These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

135 related items for PubMed ID: 10545041

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. 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]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Merosin and congenital muscular dystrophy.
    Miyagoe-Suzuki Y, Nakagawa M, Takeda S.
    Microsc Res Tech; 1996 Oct; 48(3-4):181-91. PubMed ID: 10679965
    [Abstract] [Full Text] [Related]

  • 13. Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients.
    Farina L, Morandi L, Milanesi I, Ciceri E, Mora M, Moroni I, Pantaleoni C, Savoiardo M.
    Neuroradiology; 1998 Dec; 40(12):807-11. PubMed ID: 9877136
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Merosin-positive congenital muscular dystrophy with mental retardation, microcephaly and central nervous system abnormalities unlinked to the Fukuyama muscular dystrophy and muscular-eye-brain loci: report of three siblings.
    Ruggieri V, Lubieniecki F, Meli F, Diaz D, Ferragut E, Saito K, Brockington M, Muntoni F, Fukuyama Y, Taratuto AL.
    Neuromuscul Disord; 2001 Sep; 11(6-7):570-8. PubMed ID: 11525887
    [Abstract] [Full Text] [Related]

  • 20. Severe classical congenital muscular dystrophy and merosin expression.
    Vajsar J, Chitayat D, Becker LE, Ho M, Ben-Zeev B, Jay V.
    Clin Genet; 1998 Sep; 54(3):193-8. PubMed ID: 9788720
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.