Publications

  1. Beecher G, Pinal-Fernandez I, Mammen AL, Liewluck T. Immune Checkpoint Inhibitor Myopathy: The Double-Edged Sword of Cancer Immunotherapy. Neurology. 2024 Dec 10; 103 (11):e210031 Epub 2024 Nov 08
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  2. Santilli AR, Ni O, Milone M, Selcen D, Mehrabyan AC, Seth A, Hsieh C, Raslan WF, Alkhalifah MM, Alenezi RM, Nicolau S, Soontrapa P, Liewluck T. Immune-Mediated Megaconial Myopathy: A Novel Subtype of Autoimmune Myopathy. Neurology. 2024 Nov 26; 103 (10):e210001 Epub 2024 Oct 30
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  3. Pinal-Fernandez I, Munoz-Braceras S, Casal-Dominguez M, Pak K, Torres-Ruiz J, Musai J, Dell'Orso S, Naz F, Islam S, Gutierrez-Cruz G, Cano MD, Matas-Garcia A, Padrosa J, Tobias-Baraja E, Garrabou G, Aldecoa I, Espinosa G, Simeon-Aznar CP, Guillen-Del-Castillo A, Gil-Vila A, Trallero-Araguas E, Christopher-Stine L, Lloyd TE, Liewluck T, Naddaf E, Stenzel W, Greenberg SA, Grau JM, Selva-O'Callaghan A, Milisenda JC, Mammen AL. Pathological autoantibody internalisation in myositis. Ann Rheum Dis. 2024 Oct 21; 83 (11):1549-1560
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  4. Putko B, Pestronk A, Van Stavern GP, Phan CL, Beecher G, Liewluck T. Ophthalmoparesis as an unusual manifestation of anti-3‑hydroxy-3-methyl-glutaryl-coenzyme A reductase antibody-associated myopathies. Neuromuscul Disord. 2024 Sep; 42:1-4 Epub 2024 June 21
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  5. Shah M, Shrestha K, Tseng CW, Goyal A, Liewluck T, Gupta L. Statin-associated muscle symptoms: A comprehensive exploration of epidemiology, pathophysiology, diagnosis, and clinical management strategies. Int J Rheum Dis. 2024 Sep; 27 (9):e15337
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  6. Skolka MP, Milone M, Litchy WJ, Laughlin RS, Rubin DI, Liewluck T. The utility of electrodiagnostic testing in unprovoked rhabdomyolysis in the era of next-generation sequencing. Muscle Nerve. 2024 Aug; 70 (2):180-186 Epub 2024 Mar 27
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  7. Shelly S, Soontrapa P, Madigan NN, Polzin MJ, Singh TD, Sista SRS, Paul P, Braksick SA, Liao B, Windebank AJ, Boon AJ, Litchy WJ, Milone M, Liewluck T. Compound Muscle Action Potential and Myosin-Loss Pathology in Patients With Critical Illness Myopathy: Correlation and Prognostication. Neurology. 2024 Jul 09; 103(1):e209496. Epub 2024 Jun 13.
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  8. Granger A, Sorenson EJ, Selcen D, Liewluck T. Myopathy With Crescent of Nuclei: A Novel Histopathologic Finding in Desminopathy. J Clin Neuromuscul Dis 2024 Jun 1; 25 (4):197-198
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  9. Soontrapa P, Shahar S, Eauchai L, Ernste FC, Liewluck T. Disease spectrum of myopathies with elevated aldolase and normal creatine kinase. Eur J Neurol. 2024 Feb; 31 (2):e16117 Epub 2023 Nov 03
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  10. Soontrapa P, Seven NA, Liewluck T, Cui G, Mer G, Milone M. Adolescent-onset multisystem proteinopathy due to a novel VCP variant. Neuromuscul Disord. 2024 Jan; 34:89-94 Epub 2023 Dec 10
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  11. Hooshmand SJ, Aragon Pinto C, Liewluck T, Pinto MV. Teaching Video NeuroImage: Response to IVIg in a Patient With Steroid-Refractory Immune Checkpoint Inhibitor-Related Ocular Myopathy. Neurology. 2023 Nov 21; 101 (21):e2204 Epub 2023 Oct 03
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  12. Soontrapa P, Tracy JA, Gonsalves WI, Liewluck T. Treatment-responsive glycogen storage myopathy in a patient with POEMS syndrome: A new monoclonal gammopathy-associated myopathy. Eur J Neurol. 2023 Oct; 30 (10):3404-3406 Epub 2023 Aug 11
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  13. Kamboj AK, Soontrapa P, Dubey D, Liewluck T, Leggett CL. Achalasia and Inclusion Body Myositis. Am J Gastroenterol. 2023 Aug 1; 118 (8):1317 Epub 2023 Apr 13
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  14. Chompoopong P, Skolka MP, Ernste FC, Milone M, Liewluck T. Symptomatic myopathies in sarcoidosis: disease spectrum and myxovirus resistance protein A expression. Rheumatology (Oxford). 2023 Jul 05; 62(7):2556-2562.
