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Items: 1 to 20 of 503

1.
Progressive proximal muscle weakness with subacute onset in an elderly patient: a case report
Ana Martins, Goreti Nadais, Miguel Pinto, Ricardo Taipa, Lúcia Costa, Sofia Pimenta
Rev Neurol. 2023; 76(1): 31–34. Published online 2023 Jan 1. doi: 10.33588/rn.7601.2021276
PMCID:
PMC10364021
ArticlePubReaderPDF–960KCite
2.
Statin-Induced Immune-Mediated Necrotizing Myopathy Resulting in Proximal Muscle Weakness
Mohammed S. Abdalla, Qishuo Zhang, Monzer O. Abdalla, Suhair S. Abdel-Jalil
J Med Cases. 2023 Feb; 14(2): 64–70. Published online 2023 Feb 25. doi: 10.14740/jmc4039
PMCID:
PMC9990704
ArticlePubReaderPDF–2.2MCite
3.
Proximal muscle weakness as the sole manifestation of Cushing’s disease, misdiagnosed as dermatomyositis: a case report
Marjan Jeddi, Mesbah Shams
J Med Case Rep. 2022; 16: 483. Published online 2022 Dec 22. doi: 10.1186/s13256-022-03649-4
PMCID:
PMC9773494
ArticlePubReaderPDF–1.0MCite
4.
Absence of proximal muscle weakness, dysarthria, and facial diplegia suggests Guillain–Barre syndrome rather than CIDP
Josef Finsterer
Egypt J Neurol Psychiatr Neurosurg. 2022; 58(1): 161. Published online 2022 Dec 15. doi: 10.1186/s41983-022-00598-z
PMCID:
PMC9753869
ArticlePubReaderPDF–611KCite
5.
ANCA-associated vasculitis and severe proximal muscle weakness
Jordan S. Dutcher, Albert Bui, Tochukwu A. Ibe, Goyal Umadat, Eugene P. Harper, Erik H. Middlebrooks, Michael M. Mohseni, Michael B. Phillips
Proc (Bayl Univ Med Cent) 2021 May; 34(3): 384–386. Published online 2021 Jan 14. doi: 10.1080/08998280.2020.1871177
PMCID:
PMC8059901
ArticlePubReaderPDF–416KCite
6.
Severe proximal muscle weakness with normal CK as a presenting feature of ANCA-associated vasculitis
Sureshkumar Nagiah, Daunda Mudiyanselage Manodhi Saranapala
BMJ Case Rep. 2020; 13(1): e232854. Published online 2020 Jan 21. doi: 10.1136/bcr-2019-232854
PMCID:
PMC7021126
ArticlePubReaderPDF–797KCite
7.
Man of Steel Syndrome: Silicone and Mineral Oil Injections With Associated Hypercalcemia, Hypophosphatemia, and Proximal Muscle Weakness
Arash Shirvani, Nadine E Palermo, Michael F Holick
JBMR Plus. 2019 Oct; 3(10): e10208. Published online 2019 Jul 29. doi: 10.1002/jbm4.10208
PMCID:
PMC6820462
ArticlePubReaderPDF–3.7MCite
8.
A Case of a 34-Year-Old Female with Acute Hypoxemic Respiratory Failure and Proximal Muscle Weakness
Alex Diaz, Surit Sharma
Case Rep Crit Care. 2017; 2017: 7941715. Published online 2017 Dec 19. doi: 10.1155/2017/7941715
PMCID:
PMC5749215
ArticlePubReaderPDF–572KCite
9.
Proximal Limb Weakness in a Patient with Celiac Disease: Copper Deficiency, Gluten Sensitivity, or Both as the Underlying Cause?
J. David Avila, David Lacomis
Case Rep Neurol Med. 2016; 2016: 5415949. Published online 2016 Nov 22. doi: 10.1155/2016/5415949
PMCID:
PMC5138455
ArticlePubReaderPDF–788KCite
10.
A Curious Case of Proximal Muscle Weakness with Eosinophilic Polymyositis
Ciel Harris, Robert Ali, Julio Perez-Downes, Firas Baidoun, Marianne DeLima, Jaimin Shah, Win Aung, Raafat F. Makary
Case Rep Rheumatol. 2016; 2016: 7810916. Published online 2016 Sep 14. doi: 10.1155/2016/7810916
PMCID:
PMC5039291
ArticlePubReaderPDF–658KCite
11.
Idiopathic spinal cord herniation of the cervical cord: unusual cause of proximal muscle weakness in upper limbs
Dilina Rajapakse, Leah Mapara, Sathiyaseelan Maniharan
BMJ Case Rep. 2016; 2016: bcr2016215022. Published online 2016 May 16. doi: 10.1136/bcr-2016-215022
PMCID:
PMC4885372
ArticlePubReaderPDF–370KCite
12.
Adult onset supranuclear ophthalmoplegia, cerebellar ataxia, and neurogenic proximal muscle weakness in a brother and sister: another hexosaminidase A deficiency syndrome.
