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 *

120 related articles for article (PubMed ID: 7249619)

  • 41. Involvement of the central nervous system in congenital muscular dystrophies.
    Egger J; Kendall BE; Erdohazi M; Lake BD; Wilson J; Brett EM
    Dev Med Child Neurol; 1983 Feb; 25(1):32-42. PubMed ID: 6832496
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Fukuyama congenital muscular dystrophy in two Australian female siblings.
    Stern LM; Albertyn L; Manson JI
    Dev Med Child Neurol; 1990 Sep; 32(9):808-13. PubMed ID: 2227144
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Congenital muscular dystrophy with complete laminin-alpha2-deficiency, cortical dysplasia, and cerebral white-matter changes in children.
    Tsao CY; Mendell JR; Rusin J; Luquette M
    J Child Neurol; 1998 Jun; 13(6):253-6. PubMed ID: 9660506
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Serial MRI in Fukuyama type congenital muscular dystrophy.
    Aihara M; Tanabe Y; Kato K
    Neuroradiology; 1992; 34(5):396-8. PubMed ID: 1407518
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Western type cerebro-muscular dystrophy and congenital merosin deficiency muscular dystrophy: two terms for the same disorder].
    Castro-Gago M; Novo-Rodríguez MI; Pintos-Martínez E; Alonso-Martín A; Morales-Redondo R; Eirís-Puñal J
    Rev Neurol; 1998 Sep; 27(157):459-62. PubMed ID: 9774819
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome.
    Kimura S; Sasaki Y; Kobayashi T; Ohtsuki N; Tanaka Y; Hara M; Miyake S; Yamada M; Iwamoto H; Misugi N
    Brain Dev; 1993; 15(3):182-91. PubMed ID: 8214343
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form.
    Kobayashi O; Hayashi Y; Arahata K; Ozawa E; Nonaka I
    Neurology; 1996 Mar; 46(3):815-8. PubMed ID: 8618689
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The cerebellar and thalamic degeneration in Fukuyama-type congenital muscular dystrophy.
    Kumada S; Tsuchiya K; Takahashi M; Takesue M; Shiotsu H; Nomura Y; Segawa M; Ikeda K; Hayashi M
    Acta Neuropathol; 2000 Feb; 99(2):209-13. PubMed ID: 10672329
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [A case of Fukuyama type congenital muscular dystrophy--cranial MRI findings prior to the onset of neuromuscular signs].
    Takanashi J; Wataki K; Iai M; Sugita K; Tanabe Y
    No To Hattatsu; 1989 Nov; 21(6):588-9. PubMed ID: 2803819
    [No Abstract]   [Full Text] [Related]  

  • 50. Two Dutch siblings with congenital muscular dystrophy (Fukuyama type).
    Vles JS; de Krom MC; Visser R; Höweler CJ
    Clin Neurol Neurosurg; 1983; 85(3):175-80. PubMed ID: 6315292
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Rapidly progressive heart failure requiring transplantation in muscular dystrophy: a need for frequent screening.
    Pick JM; Ellis ZD; Alejos JC; Chang AC
    Cardiol Young; 2017 Nov; 27(9):1836-1840. PubMed ID: 28689515
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Congenital muscular dystrophy].
    Mumenthaler M
    Z Kinderheilkd; 1969; 106(2):131-62. PubMed ID: 5802055
    [No Abstract]   [Full Text] [Related]  

  • 54. 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]  

  • 55. Selective involvement of the quadriceps muscle in congenital muscular dystrophies: an ultrasonographic study.
    Topaloğlu H; Gücüyener K; Yalaz K; Renda Y; Topçu M; Aysun S; Ozdirim E; Anlar B
    Brain Dev; 1992 Mar; 14(2):84-7. PubMed ID: 1621930
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Congenital muscular dystrophy with leukoencephalopathy.
    Streib EW; Lucking CH
    Eur Neurol; 1989; 29(4):211-5. PubMed ID: 2759146
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy.
    Yoshioka M; Kuroki S; Nigami H; Kawai T; Nakamura H
    Brain Dev; 1992 Sep; 14(5):334-7. PubMed ID: 1456390
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A case of Fukuyama-type congenital muscular dystrophy with a very mild mental deficit.
    Hino-Fukuyo N; Haginoya K; Hayashi YK; Nishino I; Murakami T; Nonaka I; Togashi K; Tanaka S; Takayanagi M; Yokoyama H; Sakamoto O; Abe T; Toda T; Iinuma K
    Neuromuscul Disord; 2006 Apr; 16(4):274-6. PubMed ID: 16545565
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].
    Koga M; Abe M; Tateishi J; Antoku Y; Iwashita H; Miyoshino S
    No To Shinkei; 1984 Nov; 36(11):1103-8. PubMed ID: 6525323
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.