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  15. Pinal-Fernandez I, Quintana A, Milisenda JC, Casal-Dominguez M, Munoz-Braceras S, Derfoul A, Torres-Ruiz J, Pak K, Dell'Orso S, Naz F, Gutierrez-Cruz G, Milone M, Shelly S, Duque-Jaimez Y, Tobias-Baraja E, Matas-Garcia A, Garrabou G, Padrosa J, Ros J, Trallero-Araguas E, Walitt B, Christopher-Stine L, Lloyd TE, Zhao C, Swift S, Rajan A, Grau-Junyent JM, Selva-O'Callaghan A, Liewluck T, Mammen AL. Transcriptomic profiling reveals distinct subsets of immune checkpoint inhibitor induced myositis. Ann Rheum Dis. 2023 Jun; 82 (6):829-836 Epub 2023 Feb 17
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  16. Chompoopong P, Oskarsson B, Madigan NN, Mirman I, Martinez-Thompson JM, Liewluck T, Milone M. Multisystem proteinopathies (MSPs) and MSP-like disorders: Clinical-pathological-molecular spectrum. Ann Clin Transl Neurol. 2023 Apr; 10 (4):632-643 Epub 2023 Mar 01
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  17. Skolka MP, Soontrapa P, Dubey D, Litchy WJ, Rezk MM, Gardon S, Liewluck T. Immune-mediated rippling muscle disease: not your usual muscle twitches and ache. Neuromuscul Disord. 2023 Mar; 33(3):239-240. Epub 2023 Jan 18.
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  18. Chompoopong P, Liewluck T. Granulomatous myopathy: Sarcoidosis and beyond. Muscle Nerve. 2023 Mar; 67 (3):193-203 Epub 2022 Nov 09
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  19. Granger A, Beecher G, Liewluck T, Nicolau S, Flanigan KM, Laughlin RS, Milone M. Inherited myopathy plus: Double-trouble from rare neuromuscular disorders. Neuromuscul Disord. 2023 Feb; 33 (2):153-160 Epub 2022 Dec 15
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  20. Shelly S, Beecher G, Milone M, Liewluck T, Ernste F, Triplett J, Naddaf E, Zekeridou A, McKeon A, Pittock SJ, Dubey D, Mills JR, Mandrekar J, Klein CJ. Cancer and immune-mediated necrotizing myopathy: a longitudinal referral case-controlled outcomes evaluation. Rheumatology (Oxford). 2022 Dec 23; 62 (1):281-289
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  21. Pritt BS, Mathison BA, Bradbury RS, Liewluck T, Nicolau S, O'Horo JC, Grunst D, Pinto MV, Swanson AA, Virk A. Imported Haycocknema perplexum Infection, United States(1). Emerg Infect Dis. 2022 Nov; 28 (11):2281-2284
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  22. Soontrapa P, Liewluck T. Anoctamin 5 (ANO5) Muscle Disorders: A Narrative Review. Genes (Basel). 2022 Sep 27; 13 (10) Epub 2022 Sept 27
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  23. Schmitt RE, Smith DY 4th, Cho DS, Kirkeby LA, Resch ZT, Liewluck T, Niu Z, Milone M, Doles JD. Myogenesis defects in a patient-derived iPSC model of hereditary GNE myopathy. NPJ Regen Med. 2022 Sep 9; 7 (1):48 Epub 2022 Sept 09
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  24. Granger A, Pinto MV, Milone M, Liewluck T. Glycogen accumulation in GNE myopathy. Neuromuscul Disord. 2022 Sep; 32 (9):774-775 Epub 2022 July 13
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  25. Dubey D, Beecher G, Hammami MB, Knight AM, Liewluck T, Triplett J, Datta A, Dasari S, Zhang Y, Roforth MM, Jerde CR, Murphy SJ, Litchy WJ, Amato A, Lennon VA, McKeon A, Mills JR, Pittock SJ, Milone M. Identification of Caveolae-Associated Protein 4 Autoantibodies as a Biomarker of Immune-Mediated Rippling Muscle Disease in Adults. JAMA Neurol. 2022 Aug 01; 79(8):808-816.
