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Journal Abstract Search

153 related items for PubMed ID: 8719743

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  • 23. Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.
    Trevisan CP, Martinello F, Ferruzza E, Fanin M, Chevallay M, Tomé FM.
    Childs Nerv Syst; 1996 Oct; 12(10):604-10. PubMed ID: 8934020
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  • 24. 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
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  • 25. Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy.
    Mercuri E, Anker S, Philpot J, Sewry C, Dubowitz V, Muntoni F.
    Pediatr Neurol; 1998 May; 18(5):399-401. PubMed ID: 9650678
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  • 26. [Diagnosis of congenital muscular dystrophy and clinical significance of merosin expression].
    Xiong H, Yao S, Yuan Y, Chang XZ, Wu Y, Bao XH, Zhang YH, Wu HS, Chen L, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2006 Dec; 44(12):918-23. PubMed ID: 17254461
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  • 29. MR imaging of pelvic and thigh muscles in congenital muscular dystrophy.
    Oto A, Aydingöz U, Başgün N, Talim B, Karaağaoğlu E, Topaloğlu H.
    Turk J Pediatr; 2001 Dec; 43(1):44-51. PubMed ID: 11297158
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  • 32. Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.
    Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V.
    Neuropediatrics; 1995 Feb; 26(1):3-7. PubMed ID: 7791947
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  • 33. Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging.
    Philpot J, Cowan F, Pennock J, Sewry C, Dubowitz V, Bydder G, Muntoni F.
    Neuromuscul Disord; 1999 Mar; 9(2):81-5. PubMed ID: 10220862
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  • 34. Merosin-negative congenital muscular dystrophy: diffusion-weighted imaging findings of brain.
    Alkan A, Sigirci A, Kutlu R, Aslan M, Doganay S, Yakinci C.
    J Child Neurol; 2007 May; 22(5):655-9. PubMed ID: 17690079
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  • 35. Immunohistochemical evaluation of merosin deficiency in congenital muscular dystrophies.
    Brett FM, Loring P, Caesar A, Burke M, Brennan RP, King M, Farrell MA.
    Arch Pathol Lab Med; 1998 Jan; 122(1):69-71. PubMed ID: 9448020
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  • 36. Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities.
    Sunada Y, Edgar TS, Lotz BP, Rust RS, Campbell KP.
    Neurology; 1995 Nov; 45(11):2084-9. PubMed ID: 7501163
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  • 37. Congenital muscular dystrophy.
    Huang FL, Mak SC, Chi CS.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Feb; 63(2):165-9. PubMed ID: 10677931
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