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 *

95 related articles for article (PubMed ID: 7458538)

  • 21. "Central core" and "multicore" disease. Clinical, histochemical and ultrastructural study of two cases with unusual hereditary transmission.
    Marolda M; Filla A; Pellegrini G; Esposito V; Maiuri F; Zotti G
    Acta Neurol (Napoli); 1985 Dec; 7(6):473-81. PubMed ID: 4091061
    [No Abstract]   [Full Text] [Related]  

  • 22. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S; Sugino S; Ohtani Y; Matsukura M; Nishino I; Ikezawa M; Sakata A; Kondo Y; Yoshioka K; Huard J; Nonaka I; Miike T
    Ann Neurol; 1998 Dec; 44(6):967-71. PubMed ID: 9851444
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Congenital fiber type disproportion associated with aortic coarctation complex: a case report].
    Noda Y; Aoki Y; Ishikita T; Tada H; Morooka K; Saji T; Matsuo N
    No To Hattatsu; 1990 Jan; 22(1):88-90. PubMed ID: 2294956
    [No Abstract]   [Full Text] [Related]  

  • 24. [Muscle biopsy. Value and limitations of the method of investigation].
    Campanacci L; Maschio G; Poli D; Mioni G
    G Clin Med; 1967 Apr; 48(4):323-65. PubMed ID: 5602956
    [No Abstract]   [Full Text] [Related]  

  • 25. Craniofacial abnormalities associated with congenital fiber type disproportion myopathy.
    Baccetti T; Defraia E; Donati MA
    J Clin Pediatr Dent; 1997; 21(2):167-71. PubMed ID: 9484111
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Clinical study of one family of central core disease (author's transl)].
    Fukunaga H; Kitano H; Tokunaga H; Okatsu Y; Igata A
    Rinsho Shinkeigaku; 1980 Apr; 20(4):248-54. PubMed ID: 7408328
    [No Abstract]   [Full Text] [Related]  

  • 27. [Congenital non-progressive myopathies].
    Kojima S; Takagi A
    Nihon Rinsho; 1990 Jul; 48(7):1464-9. PubMed ID: 2402063
    [No Abstract]   [Full Text] [Related]  

  • 28. Lafora's disease--a distinct genetically determined form of Unverricht's syndrome.
    Yanoff M; Schwarz GA
    J Genet Hum; 1965 Sep; 14(2):235-44. PubMed ID: 5849253
    [No Abstract]   [Full Text] [Related]  

  • 29. Proteolysis of beta-dystroglycan in muscular diseases.
    Matsumura K; Zhong D; Saito F; Arai K; Adachi K; Kawai H; Higuchi I; Nishino I; Shimizu T
    Neuromuscul Disord; 2005 May; 15(5):336-41. PubMed ID: 15833425
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital fiber-type disproportion myopathy with type I fiber predominance and type II fiber smallness and atrophy--a sterological analysis.
    Rao TV; Koul RL; Inuwa IM
    Clin Neuropathol; 2005; 24(1):26-31. PubMed ID: 15696781
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The clinical significance of type 1 fiber predominance.
    Kyriakides T; Silberstein JM; Jongpiputvanich S; Silberstein EP; Walsh PJ; Gubbay SS; Kakulas BA
    Muscle Nerve; 1993 Apr; 16(4):418-23. PubMed ID: 8455657
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Multi-minicore disease--searching for boundaries: phenotype analysis of 38 cases.
    Ferreiro A; Estournet B; Chateau D; Romero NB; Laroche C; Odent S; Toutain A; Cabello A; Fontan D; dos Santos HG; Haenggeli CA; Bertini E; Urtizberea JA; Guicheney P; Fardeau M
    Ann Neurol; 2000 Nov; 48(5):745-57. PubMed ID: 11079538
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Autosomal dominant distal myopathy with desmin storage: a clinicopathologic and electrophysiologic study of a large kinship.
    Horowitz SH; Schmalbruch H
    Muscle Nerve; 1994 Feb; 17(2):151-60. PubMed ID: 8114783
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Case of congenital fiber type disproportion].
    Fukuda T; Kobayashi S; Yamamoto Y; Kamoshita S
    No To Hattatsu; 1983 Sep; 15(5):425-31. PubMed ID: 6661328
    [No Abstract]   [Full Text] [Related]  

  • 35. [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]  

  • 36. Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.
    Sharma MC; Ralte AM; Atri SK; Gulati S; Kalra V; Sarkar C
    Neurol India; 2004 Jun; 52(2):254-6. PubMed ID: 15269486
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Muscular echinococcosis].
    Klush T; Alimov TU; Esenov KT; Urfella V; Sebti S
    Khirurgiia (Mosk); 1982 Sep; (9):106-7. PubMed ID: 7143964
    [No Abstract]   [Full Text] [Related]  

  • 38. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.
    Sivakumar K; Kyriakides T; Puls I; Nicholson GA; Funalot B; Antonellis A; Sambuughin N; Christodoulou K; Beggs JL; Zamba-Papanicolaou E; Ionasescu V; Dalakas MC; Green ED; Fischbeck KH; Goldfarb LG
    Brain; 2005 Oct; 128(Pt 10):2304-14. PubMed ID: 16014653
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A study of morphometric and histopathological features of muscle biopsies from patients of myopathy.
    Chakrabarti S; Chatterjee U; Sarkar S; Senapati A; Guha D; Mukherjee K
    Indian J Pathol Microbiol; 2007 Apr; 50(2):288-92. PubMed ID: 17883047
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A child with both congenital fiber type disproportion and giant congenital melanocytic nevi with malignant melanoma.
    Seigler RS; Golding EM; Rogers C
    J S C Med Assoc; 1997 Oct; 93(10):374-6. PubMed ID: 9343958
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.