Milone M - Search Results

1

LRP4-IgG service line testing in seronegative myasthenia gravis and controls.

Klein CJ, Beecher G, Lamb C, Naddaf E, Milone M, Liewluck T, Dubey D, Zekeridou A, Shelly S, Mills JR. Klein CJ, et al. Among authors: milone m. J Neuroimmunol. 2022 Jul 15;368:577895. doi: 10.1016/j.jneuroim.2022.577895. Epub 2022 May 18. J Neuroimmunol. 2022. PMID: 35617719

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

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

6

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

7

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

8

Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations.

Liewluck T, Milone M, Tian X, Engel AG, Staff NP, Wong LJ. Liewluck T, et al. Among authors: milone m. Muscle Nerve. 2016 Jun;53(6):984-8. doi: 10.1002/mus.25054. Epub 2016 Apr 25. Muscle Nerve. 2016. PMID: 26802438

9

Hereditary myopathies with early respiratory insufficiency in adults.

Naddaf E, Milone M. Naddaf E, et al. Among authors: milone m. Muscle Nerve. 2017 Nov;56(5):881-886. doi: 10.1002/mus.25602. Epub 2017 Apr 11. Muscle Nerve. 2017. PMID: 28181274

10

Autosomal dominant distal myopathy due to a novel ACTA1 mutation.

Liewluck T, Sorenson EJ, Walkiewicz MA, Rumilla KM, Milone M. Liewluck T, et al. Among authors: milone m. Neuromuscul Disord. 2017 Aug;27(8):742-746. doi: 10.1016/j.nmd.2017.05.003. Epub 2017 May 5. Neuromuscul Disord. 2017. PMID: 28606400

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