BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 3736585)

  • 1. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site.
    Bodensteiner JB; Schochet SS
    Muscle Nerve; 1986; 9(6):544-7. PubMed ID: 3736585
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Facioscapulohumeral neuromuscular syndromes--problems of differential and early diagnosis and genetic counseling].
    Bachmann H; Ziegan J; Steinbicker V; von Rohden L; Wagner A
    Psychiatr Neurol Med Psychol (Leipz); 1989 Oct; 41(10):586-95. PubMed ID: 2608758
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Becker-type muscular dystrophy.
    Bradley WG; Jones MZ; Mussini JM; Fawcett PR
    Muscle Nerve; 1978; 1(2):111-32. PubMed ID: 571527
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Differential diagnosis of a benign course of muscular dystrophy using molecular genetic methods].
    Wagner M; Diedrich U; Pozsàr C; Becker PE; Reiss J
    Nervenarzt; 1990 Apr; 61(4):244-7. PubMed ID: 2352571
    [No Abstract]   [Full Text] [Related]  

  • 5. Distal muscular dystrophy. Case reports.
    Ishpekova B; Milanov I
    Electromyogr Clin Neurophysiol; 1997; 37(4):201-5. PubMed ID: 9208214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE; Strehler DA
    Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795
    [No Abstract]   [Full Text] [Related]  

  • 7. Clinico-morphological correlative aspects in progressive muscular dystrophy.
    Andreicuţ S; Dulău E; Popoviciu L; Simu G
    Morphol Embryol (Bucur); 1984; 30(2):123-8. PubMed ID: 6234457
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Scapuloperoneal myopathy.
    Todman DH; Cooke RA
    Clin Exp Neurol; 1984; 20():169-74. PubMed ID: 6568938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital muscular dystrophy: case reports and reappraisal.
    Lazaro RP; Fenichel GM; Kilroy AW
    Muscle Nerve; 1979; 2(5):349-55. PubMed ID: 492211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
    Lischka A; Grisold W; Weninger M; Toifl K; Tatzer E
    Klin Padiatr; 1986; 198(2):119-21. PubMed ID: 3702273
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement.
    van der Kooi AJ; Ledderhof TM; de Voogt WG; Res CJ; Bouwsma G; Troost D; Busch HF; Becker AE; de Visser M
    Ann Neurol; 1996 May; 39(5):636-42. PubMed ID: 8619549
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Emery-Dreifuss muscular dystrophy with unusual features.
    Deymeer F; Oge AE; Bayindir C; Kaymaz C; Nişanci Y; Adalet K; Yates JR; Ozdemir C
    Muscle Nerve; 1993 Dec; 16(12):1359-65. PubMed ID: 8232393
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A study of Duchenne's muscular dystrophy in females. A clinical, biochemical, pathological and chromosomal study of two families.
    Reddy MV; Prabhakar V; Sadasivan G; Ebenezer LN
    Neurol India; 1968; 16(2):41-5. PubMed ID: 5682570
    [No Abstract]   [Full Text] [Related]  

  • 15. [Tibial muscular dystrophy. A rare form of distal myopathy].
    de Seze J; Udd B; Vermersch P
    Rev Neurol (Paris); 1999 Apr; 155(4):296-305. PubMed ID: 10367327
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Muscle LDH isoenzymes in neuromuscular diseases and in carriers of recessive X-linked muscular dystrophy (duchenne)].
    Kowalewski S; Rotthauwe HW
    Z Kinderheilkd; 1972; 113(1):55-70. PubMed ID: 5056500
    [No Abstract]   [Full Text] [Related]  

  • 17. [Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg].
    Udd B; Partanen J; Halonen P; Somer H; Falck B; Hakamies L; Heikkilä H; Ingo S; Kalimo H; Laulumaa V
    Duodecim; 1992; 108(15):1331-8. PubMed ID: 1366093
    [No Abstract]   [Full Text] [Related]  

  • 18. Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy.
    Tachi N; Tachi M; Sasaki K; Nagata N; Chiba S
    Pediatr Neurol; 1990; 6(4):265-8. PubMed ID: 2206159
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Ocular myopathy. A familial case of oculo-pharyngeal and skeletal muscular dystrophy with late onset].
    Manigand G; Lucsko M; Deparis M
    Sem Hop; 1969 Nov; 45(45):2803-8. PubMed ID: 4312491
    [No Abstract]   [Full Text] [Related]  

  • 20. Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation.
    Nonaka I; Sunohara N; Satoyoshi E; Terasawa K; Yonemoto K
    Ann Neurol; 1985 Jan; 17(1):51-9. PubMed ID: 3985587
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.