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 *

66 related articles for article (PubMed ID: 20540866)

  • 1. [Congenital neuromuscular disease with uniform type 1 fiber complicated by brain atrophy: a case report].
    Li XH; Zhang J; Cui XE
    Zhongguo Dang Dai Er Ke Za Zhi; 2010 Jun; 12(6):496-8. PubMed ID: 20540866
    [No Abstract]   [Full Text] [Related]  

  • 2. Brain atrophy in congenital neuromuscular disease with uniform type 1 fibers.
    Jung EY; Hattori H; Higuchi Y; Mitsuyoshi I; Kanda T
    Pediatr Neurol; 1997 Jan; 16(1):56-8. PubMed ID: 9044404
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of congenital neuromuscular disease with uniform type 1 fiber.
    Na SJ; Kang SW; Lee KO; Lee KY; Kim TS; Choi YC
    Yonsei Med J; 2004 Feb; 45(1):150-2. PubMed ID: 15004883
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Patient with adult-onset congenital neuromuscular disease with uniform type 1 fibers.
    Shimohata T; Sano H; Takado Y; Tada M; Tanaka K; Nishizawa M
    Eur J Neurol; 2006 Nov; 13(11):e10-1. PubMed ID: 17038021
    [No Abstract]   [Full Text] [Related]  

  • 5. Anesthetic case in a child with congenital neuromuscular disease with uniform type 1 fibers (CNMDU1).
    Okutani R; Arashi D; Tsujii K
    J Anesth; 2010 Oct; 24(5):797-800. PubMed ID: 20585812
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital myopathy with uniform type 1 fibers.
    Rakocevic-Stojanovic V; Lavrnic D; Nestorovic B; Dozic S; Cvetkovic D
    Acta Myol; 2005 Oct; 24(2):162-3. PubMed ID: 16550934
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The significance of type 1 fiber atrophy (hypotrophy) in childhood neuromuscular disorders.
    Imoto C; Nonaka I
    Brain Dev; 2001 Aug; 23(5):298-302. PubMed ID: 11504599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A case of congenital neuromuscular disease with uniform type 1 fibers.
    Sakamoto HM; Yoshioka M; Tsuji M; Kuroki S; Higuchi Y; Nonaka I; Nishino I
    Brain Dev; 2006 Apr; 28(3):202-5. PubMed ID: 16413720
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line.
    Pellegrini G; Barbieri S; Moggio M; Cheldi A; Scarlato G; Minetti C
    Neuropediatrics; 1985 Aug; 16(3):162-6. PubMed ID: 4047349
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital muscle fiber-type disproportion in a patient with congenital central hypoventilation syndrome due to PHOX2B mutations.
    Khan A; Sarnat HB; Spaetgens R
    J Child Neurol; 2008 Jul; 23(7):829-31. PubMed ID: 18658083
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Congenital neuromuscular disease with uniform type 1 fibers : a case report].
    Araki A; Kurokawa T; Sakuragawa N; Nonaka I
    No To Hattatsu; 1991 May; 23(3):295-8. PubMed ID: 2043374
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital neuromuscular disease with uniform type-1 fibers, presenting early stage dystrophic muscle pathology.
    Korematsu S; Imai K; Sato K; Maeda T; Suenobu S; Kojo M; Izumi T
    Brain Dev; 2006 Jan; 28(1):63-6. PubMed ID: 16168598
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nonprogressive congenital neuromuscular disease with uniform type 1 fiber.
    Oh SJ; Danon MJ
    Arch Neurol; 1983 Mar; 40(3):147-50. PubMed ID: 6830453
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Muscle atrophy and hormonal regulation in women in 120 day bed rest.
    Larina IM; Tcheglova IA; Shenkman BS; Nemirovskaya TL
    J Gravit Physiol; 1997 Jul; 4(2):P121-2. PubMed ID: 11540671
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Morphologic changes in the vastus medialis muscle in patients with osteoarthritis of the knee.
    Fink B; Egl M; Singer J; Fuerst M; Bubenheim M; Neuen-Jacob E
    Arthritis Rheum; 2007 Nov; 56(11):3626-33. PubMed ID: 17968889
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Reperfusion injury to skeletal muscle affects primarily type II muscle fibers.
    Chan RK; Austen WG; Ibrahim S; Ding GY; Verna N; Hechtman HB; Moore FD
    J Surg Res; 2004 Nov; 122(1):54-60. PubMed ID: 15522315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Age-related skeletal muscle atrophy in humans: an immunohistochemical and morphometric study.
    Nikolić M; Malnar-Dragojević D; Bobinac D; Bajek S; Jerković R; Soić-Vranić T
    Coll Antropol; 2001 Dec; 25(2):545-53. PubMed ID: 11811285
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Congenital type I fiber hypotrophy myopathy (author's transl)].
    Hernández M; Ricoy JR; Santolaya JM; Escudero R
    An Esp Pediatr; 1978; 11(6-7):471-84. PubMed ID: 697216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital myopathy with type 2A muscle fiber uniformity and smallness.
    Gallanti A; Prelle A; Chianese L; Barbieri S; Jann S; Schiaffino S; Comini A; Scarpini E; Pellegrini G; Moggio M
    Neuropediatrics; 1992 Feb; 23(1):10-3. PubMed ID: 1565211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.