Milone M - Search Results

1

Diagnostic modelling and therapeutic monitoring of immune-mediated necrotizing myopathy: role of electrical myotonia.

Triplett JD, Shelly S, Livne G, Milone M, Kassardjian CD, Liewluck T, Kelly C, Naddaf E, Laughlin RS, Lamb CJ, Rubin D, Dimberg EL, Dubey D, Mills JR, Mandrekar J, Klein CJ. Triplett JD, et al. Among authors: milone m. Brain Commun. 2020 Dec 13;2(2):fcaa191. doi: 10.1093/braincomms/fcaa191. eCollection 2020. Brain Commun. 2020. PMID: 33364599 Free PMC article.

2

Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia.

Liewluck T, Shen XM, Milone M, Engel AG. Liewluck T, et al. Among authors: milone m. Neuromuscul Disord. 2011 Jun;21(6):387-95. doi: 10.1016/j.nmd.2011.03.002. Epub 2011 Apr 8. Neuromuscul Disord. 2011. PMID: 21482111 Free PMC article.

3

Novel POLG splice site mutation and optic atrophy.

Milone M, Wang J, Liewluck T, Chen LC, Leavitt JA, Wong LJ. Milone M, et al. Arch Neurol. 2011 Jun;68(6):806-11. doi: 10.1001/archneurol.2011.124. Arch Neurol. 2011. PMID: 21670405

4

Amyloidosis and exercise intolerance in ANO5 muscular dystrophy.

Milone M, Liewluck T, Winder TL, Pianosi PT. Milone M, et al. Neuromuscul Disord. 2012 Jan;22(1):13-5. doi: 10.1016/j.nmd.2011.07.005. Epub 2011 Aug 4. Neuromuscul Disord. 2012. PMID: 21820307

5

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations.

Tang S, Dimberg EL, Milone M, Wong LJ. Tang S, et al. Among authors: milone m. J Neurol. 2012 May;259(5):862-8. doi: 10.1007/s00415-011-6268-6. Epub 2011 Oct 13. J Neurol. 2012. PMID: 21993618

6

Electrically active immune-mediated rippling muscle disease preceding breast cancer.

Liewluck T, Goodman BP, Milone M. Liewluck T, et al. Among authors: milone m. Neurologist. 2012 May;18(3):155-8. doi: 10.1097/NRL.0b013e318251e70f. Neurologist. 2012. PMID: 22549359

7

ANO5-muscular dystrophy: clinical, pathological and molecular findings.

Liewluck T, Winder TL, Dimberg EL, Crum BA, Heppelmann CJ, Wang Y, Bergen HR 3rd, Milone M. Liewluck T, et al. Among authors: milone m. Eur J Neurol. 2013 Oct;20(10):1383-9. doi: 10.1111/ene.12191. Epub 2013 May 12. Eur J Neurol. 2013. PMID: 23663589

8

Coexistence of DMPK gene expansion and CLCN1 missense mutation in the same patient.

Kassardjian CD, Milone M. Kassardjian CD, et al. Among authors: milone m. Neurogenetics. 2014 Aug;15(3):213-4. doi: 10.1007/s10048-014-0402-4. Epub 2014 Apr 5. Neurogenetics. 2014. PMID: 24705798 No abstract available.

9

A novel VCP mutation underlies scapuloperoneal muscular dystrophy and dropped head syndrome featuring lobulated fibers.

Liewluck T, Milone M, Mauermann ML, Castro-Couch M, Cerhan JH, Murthy NS. Liewluck T, et al. Among authors: milone m. Muscle Nerve. 2014 Aug;50(2):295-9. doi: 10.1002/mus.24290. Epub 2014 Jul 14. Muscle Nerve. 2014. PMID: 24838343

10

Myopathy during treatment with the antianginal drug ranolazine.

Kassardjian CD, Tian X, Vladutiu G, Wong LJ, Milone M. Kassardjian CD, et al. Among authors: milone m. J Neurol Sci. 2014 Dec 15;347(1-2):380-2. doi: 10.1016/j.jns.2014.10.037. Epub 2014 Oct 31. J Neurol Sci. 2014. PMID: 25466697

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