BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

86 related articles for article (PubMed ID: 13802)

  • 1. [Further remarks on histochemistry applied to myodiagnosis: findings of "type predominance" (author's transl)].
    Marbini A; Parma M; Zampollo A
    Ateneo Parmense Acta Biomed; 1976; 47(2):149-54. PubMed ID: 13802
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)].
    Anosov NN; Saĭkova LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):22-5. PubMed ID: 6952668
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Histochemical aspects of primary and secondary myopathies (author's transl)].
    Bundschu HD; Suchenwirth R
    Fortschr Neurol Psychiatr Grenzgeb; 1973 Aug; 41(8):419-49. PubMed ID: 4147575
    [No Abstract]   [Full Text] [Related]  

  • 4. Motor innervation and fiber type pattern in amyotrophic lateral sclerosis and in Charcot-Marie-Tooth disease.
    Telerman-Toppet N; Coërs C
    Muscle Nerve; 1978; 1(2):133-9. PubMed ID: 155778
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Three cases of Charcot-Marie-Tooth disease with neural deafness-the classification and sural nerve pathology (author's transl)].
    Kim I; Ohnishi A; Kuroiwa Y
    Rinsho Shinkeigaku; 1980 Apr; 20(4):264-70. PubMed ID: 7408330
    [No Abstract]   [Full Text] [Related]  

  • 6. [Histochemico-clinical contribution to the study of infantile myopathies].
    Preto Parvis V; Piria F
    Riv Istochim Norm Patol; 1971 Dec; 17(6):343-71. PubMed ID: 4276022
    [No Abstract]   [Full Text] [Related]  

  • 7. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
    Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM
    Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
    [No Abstract]   [Full Text] [Related]  

  • 8. [Histochemical studies of neuromuscular diseases].
    Okada K
    Shinkei Kenkyu No Shimpo; 1966 Oct; 10(3):565-81. PubMed ID: 6009309
    [No Abstract]   [Full Text] [Related]  

  • 9. [Contribution to enzymatic study in liquor and serum of different amyotrophic entities (author's transl)].
    Nieto Vales JM; Rodríguez Navarro I
    Folia Clin Int (Barc); 1973 Feb; 23(2):86-109. PubMed ID: 4804725
    [No Abstract]   [Full Text] [Related]  

  • 10. [Proceedings: Enzymology of the muscular myelopathic atrophies: enzymologic and ultrastructural study on Charcot-Marie-Tooth disease].
    Rizzoli AA
    Quad Sclavo Diagn; 1973 Mar; 9(1):166-75. PubMed ID: 4788705
    [No Abstract]   [Full Text] [Related]  

  • 11. [Morphological studies of peripheral nerves for a better understanding of Charcot-Marie-Tooth atrophy and Roussy-Lévy hereditary areflexic dysstasia].
    Lapresle J
    Ann Med Interne (Paris); 1980; 131(7):397-400. PubMed ID: 7224445
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Chronic distal spinal amyotrophy or spinal forms of Charcot-Marie disease. A report on six sporadic adult cases (author's transl)].
    Serratrice G; Gastaut JL
    Rev Neurol (Paris); 1979; 135(11):815-26. PubMed ID: 555021
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Early diagnosis and differentiation of Charcot-Marie neural atrophy].
    Lobzin VS; Saĭkova LA; Poliakova LA; Kosachev VD
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1601-5. PubMed ID: 6524176
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enzyme histochemistry of skeletal muscle. 3. Neurogenic muscular atrophies.
    Dubowitz V
    J Neurol Neurosurg Psychiatry; 1966 Feb; 29(1):23-8. PubMed ID: 4379649
    [No Abstract]   [Full Text] [Related]  

  • 15. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)].
    Sadaba Garay F; Franco Vicario R; Miguel de la Villa F; Ibarmia Lahuerta J; Bustamante Murga V
    Med Clin (Barc); 1980 Oct; 75(6):240-6. PubMed ID: 7421358
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Charcot-Marie-Tooth neural muscular atrophy (HMSN type I) with isolated tumerous hypertrophy of the median nerve].
    Berger W; Goth D; Ketelsen U
    Nervenarzt; 1982 Dec; 53(12):725-8. PubMed ID: 7155235
    [No Abstract]   [Full Text] [Related]  

  • 17. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K; Tsubaki T; Ikuta F
    Rinsho Shinkeigaku; 1977 Jan; 17(1):52-7. PubMed ID: 557401
    [No Abstract]   [Full Text] [Related]  

  • 18. Serum enzymes in peroneal muscular atrophy (Charcot-Marie-Tooth disease).
    Switala KJ; Robinson N; Sances A; Larson S; Evans SM; Pintar K
    Wis Med J; 1977 Jan; 76(1):S4-6. PubMed ID: 835307
    [No Abstract]   [Full Text] [Related]  

  • 19. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A case of central core disease. Light microscopic and histochemical studies (author's transl)].
    Meerbach W; Gräbner R
    Zentralbl Allg Pathol; 1977; 121(1-2):169-76. PubMed ID: 848174
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.