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Items: 1 to 50 of 69

1.

Transthyretin Amyloidosis: Putting Myopathy On The Map.

Pinto MV, Milone M, Mauermann ML, Dyck PJB, Alhammad R, McPhail ED, Grogan M, Liewluck T.

Muscle Nerve. 2019 Oct 6. doi: 10.1002/mus.26723. [Epub ahead of print]

PMID:
31587306
2.

Dominant collagen XII mutations cause a distal myopathy.

Mohassel P, Liewluck T, Hu Y, Ezzo D, Ogata T, Saade D, Neuhaus S, Bolduc V, Zou Y, Donkervoort S, Medne L, Sumner CJ, Dyck PJB, Wierenga KJ, Tennekoon G, Finkel RS, Chen J, Winder TL, Staff NP, Foley AR, Koch M, Bönnemann CG.

Ann Clin Transl Neurol. 2019 Sep 11. doi: 10.1002/acn3.50882. [Epub ahead of print]

3.

TFG: At the crossroads of motor neuron disease and myopathy.

Nicolau S, Liewluck T.

Muscle Nerve. 2019 Sep 3. doi: 10.1002/mus.26692. [Epub ahead of print] No abstract available.

PMID:
31478205
4.

Trouble at the junction: When myopathy and myasthenia overlap.

Nicolau S, Kao JC, Liewluck T.

Muscle Nerve. 2019 Aug 26. doi: 10.1002/mus.26676. [Epub ahead of print] Review.

PMID:
31449669
5.

Necrotizing autoimmune myopathy with tubular aggregates.

Madigan NN, Liewluck T, Milone M, Naddaf E.

Neurology. 2019 Aug 13;93(7):313-314. doi: 10.1212/WNL.0000000000007952. No abstract available.

PMID:
31405936
6.

A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmission.

Nicolau S, Liewluck T, Shen XM, Selcen D, Engel AG, Milone M.

Neuromuscul Disord. 2019 Aug;29(8):614-617. doi: 10.1016/j.nmd.2019.07.001. Epub 2019 Jul 5.

PMID:
31378432
7.

Reader response: Pearls & Oy-sters: Pembrolizumab-induced myasthenia gravis.

Robbins NM, Mozaffar T, Mammen AL, Liewluck T, Guidon A, Lawson VH.

Neurology. 2019 Jul 23;93(4):183-184. doi: 10.1212/WNL.0000000000007845. No abstract available.

PMID:
31332091
8.

Congenital myopathies in the adult neuromuscular clinic: Diagnostic challenges and pitfalls.

Nicolau S, Liewluck T, Tracy JA, Laughlin RS, Milone M.

Neurol Genet. 2019 Jun 4;5(4):e341. doi: 10.1212/NXG.0000000000000341. eCollection 2019 Aug.

9.

Neuromuscular transmission defects in myopathies.

Liewluck T, Laughlin RS, Litchy WJ, Milone M.

Muscle Nerve. 2019 Jul;60(1):E8-E9. doi: 10.1002/mus.26503. Epub 2019 May 13. No abstract available.

PMID:
31050017
10.

ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles.

Liewluck T, Niu Z, Moore SA, Alsharabati M, Milone M.

Neuromuscul Disord. 2019 May;29(5):388-391. doi: 10.1016/j.nmd.2019.02.012. Epub 2019 Mar 2.

PMID:
30987788
11.

Centronuclear myopathy with cardiomyopathy due to recessive titinopathy.

Martinez-Thompson JM, Winder TL, Liewluck T.

Muscle Nerve. 2019 Apr;59(4):E26-E27. doi: 10.1002/mus.26429. Epub 2019 Feb 12. No abstract available.

PMID:
30681174
12.

Myopathies featuring non-caseating granulomas: Sarcoidosis, inclusion body myositis and an unfolding overlap.

Alhammad RM, Liewluck T.

