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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

238 related items for PubMed ID: 9225685

  • 21.
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  • 26. A case of Walker-Warburg syndrome resulting from a homozygous POMT1 mutation.
    Yis U, Uyanik G, Kurul S, Dirik E, Ozer E, Gross C, Hehr U.
    Eur J Paediatr Neurol; 2007 Jan; 11(1):46-9. PubMed ID: 17161965
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  • 27. Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.
    Toda T, Watanabe T, Matsumura K, Sunada Y, Yamada H, Nakano I, Mannen T, Kanazawa I, Shimizu T.
    Muscle Nerve; 1995 May; 18(5):508-17. PubMed ID: 7739638
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  • 29. 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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  • 30. Cobblestone lissencephaly with normal eyes and muscle.
    Dobyns WB, Patton MA, Stratton RF, Mastrobattista JM, Blanton SH, Northrup H.
    Neuropediatrics; 1996 Apr; 27(2):70-5. PubMed ID: 8737821
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  • 31. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
    Seidahmed MZ, Sunada Y, Ozo CO, Hamid F, Campbell KP, Salih MA.
    Neuropediatrics; 1996 Dec; 27(6):305-10. PubMed ID: 9050048
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  • 32. 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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  • 33. 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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  • 34. Report on a patient with congenital muscular dystrophy, hydrocephalus, Dandy-Walker malformation and leukodystrophy.
    Di Rocco M, Leveratto L, Cama A, Bado M, Tortori Donati P, Andreussi L, Borrone C.
    Genet Couns; 1993 Nov; 4(4):295-8. PubMed ID: 8110418
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  • 35. 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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  • 36. 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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  • 37. [MRI in congenital nystagmus].
    Denis D, Girard N, Toesca E, Zanin E, Gambarelli N, Lebranchu P, Mancini J.
    J Fr Ophtalmol; 2010 Mar; 33(3):189-205. PubMed ID: 20138687
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  • 38. An unusual case of congenital muscular dystrophy with normal serum CK level, external ophtalmoplegia, and white matter changes on brain MRI.
    Vondracek P, Hermanova M, Vodickova K, Fajkusova L, Blakely EL, He L, Turnbull DM, Taylor RW, Tajsharghi H.
    Eur J Paediatr Neurol; 2007 Nov; 11(6):381-4. PubMed ID: 17395506
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  • 39. Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome.
    Sasaki M, Yoshioka K, Yanagisawa T, Nemoto A, Takasago Y, Nagano T.
    Childs Nerv Syst; 1989 Feb; 5(1):35-7. PubMed ID: 2495176
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