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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

35 related articles for article (PubMed ID: 10980312)

  • 21. [Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)].
    Toda T
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1419-21. PubMed ID: 8752416
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
    Toda T; Kobayashi K
    Nihon Rinsho; 1997 Dec; 55(12):3169-75. PubMed ID: 9436430
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Beyond dystrophin: current progress in the muscular dystrophies.
    Bönnemann CG; McNally EM; Kunkel LM
    Curr Opin Pediatr; 1996 Dec; 8(6):569-82. PubMed ID: 9018440
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Walker-Warburg syndrome: neurologic features and muscle membrane structure.
    Kanoff RJ; Curless RG; Petito C; Falcone S; Siatkowski RM; Pegoraro E
    Pediatr Neurol; 1998 Jan; 18(1):76-80. PubMed ID: 9492098
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review.
    Jones KJ; Morgan G; Johnston H; Tobias V; Ouvrier RA; Wilkinson I; North KN
    J Med Genet; 2001 Oct; 38(10):649-57. PubMed ID: 11584042
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Non-Fukuyama type congenital muscular dystrophy--merosin deficient and positive forms].
    Nonaka I
    Nihon Rinsho; 1997 Dec; 55(12):3176-80. PubMed ID: 9436431
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Type II lissencephaly: presentation of intermediate form].
    Palomero-Domínguez MA; Ramos-Fernández JM; Domínguez-Santurino F; Ruiz-Gómez M
    Rev Neurol; 1998 Oct; 27(158):594-6. PubMed ID: 9803503
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital muscular dystrophy: from muscle to brain.
    Falsaperla R; Praticò AD; Ruggieri M; Parano E; Rizzo R; Corsello G; Vitaliti G; Pavone P
    Ital J Pediatr; 2016 Aug; 42(1):78. PubMed ID: 27576556
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Muscle and brain disease: an update.
    Gordon N
    Child Care Health Dev; 1994; 20(4):279-87. PubMed ID: 7955139
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy.
    Chadani Y; Kondoh T; Kamimura N; Matsumoto T; Matsuzaka T; Kobayashi O; Kondo-Iida E; Kobayashi K; Nonaka I; Toda T
    J Neurol Sci; 2000 Aug; 177(2):150-3. PubMed ID: 10980312
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis.
    Yoshioka M; Toda T; Kuroki S; Hamano K
    J Child Neurol; 1999 Nov; 14(11):711-5. PubMed ID: 10593547
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital muscular dystrophies.
    Arahata K; Ishii H; Hayashi YK
    Curr Opin Neurol; 1995 Oct; 8(5):385-90. PubMed ID: 8542045
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Walker-Warburg syndrome in a Japanese patient.
    Tachi N; Tachi M; Sasaki K; Tanabe C; Minagawa K
    Pediatr Neurol; 1988; 4(4):236-40. PubMed ID: 3072008
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The Fukuyama congenital muscular dystrophy story.
    Toda T; Kobayashi K; Kondo-Iida E; Sasaki J; Nakamura Y
    Neuromuscul Disord; 2000 Mar; 10(3):153-9. PubMed ID: 10734260
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome. Commentary to Kimura's paper (pp. 182-91).
    Takada K
    Brain Dev; 1993; 15(3):244-5. PubMed ID: 8214355
    [No Abstract]   [Full Text] [Related]  

    [Previous]     [New Search]
    of 2.