메뉴 건너뛰기




Volumn 21, Issue 4, 1999, Pages 244-247

Duchenne and Becker muscular dystrophies: An Estonian experience

Author keywords

Becker muscular dystrophy; Duchenne muscular dystrophy; Dystrophin; Motor developmental delay; Risk sign

Indexed keywords

DYSTROPHIN;

EID: 0033040413     PISSN: 03877604     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0387-7604(99)00016-9     Document Type: Article
Times cited : (5)

References (18)
  • 1
    • 0023614271 scopus 로고
    • Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
    • Koenig M., Hoffman E.P., Bertelson C.J., Monaco A.P., Feener C., Kunkel L.M. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell. 50:1987;509-517.
    • (1987) Cell , vol.50 , pp. 509-517
    • Koenig, M.1    Hoffman, E.P.2    Bertelson, C.J.3    Monaco, A.P.4    Feener, C.5    Kunkel, L.M.6
  • 3
    • 0027052612 scopus 로고
    • Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability
    • Hodgson S.V., Abbs S., Manzur A., Heckmatt J.Z.H., Dubowitz V., Bobrow M. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability. Neuromusc Disord. 4:1992;262-276.
    • (1992) Neuromusc Disord , vol.4 , pp. 262-276
    • Hodgson, S.V.1    Abbs, S.2    Manzur, A.3    Heckmatt, J.Z.H.4    Dubowitz, V.5    Bobrow, M.6
  • 4
    • 0027936884 scopus 로고
    • Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected
    • Ballo R., Viljoen D., Beighton P. Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected. S Afr Med J. 84:1994;494-497.
    • (1994) S Afr Med J , vol.84 , pp. 494-497
    • Ballo, R.1    Viljoen, D.2    Beighton, P.3
  • 6
    • 0030256839 scopus 로고    scopus 로고
    • Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan (in Russian)
    • Odinokova O.N., Puzyrev V.P., Radzhabaliev S.F., Rakhmonov R.A. Deletion analysis of the dystrophin gene in patients with Duchenne's muscular dystrophy in Tajikistan (in Russian). Genetica. 32:1996;1392-1395.
    • (1996) Genetica , vol.32 , pp. 1392-1395
    • Odinokova, O.N.1    Puzyrev, V.P.2    Radzhabaliev, S.F.3    Rakhmonov, R.A.4
  • 7
    • 0031034656 scopus 로고    scopus 로고
    • Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients
    • Singh V., Sinha S., Mishra S., Chaturvedi L.S., Pradhan S., Mittal R.D.et al. Proportion and pattern of dystrophin gene deletions in North Indian Duchenne and Becker muscular dystrophy patients. Hum Genet. 99:1997;206-208.
    • (1997) Hum Genet , vol.99 , pp. 206-208
    • Singh, V.1    Sinha, S.2    Mishra, S.3    Chaturvedi, L.S.4    Pradhan, S.5    Mittal, R.D.6
  • 8
    • 0031885739 scopus 로고    scopus 로고
    • Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy
    • Haider M.Z., Bastaki L., Habib Y., Moosa A. Screening 25 dystrophin gene exons for deletions in Arab children with Duchenne muscular dystrophy. Hum Hered. 48:1998;61-66.
    • (1998) Hum Hered , vol.48 , pp. 61-66
    • Haider, M.Z.1    Bastaki, L.2    Habib, Y.3    Moosa, A.4
  • 11
    • 0002503692 scopus 로고
    • Multiplex PCR for diagnosis of Duchenne muscular dystrophy
    • In: Innis M, Gelfand D, Sninski J, White T, editors. New York: Academic Press
    • Chamberlain JS, Gibbs RA, Rainer JE, Caskey CT. Multiplex PCR for diagnosis of Duchenne muscular dystrophy. In: Innis M, Gelfand D, Sninski J, White T, editors. PCR: protocols and applications- a laboratory manual. New York: Academic Press, 1990: 272-281.
    • (1990) PCR: Protocols and Applications- A Laboratory Manual , pp. 272-281
    • Chamberlain, J.S.1    Gibbs, R.A.2    Rainer, J.E.3    Caskey, C.T.4
  • 12
    • 0004062117 scopus 로고    scopus 로고
    • Multiplex PCR for identifying dystrophin gene deletions
    • In: Diacopoli NC, Haines JL, Korf BR, et al., editors. New York: Wiley
    • Beggs AH. Multiplex PCR for identifying dystrophin gene deletions. In: Diacopoli NC, Haines JL, Korf BR, et al., editors. Current protocols in human genetics. New York: Wiley 1996:9.3.1.-9.3.19.
    • (1996) Current Protocols in Human Genetics , pp. 931-9319
    • Beggs, A.H.1
  • 13
    • 0025244924 scopus 로고
    • Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
    • Beggs A.H., Koenig M., Boyce F.M., Kunkel L.M. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Hum Genet. 86:1990;45-48.
    • (1990) Hum Genet , vol.86 , pp. 45-48
    • Beggs, A.H.1    Koenig, M.2    Boyce, F.M.3    Kunkel, L.M.4
  • 14
    • 0014118255 scopus 로고
    • The Denver developmental screening test
    • Frankenburg W.K., Dodds J.B. The Denver developmental screening test. J Pediatr. 79:1971;181-191.
    • (1971) J Pediatr , vol.79 , pp. 181-191
    • Frankenburg, W.K.1    Dodds, J.B.2
  • 15
    • 0020959996 scopus 로고
    • Implications of diagnostic delay in Duchenne muscular dystrophy
    • O'Brien T., Sibert J.R., Harper P.S. Implications of diagnostic delay in Duchenne muscular dystrophy. Br Med J. 287:1983;1106-1107.
    • (1983) Br Med J , vol.287 , pp. 1106-1107
    • O'Brien, T.1    Sibert, J.R.2    Harper, P.S.3
  • 16
    • 0028898858 scopus 로고
    • No improvement in delay in diagnosis of Duchenne muscular dystrophy
    • Marshall P.D., Galasko C.S.B. No improvement in delay in diagnosis of Duchenne muscular dystrophy. Lancet. 345:1995;590-591.
    • (1995) Lancet , vol.345 , pp. 590-591
    • Marshall, P.D.1    Galasko, C.S.B.2
  • 17
    • 84906416974 scopus 로고
    • Intellectual impairment in muscular dystrophy
    • Dubowitz V. Intellectual impairment in muscular dystrophy. Arch Dis Child. 40:1965;296-301.
    • (1965) Arch Dis Child , vol.40 , pp. 296-301
    • Dubowitz, V.1
  • 18
    • 0026766161 scopus 로고
    • Genetic and clinical correlations of Xp21 muscular dystrophy
    • Bushby K.M.D. Genetic and clinical correlations of Xp21 muscular dystrophy. J Inher Metab Dis. 15:1992;551-564.
    • (1992) J Inher Metab Dis , vol.15 , pp. 551-564
    • Bushby, K.M.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.