BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 6859110)

  • 1. Oculogastrointestinal muscular dystrophy.
    Ionasescu V
    Am J Med Genet; 1983 May; 15(1):103-12. PubMed ID: 6859110
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Late-onset oculogastrointestinal muscular dystrophy.
    Ionasescu VV; Thompson HS; Aschenbrener C; Anuras S; Risk WS
    Am J Med Genet; 1984 Aug; 18(4):781-8. PubMed ID: 6548335
    [No Abstract]   [Full Text] [Related]  

  • 3. Oculopharyngeal and distal myopathy: a case study from Papua New Guinea.
    Scrimgeour EM; Mastaglia FL
    Am J Med Genet; 1984 Apr; 17(4):763-71. PubMed ID: 6720743
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A familial visceral myopathy with external ophthalmoplegia and autosomal recessive transmission.
    Anuras S; Mitros FA; Nowak TV; Ionasescu VV; Gurll NJ; Christensen J; Green JB
    Gastroenterology; 1983 Feb; 84(2):346-53. PubMed ID: 6687359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oculopharyngodistal myopathy.
    Satoyoshi E; Kinoshita M
    Arch Neurol; 1977 Feb; 34(2):89-92. PubMed ID: 836191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J; Sunohara N; Saito Y
    Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited ophthalmoplegia with intestinal pseudo-obstruction.
    Ionasescu V; Thompson SH; Ionasescu R; Searby C; Anuras S; Christensen J; Mitros F; Hart M; Bosch P
    J Neurol Sci; 1983 May; 59(2):215-28. PubMed ID: 6687898
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Oculopharyngeal muscular dystrophy. Clinical, electromyography and muscle biopsy findings in 2 cases].
    Klostermann W; Wessel K; Reusche E; Kessler C; Kömpf D
    Nervenarzt; 1990 Jun; 61(6):351-5. PubMed ID: 2377260
    [No Abstract]   [Full Text] [Related]  

  • 9. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M; Attia N; Chabouni H; Fardeau M
    Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary ptosis.
    Aberfeld DC
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):63-5. PubMed ID: 5173128
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinicopathological study of a case of oculopharyngeal muscular dystrophy].
    Moreno Martínez JM; Martín Araguz A; García de la Rocha ML; Masjuán Vallejo J; Barón Rubio M; Ginel Feito MD
    Arch Neurobiol (Madr); 1991; 54(5):229-32. PubMed ID: 1804038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuropathic findings in oculopharyngeal muscular dystrophy. A report of seven cases and a review of the literature.
    Hardiman O; Halperin JJ; Farrell MA; Shapiro BE; Wray SH; Brown RH
    Arch Neurol; 1993 May; 50(5):481-8. PubMed ID: 8387769
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial visceral neuropathy as part of a diffuse neuronal syndrome: four fatal cases in one sibship.
    Matulis SR; McJunkin B; Chang HH
    Am J Gastroenterol; 1994 May; 89(5):792-6. PubMed ID: 8172158
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oculopharyngeal muscular dystrophy.
    Champion P; Harrison RJ
    Proc R Soc Med; 1971 Jan; 64(1):45. PubMed ID: 5551455
    [No Abstract]   [Full Text] [Related]  

  • 15. Girls with muscular dystrophy.
    Reddy BK; Kumari CK; Reddy MV; Reddi OS
    Acta Anthropogenet; 1984; 8(3-4):209-16. PubMed ID: 6545753
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
    Schmitt HP; Krause KH
    Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.
    Illa I; Serrano-Munuera C; Gallardo E; Lasa A; Rojas-García R; Palmer J; Gallano P; Baiget M; Matsuda C; Brown RH
    Ann Neurol; 2001 Jan; 49(1):130-4. PubMed ID: 11198284
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency.
    Romero NB; Tomé FM; Leturcq F; el Kerch FE; Azibi K; Bachner L; Anderson RD; Roberds SL; Campbell KP; Fardeau M
    C R Acad Sci III; 1994 Jan; 317(1):70-6. PubMed ID: 7987694
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A case of distal muscular dystrophy (Miyoshi), characterized by early involvement in paravertebral muscle and atypical changes in muscle biopsy specimen].
    Kamakura K; Shimomura S; Higuchi I; Takatani O
    Rinsho Shinkeigaku; 1988 Jun; 28(6):665-9. PubMed ID: 3233839
    [No Abstract]   [Full Text] [Related]  

  • 20. Surgery for progressive familial myopathic ptosis.
    Fox SA
    Ann Ophthalmol; 1971 Sep; 3(9):1033-8. PubMed ID: 5163784
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.