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 *

69 related articles for article (PubMed ID: 3409612)

  • 1. [A case of congenital myopathy with type 2 fiber hypotrophy].
    Touge T; Nasu Y; Yamada A; Miki H; Takeuchi H
    Rinsho Shinkeigaku; 1988 Feb; 28(2):147-50. PubMed ID: 3409612
    [No Abstract]   [Full Text] [Related]  

  • 2. [Clinical and ultrastructural study of a case of centronuclear myopathy (myotubular myopathy) in an adult].
    Vital C; Vallat JM; Martin F; Le Blanc M; Bergouignan M
    Rev Neurol (Paris); 1970 Aug; 123(2):117-30. PubMed ID: 5516059
    [No Abstract]   [Full Text] [Related]  

  • 3. [Granular body myopathy (so-called reducing body myopathy)].
    Hübner G; Pongratz D
    Pathologe; 1982 Mar; 3(2):111-3. PubMed ID: 7088899
    [No Abstract]   [Full Text] [Related]  

  • 4. [Congenital muscle fiber disproportion (congenital muscle fiber type 1 fiber atrophy)].
    Szokol M; György I; Soltész M
    Orv Hetil; 1980 Aug; 121(31):1895-8. PubMed ID: 7454302
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial type I fiber atrophy.
    Kinoshita M; Satoyoshi E; Kumagai M
    J Neurol Sci; 1975 May; 25(1):11-7. PubMed ID: 1141954
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case of neurogenic muscular atrophy with selective type I fiber atrophy].
    Ono S; Miyajima H; Nishimura Y; Honda N
    Rinsho Shinkeigaku; 1986 Jul; 26(7):704-7. PubMed ID: 3769318
    [No Abstract]   [Full Text] [Related]  

  • 7. A progressive congenital myopathy. Initial involvement of the diaphragm with type I muscle fiber atrophy.
    De Reuck J; Hooft C; De Coster W; van den Bossche H; Cuvelier C
    Eur Neurol; 1977; 15(4):217-56. PubMed ID: 872842
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital cervical spinal atrophy.
    Darwish H; Sarnat H; Archer C; Brownell K; Kotagal S
    Muscle Nerve; 1981; 4(2):106-10. PubMed ID: 7207500
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Type I fiber atrophy and centrally limited muscle fiber abnormality in a family].
    Kinoshita M; Kawasaki K; Matsuo N; Kumagai M
    Rinsho Shinkeigaku; 1975 Apr; 15(4):205-11. PubMed ID: 1170059
    [No Abstract]   [Full Text] [Related]  

  • 10. [Case of the rigid spine syndrome in a female patient].
    Ben Hamida M; Hentati F; Ben Hamida C; Slimane N; Ben Othman T; Chebbi N; Letaief F
    Tunis Med; 1986; 64(6-7):645-8. PubMed ID: 3787754
    [No Abstract]   [Full Text] [Related]  

  • 11. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.
    Sugie H; Hanson R; Rasmussen G; Verity MA
    J Neurol Neurosurg Psychiatry; 1982 Jun; 45(6):507-12. PubMed ID: 7119813
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Congenital fiber disproportion: atrophy of type I fibers. Report of 11 cases].
    Levy JA; Alegro MS; Lusvarghi ES; Salum PN; Tsanaclis AM; Levy A
    Arq Neuropsiquiatr; 1987 Jun; 45(2):153-8. PubMed ID: 3426422
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Study of skeletal muscle glycogenolysis and glycolysis in chronic steroid myopathy, non-steroid histochemical type-2 fiber atrophy, and denervation.
    Danon MJ; Schliselfeld LH
    Clin Biochem; 2007 Jan; 40(1-2):46-51. PubMed ID: 17054931
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital non-progressive myopathy with type II fibre atrophy and internal nuclei.
    Scelsi R; Lanzi G; Nespoli L; Poggi P
    Eur Neurol; 1976; 14(4):285-93. PubMed ID: 954775
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Arthrogryposis accompanying congenital spinal-type muscular atrophy.
    Besser M; Behar A
    Arch Dis Child; 1967 Dec; 42(226):666-70. PubMed ID: 6073835
    [No Abstract]   [Full Text] [Related]  

  • 16. Congenital myopathy with type II muscle fiber hypoplasia.
    Yoshioka M; Kuroki S; Ohkura K; Itagaki Y; Saida K
    Neurology; 1987 May; 37(5):860-3. PubMed ID: 3574691
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital muscle disorders].
    Ferrer S; Muñoz A; Madrid R; Vergara F; Grismali J
    Rev Med Chil; 1969 Nov; 97(11):720-6. PubMed ID: 5385879
    [No Abstract]   [Full Text] [Related]  

  • 18. [Histological characteristics of stress-induced myopathy of the musculus longissimus dorsi in swine].
    Sośnicki A
    Patol Pol; 1985; 36(3):302-20. PubMed ID: 3835514
    [No Abstract]   [Full Text] [Related]  

  • 19. Predominant fiber atrophy and fiber type disproportion in early ullrich disease.
    Schessl J; Goemans NM; Magold AI; Zou Y; Hu Y; Kirschner J; Sciot R; Bönnemann CG
    Muscle Nerve; 2008 Sep; 38(3):1184-91. PubMed ID: 18720506
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Peculiar congenital myopathy in two siblings. Congenital fibre type disproportion or type II fibres hypotrophy?
    Pavone L; Scelsi R; Gullotta F; La Rosa M; Grasso A
    Acta Neurol (Napoli); 1984 Aug; 6(4):309-12. PubMed ID: 6485910
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.