1385 related articles for article (PubMed ID: 16487936)
1. Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
Taniguchi M; Kurahashi H; Noguchi S; Sese J; Okinaga T; Tsukahara T; Guicheney P; Ozono K; Nishino I; Morishita S; Toda T
Biochem Biophys Res Commun; 2006 Apr; 342(2):489-502. PubMed ID: 16487936
[TBL] [Abstract][Full Text] [Related]
2. The childhood muscular dystrophies: making order out of chaos.
Tsao CY; Mendell JR
Semin Neurol; 1999; 19(1):9-23. PubMed ID: 10711985
[TBL] [Abstract][Full Text] [Related]
3. Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy.
Voit T; Sewry CA; Meyer K; Hermann R; Straub V; Muntoni F; Kahn T; Unsöld R; Helliwell TR; Appleton R
Neuropediatrics; 1995 Jun; 26(3):148-55. PubMed ID: 7477753
[TBL] [Abstract][Full Text] [Related]
4. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy.
Pegoraro E; Mancias P; Swerdlow SH; Raikow RB; Garcia C; Marks H; Crawford T; Carver V; Di Cianno B; Hoffman EP
Ann Neurol; 1996 Nov; 40(5):782-91. PubMed ID: 8957020
[TBL] [Abstract][Full Text] [Related]
5. Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy.
Guo C; Willem M; Werner A; Raivich G; Emerson M; Neyses L; Mayer U
Hum Mol Genet; 2006 Mar; 15(6):989-98. PubMed ID: 16476707
[TBL] [Abstract][Full Text] [Related]
6. [Muscular dystrophies due to alterations at extracellular space level: congenital muscular dystrophy caused by merosin deficiency].
Smeyers P
Rev Neurol; 1999 Jan 16-31; 28(2):141-9. PubMed ID: 10101782
[TBL] [Abstract][Full Text] [Related]
7. Congenital muscular dystrophy with merosin deficiency.
Tomé FM; Evangelista T; Leclerc A; Sunada Y; Manole E; Estournet B; Barois A; Campbell KP; Fardeau M
C R Acad Sci III; 1994 Apr; 317(4):351-7. PubMed ID: 8000914
[TBL] [Abstract][Full Text] [Related]
8. Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle.
Cohn RD; Mayer U; Saher G; Herrmann R; van der Flier A; Sonnenberg A; Sorokin L; Voit T
J Neurol Sci; 1999 Mar; 163(2):140-52. PubMed ID: 10371075
[TBL] [Abstract][Full Text] [Related]
9. Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy.
Sewry CA; D'Alessandro M; Wilson LA; Sorokin LM; Naom I; Bruno S; Ferlini A; Dubowitz V; Muntoni F
Neuropediatrics; 1997 Aug; 28(4):217-22. PubMed ID: 9309712
[TBL] [Abstract][Full Text] [Related]
10. Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.
Taniguchi M; Kurahashi H; Noguchi S; Fukudome T; Okinaga T; Tsukahara T; Tajima Y; Ozono K; Nishino I; Nonaka I; Toda T
Hum Mol Genet; 2006 Apr; 15(8):1279-89. PubMed ID: 16531417
[TBL] [Abstract][Full Text] [Related]
11. Genetically confirmed patients with merosin-deficient congenital muscular dystrophy in China.
Yuan J; Takashima H; Higuchi I; Arimura K; Li N; Zhao Z; Shen H; Hu J
Neuropediatrics; 2008 Oct; 39(5):264-7. PubMed ID: 19294599
[TBL] [Abstract][Full Text] [Related]
12. Severe congenital muscular dystrophy in a Mexican family with a new nonsense mutation (R2578X) in the laminin alpha-2 gene.
Coral-Vazquez RM; Rosas-Vargas H; Meza-Espinosa P; Mendoza I; Huicochea JC; Ramon G; Salamanca F
J Hum Genet; 2003; 48(2):91-5. PubMed ID: 12601554
[TBL] [Abstract][Full Text] [Related]
13. Merosin-deficient congenital muscular dystrophy type 1A.
Buteică E; Roşulescu E; Burada F; Stănoiu B; Zăvăleanu M
Rom J Morphol Embryol; 2008; 49(2):229-33. PubMed ID: 18516331
[TBL] [Abstract][Full Text] [Related]
14. Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy.
Porter JD; Merriam AP; Leahy P; Gong B; Feuerman J; Cheng G; Khanna S
Hum Mol Genet; 2004 Feb; 13(3):257-69. PubMed ID: 14681298
[TBL] [Abstract][Full Text] [Related]
15. [Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
Toda T; Kobayashi K
Nihon Rinsho; 1997 Dec; 55(12):3169-75. PubMed ID: 9436430
[TBL] [Abstract][Full Text] [Related]
16. Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin.
Rooney JE; Welser JV; Dechert MA; Flintoff-Dye NL; Kaufman SJ; Burkin DJ
J Cell Sci; 2006 Jun; 119(Pt 11):2185-95. PubMed ID: 16684813
[TBL] [Abstract][Full Text] [Related]
17. Muscle regeneration and satellite cells in Fukuyama type congenital muscular dystrophy.
Terasawa K
Muscle Nerve; 1986 Jun; 9(5):465-70. PubMed ID: 3724791
[TBL] [Abstract][Full Text] [Related]
18. Merosin-positive congenital muscular dystrophy: a large inbred family.
Mahjneh I; Bushby K; Anderson L; Muntoni F; Tolvanen-Mahjneh H; Bashir R; Pizzi A; Brockington M; Marconi G
Neuropediatrics; 1999 Feb; 30(1):22-8. PubMed ID: 10222457
[TBL] [Abstract][Full Text] [Related]
19. Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
Gawlik K; Miyagoe-Suzuki Y; Ekblom P; Takeda S; Durbeej M
Hum Mol Genet; 2004 Aug; 13(16):1775-84. PubMed ID: 15213105
[TBL] [Abstract][Full Text] [Related]
20. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
Nonaka I
Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
