{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,2,10]],"date-time":"2024-02-10T00:20:55Z","timestamp":1707524455907},"reference-count":13,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2022,1,18]]},"DOI":"10.7759\/cureus.21353","type":"journal-article","created":{"date-parts":[[2022,1,18]],"date-time":"2022-01-18T09:43:25Z","timestamp":1642499005000},"source":"Crossref","is-referenced-by-count":1,"title":["Calpainopathy (Leyden-Mobius Limb-Girdle Muscular Dystrophy Type 2A Phenotype) and Dysferlinopathy (Miyoshi Distal Myopathy Limb-Girdle Muscular Dystrophy Type 2B Phenotype) of Preadolescent Onset: Case Reports of Two Male Filipinos"],"prefix":"10.7759","author":[{"given":"Joanna May S","family":"Quilacio","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raymond L","family":"Rosales","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Encarnita R","family":"Ampil","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1515\/rjim-2015-0002","article-title":"The growing family of limb-girdle muscular dystrophies: old and newly identified members","volume":"53","author":"Bastian A","year":"2015","unstructured":"Bastian A, Mageriu V, Micu G, Manole E. The growing family of limb-girdle muscular dystrophies: old and newly identified members. Rom J Intern Med. 2015, 53:13-24. 10.1515\/rjim-2015-0002","journal-title":"Rom J Intern Med"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1179\/174313209X380847","article-title":"The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)","volume":"32","author":"Angelini C","year":"2010","unstructured":"Angelini C, Nardetto L, Borsato C, Padoan R, Fanin M, Nascimbeni AC, Tasca E. The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B). Neurol Res. 2010, 32:41-6. 10.1179\/174313209X380847","journal-title":"Neurol Res"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.0000000000000892","article-title":"Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine","volume":"83","author":"Narayanaswami P","year":"2014","unstructured":"Narayanaswami P, Weiss M, Selcen D, et al.. Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. Neurology. 2014, 83:1453-63. 10.1212\/WNL.0000000000000892","journal-title":"Neurology"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.1016\/j.ncl.2014.04.005","article-title":"The limb-girdle muscular dystrophies","volume":"32","author":"Wicklund MP","year":"2014","unstructured":"Wicklund MP, Kissel JT. The limb-girdle muscular dystrophies. Neurol Clin. 2014, 32:729-49. 10.1016\/j.ncl.2014.04.005","journal-title":"Neurol Clin"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.2004.028738","article-title":"Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes","volume":"42","author":"Piluso G","year":"2005","unstructured":"Piluso G, Politano L, Aurino S, et al.. Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes. J Med Genet. 2005, 42:686-93. 10.1136\/jmg.2004.028738","journal-title":"J Med Genet"},{"key":"ref6","article-title":"Limb-girdle muscular dystrophy overview - retired chapter, for historical reference only","author":"Pegoraro E","year":"2000","unstructured":"Pegoraro E, Hoffman EP. Limb-girdle muscular dystrophy overview - retired chapter, for historical reference only. GeneReviews. 2000,","journal-title":"GeneReviews"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.3969\/j.issn.1673-5374.2013.20.010","article-title":"Limb-girdle muscular dystrophy subtypes: first-reported cohort from northeastern China","volume":"8","author":"Mahmood OA","year":"2013","unstructured":"Mahmood OA, Jiang X, Zhang Q. Limb-girdle muscular dystrophy subtypes: first-reported cohort from northeastern China. Neural Regen Res. 2013, 8:1907-18. 10.3969\/j.issn.1673-5374.2013.20.010","journal-title":"Neural Regen Res"},{"key":"ref8","article-title":"Limb-girdle muscular dystrophy: update","volume":"44","author":"Sunda Y","year":"2004","unstructured":"Sunda Y. Limb-girdle muscular dystrophy: update. Rinsho Shinkeigaku. 2004, 44:995-7.","journal-title":"Rinsho Shinkeigaku"},{"key":"ref9","article-title":"Miyoshi type distal myopathy with Dysferlin mutation in a Filipino patient","volume":"33","author":"Barja RA","year":"2005","unstructured":"Barja RA, Rosales RL, Malicdan MC, Romario R. Miyoshi type distal myopathy with Dysferlin mutation in a Filipino patient. Philippine Journal of Neurology. 2005, 33:9-2.","journal-title":"Philippine Journal of Neurology"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.4103\/aian.AIAN_81_17","article-title":"Limb-girdle muscular dystrophies in India: a review","volume":"20","author":"Khadilkar SV","year":"2017","unstructured":"Khadilkar SV, Faldu HD, Patil SB, Singh R. Limb-girdle muscular dystrophies in India: a review. Ann Indian Acad Neurol. 2017, 20:87-95. 10.4103\/aian.AIAN_81_17","journal-title":"Ann Indian Acad Neurol"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1002\/mus.24682","article-title":"Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: the yield and the pitfalls","volume":"52","author":"Fanin M","year":"2015","unstructured":"Fanin M, Angelini C. Protein and genetic diagnosis of limb girdle muscular dystrophy type 2A: the yield and the pitfalls. Muscle Nerve. 2015, 52:163-73. 10.1002\/mus.24682","journal-title":"Muscle Nerve"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1002\/humu.9424","article-title":"Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding","volume":"27","author":"Wenzel K","year":"2006","unstructured":"Wenzel K, Carl M, Perrot A, et al.. Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding. Hum Mutat. 2006, 27:599-600. 10.1002\/humu.9424","journal-title":"Hum Mutat"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddi217","article-title":"Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway","volume":"14","author":"Kramerova I","year":"2005","unstructured":"Kramerova I, Kudryashova E, Venkatraman G, Spencer MJ. Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway. Hum Mol Genet. 2005, 14:2125-34. 10.1093\/hmg\/ddi217","journal-title":"Hum Mol Genet"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/81739-calpainopathy-leyden-mobius-limb-girdle-muscular-dystrophy-type-2a-phenotype-and-dysferlinopathy-miyoshi-distal-myopathy-limb-girdle-muscular-dystrophy-type-2b-phenotype-of-preadolescent-onset-case-reports-of-two-male-filipinos","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:36:07Z","timestamp":1707507367000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/81739-calpainopathy-leyden-mobius-limb-girdle-muscular-dystrophy-type-2a-phenotype-and-dysferlinopathy-miyoshi-distal-myopathy-limb-girdle-muscular-dystrophy-type-2b-phenotype-of-preadolescent-onset-case-reports-of-two-male-filipinos"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,1,18]]},"references-count":13,"URL":"https:\/\/doi.org\/10.7759\/cureus.21353","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2022,1,18]]}}}