Beecher G - Search Results

1

Mitochondrial myopathies diagnosed in adulthood: clinico-genetic spectrum and long-term outcomes.

Beecher G, Gavrilova RH, Mandrekar J, Naddaf E. Beecher G, et al. Brain Commun. 2024 Feb 14;6(2):fcae041. doi: 10.1093/braincomms/fcae041. eCollection 2024. Brain Commun. 2024. PMID: 38434220 Free PMC article.

2

Pure Motor Onset and IgM-Gammopathy Occurrence in Multifocal Acquired Demyelinating Sensory and Motor Neuropathy.

Beecher G, Shelly S, Dyck PJB, Mauermann ML, Martinez-Thompson JM, Berini SE, Naddaf E, Shouman K, Taylor BV, Dyck PJ, Engelstad J, Howe BM, Mills JR, Dubey D, Spinner RJ, Klein CJ. Beecher G, et al. Neurology. 2021 Oct 4;97(14):e1392-e1403. doi: 10.1212/WNL.0000000000012618. Neurology. 2021. PMID: 34376509

3

Cancer and immune-mediated necrotizing myopathy: a longitudinal referral case-controlled outcomes evaluation.

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. Shelly S, et al. Among authors: beecher g. Rheumatology (Oxford). 2022 Dec 23;62(1):281-289. doi: 10.1093/rheumatology/keac144. Rheumatology (Oxford). 2022. PMID: 35285492

4

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: beecher g. J Neuroimmunol. 2022 Jul 15;368:577895. doi: 10.1016/j.jneuroim.2022.577895. Epub 2022 May 18. J Neuroimmunol. 2022. PMID: 35617719

5

Hereditary myopathies associated with hematological abnormalities.

Beecher G, Fleming MD, Liewluck T. Beecher G, et al. Muscle Nerve. 2022 Apr;65(4):374-390. doi: 10.1002/mus.27474. Epub 2022 Jan 5. Muscle Nerve. 2022. PMID: 34985130 Review.

6

Identification of Caveolae-Associated Protein 4 Autoantibodies as a Biomarker of Immune-Mediated Rippling Muscle Disease in Adults.

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. Dubey D, et al. Among authors: beecher g. JAMA Neurol. 2022 Aug 1;79(8):808-816. doi: 10.1001/jamaneurol.2022.1357. JAMA Neurol. 2022. PMID: 35696196 Free PMC article.

7

Adult-Onset Sandhoff Disease in a Filipino Patient: Asymmetric Weakness, Whole HEXB Gene Deletion, and Coexisting MYH7 Pathogenic Variant.

Beecher G, Liewluck T, Milone M. Beecher G, et al. Neurol Genet. 2022 Apr 26;8(3):e672. doi: 10.1212/NXG.0000000000000672. eCollection 2022 Jun. Neurol Genet. 2022. PMID: 35711818 Free PMC article.

8

Novel p.Asp27Glu ACTA1 variant features congenital myopathy with finger flexor weakness, cardiomyopathy, and cardiac conduction defects.

Mulvany-Robbins B, Putko B, Schmitt L, Oudit G, Phan C, Beecher G. Mulvany-Robbins B, et al. Among authors: beecher g. Neuromuscul Disord. 2023 Jul;33(7):546-550. doi: 10.1016/j.nmd.2023.05.009. Epub 2023 May 30. Neuromuscul Disord. 2023. PMID: 37315422

9

Plexus MRI helps distinguish the immune-mediated neuropathies MADSAM and MMN.

Beecher G, Howe BM, Shelly S, Staff NP, Mauermann ML, Taylor BV, Spinner RJ, Tracy JA, Dyck PJB, Klein CJ. Beecher G, et al. J Neuroimmunol. 2022 Oct 15;371:577953. doi: 10.1016/j.jneuroim.2022.577953. Epub 2022 Aug 18. J Neuroimmunol. 2022. PMID: 36007424

10

Axillary and musculocutaneous neuropathies.

Beecher G, Dyck PJB, Zochodne DW. Beecher G, et al. Handb Clin Neurol. 2024;201:135-148. doi: 10.1016/B978-0-323-90108-6.00004-1. Handb Clin Neurol. 2024. PMID: 38697736 Review.

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