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 *

132 related articles for article (PubMed ID: 2451237)

  • 21. Familial congenital fiber type disproportion (CFTD) with an autosomal recessive inheritance.
    Jaffe M; Shapira J; Borochowitz Z
    Clin Genet; 1988 Jan; 33(1):33-7. PubMed ID: 3342545
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Neonatal perifascicular myopathy.
    Nevo Y; Pestronk A
    Pediatr Neurol; 1996 Sep; 15(2):150-2. PubMed ID: 8888050
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Congenital familial myopathy with type 2 fiber hypoplasia and type 1 fiber predominance.
    Muranaka H; Osari S; Fujita H; Kimura Y; Goto A; Imoto C; Nonaka I
    Brain Dev; 1997 Jul; 19(5):362-5. PubMed ID: 9253491
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Muscle fiber type transformation in nemaline myopathy and congenital fiber type disproportion.
    Miike T; Ohtani Y; Tamari H; Ishitsu T; Une Y
    Brain Dev; 1986; 8(5):526-32. PubMed ID: 3799921
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Muscle ultrasonography and electromyography correlation for evaluation of floppy infants.
    Aydinli N; Baslo B; Calişkan M; Ertaş M; Ozmen M
    Brain Dev; 2003 Jan; 25(1):22-4. PubMed ID: 12536029
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical and skeletal muscle biopsy characteristics of 25 patients with floppy infant syndrome.
    Bing Q; Hu J; Li N; Shen HR; Zhao Z
    Clin Neuropathol; 2013; 32(6):471-9. PubMed ID: 23743156
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Muscle biopsy in hypotonic children.
    Jirásek A; Kocura P
    Acta Univ Carol Med Monogr; 1976; (75):35-6. PubMed ID: 1052638
    [No Abstract]   [Full Text] [Related]  

  • 28. Dysmaturative myopathy. Evolution of the morphological picture in three cases.
    Ricoy JR; Cabello A
    Acta Neuropathol Suppl; 1981; 7():313-6. PubMed ID: 6939261
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Congenital muscular dystrophy. A histochemical study with morphometric analysis on biopsied muscles.
    Kihira S; Nonaka I
    J Neurol Sci; 1985 Sep; 70(2):139-49. PubMed ID: 4056819
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Complete external ophthalmoplegia in a patient with congenital myopathy without specific features (minimal change myopathy).
    Ohtaki E; Yamaguchi Y; Yamashita Y; Matsuishi T; Terasawa K; Katafuchi Y; Nonaka I
    Brain Dev; 1990; 12(4):427-30. PubMed ID: 2240464
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Neonatal hypotonia of muscular origin: analysis of 50 cases].
    Floriach-Robert M; Cabello A; Simón De Las Heras R; Mateos Beato F
    Neurologia; 2001; 16(6):245-53. PubMed ID: 11423041
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Delay in the maturation of muscle fibers in infants with congenital hypotonia.
    Farkas-Bargeton E; Aicardi J; Arsenio-Nunes ML; Wehrle R
    J Neurol Sci; 1978 Nov; 39(1):17-29. PubMed ID: 731270
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Muscle histochemistry in the Prader-Willi syndrome.
    Sone S
    Brain Dev; 1994; 16(3):183-8. PubMed ID: 7943601
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The floppy weak infant revisited.
    Johnston HM
    Brain Dev; 2003 Apr; 25(3):155-8. PubMed ID: 12689691
    [No Abstract]   [Full Text] [Related]  

  • 35. Dysmaturation neuromyopathy: correlation with minimal neuropathy in sural nerve biopsies.
    Verity MA; Gao YH
    J Child Neurol; 1988 Oct; 3(4):276-91. PubMed ID: 3198895
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical variability in congenital fiber type disproportion.
    Clancy RR; Kelts KA; Oehlert JW
    J Neurol Sci; 1980 Jun; 46(3):257-66. PubMed ID: 7381515
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A fluorescent microscopy study of biopsied muscles from infantile neuromuscular disorders.
    Miike T; Tamari H; Ohtani Y; Nakamura H; Matsuda I; Miyoshino S
    Acta Neuropathol; 1983; 59(1):48-52. PubMed ID: 6837268
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital inflammatory myopathy.
    Shevell M; Rosenblatt B; Silver K; Carpenter S; Karpati G
    Neurology; 1990 Jul; 40(7):1111-4. PubMed ID: 2192302
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital muscular dystrophies and unstructured congenital myopathies.
    Lenard HG; Goebel HH
    Brain Dev; 1980; 2(2):119-25. PubMed ID: 7435873
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Comparison of clinical characteristics between congenital fiber type disproportion myopathy and congenital myopathy with type 1 fiber predominance.
    Na SJ; Kim WK; Kim TS; Kang SW; Lee EY; Choi YC
    Yonsei Med J; 2006 Aug; 47(4):513-8. PubMed ID: 16941741
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.