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  26. Klein CJ, Beecher G, Lamb C, Naddaf E, Milone M, Liewluck T, Dubey D, Zekeridou A, Shelly S, Mills JR. LRP4-IgG service line testing in seronegative myasthenia gravis and controls. J Neuroimmunol. 2022 Jul 15; 368:577895 Epub 2022 May 18
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  27. Beecher G, Liewluck T, Milone M. Adult-Onset Sandhoff Disease in a Filipino Patient: Asymmetric Weakness, Whole HEXB Gene Deletion, and Coexisting MYH7 Pathogenic Variant. Neurol Genet. 2022 Jun; 8 (3):e672 Epub 2022 Apr 26
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  28. Chompoopong P, Milone M, Niu Z, Cui G, Mer G, Liewluck T. A novel missense HNRNPA1 variant in the PY-NLS domain in a patient with late-onset distal myopathy. Neuromuscul Disord. 2022 Jun; 32 (6):521-526 Epub 2022 Mar 31
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  29. Naddaf E, Shelly S, Mandrekar J, Chamberlain AM, Hoffman EM, Ernste FC, Liewluck T. Survival and associated comorbidities in inclusion body myositis. Rheumatology (Oxford). 2022 May 5; 61 (5):2016-2024
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  30. Shelly S, Mielke MM, Paul P, Milone M, Tracy JA, Mills JR, Klein CJ, Ernste FC, Mandrekar J, Liewluck T. Incidence and prevalence of immune-mediated necrotizing myopathy in adults in Olmsted County, Minnesota. Muscle Nerve. 2022 May; 65 (5):541-546 Epub 2022 Feb 28
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  31. Beecher G, Fleming MD, Liewluck T. Hereditary myopathies associated with hematological abnormalities. Muscle Nerve. 2022 Apr; 65 (4):374-390 Epub 2022 Jan 05
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  32. Nicolau S, Milone M, Tracy JA, Mills JR, Triplett JD, Liewluck T. Immune-mediated necrotizing myopathy: Unusual presentations of a treatable disease. Muscle Nerve. 2021 Dec; 64 (6):734-739 Epub 2021 Oct 15
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  33. Alamr M, Milone M, Naddaf E, Ytterberg SR, Steel SJ, Jones LK Jr, Liewluck T. Interstitial amyloidosis in sporadic inclusion body myositis. Muscle Nerve. 2021 Nov; 64 (5):590-594 Epub 2021 July 16
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  34. Chompoopong P, Liewluck T, McMenomy BP, Harper CM Jr. Diffuse Soft-Tissue Swelling in Antinuclear Matrix Protein-2 Antibody-Associated Dermatomyositis Sine Dermatitis. Mayo Clin Proc. 2021 Oct; 96 (10):2517-2518 Epub 2021 Aug 21
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  35. Nicolau S, Milone M, Liewluck T. Guidelines for genetic testing of muscle and neuromuscular junction disorders. Muscle Nerve. 2021 Sep; 64 (3):255-269 Epub 2021 June 16
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  36. Pinto MV, Dyck PJB, Liewluck T. Neuromuscular amyloidosis: Unmasking the master of disguise. Muscle Nerve. 2021 Jul; 64 (1):23-36 Epub 2021 Jan 17
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  37. Paul P, Vazquez Do Campo R, Liewluck T, Naddaf E. Ranolazine-induced lipid storage myopathy presenting with respiratory failure and head drop. Neuromuscul Disord. 2021 Jun; 31 (6):546-550 Epub 2021 Mar 22
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  38. Shelly S, Mielke MM, Mandrekar J, Milone M, Ernste FC, Naddaf E, Liewluck T. Epidemiology and Natural History of Inclusion Body Myositis: A 40-Year Population-Based Study. Neurology. 2021 May 25; 96 (21):e2653-e2661 Epub 2021 Apr 20
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  39. Madigan NN, Polzin MJ, Cui G, Liewluck T, Alsharabati MH, Klein CJ, Windebank AJ, Mer G, Milone M. Filamentous tangles with nemaline rods in MYH2 myopathy: a novel phenotype. Acta Neuropathol Commun. 2021 Apr 29; 9 (1):79
