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 *

104 related articles for article (PubMed ID: 4807104)

  • 1. [Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example].
    Berg RL; Kryshova NA; Ozeretskovskaia NG; Artemchuk NL; Begzhanov KB
    Genetika; 1973 Oct; 9(10):127-38. PubMed ID: 4807104
    [No Abstract]   [Full Text] [Related]  

  • 2. [Incidence and clinical polymorphism of Charcot-Marie neural amyotrophy in the Amur region].
    Khomenko EI
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):22-6. PubMed ID: 7180298
    [No Abstract]   [Full Text] [Related]  

  • 3. [Clinico-genalogic characteristics of hereditary diseases of the nervous system in the Kuibyshev region].
    Nesterov LN; Sushcheva GP; Viatkina SIa
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1506-12. PubMed ID: 152555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Evoked potentials of the somatosensory system in patients with progressive muscular dystrophies].
    Avakian GN
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1628-32. PubMed ID: 6675359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Clinico-epidemiological aspects of hereditary neuromuscular diseases in the Krasnodar territory].
    Krivopusk ME
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(9):3-5. PubMed ID: 1664610
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Scapuloperoneal syndromes].
    Serratrice G; Pellissier JF; Pouget J; Gastaut JL; Cros D
    Rev Neurol (Paris); 1982; 138(10):691-711. PubMed ID: 7156632
    [No Abstract]   [Full Text] [Related]  

  • 7. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
    Beighton PH
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):105. PubMed ID: 5173114
    [No Abstract]   [Full Text] [Related]  

  • 8. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG; Hadro TA; Treiber DL; Wollner T; Morris C
    Birth Defects Orig Artic Ser; 1982; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract]   [Full Text] [Related]  

  • 9. [Plasma and erythrocyte free amino acids in patients with progressive muscular dystrophy].
    Temin PA; Toguzov RT; Griniu LP; Kushelev AR; Dzhutova ED
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):29-33. PubMed ID: 7180300
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Malignant melanoma and Charcot-Marie-Tooth disease.
    Greene MH; Mead GD; Reimer RR; Bergfeld WF; Fraumeni JF
    Am J Med Genet; 1980; 5(1):69-71. PubMed ID: 7395902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prevalence of peroneal muscular atrophy in Cantabria].
    Combarros O; Rebollo M; Calleja J; Berciano J
    Rev Clin Esp; 1982 Sep; 166(6):281-4. PubMed ID: 7178569
    [No Abstract]   [Full Text] [Related]  

  • 12. [Charcot-Marie-Tooth disease. Report of a family (author's transl)].
    Alonso ME; Figueroa HH; Zermeño F; Escobar A; Flores T
    Rev Invest Clin; 1981; 33(3):303-7. PubMed ID: 7330503
    [No Abstract]   [Full Text] [Related]  

  • 13. [Effect of myoelectrostimulation on the status of peripheral hemodynamics in progressive muscular dystrophy].
    Avakian GN; Sadykova NF; Iakovlev IuV; Timonina OV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(11):33-7. PubMed ID: 6983797
    [No Abstract]   [Full Text] [Related]  

  • 14. [Report of 9 cases of hereditary neuromuscular atrophy and investigation of its genetic patterns].
    Li ZX
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Aug; 16(4):210-2. PubMed ID: 6641396
    [No Abstract]   [Full Text] [Related]  

  • 15. Controversy in genetic disorders.
    Sybert VP
    Arch Dermatol; 1981 Jul; 117(7):380-1. PubMed ID: 6455091
    [No Abstract]   [Full Text] [Related]  

  • 16. Molecular basis of neuromuscular diseases.
    Chance PF; Ashizawa T; Hoffman EP; Crawford TO
    Phys Med Rehabil Clin N Am; 1998 Feb; 9(1):49-81, vi. PubMed ID: 9894134
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results].
    Fardin P; Micaglio GF; Angelini C; Negrin P; Siciliano G
    Riv Neurobiol; 1984; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract]   [Full Text] [Related]  

  • 18. Molecular genetics in neurologic diseases.
    Bird TD
    West J Med; 1993 Aug; 159(2):180-1. PubMed ID: 8212684
    [No Abstract]   [Full Text] [Related]  

  • 19. [The activity of carbohydrate-metabolizing enzymes in muscle biopsies from humans with various myodystrophies].
    Il'in VS; Anosov NN; Soliternova IB; Razumovskaia NI; Deriabina EI
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(9):1312-6. PubMed ID: 4416986
    [No Abstract]   [Full Text] [Related]  

  • 20. [On the social aspect of muscular dystrophies and progressive muscular atrophies in children].
    Majewska Z; Kamraj-Mazurkiewicz K
    Pediatr Pol; 1972 Dec; 47(12):1557-61. PubMed ID: 4643090
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.