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 *

121 related articles for article (PubMed ID: 11679216)

  • 1. Oculopharyngeal muscular dystrophy: clinical and CT findings.
    Bilgen C; Bilgen IG; Sener RN
    Comput Med Imaging Graph; 2001; 25(6):527-9. PubMed ID: 11679216
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)(11) in PABP2 gene.
    Nagashima T; Kato H; Kase M; Maguchi S; Mizutani Y; Matsuda K; Chuma T; Mano Y; Goto Y; Minami N; Nonaka I; Nagashima K
    Neuromuscul Disord; 2000 Mar; 10(3):173-7. PubMed ID: 10734263
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oculopharyngeal muscular dystrophy in Japan.
    Uyama E; Nohira O; Tomé FM; Chateau D; Tokunaga M; Ando M; Maki M; Okabe T; Uchino M
    Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S41-9. PubMed ID: 9392015
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. CT manifestation of ocular muscular dystrophy.
    Wosick WF; Alker G
    Comput Radiol; 1984; 8(6):391-3. PubMed ID: 6529909
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evidence for a chronic axonal atrophy in oculopharyngeal "muscular dystrophy".
    Probst A; Tackmann W; Stoeckli HR; Jerusalem F; Ulrich J
    Acta Neuropathol; 1982; 57(2-3):209-16. PubMed ID: 7124348
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [X-ray computed tomographic scans of lower limb and trunk muscles in facioscapulohumeral muscular dystrophy].
    Horikawa H; Takahashi K; Nishio H; Mano Y; Takayanagi T
    Rinsho Shinkeigaku; 1992 Oct; 32(10):1061-6. PubMed ID: 1297548
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial abnormalities in oculopharyngeal muscular dystrophy.
    Pauzner R; Blatt I; Mouallem M; Ben-David E; Farfel Z; Sadeh M
    Muscle Nerve; 1991 Oct; 14(10):947-52. PubMed ID: 1944407
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Late onset foot-drop muscular dystrophy with rimmed vacuoles.
    Partanen J; Laulumaa V; Paljärvi L; Partanen K; Naukkarinen A
    J Neurol Sci; 1994 Sep; 125(2):158-67. PubMed ID: 7807161
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Mechanism to induce scoliosis in Duchenne muscular dystrophy--a study of paraspinal muscle by X-ray computed tomography].
    Ando N; Takayanagi T; Fujimoto Y; Mano Y
    Rinsho Shinkeigaku; 1992 Sep; 32(9):956-61. PubMed ID: 1300267
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Skeletal muscle MRI findings in autosomal recessive distal muscular dystrophy (Miyoshi)].
    Ohsuga H; Ohsuga S; Yamamoto M; Shinohara Y
    Rinsho Shinkeigaku; 1988 Nov; 28(11):1304-11. PubMed ID: 3233830
    [No Abstract]   [Full Text] [Related]  

  • 12. Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients.
    Linssen WH; Notermans NC; Van der Graaf Y; Wokke JH; Van Doorn PA; Höweler CJ; Busch HF; De Jager AE; De Visser M
    Brain; 1997 Nov; 120 ( Pt 11)():1989-96. PubMed ID: 9397016
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Early onset muscular dystrophy with autosomal dominant heredity. Report of a family and CT findings of skeletal muscle.
    Tohyama J; Inagaki M; Nonaka I
    Brain Dev; 1994; 16(5):402-6. PubMed ID: 7892962
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oculopharyngeal muscular dystrophy. An autopsied case from the French-Canadian kindred.
    Little BW; Perl DP
    J Neurol Sci; 1982 Feb; 53(2):145-58. PubMed ID: 7057207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Oculopharyngeal dystrophy: ultrastructure of muscles distinct from the primary myopathy.
    Kozachek JW; Wilson FJ
    Acta Neuropathol; 1982; 57(1):7-12. PubMed ID: 7090744
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial difference in the onset and distribution of muscular involvement.
    Fukuhara N; Kumamoto T; Tsubaki T; Mayuzumi T; Nitta H
    Acta Neurol Scand; 1982 May; 65(5):458-67. PubMed ID: 7113658
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A) binding protein 2.
    Becher MW; Kotzuk JA; Davis LE; Bear DG
    Ann Neurol; 2000 Nov; 48(5):812-5. PubMed ID: 11079550
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A case of Fukuyama type congenital muscular dystrophy with progressive changes in brain CT scanning].
    Mori K; Saijo T; Hamaguchi H; Tayama M; Kawano N; Hashimoto T; Miyao M
    No To Hattatsu; 1988; 20(5):418-22. PubMed ID: 3224015
    [No Abstract]   [Full Text] [Related]  

  • 19. Familial oculopharyngeal muscular dystrophy with distal spread.
    Vita G; Dattola R; Santoro M; Messina C
    J Neurol; 1983; 230(1):57-64. PubMed ID: 6194273
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Computed tomographic findings in manifesting carriers of Duchenne muscular dystrophy.
    de Visser M; Verbeeten B
    Clin Genet; 1985 Mar; 27(3):269-75. PubMed ID: 3987077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.