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  40. Paul P, Liewluck T, Ernste FC, Mandrekar J, Milone M. Anti-cN1A antibodies do not correlate with specific clinical, electromyographic, or pathological findings in sporadic inclusion body myositis. Muscle Nerve. 2021 Apr; 63 (4):490-496 Epub 2021 Jan 12
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  41. Patel SR, Saliba AN, Steel S, Liewluck T, Mahipal A. Metastatic Colon Cancer Presenting With Immune-mediated Necrotizing Myopathy. Clin Colorectal Cancer. 2021 Mar; 20 (1):e71-e73 Epub 2020 Aug 29
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  42. Ducharme-Smith A, Nicolau S, Chahal CAA, Ducharme-Smith K, Rehman S, Jaliparthy K, Khan N, Scott CG, St Louis EK, Liewluck T, Somers VK, Lin G, Brady PA, Milone M. Cardiac Involvement in Facioscapulohumeral Muscular Dystrophy (FSHD). Front Neurol. 2021; 12:668180 Epub 2021 May 24
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  43. Shelly S, Paul P, Bi H, Dubey D, Milone M, Sorenson EJ, Crum BA, Laughlin RS, Liewluck T, Mandrekar J, Pittock SJ, Zekeridou A, McKeon A, Harper MC, Mills JR, Klein CJ. Improving accuracy of myasthenia gravis autoantibody testing by reflex algorithm. Neurology. 2020 Dec 1; 95 (22):e3002-e3011 Epub 2020 Sept 16
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  44. Sechi E, Markovic SN, McKeon A, Dubey D, Liewluck T, Lennon VA, Lopez-Chiriboga AS, Klein CJ, Mauermann M, Pittock SJ, Flanagan EP, Zekeridou A. Neurologic autoimmunity and immune checkpoint inhibitors: Autoantibody profiles and outcomes. Neurology. 2020 Oct 27; 95 (17):e2442-e2452 Epub 2020 Aug 13
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  45. Nicolau S, Liewluck T, Milone M. Myopathies with finger flexor weakness: Not only inclusion-body myositis. Muscle Nerve. 2020 Oct; 62 (4):445-454 Epub 2020 June 01
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  46. Triplett J, Kassardjian CD, Liewluck T, Tahir A, Lennon V, Kopecky S, Milone M. Cardiac and Respiratory Complications of Necrotizing Autoimmune Myopathy. Mayo Clin Proc. 2020 Oct; 95 (10):2144-2149 Epub 2020 Aug 14
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  47. Triplett JD, Pinto MV, Hosfield EA, Milone M, Liewluck T. Myopathies featuring early or prominent dysphagia. Muscle Nerve. 2020 Sep; 62 (3):344-350 Epub 2020 June 18
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  48. Pinto MV, Tracy JA, Liewluck T. Teaching NeuroImages: Amyloid myopathy: Not your usual suspects. Neurology. 2020 Sep 1; 95 (9):e1290-e1291 Epub 2020 July 01
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  49. Nicolau S, Liewluck T, Elliott JL, Engel AG, Milone M. A novel heterozygous mutation in the C-terminal region of HSPB8 leads to limb-girdle rimmed vacuolar myopathy. Neuromuscul Disord. 2020 Mar; 30 (3):236-240 Epub 2020 Feb 12
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  50. Pinto MV, Milone M, Mauermann ML, Dyck PJB, Alhammad R, McPhail ED, Grogan M, Liewluck T. Transthyretin amyloidosis: Putting myopathy on the map. Muscle Nerve. 2020 Jan; 61 (1):95-100 Epub 2019 Oct 21
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  51. 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. Diagnostic modelling and therapeutic monitoring of immune-mediated necrotizing myopathy: role of electrical myotonia. Brain Commun. 2020; 2 (2):fcaa191 Epub 2020 Dec 13
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  52. Shelly S, Triplett JD, Pinto MV, Milone M, Diehn FE, Zekeridou A, Liewluck T. Immune checkpoint inhibitor-associated myopathy: a clinicoseropathologically distinct myopathy. Brain Commun. 2020; 2 (2):fcaa181 Epub 2020 Nov 02
