10.1152/japplphysiol.00544.2014. Epub 2014 Aug 7.

13.

Focal and abnormally persistent paralysis associated with congenital paramyotonia.

Magot A, David A, Sternberg D, Péréon Y.

BMJ Case Rep. 2014 Jun 17;2014. pii: bcr2014204430. doi: 10.1136/bcr-2014-204430.

PMID:
24939454
14.

Insufficiency of electrocardiogram alone in predicting infrahisian abnormalities in patients with type 1 myotonic dystrophy.

Siméon E, Patier-Dussauge A, Bernard-Brunet A, Clémenty N, Gouraud JB, Guyomarch B, Magot A, Probst V, Babuty D.

Int J Cardiol. 2014 Apr 1;172(3):625-7. doi: 10.1016/j.ijcard.2014.02.001. Epub 2014 Feb 11. No abstract available.

PMID:
24560399
15.

Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.

Mercier S, Küry S, Shaboodien G, Houniet DT, Khumalo NP, Bou-Hanna C, Bodak N, Cormier-Daire V, David A, Faivre L, Figarella-Branger D, Gherardi RK, Glen E, Hamel A, Laboisse C, Le Caignec C, Lindenbaum P, Magot A, Munnich A, Mussini JM, Pillay K, Rahman T, Redon R, Salort-Campana E, Santibanez-Koref M, Thauvin C, Barbarot S, Keavney B, Bézieau S, Mayosi BM.

Am J Hum Genet. 2013 Dec 5;93(6):1100-7. doi: 10.1016/j.ajhg.2013.10.013. Epub 2013 Nov 21.

16.

Antibodies to clustered acetylcholine receptor: expanding the phenotype.

Devic P, Petiot P, Simonet T, Stojkovic T, Delmont E, Franques J, Magot A, Vial C, Lagrange E, Nicot AS, Risson V, Eymard B, Schaeffer L.

Eur J Neurol. 2014;21(1):130-4. doi: 10.1111/ene.12270. Epub 2013 Sep 21.

PMID:
24112557
17.

Evolution of life expectancy of patients with Duchenne muscular dystrophy at AFM Yolaine de Kepper centre between 1981 and 2011.

Kieny P, Chollet S, Delalande P, Le Fort M, Magot A, Pereon Y, Perrouin Verbe B.

Ann Phys Rehabil Med. 2013 Sep;56(6):443-54. doi: 10.1016/j.rehab.2013.06.002. Epub 2013 Jun 24.

18.

Guillain-Barré syndrome during childhood: particular clinical and electrophysiological features.

Devos D, Magot A, Perrier-Boeswillwald J, Fayet G, Leclair-Visonneau L, Ollivier Y, Nguyen The Tich S, Pereon Y.

Muscle Nerve. 2013 Aug;48(2):247-51. doi: 10.1002/mus.23749. Epub 2013 Jun 29.

PMID:
23813561
19.

Maculopathy and spinocerebellar ataxia type 1: a new association?

Lebranchu P, Le Meur G, Magot A, David A, Verny C, Weber M, Milea D.

J Neuroophthalmol. 2013 Sep;33(3):225-31. doi: 10.1097/WNO.0b013e31828d4add.

PMID:
23584155
20.

Immune response and mitochondrial metabolism are commonly deregulated in DMD and aging skeletal muscle.

Baron D, Magot A, Ramstein G, Steenman M, Fayet G, Chevalier C, Jourdon P, Houlgatte R, Savagner F, Pereon Y.

PLoS One. 2011;6(11):e26952. doi: 10.1371/journal.pone.0026952. Epub 2011 Nov 9.

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