Neuromuscul Disord. 2019 Jan;29(1):39-47. doi: 10.1016/j.nmd.2018.10.007. Epub 2018 Nov 9.

PMID:
30578101
13.

Neuromuscular transmission defects in myopathies: Rare but worth searching for.

Elahi B, Laughlin RS, Litchy WJ, Milone M, Liewluck T.

Muscle Nerve. 2019 Apr;59(4):475-478. doi: 10.1002/mus.26393. Epub 2019 Jan 6.

PMID:
30536954
14.

Intramuscular interstitial amyloid deposition does not impact anoctaminopathy-5 phenotype.

Anandan C, Milone M, Liewluck T.

Muscle Nerve. 2019 Jan;59(1):133-137. doi: 10.1002/mus.26349. Epub 2018 Oct 17.

PMID:
30320887
15.

Congenital myasthenic syndromes in adult neurology clinic: A long road to diagnosis and therapy.

Kao JC, Milone M, Selcen D, Shen XM, Engel AG, Liewluck T.

Neurology. 2018 Nov 6;91(19):e1770-e1777. doi: 10.1212/WNL.0000000000006478. Epub 2018 Oct 5.

PMID:
30291185
16.

The unfolding spectrum of inherited distal myopathies.

Milone M, Liewluck T.

Muscle Nerve. 2019 Mar;59(3):283-294. doi: 10.1002/mus.26332. Epub 2018 Nov 28. Review.

PMID:
30171629
17.

Neuromuscular Complications of Programmed Cell Death-1 (PD-1) Inhibitors.

Kao JC, Brickshawana A, Liewluck T.

Curr Neurol Neurosci Rep. 2018 Aug 4;18(10):63. doi: 10.1007/s11910-018-0878-7. Review.

PMID:
30078154
18.

Author response: Anti-cytosolic 5'-nucleotidase 1A (cN1A) autoantibodies in motor neuron diseases.

Liewluck T.

Neurology. 2018 May 22;90(21):990. doi: 10.1212/WNL.0000000000005575. No abstract available.

PMID:
29784724
19.

A novel ACTA1 mutation causing progressive facioscapuloperoneal myopathy in an adult.

Kao JC, Liewluck T, Milone M.

J Clin Neurosci. 2018 Jul;53:261-262. doi: 10.1016/j.jocn.2018.04.044. Epub 2018 May 3.

PMID:
29731279
20.

A novel CAPN3 mutation in late-onset limb-girdle muscular dystrophy with early respiratory insufficiency.

Martinez-Thompson JM, Moore SA, Liewluck T.

J Clin Neurosci. 2018 Jul;53:229-231. doi: 10.1016/j.jocn.2018.04.025. Epub 2018 Apr 21.

21.

Untangling the complexity of limb-girdle muscular dystrophies.

Liewluck T, Milone M.

Muscle Nerve. 2018 Aug;58(2):167-177. doi: 10.1002/mus.26077. Epub 2018 Feb 7. Review.

PMID:
29350766
22.

Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases.

Dhawan PS, Liewluck T, Knapik J, Milone M.

Muscle Nerve. 2018 May;57(5):E124-E126. doi: 10.1002/mus.26036. Epub 2017 Dec 20. No abstract available.

PMID:
29211919
23.

PD-1 Inhibitor-associated Myopathies: Emerging Immune-mediated Myopathies.

Liewluck T, Kao JC, Mauermann ML.

J Immunother. 2018 May;41(4):208-211. doi: 10.1097/CJI.0000000000000196.

PMID:
29200081
24.

Anti-cytosolic 5'-nucleotidase 1A (cN1A) autoantibodies in motor neuron diseases.

Liewluck T.

Neurology. 2017 Nov 7;89(19):2017-2018. doi: 10.1212/WNL.0000000000004610. Epub 2017 Sep 27. No abstract available.

PMID:
28954884
25.

Characterization of isolated amyloid myopathy.

Liewluck T, Milone M.

