Muscle disorders in pediatric patients in King Chulalongkorn Memorial Hospital

Journal of the Medical Association of Thailand

Volumn 87, Issue SUPPL. 2, 2004, Pages

  Jongpiputvanich, Sungkom ^a   Norapucsunton, Terasak ^a   Shuangshoti, Shanop ^a  

^a CHULALONGKORN UNIVERSITY   (Thailand)

Author keywords

Children; Muscle disorders

Indexed keywords

ADOLESCENT; ARTICLE; BECKER MUSCULAR DYSTROPHY; CHILD; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DUCHENNE MUSCULAR DYSTROPHY; HISTOPATHOLOGY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MUSCLE BIOPSY; MYOPATHY; MYOSITIS; NEUROMUSCULAR DISEASE; SPINAL MUSCULAR ATROPHY;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CREATINE KINASE; FEMALE; HUMANS; INFANT; MALE; MUSCULAR ATROPHY, SPINAL; MUSCULAR DISEASES; MUSCULAR DYSTROPHIES; RETROSPECTIVE STUDIES; THAILAND;

EID: 22744431747     PISSN: 01252208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. nd edition. WB Saunders Company Ltd, London, England 1985.
2. nd edition. WB Saunders Company Ltd, London, England 1995
3. Emery AEH. In Oxford monographs on medical genetics, No. 24, 1993. Oxford University Press, Oxford, England.
4. Kunkel LM. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 1986; 322: 73-7.
5. Darras BT, Franke U. Normal human genomic restriction fragment patterns and polymorphism revealed by hybridization with the entire dystrophin cDNA. Am J Hum Genet 1988; 43: 612-9.
6. Beggs AH, Koenig M, Boyce FM, Kunkel LM. Detection of 98% of DMD/BMD deletion by polymerase chain reaction. Hum Genet 1990; 86: 45-8.
7. Mutirangura A, Jongpiputvanich S, Norapucsunton T, et al. Multiplex PCR to Detect the Dystrophin Gene Deletion in Thai patients. J Med Assoc Thai 1995; 78: 460-5.
8. Gilliam TC, Bruzustowicz LM, Castilla LH, et al. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Nature 1990; 345: 823-5.
9. Melki J, Lefebvre S, Burglen L, et al. De novo and inherited deletions of the 5q13 region in spinal muscular atrophies. Science 1994; 264: 1474-7.
10. Munsat TL. Workshop report. International SMA collaboration. Neuromusc Disord 1991; 1: 81.
11. Bodensteiner J. Congenital Myopathies. Neurol Clin 1988; 6: 499-512.
12. Byrne E, Dennett X, Trounce I, et al. Partial cytochrome c oxidase deficiency in chronic progressive external opthalmoplegia. J Neurol Sci 1985; 71: 257-71.