Value of immunocytochemical analysis of dystrophin in the diagnosis of X-chromosome linked muscular dystrophy
Roig Quilis, M.; Bonilla, E.
Anales Espanoles de Pediatria 36(4): 251-260
1992
ISSN/ISBN: 0302-4342 PMID: 1605405 Document Number: 391145
Document emailed within 1 workday
Related Documents
Cabello, A. 1995: Histological and immunohistochemical analysis of dystrophin++ in muscular dystrophy of Duchenne and Becker type Revista de Neurologia 23(Suppl 3): S395-S399Jain, S.; Jha, S.K.; Thomas, M.; Sarkar, C.; Maheshwari, M.C. 1994: Distinction of Becker's muscular dystrophy from limb-girdle type by dystrophin analysis Journal of the Association of Physicians of India 42(8): 624-625
Coral-Vázquez, R.; Arenas, D.; Cisneros, B.; Peñaloza, L.; Kofman, S.; Salamanca, F.; Montañez, C. 1993: Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy Archives of Medical Research 24(1): 1-6
Kinoshita, M.; Ikeda, K.; Yoshimura, M.; Saku, A.; Watanabe, K. 1990: Duchenne muscular dystrophy carrier presenting with mosaic X chromosome constitution and muscular symptoms--with analysis of the barr bodies in the muscle Rinsho Shinkeigaku 30(6): 643-646
Handa, V.; Mital, A.; Gupta, M.; Goyle, S. 2001: Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects Neurology India 49(1): 19-24
Saito, K.; Tanaka, A.; Harada, T.; Ikeya, K.; Fukuyama, Y.; Arahata, K.; Sugita, H.; Osawa, M.; Shishikura, K.; Suzuki, H. 1989: Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA No to Hattatsu 21(4): 361-368
Voit, T.; Patel, K.; Sewry, C.A.; Strong, P.N.; Dubowitz, V.; Dunn, M.J. 1989: Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 137(1): 20-27
El Sherif, R.M.; Fahmy, N.A.; Nonaka, I.; Etribi, M.A. 2007: Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the Mediterranean Society of Myology 26(3): 145-150
Lisiecka, D.; Wigowska-Sowińska, J.; Kwiatkowska, J.; Galas-Zgorzalewicz, B.; Słomski, R. 1998: Molecular-genetic characteristics of mutations in dystrophin gene and clinical symptoms in Duchenne muscular dystrophy Neurologia i Neurochirurgia Polska 32(5): 1069-1079
Fujishita, S.; Shibuya, N.; Sugino, S.; Matsumoto, T.; Niikawa, N. 1989: Strategy for molecular diagnosis of Duchenne muscular dystrophy: alleles frequency in RFLPs detected with X-linked probes in normal Japanese Rinsho Shinkeigaku 29(5): 554-557
Kawamura, J.; Kato, S.; Ishihara, T.; Hiraishi, Y.; Kawashiro, T. 1997: Difference of new mutation rates in dystrophin gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy Rinsho Shinkeigaku 37(3): 212-217
Chyatte, S.B.; Rudman, D.; Patterson, J.H.; Ahmann, P.; Jordan, A. 1974: Human growth hormone in myopathy: myotonic dystrophy, duchenne muscular dystrophy, and limb-girdle muscular dystrophy Southern Medical Journal 67(2): 170-172
Akaike, M.; Kawai, H. 1997: Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy Rinsho Byori. Japanese Journal of Clinical Pathology 45(2): 136-140
Mittal, S.R.; Jain, S.; Khattri, H.N.; Bidwai, P.S. 1980: Sex linked 'benign' muscular dystrophy with severe cardiac involvement-a case report Journal of the Association of Physicians of India 28(11): 483-486
Jongpiputvanich, S.; Norapucsunton, T.; Mutirangura, A. 1996: Diagnosis and carrier detection in a Duchenne muscular dystrophy family by multiplex polymerase chain reaction and microsatellite analysis Journal of the Medical Association of Thailand 79(Suppl): S15-S21
Lukás, Z.; Foretová, L.; Vojtísková, M.; Dráber, P.; Hájek, J. 1994: Monoclonal antibodies to dystrophin in biopsy diagnosis of Duchenne and Becker progressive muscular dystrophies Ceskoslovenska Patologie 30(2): 37-42
DeVore, G.R.; Mahoney, M.J.; Hobbins, J.C. 1980: Antenatal diagnosis of haemoglobinopathies, haemophilia, von Willebrand's disease, Duchenne's muscular dystrophy, and chronic granulomatous disease by fetal blood analysis Clinics in Obstetrics and Gynaecology 7(1): 41-72
Apold, J.; Eiken, H.G.; Engebretsen, L.F.; Boman, H. 1993: Analysis of the Duchenne muscular dystrophy gene with PCR analysis in paraffin-embedded tissue. a new diagnostic possibility Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 113(26): 3233-3235
Dubowitz, V. 1976: Early diagnosis of muscular dystrophy Practitioner 216(1294): 389-393
Ketenjian, A.Y. 1978: Muscular dystrophy: diagnosis and treatment Orthopedic Clinics of North America 9(1): 25-42