Eur J Neurol. 2017 Dec;24(12):1437-1445. doi: 10.1111/ene.13448. Epub 2017 Oct 5.

PMID:
28888072
26.

Neurological Complications Associated With Anti-Programmed Death 1 (PD-1) Antibodies.

Kao JC, Liao B, Markovic SN, Klein CJ, Naddaf E, Staff NP, Liewluck T, Hammack JE, Sandroni P, Finnes H, Mauermann ML.

JAMA Neurol. 2017 Oct 1;74(10):1216-1222. doi: 10.1001/jamaneurol.2017.1912. Erratum in: JAMA Neurol. 2017 Oct 1;74(10):1271.

27.

Autosomal dominant distal myopathy due to a novel ACTA1 mutation.

Liewluck T, Sorenson EJ, Walkiewicz MA, Rumilla KM, Milone M.

Neuromuscul Disord. 2017 Aug;27(8):742-746. doi: 10.1016/j.nmd.2017.05.003. Epub 2017 May 5.

PMID:
28606400
28.

Facial diplegia after pembrolizumab treatment.

Yost MD, Chou CZ, Botha H, Block MS, Liewluck T.

Muscle Nerve. 2017 Sep;56(3):E20-E21. doi: 10.1002/mus.25663. Epub 2017 May 6. No abstract available.

PMID:
28398689
29.

Immunotherapy-responsive allodynia due to distal acquired demyelinating symmetric (DADS) neuropathy.

Liewluck T, Engelstad JK, Mauermann ML.

Muscle Nerve. 2016 Nov;54(5):973-977. doi: 10.1002/mus.25206. Epub 2016 Aug 17.

PMID:
27251375
30.

Systemic Immunoglobulin Light Chain Amyloidosis-Associated Myopathy: Presentation, Diagnostic Pitfalls, and Outcome.

Muchtar E, Derudas D, Mauermann M, Liewluck T, Dispenzieri A, Kumar SK, Dingli D, Lacy MQ, Buadi FK, Hayman SR, Kapoor P, Leung N, Chakraborty R, Gonsalves W, Russell S, Lust JA, Lin Y, Go RS, Zeldenrust S, Kyle RA, Rajkumar SV, Gertz MA.

Mayo Clin Proc. 2016 Oct;91(10):1354-1361. doi: 10.1016/j.mayocp.2016.06.027.

PMID:
27712634
31.

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.

Muscle Nerve. 2016 Jun;53(6):984-8. doi: 10.1002/mus.25054. Epub 2016 Apr 25.

PMID:
26802438
32.

Anticholinesterase Therapy Worsening Head Drop and Limb Weakness Due to a Novel DOK7 Mutation.

Lozowska D, Ringel SP, Winder TL, Liu J, Liewluck T.

J Clin Neuromuscul Dis. 2015 Dec;17(2):72-7. doi: 10.1097/CND.0000000000000095.

PMID:
26583494
33.

Progressive Muscular Atrophy.

Liewluck T, Saperstein DS.

Neurol Clin. 2015 Nov;33(4):761-73. doi: 10.1016/j.ncl.2015.07.005. Review.

PMID:
26515620
34.

Exertional rhabdomyolysis associated with high intensity exercise.

Lozowska D, Liewluck T, Quan D, Ringel SP.

Muscle Nerve. 2015 Dec;52(6):1134-5. doi: 10.1002/mus.24784. Epub 2015 Sep 10. No abstract available.

PMID:
26212224
35.

Immune-Mediated Neurological Disorders.

Liewluck T, Miravalle A.

Curr Neurol Neurosci Rep. 2015 Sep;15(9):61. doi: 10.1007/s11910-015-0581-x. Review.

PMID:
26202897
36.

Dystrophinopathy mimicking metabolic myopathies.

Liewluck T, Tian X, Wong LJ, Pestronk A.

Neuromuscul Disord. 2015 Aug;25(8):653-7. doi: 10.1016/j.nmd.2015.04.001. Epub 2015 Apr 11.

