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 *

125 related articles for article (PubMed ID: 8745394)

  • 41. [Muscle biopsy (author's transl)].
    Goebel HH; Schaake T
    MMW Munch Med Wochenschr; 1977 Jul; 119(27):923-6. PubMed ID: 142918
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Congenital fiber-type disproportion.
    Clarke NF
    Semin Pediatr Neurol; 2011 Dec; 18(4):264-71. PubMed ID: 22172422
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Abundant minute myotubes in a patient who later developed centronuclear myopathy.
    Wöckel L; Ketelsen UP; Stötter M; Laule S; Meyermann R; Bornemann A
    Acta Neuropathol; 1998 May; 95(5):547-51. PubMed ID: 9600602
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Skeletal muscle in preterm infants with congenital myotonic dystrophy. Morphologic and histochemical study.
    Sahgal V; Bernes S; Sahgal S; Lischwey C; Subramani V
    J Neurol Sci; 1983 Apr; 59(1):47-55. PubMed ID: 6222163
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Central nervous system lesion in myotonic dystrophy--demonstrated by X-ray computed tomography and magnetic resonance imaging].
    Yoneyama S; Honda H; Konagaya M; Iida M; Takahashi A
    Rinsho Shinkeigaku; 1992 Sep; 32(9):969-72. PubMed ID: 1300269
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Congenital myopathies in Israeli families.
    Weiss K; Shapira Y; Glick B; Lerman-Sagie T; Shahar E; Goez H; Kutai M; Nevo Y
    J Child Neurol; 2007 Jun; 22(6):732-6. PubMed ID: 17641259
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Batten disease: ocular features, differential diagnosis and diagnosis by enzyme analysis.
    Zeman W
    Birth Defects Orig Artic Ser; 1976; 12(3):441-53. PubMed ID: 782600
    [No Abstract]   [Full Text] [Related]  

  • 48. [NMR tomography of the skeletal muscles in neuromuscular diseases].
    Rodiek SO
    Rofo; 1985 Oct; 143(4):418-25. PubMed ID: 2997868
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Congenital myotonic dystrophy. Changes in muscle pathology with ageing.
    Tanabe Y; Nonaka I
    J Neurol Sci; 1987 Jan; 77(1):59-68. PubMed ID: 3806137
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Central nervous system complications of congenital myotonic dystrophy].
    Shimozawa N; Inagaki M; Mito T; Ando Y; Takashima S; Takeshita K; Becker LE
    No To Hattatsu; 1986 Jul; 18(4):280-5. PubMed ID: 3730189
    [No Abstract]   [Full Text] [Related]  

  • 51. [Congenital myotonic dystrophy].
    Oliván Gonzalvo G; Alonso Gregorio M; López Moreno MJ; Domínguez Arranz MM; Olivares López JL; Pérez González JM
    An Esp Pediatr; 1990 May; 32(5):460-3. PubMed ID: 2400164
    [No Abstract]   [Full Text] [Related]  

  • 52. Prevalence of unsuspected myopathy in infants presenting for clubfoot surgery.
    Zanette G; Manani G; Pittoni G; Angelini C; Trevisan CP; Turra S
    Paediatr Anaesth; 1995; 5(3):165-70. PubMed ID: 7489436
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Nerve contact with muscle component in neuromuscular hamartoma.
    Kusuzaki K; Emoto K; Murata H; Katsura K; Sugihara H; Tsuchihashi Y; Hirasawa Y
    Anticancer Res; 2000; 20(5C):3807-11. PubMed ID: 11268458
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Longitudinal in vivo muscle function analysis of the DMSXL mouse model of myotonic dystrophy type 1.
    Decostre V; Vignaud A; Matot B; Huguet A; Ledoux I; Bertil E; Gjata B; Carlier PG; Gourdon G; Hogrel JY
    Neuromuscul Disord; 2013 Dec; 23(12):1016-25. PubMed ID: 24139022
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. [Comparison of the diagnostic value of electrophysiologic and muscle biopsy studies in myopathies].
    Haupt WF; Schädlich HJ
    Nervenarzt; 1982 Dec; 53(12):679-83. PubMed ID: 6130484
    [No Abstract]   [Full Text] [Related]  

  • 57. Experienced and physiological fatigue in neuromuscular disorders.
    Schillings ML; Kalkman JS; Janssen HM; van Engelen BG; Bleijenberg G; Zwarts MJ
    Clin Neurophysiol; 2007 Feb; 118(2):292-300. PubMed ID: 17166763
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. Thin ribs on chest X-ray: a useful sign in the differential diagnosis of the floppy newborn.
    Osborne JP; Murphy EG; Hill A
    Dev Med Child Neurol; 1983 Jun; 25(3):343-5. PubMed ID: 6873496
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Muscle fiber type disproportion with an autosomal dominant inheritance.
    Kim WK; Choi BO; Cheon HY; Sunwoo IN; Kim TS
    Yonsei Med J; 2000 Apr; 41(2):281-4. PubMed ID: 10817032
    [TBL] [Abstract][Full Text] [Related]  

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