A E Harding, E P Young, F Schon
J Neurol Neurosurg Psychiatry. 1987 Jun; 50(6): 687–690. doi: 10.1136/jnnp.50.6.687
PMCID:
PMC1032071
SummaryPage BrowsePDF–713KCite
13.
The clinical, pathological, and genetic characteristics of lipid storage myopathy in northern China
Jingzhe HAN, Shan LU, Xueqin SONG, Guang JI, Yanan XIE, Hongran WU
Turk J Med Sci. 2022; 52(4): 1256–1265. Published online 2022 May 12. doi: 10.55730/1300-0144.5431
PMCID:
PMC10388001
ArticlePubReaderPDF–907KCite
14.
X-linked SBMA model mice display relevant non-neurological phenotypes and their expression of mutant androgen receptor protein in motor neurons is not required for neuromuscular disease
Anastasia Gromova, Byeonggu Cha, Erica M. Robinson, Laura M. Strickland, Nhat Nguyen, Mai K. ElMallah, Constanza J. Cortes, Albert R. La Spada
Acta Neuropathol Commun. 2023; 11: 90. Published online 2023 Jun 2. doi: 10.1186/s40478-023-01582-1
PMCID:
PMC10239133
ArticlePubReaderPDF–1.8MCite
15.
Dominantly inherited myosin IIa myopathy caused by aberrant splicing of MYH2
Carola Hedberg-Oldfors, Ólöf Elíasdóttir, Mats Geijer, Christopher Lindberg, Anders Oldfors
BMC Neurol. 2022; 22: 428. Published online 2022 Nov 15. doi: 10.1186/s12883-022-02935-4
PMCID:
PMC9664609
ArticlePubReaderPDF–2.2MCite
16.
Expansion of a novel population of NK cells with low ribosome expression in juvenile dermatomyositis
Kinsey A. Hilliard, Allison A. Throm, Jeanette T. Pingel, Nermina Saucier, Hani S. Zaher, Anthony R. French
Front Immunol. 2022; 13: 1007022. Published online 2022 Oct 31. doi: 10.3389/fimmu.2022.1007022
PMCID:
PMC9660249
ArticlePubReaderPDF–7.2MCite
17.
FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum
Magdalena Mroczek, Cheryl Longman, Maria Elena Farrugia, Solange Kapetanovic Garcia, Didem Ardicli, Haluk Topaloglu, Aurelio Hernández Laín, Diclehan Orhan, Mehmet Alikasifoglu, Jennifer Duff, Sabine Specht, Kristen J Nowak, Gianina Ravenscroft, Katherine R Chao, Zaheer Valivullah, Sandra Donkervoort, Dimah Saade, Carsten G Bönnemann, Volker Straub, Grace Yoon
J Med Genet. Author manuscript; available in PMC 2022 Nov 1.
Published in final edited form as: J Med Genet. 2022 Nov; 59(11): 1069–1074. Published online 2022 Apr 7. doi: 10.1136/jmedgenet-2021-108341
PMCID:
PMC9537361
ArticlePubReaderPDF–718KCite
18.
Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene
Francesca Magri, Simona Zanotti, Sabrina Salani, Francesco Fortunato, Patrizia Ciscato, Simonetta Gerevini, Lorenzo Maggi, Monica Sciacco, Maurizio Moggio, Stefania Corti, Nereo Bresolin, Giacomo Pietro Comi, Dario Ronchi
Int J Mol Sci. 2022 Sep; 23(17): 9817. Published online 2022 Aug 29. doi: 10.3390/ijms23179817
PMCID:
PMC9456520
ArticlePubReaderPDF–1.3MCite
19.
MicroRNAs as serum biomarkers in Becker muscular dystrophy
Delia Gagliardi, Mafalda Rizzuti, Roberta Brusa, Michela Ripolone, Simona Zanotti, Elisa Minuti, Valeria Parente, Laura Dioni, Sara Cazzaniga, Paolo Bettica, Nereo Bresolin, Giacomo Pietro Comi, Stefania Corti, Francesca Magri, Daniele Velardo
J Cell Mol Med. 2022 Sep; 26(17): 4678–4685. Published online 2022 Jul 26. doi: 10.1111/jcmm.17462
PMCID:
PMC9443944
ArticlePubReaderPDF–3.3MCite
20.
A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pair
Sonja Strang-Karlsson, Katherine Johnson, Ana Töpf, Liwen Xu, Monkol Lek, Daniel G. MacArthur, Olivera Casar-Borota, Maria Williams, Volker Straub, Carina Wallgren-Pettersson
Neuromuscul Disord. Author manuscript; available in PMC 2022 Aug 31.
Published in final edited form as: Neuromuscul Disord. 2018 Jul; 28(7): 614–618. Published online 2018 May 16. doi: 10.1016/j.nmd.2018.04.012
PMCID:
PMC9429833
ArticlePubReaderPDF–1.1MCite

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