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  53. Nicolau S, Kao JC, Liewluck T. Trouble at the junction: When myopathy and myasthenia overlap. Muscle Nerve. 2019 Dec; 60 (6):648-657 Epub 2019 Sept 10
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  54. 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, Bonnemann CG. Dominant collagen XII mutations cause a distal myopathy. Ann Clin Transl Neurol. 2019 Oct; 6 (10):1980-1988 Epub 2019 Sept 11
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  55. Madigan NN, Liewluck T, Milone M, Naddaf E. Necrotizing autoimmune myopathy with tubular aggregates. Neurology. 2019 Aug 13; 93 (7):313-314
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  56. Nicolau S, Liewluck T, Tracy JA, Laughlin RS, Milone M. Congenital myopathies in the adult neuromuscular clinic: Diagnostic challenges and pitfalls. Neurol Genet. 2019 Aug; 5 (4):e341 Epub 2019 June 04
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  57. Nicolau S, Liewluck T, Shen XM, Selcen D, Engel AG, Milone M. A homozygous mutation in GMPPB leads to centronuclear myopathy with combined pre- and postsynaptic defects of neuromuscular transmission. Neuromuscul Disord. 2019 Aug; 29 (8):614-617 Epub 2019 July 05
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  58. Liewluck T, Niu Z, Moore SA, Alsharabati M, Milone M. ACTA1-myopathy with prominent finger flexor weakness and rimmed vacuoles. Neuromuscul Disord. 2019 May; 29 (5):388-391 Epub 2019 Mar 02
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  59. Martinez-Thompson JM, Winder TL, Liewluck T. Centronuclear myopathy with cardiomyopathy due to recessive titinopathy. Muscle Nerve. 2019 Apr; 59 (4):E26-E27 Epub 2019 Feb 12
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  60. Elahi B, Laughlin RS, Litchy WJ, Milone M, Liewluck T. Neuromuscular transmission defects in myopathies: Rare but worth searching for. Muscle Nerve. 2019 Apr; 59 (4):475-478 Epub 2019 Jan 06
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  61. Milone M, Liewluck T. The unfolding spectrum of inherited distal myopathies. Muscle Nerve. 2019 Mar; 59 (3):283-294 Epub 2018 Nov 28
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  62. Anandan C, Milone M, Liewluck T. Intramuscular interstitial amyloid deposition does not impact anoctaminopathy-5 phenotype. Muscle Nerve. 2019 Jan; 59 (1):133-137 Epub 2018 Oct 17
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  63. Alhammad RM, Liewluck T. Myopathies featuring non-caseating granulomas: Sarcoidosis, inclusion body myositis and an unfolding overlap. Neuromuscul Disord. 2019 Jan; 29 (1):39-47 Epub 2018 Nov 09
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  64. Kao JC, Milone M, Selcen D, Shen XM, Engel AG, Liewluck T. Congenital myasthenic syndromes in adult neurology clinic: A long road to diagnosis and therapy. Neurology. 2018 Nov 6; 91 (19):e1770-e1777 Epub 2018 Oct 05
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  65. Kao JC, Brickshawana A, Liewluck T. Neuromuscular Complications of Programmed Cell Death-1 (PD-1) Inhibitors. Curr Neurol Neurosci Rep. 2018 Aug 4; 18 (10):63 Epub 2018 Aug 04
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  66. Liewluck T, Milone M. Untangling the complexity of limb-girdle muscular dystrophies. Muscle Nerve. 2018 Aug; 58 (2):167-177 Epub 2018 Feb 07
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  67. Martinez-Thompson JM, Moore SA, Liewluck T. A novel CAPN3 mutation in late-onset limb-girdle muscular dystrophy with early respiratory insufficiency. J Clin Neurosci. 2018 Jul; 53:229-231 Epub 2018 Apr 21