PMID:
25998609
37.

Clinical reasoning: a 52-year-old woman with progressive proximal weakness.

Enduri S, Taylor MR, Liewluck T.

Neurology. 2014 Sep 2;83(10):e106-9. doi: 10.1212/WNL.0000000000000757. No abstract available.

38.

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.

Muscle Nerve. 2014 Aug;50(2):295-9. doi: 10.1002/mus.24290. Epub 2014 Jul 14.

PMID:
24838343
39.

Frequency and spectrum of myopathies in patients with psoriasis.

Liewluck T, Ernste FC, Tracy JA.

Muscle Nerve. 2013 Nov;48(5):716-21. doi: 10.1002/mus.23812. Epub 2013 Aug 30.

PMID:
24037820
40.

Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.

Liewluck T, Mundi MS, Mauermann ML.

Muscle Nerve. 2013 Dec;48(6):989-91. doi: 10.1002/mus.23959. Epub 2013 Oct 25.

PMID:
23868323
41.

Cramp-fasciculation syndrome in patients with and without neural autoantibodies.

Liewluck T, Klein CJ, Jones LK Jr.

Muscle Nerve. 2014 Mar;49(3):351-6. doi: 10.1002/mus.23935. Epub 2013 Dec 17.

PMID:
23836298
42.

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.

Eur J Neurol. 2013 Oct;20(10):1383-9. doi: 10.1111/ene.12191. Epub 2013 May 12.

PMID:
23663589
43.

Camptocormia due to inclusion body myositis.

Goodman BP, Liewluck T, Crum BA, Spinner RJ.

J Clin Neuromuscul Dis. 2012 Dec;14(2):78-81. doi: 10.1097/CND.0b013e3182650718.

PMID:
23172388
44.

Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota Hutterite.

Liewluck T, Tracy JA, Sorenson EJ, Engel AG.

Neuromuscul Disord. 2013 Feb;23(2):133-8. doi: 10.1016/j.nmd.2012.09.010. Epub 2012 Nov 9. Review.

PMID:
23142638
45.

Late-onset axial myopathy and camptocormia in a calpainopathy carrier.

Liewluck T, Goodman BP.

J Clin Neuromuscul Dis. 2012 Jun;13(4):209-13. doi: 10.1097/CND.0b013e3182461a9c.

PMID:
22622166
46.

Myalgic phenotype and preserved muscle strength in adult-onset acid maltase deficiency.

Jones LK Jr, Liewluck T, Gavrilova RH.

Neuromuscul Disord. 2012 Aug;22(8):763-6. doi: 10.1016/j.nmd.2012.02.003. Epub 2012 May 16.

PMID:
22595200
47.

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

Liewluck T, Goodman BP, Milone M.

Neurologist. 2012 May;18(3):155-8. doi: 10.1097/NRL.0b013e318251e70f.

PMID:
22549359
48.

Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok-7 myasthenia.

Liewluck T, Selcen D, Engel AG.

Muscle Nerve. 2011 Nov;44(5):789-94. doi: 10.1002/mus.22176. Epub 2011 Sep 23.

49.

Amyloidosis and exercise intolerance in ANO5 muscular dystrophy.

Milone M, Liewluck T, Winder TL, Pianosi PT.

Neuromuscul Disord. 2012 Jan;22(1):13-5. doi: 10.1016/j.nmd.2011.07.005. Epub 2011 Aug 4.

PMID:
21820307
50.

Novel POLG splice site mutation and optic atrophy.

Milone M, Wang J, Liewluck T, Chen LC, Leavitt JA, Wong LJ.

Arch Neurol. 2011 Jun;68(6):806-11. doi: 10.1001/archneurol.2011.124. Erratum in: Arch Neurol. 2011 Aug;68(8):1084. Arch Neurol. 2011 Nov;68(11):1446.

PMID:
21670405

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