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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1988 1
1990 1
1992 1
1993 1
1994 1
1996 1
1997 1
1998 1
1999 2
2000 1
2001 1
2002 3
2005 4
2007 2
2008 5
2009 1
2010 1
2011 1
2012 2
2014 1
2015 1
2016 3
2018 3
2019 1
2020 2
2021 1
2022 5
2024 0

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48 results

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Page 1
Juvenile Dermatomyositis: Advances in Pathogenesis, Assessment, and Management.
Leung AKC, Lam JM, Alobaida S, Leong KF, Wong AHC. Leung AKC, et al. Curr Pediatr Rev. 2021;17(4):273-287. doi: 10.2174/1573396317666210426105045. Curr Pediatr Rev. 2021. PMID: 33902423 Review.
BACKGROUND: Juvenile dermatomyositis is the most common inflammatory myopathy in the pediatric age group and a major cause of mortality and morbidity in individuals with childhood rheumatic diseases. ...In the absence of muscle biopsy, a definite diagnosis of idiopathic in …
BACKGROUND: Juvenile dermatomyositis is the most common inflammatory myopathy in the pediatric age group and a major cause of mortali …
Oculopharyngodistal myopathy.
Yu J, Deng J, Wang Z. Yu J, et al. Curr Opin Neurol. 2022 Oct 1;35(5):637-644. doi: 10.1097/WCO.0000000000001089. Epub 2022 Aug 4. Curr Opin Neurol. 2022. PMID: 35942670 Review.
PURPOSE OF REVIEW: Oculopharyngodistal myopathy (OPDM) is a rare adolescent or adult-onset neuromuscular disease that is characterized by progressive ocular, facial, pharyngeal and distal limb muscle weakness. ...In this review, the latest findings related to the ge …
PURPOSE OF REVIEW: Oculopharyngodistal myopathy (OPDM) is a rare adolescent or adult-onset neuromuscular disease that is characterize …
Distal myopathies.
Nonaka I. Nonaka I. Curr Opin Neurol. 1999 Oct;12(5):493-9. doi: 10.1097/00019052-199910000-00002. Curr Opin Neurol. 1999. PMID: 10590885 Review.
Since the discovery of the gene loci for several distal myopathies, several diseases previously categorized as different disorders have now proven to be the same or allelic disorders (e.g. distal myopathy with rimmed vacuoles and hereditary inclusion b …
Since the discovery of the gene loci for several distal myopathies, several diseases previously categorized as different disor …
Distal myopathies.
Udd B, Griggs R. Udd B, et al. Curr Opin Neurol. 2001 Oct;14(5):561-6. doi: 10.1097/00019052-200110000-00003. Curr Opin Neurol. 2001. PMID: 11562566 Review.
Distal myopathies are frequently encountered in the Nordic countries, and are now being increasingly recognized elsewhere. Three new descriptions of distal myopathy phenotypes have been published in the past year. At the same time there has been consid
Distal myopathies are frequently encountered in the Nordic countries, and are now being increasingly recognized elsewhere. Thr
Distal myopathies.
Mastaglia FL, Lamont PJ, Laing NG. Mastaglia FL, et al. Curr Opin Neurol. 2005 Oct;18(5):504-10. doi: 10.1097/01.wco.0000175936.23945.b6. Curr Opin Neurol. 2005. PMID: 16155432 Review.
PURPOSE OF REVIEW: The distal myopathies are a heterogeneous group of disorders that pose a challenge to both the clinician and geneticist. ...Recent studies have led to the identification of the genes and mutations responsible for early onset (Laing) myopathy
PURPOSE OF REVIEW: The distal myopathies are a heterogeneous group of disorders that pose a challenge to both the clinician an …
Myofibrillar myopathies.
Selcen D. Selcen D. Curr Opin Neurol. 2008 Oct;21(5):585-9. doi: 10.1097/WCO.0b013e32830a752b. Curr Opin Neurol. 2008. PMID: 18769253 Free PMC article. Review.
PURPOSE OF REVIEW: The aim of this communication is to provide an up-to-date overview of myofibrillar myopathies. RECENT FINDINGS: The most important recent advance in the myofibrillar myopathies has been the discovery that mutations in Z band alternatively spliced …
PURPOSE OF REVIEW: The aim of this communication is to provide an up-to-date overview of myofibrillar myopathies. RECENT FINDINGS: Th …
Hereditary myosin myopathies.
Oldfors A. Oldfors A. Neuromuscul Disord. 2007 May;17(5):355-67. doi: 10.1016/j.nmd.2007.02.008. Epub 2007 Apr 16. Neuromuscul Disord. 2007. PMID: 17434305 Review.
The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or symptoms of skeletal myopathy. Several mutations in two different parts of the slow/beta-cardiac MyHC rod region are associated with t …
The majority of more than 200 dominant missense mutations in MYH7 are associated with hypertrophic/dilated cardiomyopathy without signs or s …
Congenital myopathies: The current status.
Goebel HH, Dittmayer C, Stenzel W. Goebel HH, et al. Indian J Pathol Microbiol. 2022 May;65(Supplement):S271-S276. doi: 10.4103/ijpm.ijpm_1031_21. Indian J Pathol Microbiol. 2022. PMID: 35562159 Free article. Review.
Within the history of neuromuscular diseases (NMD), congenital myopathies (CM) represent a relatively new category introduced in the mid-nineteen hundreds upon advent and subsequent application of enzyme histochemistry and electron microscopy by establishing the three majo …
Within the history of neuromuscular diseases (NMD), congenital myopathies (CM) represent a relatively new category introduced in the …
Progress and challenges in diagnosis of dysferlinopathy.
Fanin M, Angelini C. Fanin M, et al. Muscle Nerve. 2016 Nov;54(5):821-835. doi: 10.1002/mus.25367. Muscle Nerve. 2016. PMID: 27501525 Review.
Dysferlin-deficient limb girdle muscular dystrophy type 2B, distal Miyoshi myopathy, and other less frequent phenotypes are a group of recessive disorders called dysferlinopathies. ...To diagnose dysferlinopathy, a clinical neuromuscular workup, including electrophy …
Dysferlin-deficient limb girdle muscular dystrophy type 2B, distal Miyoshi myopathy, and other less frequent phenotypes are a …
Congenital myopathies.
Sewry CA, Jimenez-Mallebrera C, Muntoni F. Sewry CA, et al. Curr Opin Neurol. 2008 Oct;21(5):569-75. doi: 10.1097/WCO.0b013e32830f93c7. Curr Opin Neurol. 2008. PMID: 18769251 Review.
PURPOSE OF REVIEW: The present review aims to discuss the pathological and clinical heterogeneity of congenital myopathies, and the overlap between the different variants highlighted by recent studies. ...The complexity of the classification of these conditions is highligh …
PURPOSE OF REVIEW: The present review aims to discuss the pathological and clinical heterogeneity of congenital myopathies, and the o …
48 results