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Journal Abstract Search

238 related items for PubMed ID: 9225685

  • 1. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.
    van der Knaap MS, Smit LM, Barth PG, Catsman-Berrevoets CE, Brouwer OF, Begeer JH, de Coo IF, Valk J.
    Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685
    [Abstract] [Full Text] [Related]

  • 2. [Merosin-positive congenital muscular dystrophy, white matter abnormalities, and bilateral posterior occipital cortical dysplasia].
    Ribeiro VT, Moreira NC, Teixeira J, Guimarães A, Cruz R, Lima L.
    Acta Med Port; 2003 Jul; 16(3):189-92. PubMed ID: 12868400
    [Abstract] [Full Text] [Related]

  • 3. Brain magnetic resonance imaging abnormalities in merosin-positive congenital muscular dystrophy.
    Philpot J, Pennock J, Cowan F, Sewry CA, Dubowitz V, Bydder G, Muntoni F.
    Eur J Paediatr Neurol; 2000 Jul; 4(3):109-14. PubMed ID: 10872105
    [Abstract] [Full Text] [Related]

  • 4. Brain MRI features of merosin-negative congenital muscular dystrophy.
    Ibrahim Abdulla JK, Vattoth S, Al Tawari AA, Pandey T, Abubacker S.
    Australas Radiol; 2007 Dec; 51 Suppl():B221-3. PubMed ID: 17991069
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y, Nakagawa M, Takeda S.
    Microsc Res Tech; 2006 May; 48(3-4):181-91. PubMed ID: 10679965
    [Abstract] [Full Text] [Related]

  • 7. Neuroimaging manifestations and classification of congenital muscular dystrophies.
    Barkovich AJ.
    AJNR Am J Neuroradiol; 1998 Sep; 19(8):1389-96. PubMed ID: 9763366
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Merosin-negative congenital muscular dystrophy: magnetic resonance spectroscopy findings.
    Aslan M, Alkan A, Yakinci C, Sonmezgoz E, Bicak U, Zorludemir S.
    Brain Dev; 2005 Jun; 27(4):308-10. PubMed ID: 15862197
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Antenatal and postnatal brain magnetic resonance imaging in muscle-eye-brain disease.
    Longman C, Mercuri E, Cowan F, Allsop J, Brockington M, Jimenez-Mallebrera C, Kumar S, Rutherford M, Toda T, Muntoni F.
    Arch Neurol; 2004 Aug; 61(8):1301-6. PubMed ID: 15313851
    [Abstract] [Full Text] [Related]

  • 12. [Congenital muscular dystrophy: report on 10 cases].
    Olivé M, Roig M, Bonaventura I, Navarro C.
    Neurologia; 1994 Nov; 9(9):387-92. PubMed ID: 7811489
    [Abstract] [Full Text] [Related]

  • 13. Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations.
    Vainzof M, Marie SK, Reed UC, Schwartzman JS, Pavanello RC, Passos-Bueno MR, Zatz M.
    Neuropediatrics; 1995 Dec; 26(6):293-7. PubMed ID: 8719743
    [Abstract] [Full Text] [Related]

  • 14. Changes in cerebral white matter in a case of congenital muscular dystrophy (non-Fukuyama type).
    Tanaka J, Mimaki T, Okada S, Fujimura H.
    Neuropediatrics; 1990 Nov; 21(4):183-6. PubMed ID: 2290477
    [Abstract] [Full Text] [Related]

  • 15. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
    Yanagisawa A, Bouchet C, Van den Bergh PY, Cuisset JM, Viollet L, Leturcq F, Romero NB, Quijano-Roy S, Fardeau M, Seta N, Guicheney P.
    Neurology; 2007 Sep 18; 69(12):1254-60. PubMed ID: 17634419
    [Abstract] [Full Text] [Related]

  • 16. Diagnostic criteria for Walker-Warburg syndrome.
    Dobyns WB, Pagon RA, Armstrong D, Curry CJ, Greenberg F, Grix A, Holmes LB, Laxova R, Michels VV, Robinow M.
    Am J Med Genet; 1989 Feb 18; 32(2):195-210. PubMed ID: 2494887
    [Abstract] [Full Text] [Related]

  • 17. Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?
    Mercuri E, Sewry CA, Brown SC, Brockington M, Jungbluth H, DeVile C, Counsell S, Manzur A, Muntoni F.
    Neuropediatrics; 2000 Aug 18; 31(4):186-9. PubMed ID: 11071142
    [Abstract] [Full Text] [Related]

  • 18. Merosin-deficient congenital muscular dystrophy in Korea.
    Chae JH, Lee JS, Hwang H, Kim KJ, Hwang YS, Park JD, Cheon JE, Kim IO, Choe GY, Park SH.
    Brain Dev; 2009 May 18; 31(5):341-6. PubMed ID: 18723302
    [Abstract] [Full Text] [Related]

  • 19. Merosin-deficient congenital muscular dystrophy type 1A.
    Buteică E, Roşulescu E, Burada F, Stănoiu B, Zăvăleanu M.
    Rom J Morphol Embryol; 2008 May 18; 49(2):229-33. PubMed ID: 18516331
    [Abstract] [Full Text] [Related]

  • 20. Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophy.
    Yoshioka M, Kuroki S.
    Am J Med Genet; 1994 Nov 15; 53(3):245-50. PubMed ID: 7856660
    [Abstract] [Full Text] [Related]

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