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  68. Kao JC, Liewluck T, Milone M. A novel ACTA1 mutation causing progressive facioscapuloperoneal myopathy in an adult. J Clin Neurosci. 2018 Jul; 53:261-262 Epub 2018 May 03
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  69. Liewluck T, Kao JC, Mauermann ML. PD-1 Inhibitor-associated Myopathies: Emerging Immune-mediated Myopathies. J Immunother. 2018 May; 41 (4):208-211
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  70. Dhawan PS, Liewluck T, Knapik J, Milone M. Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases. Muscle Nerve. 2018 May; 57 (5):E124-E126 Epub 2017 Dec 20
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  71. Liewluck T, Milone M. Characterization of isolated amyloid myopathy. Eur J Neurol. 2017 Dec; 24 (12):1437-1445 Epub 2017 Oct 05
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  72. Liewluck T. Anti-cytosolic 5'-nucleotidase 1A (cN1A) autoantibodies in motor neuron diseases. Neurology. 2017 Nov 7; 89 (19):2017-2018 Epub 2017 Sept 27
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  73. Kao JC, Liao B, Markovic SN, Klein CJ, Naddaf E, Staff NP, Liewluck T, Hammack JE, Sandroni P, Finnes H, Mauermann ML. Neurological Complications Associated With Anti-Programmed Death 1 (PD-1) Antibodies. JAMA Neurol. 2017 Oct 1; 74 (10):1216-1222
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  74. Yost MD, Chou CZ, Botha H, Block MS, Liewluck T. Facial diplegia after pembrolizumab treatment. Muscle Nerve. 2017 Sep; 56 (3):E20-E21 Epub 2017 May 06
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  75. Liewluck T, Sorenson EJ, Walkiewicz MA, Rumilla KM, Milone M. Autosomal dominant distal myopathy due to a novel ACTA1 mutation. Neuromuscul Disord. 2017 Aug; 27 (8):742-746 Epub 2017 May 05
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  76. Liewluck T, Engelstad JK, Mauermann ML. Immunotherapy-responsive allodynia due to distal acquired demyelinating symmetric (DADS) neuropathy. Muscle Nerve. 2016 Nov; 54 (5):973-977 Epub 2016 Aug 17
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  77. 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. Systemic Immunoglobulin Light Chain Amyloidosis-Associated Myopathy: Presentation, Diagnostic Pitfalls, and Outcome. Mayo Clin Proc. 2016 Oct; 91: (10)1354-1361.
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  78. Liewluck T, Milone M, Tian X, Engel AG, Staff NP, Wong LJ. Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations. Muscle Nerve. 2016 Jun; 53 (6):984-8 Epub 2016 Apr 25
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  79. Lozowska D, Ringel SP, Winder TL, Liu J, Liewluck T. Anticholinesterase Therapy Worsening Head Drop and Limb Weakness Due to a Novel DOK7 Mutation. J Clin Neuromuscul Dis. 2015 Dec; 17(2):72-7.
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  80. Liewluck T, Saperstein DS. Progressive Muscular Atrophy. Neurol Clin. 2015 Nov; 33: (4)761-73.
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  81. Liewluck T, Miravalle A. Immune-Mediated Neurological Disorders. Curr Neurol Neurosci Rep. 2015 Sep; 15(9):61.
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  82. Liewluck T, Tian X, Wong LJ, Pestronk A. Dystrophinopathy mimicking metabolic myopathies. Neuromuscul Disord. 2015 Aug; 25(8):653-7. Epub 2015 Apr 11.
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  83. Enduri S, Taylor MR, Liewluck T. Clinical reasoning: a 52-year-old woman with progressive proximal weakness. Neurology. 2014 Sep 2; 83(10):e106-9.
