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Journal Abstract Search

320 related items for PubMed ID: 10872105

  • 21. Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.
    Quijano-Roy S, Martí-Carrera I, Makri S, Mayer M, Maugenre S, Richard P, Berard C, Viollet L, Leheup B, Guicheney P, Pinard JM, Estournet B, Carlier RY.
    Brain Dev; 2006 May; 28(4):232-42. PubMed ID: 16368217
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  • 22. 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
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  • 23. 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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  • 24. Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changes.
    Mercuri E, Dubowitz L, Berardinelli A, Pennock J, Jongmans M, Henderson S, Muntoni F, Sewry C, Philpot J, Dubowitz V.
    Neuropediatrics; 1995 Jun; 26(3):156-62. PubMed ID: 7477754
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  • 25. Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI.
    Leite CC, Lucato LT, Martin MG, Ferreira LG, Resende MB, Carvalho MS, Marie SK, Jinkins JR, Reed UC.
    Pediatr Radiol; 2005 Jun; 35(6):572-9. PubMed ID: 15750812
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  • 26. Congenital muscular dystrophy: use of brain MR imaging findings to predict merosin deficiency.
    Lamer S, Carlier RY, Pinard JM, Mompoint D, Bagard C, Burdairon E, Estournet B, Barois A, Vallée C.
    Radiology; 1998 Mar; 206(3):811-6. PubMed ID: 9494506
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  • 27. 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 Mar; 43(1):44-51. PubMed ID: 11297158
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  • 28. A large series of immunohistochemically confirmed cases of congenital muscular dystrophy seen over a period of one decade.
    Nagappa M, Atchayaram N, Narayanappa G.
    Neurol India; 2013 Mar; 61(5):481-7. PubMed ID: 24262449
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  • 31. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
    Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M.
    Ann Neurol; 2000 Feb; 47(2):152-61. PubMed ID: 10665485
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  • 32. Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status.
    Mercuri E, Gruter-Andrew J, Philpot J, Sewry C, Counsell S, Henderson S, Jensen A, Naom I, Bydder G, Dubowitz V, Muntoni F.
    Neuromuscul Disord; 1999 Oct; 9(6-7):383-7. PubMed ID: 10545041
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  • 33. [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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  • 37. Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency.
    Villanova M, Malandrini A, Toti P, Salvestroni R, Six J, Martin JJ, Guazzi GC.
    J Submicrosc Cytol Pathol; 1996 Jan; 28(1):1-4. PubMed ID: 8929621
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  • 39. [Congenital muscular dystrophy with laminin-a2 deficiency in early infancy: diagnosis and long-term follow-up].
    Panteliadis C, Karatza E, Xinias I, Flaris N, Tzitiridou M, Ramantani G.
    Klin Padiatr; 2005 Jan; 217(5):281-5. PubMed ID: 16167276
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  • 40. Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy.
    Martinello F, Angelini C, Trevisan CP.
    Eur Neurol; 1998 Jul; 40(1):37-45. PubMed ID: 9693231
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