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 *

91 related articles for article (PubMed ID: 4257931)

  • 1. [Some data on the characteristics of myopathy in the Orenburg region].
    Shtil' RG
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1461-5. PubMed ID: 4257931
    [No Abstract]   [Full Text] [Related]  

  • 2. [Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy].
    Gil'manov VKh
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1309-12. PubMed ID: 5511109
    [No Abstract]   [Full Text] [Related]  

  • 3. [Variant of the facial-scapular-humeral-gluteal-femoral form of primary myopathy in children].
    Grinio LP
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1338-41. PubMed ID: 494906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Serum aldolase activity in patients with myopathies and in their close reltives].
    Dzhuraev A
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(8):1159-63. PubMed ID: 5136820
    [No Abstract]   [Full Text] [Related]  

  • 5. [Malate dehydrogenase activity in children with myopathy].
    Gil'manov VKh
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):829-31. PubMed ID: 4753593
    [No Abstract]   [Full Text] [Related]  

  • 6. [Various epidemiologic and genetic aspects of the basic neurohereditary diseases].
    Skudarnova ZA; Sakharov LN; Makeenkova LI; Torbochkina MD; Filonova AV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):848-53. PubMed ID: 4270984
    [No Abstract]   [Full Text] [Related]  

  • 7. Scoliosis in muscular dystrophy. Some comments about diagnosis, observations on prognosis, and suggestions for therapy.
    Siegel IM
    Clin Orthop Relat Res; 1973 Jun; (93):235-8. PubMed ID: 4722946
    [No Abstract]   [Full Text] [Related]  

  • 8. [A case of Landouzy-Déjérine disease with ptosis].
    Desvignes P; Blanck MF; Mougeot M; Cassan JL
    Bull Soc Ophtalmol Fr; 1971; 71(9):874-7. PubMed ID: 5151032
    [No Abstract]   [Full Text] [Related]  

  • 9. Scapulo-thoracic fusion.
    Bunch WH
    Minn Med; 1973 May; 56(5):391-4. PubMed ID: 4698409
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Poikiloderma atrophicans vasculare associated with muscular dystrophy.
    Woolfson H; McQueen A
    Arch Dermatol; 1973 Jan; 107(1):115-7. PubMed ID: 4682534
    [No Abstract]   [Full Text] [Related]  

  • 12. [Identification of primary and secondary forms of progressive muscular dystrophy, from data of clinico-genetic and biochemical studies].
    Bondarenko ES; Tamarkina AD; Zakoshchikova LV
    Vestn Akad Med Nauk SSSR; 1973; 28(7):38-44. PubMed ID: 4786657
    [No Abstract]   [Full Text] [Related]  

  • 13. [Muscle innervation in Werdnig-Hoffmann spinal amyotrophy and several other atrophies in children].
    Olenev SN; Savel'eva-Vasil'eva ; Zav'ialova NS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1972; 72(10):1445-9. PubMed ID: 4660417
    [No Abstract]   [Full Text] [Related]  

  • 14. Early signs of Landouzy-Déjerine disease: wrist and finger weakness.
    Siegel IM
    JAMA; 1972 Jul; 221(3):302. PubMed ID: 5067800
    [No Abstract]   [Full Text] [Related]  

  • 15. [A geno-geographic study of myopathy patients in various areas of the Kalinin region].
    Artemchuk NL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(6):807-10. PubMed ID: 4243650
    [No Abstract]   [Full Text] [Related]  

  • 16. [Heredity of myopathy, with special reference to progressive muscular dystrophy].
    Sugita H
    Naika; 1970 Apr; 25(4):611-9. PubMed ID: 4912548
    [No Abstract]   [Full Text] [Related]  

  • 17. The facio-scapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases.
    Kazakov VM; Bogorodinsky DK; Znoyko ZV; Skorometz AA
    Eur Neurol; 1974; 11(4):236-60. PubMed ID: 4854830
    [No Abstract]   [Full Text] [Related]  

  • 18. [Facial-scapular-humeral myodystrophy (genetic and clinical features)].
    Bogorodinskiĭ DK; Znoĭko ZV; Kazakov VM; Skoromets AA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973; 73(6):801-9. PubMed ID: 4753589
    [No 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. Limb-girdle musclar dystrophy: its larger significance.
    Pediatrics; 1968 Feb; 41(2):382-4. PubMed ID: 5637790
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.