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  84. Liewluck T, Klein CJ, Jones LK Jr. Cramp-fasciculation syndrome in patients with and without neural autoantibodies. Muscle Nerve. 2014 Mar; 49 (3):351-6 Epub 2013 Dec 17
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  85. Liewluck T, Milone M, Mauermann ML, Castro-Couch M, Cerhan JH, Murthy NS. A novel VCP mutation underlies scapuloperoneal muscular dystrophy and dropped head syndrome featuring lobulated fibers. Muscle Nerve. 2014; 50(2):295-9.
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  86. Liewluck T, Mundi MS, Mauermann ML. Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis. Muscle Nerve. 2013 Dec; 48(6):989-91. Epub 2013 Oct 25.
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  87. Liewluck T, Ernste FC, Tracy JA. Frequency and spectrum of myopathies in patients with psoriasis. Muscle Nerve. 2013 Nov; 48(5):716-21. Epub 2013 Aug 30.
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  88. Liewluck T, Winder TL, Dimberg EL, Crum BA, Heppelmann CJ, Wang Y, Bergen HR 3rd, Milone M. ANO5-muscular dystrophy: clinical, pathological and molecular findings. Eur J Neurol. 2013 Oct; 20 (10):1383-9 Epub 2013 May 12
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  89. Liewluck T, Tracy JA, Sorenson EJ, Engel AG. Scapuloperoneal muscular dystrophy phenotype due to TRIM32-sarcotubular myopathy in South Dakota Hutterite. Neuromuscul Disord. 2013 Feb; 23(2):133-8. Epub 2012 Nov 9
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  90. Goodman BP, Liewluck T, Crum BA, Spinner RJ. Camptocormia due to inclusion body myositis. J Clin Neuromuscul Dis. 2012 Dec; 14 (2):78-81
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  91. Jones LK Jr, Liewluck T, Gavrilova RH. Myalgic phenotype and preserved muscle strength in adult-onset acid maltase deficiency. Neuromuscul Disord. 2012 Aug; 22(8):763-6. Epub 2012 May 16.
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  92. Liewluck T, Goodman BP. Late-onset axial myopathy and camptocormia in a calpainopathy carrier. J Clin Neuromuscul Dis. 2012 Jun; 13 (4):209-13
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  93. Liewluck T, Goodman BP, Milone M. Electrically active immune-mediated rippling muscle disease preceding breast cancer. Neurologist. 2012 May; 18(3):155-8.
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  94. Milone M, Liewluck T, Winder TL, Pianosi PT. Amyloidosis and exercise intolerance in ANO5 muscular dystrophy. Neuromuscul Disord. 2012 Jan; 22 (1):13-5 Epub 2011 Aug 04
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  95. Liewluck T, Selcen D, Engel AG. Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok-7 myasthenia. Muscle Nerve. 2011 Nov; 44 (5):789-94 Epub 2011 Sept 23
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  96. Liewluck T, Sacharow SJ, Fan Y, Lopez-Alberola R. A novel sporadic 614-Kb duplication of the 22q11.2 chromosome in a child with amyoplasia. J Child Neurol. 2011 Aug; 26 (8):1005-8 Epub 2011 May 13
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  97. Milone M, Wang J, Liewluck T, Chen LC, Leavitt JA, Wong LJ. Novel POLG splice site mutation and optic atrophy. Arch Neurol. 2011 Jun; 68 (6):806-11
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  98. Liewluck T, Shen XM, Milone M, Engel AG. Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia. Neuromuscul Disord. 2011 Jun; 21 (6):387-95 Epub 2011 Apr 08
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  99. Liewluck T, Sangruchi T. Pitfalls in diagnostic myopathology of sporadic inclusion body myositis. Siriraj Med J. 2011; 63:177-84.
  100. Kintarak J, Sangruchi T, Liewluck T, Kulkantrakorn K, Muengtaweepongsa S. Primary muscle diseases in Thammasat University Hospital: muscle biopsy study of 12 cases. J Med Assoc Thai. 2010 Dec; 93 Suppl 7:S236-40.
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  101. Liewluck T, Lovell TL, Bite AV, Engel AG. Sporadic centronuclear myopathy with muscle pseudohypertrophy, neutropenia, and necklace fibers due to a DNM2 mutation. Neuromuscul Disord. 2010 Dec; 20 (12):801-4
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