Gherardi RK - Search Results

1

Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up.

Desguerre I, Christov C, Mayer M, Zeller R, Becane HM, Bastuji-Garin S, Leturcq F, Chiron C, Chelly J, Gherardi RK. Desguerre I, et al. Among authors: gherardi rk. PLoS One. 2009;4(2):e4347. doi: 10.1371/journal.pone.0004347. Epub 2009 Feb 5. PLoS One. 2009. PMID: 19194511 Free PMC article.

2

Endomysial fibrosis in Duchenne muscular dystrophy: a marker of poor outcome associated with macrophage alternative activation.

Desguerre I, Mayer M, Leturcq F, Barbet JP, Gherardi RK, Christov C. Desguerre I, et al. Among authors: gherardi rk. J Neuropathol Exp Neurol. 2009 Jul;68(7):762-73. doi: 10.1097/NEN.0b013e3181aa31c2. J Neuropathol Exp Neurol. 2009. PMID: 19535995

3

A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophy.

Desguerre I, Arnold L, Vignaud A, Cuvellier S, Yacoub-Youssef H, Gherardi RK, Chelly J, Chretien F, Mounier R, Ferry A, Chazaud B. Desguerre I, et al. Among authors: gherardi rk. Muscle Nerve. 2012 Jun;45(6):803-14. doi: 10.1002/mus.23341. Muscle Nerve. 2012. PMID: 22581532

4

Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age.

Mercier S, Toutain A, Toussaint A, Raynaud M, de Barace C, Marcorelles P, Pasquier L, Blayau M, Espil C, Parent P, Journel H, Lazaro L, Andoni Urtizberea J, Moerman A, Faivre L, Eymard B, Maincent K, Gherardi R, Chaigne D, Ben Yaou R, Leturcq F, Chelly J, Desguerre I. Mercier S, et al. Eur J Hum Genet. 2013 Aug;21(8):855-63. doi: 10.1038/ejhg.2012.269. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299919 Free PMC article.

5

In vivo fusion of circulating fluorescent cells with dystrophin-deficient myofibers results in extensive sarcoplasmic fluorescence expression but limited dystrophin sarcolemmal expression.

Chretien F, Dreyfus PA, Christov C, Caramelle P, Lagrange JL, Chazaud B, Gherardi RK. Chretien F, et al. Among authors: gherardi rk. Am J Pathol. 2005 Jun;166(6):1741-8. doi: 10.1016/S0002-9440(10)62484-4. Am J Pathol. 2005. PMID: 15920159 Free PMC article.

6

Gitiaux C, De Antonio M, Aouizerate J, Gherardi RK, Guilbert T, Barnerias C, Bodemer C, Brochard-Payet K, Quartier P, Musset L, Chazaud B, Desguerre I, Bader-Meunier B. Gitiaux C, et al. Among authors: gherardi rk. Rheumatology (Oxford). 2016 Mar;55(3):470-9. doi: 10.1093/rheumatology/kev359. Epub 2015 Sep 30. Rheumatology (Oxford). 2016. PMID: 26424834

7

Whole microvascular unit deletions in dermatomyositis.

Gitiaux C, Kostallari E, Lafuste P, Authier FJ, Christov C, Gherardi RK. Gitiaux C, et al. Among authors: gherardi rk. Ann Rheum Dis. 2013 Mar;72(3):445-52. doi: 10.1136/annrheumdis-2012-201822. Epub 2012 Sep 8. Ann Rheum Dis. 2013. PMID: 22962315

8

Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositis.

Aouizerate J, De Antonio M, Bader-Meunier B, Barnerias C, Bodemer C, Isapof A, Quartier P, Melki I, Charuel JL, Bassez G, Desguerre I, Gherardi RK, Authier FJ, Gitiaux C. Aouizerate J, et al. Among authors: gherardi rk. Rheumatology (Oxford). 2018 May 1;57(5):873-879. doi: 10.1093/rheumatology/kex516. Rheumatology (Oxford). 2018. PMID: 29474663

9

Sporadic lower limb hypertrophy and exercise induced myalgia in a woman with dystrophin gene deletion.

Malapert D, Recan D, Leturcq F, Degos JD, Gherardi RK. Malapert D, et al. Among authors: gherardi rk. J Neurol Neurosurg Psychiatry. 1995 Nov;59(5):552-4. doi: 10.1136/jnnp.59.5.552. J Neurol Neurosurg Psychiatry. 1995. PMID: 8530947 Free PMC article.

10

Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophy.

Bassez G, Chapoy E, Bastuji-Garin S, Radvanyi-Hoffman H, Authier FJ, Pellissier JF, Eymard B, Gherardi RK. Bassez G, et al. Among authors: gherardi rk. J Neuropathol Exp Neurol. 2008 Apr;67(4):319-25. doi: 10.1097/NEN.0b013e31816b4acc. J Neuropathol Exp Neurol. 2008. PMID: 18379436

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