These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
160 related articles for article (PubMed ID: 8004806)
1. Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family. Oldfors A; Martinsson T; Tessin I; Wahlström J; Wang S Clin Genet; 1994 Feb; 45(2):97-103. PubMed ID: 8004806 [TBL] [Abstract][Full Text] [Related]
2. A Japanese family with two types of muscular dystrophy: DNA analysis and the dystrophin test. Matsumura K; Toda T; Hasegawa T; Kamei M; Imoto N; Shimizu T J Child Neurol; 1991 Jul; 6(3):251-6. PubMed ID: 1875028 [TBL] [Abstract][Full Text] [Related]
3. Dystrophin protein and RFLP analysis for fetal diagnosis and carrier confirmation of Duchenne muscular dystrophy. Boelter WD; Burt BA; Spector EB; Hinton DR; Pavlova Z; Fujimoto A Prenat Diagn; 1990 Nov; 10(11):703-15. PubMed ID: 1980950 [TBL] [Abstract][Full Text] [Related]
5. A symptomatic female patient with Duchenne muscular dystrophy diagnosed by dystrophin-staining: a case report. Shigihara-Yasuda K; Tonoki H; Goto Y; Arahata K; Ishikawa N; Kajii N; Fujieda K Eur J Pediatr; 1992 Jan; 151(1):66-8. PubMed ID: 1370218 [TBL] [Abstract][Full Text] [Related]
6. Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy. Dastur DK; Razzak ZA J Neurol Neurosurg Psychiatry; 1973 Jun; 36(3):399-410. PubMed ID: 4714102 [TBL] [Abstract][Full Text] [Related]
7. [Therapy of Duchenne muscular dystrophy with umbilical cord blood stem cell transplantation]. Zhang C; Feng HY; Huang SL; Fang JP; Xiao LL; Yao XL; Chen C; Ye X; Zeng Y; Lu XL; Wen JM; Zhang WX; Li Z; Feng SW; Xu HG; Huang K; Zhou DH; Chen W; Xie YM; Xi J; Zhang M; Li Y; Liu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):399-405. PubMed ID: 16086277 [TBL] [Abstract][Full Text] [Related]
8. Mosaic pattern of dystrophins in Duchenne muscular dystrophy. Tachi N; Sasaki K; Yamada T; Imamura S; Mike T Pediatr Neurol; 1990; 6(1):54-6. PubMed ID: 2178618 [TBL] [Abstract][Full Text] [Related]
9. Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family. Frydman M; Straussberg R; Shomrat R; Goebel H; Legum C; Shiloh Y Am J Med Genet; 1995 Sep; 58(3):209-12. PubMed ID: 8533818 [TBL] [Abstract][Full Text] [Related]
10. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)]. Lukás Z; Vojtísková M; Fajkusová L; Bednarík J; Kadanka Z; Hájek J; Hermanová M; Vohánka S; Vytopil M Cesk Patol; 2001 Nov; 37(4):137-45. PubMed ID: 11813630 [TBL] [Abstract][Full Text] [Related]
11. Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry. Oliveira AS; Gabbai AA; Schmidt B; Kiyomoto BH; Lima JG; Minetti C; Bonilla E Arq Neuropsiquiatr; 1992 Dec; 50(4):478-85. PubMed ID: 1309152 [TBL] [Abstract][Full Text] [Related]
12. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family. Wilton SD; Chandler DC; Kakulas BA; Laing NG Hum Mutat; 1994; 3(2):133-40. PubMed ID: 8199594 [TBL] [Abstract][Full Text] [Related]
13. Duchenne muscular dystrophy and myotonic dystrophy in the same patient. Dubrovsky AL; Taratuto AL; Sevlever G; Schultz M; Pegoraro E; Hoop RC; Hoffman EP Am J Med Genet; 1995 Jan; 55(3):342-8. PubMed ID: 7726234 [TBL] [Abstract][Full Text] [Related]
14. [Analysis of deletion mutations of the dystrophin gene by the multiplex polymerase chain reaction method in the diagnosis of Duchenne muscular dystrophy]. Baranov Vs; Gorbunova VN; Malysheva OV; Krasil'nikov VV Mol Gen Mikrobiol Virusol; 1991 Sep; (9):13-5. PubMed ID: 1745268 [TBL] [Abstract][Full Text] [Related]
15. Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects. Mizuno Y; Nonaka I; Hirai S; Ozawa E J Neurol Sci; 1993 Oct; 119(1):43-52. PubMed ID: 8246010 [TBL] [Abstract][Full Text] [Related]
16. Child neuromuscular disease in southern Norway. Prevalence, age and distribution of diagnosis with special reference to "non-Duchenne muscular dystrophy". Tangsrud SE; Halvorsen S Clin Genet; 1988 Sep; 34(3):145-52. PubMed ID: 3263224 [TBL] [Abstract][Full Text] [Related]
17. Germinal mosaicism in a Duchenne muscular dystrophy family: implications for genetic counselling. Melis MA; Cau M; Congiu R; Puddu R; Muntoni F; Cao A Clin Genet; 1993 May; 43(5):247-9. PubMed ID: 8375105 [TBL] [Abstract][Full Text] [Related]