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 *

138 related articles for article (PubMed ID: 6837270)

  • 1. Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings.
    Pellegrini G; Moggio M; Cheldi A; Scarlato G; Pistone FM; Picco P
    Acta Neuropathol; 1983; 59(1):70-4. PubMed ID: 6837270
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria.
    Tamura K; Santa T; Kuroiwa Y
    Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial mitochondrial myopathies.
    Walter GF; Tassin S; Brucher JM
    Acta Neuropathol Suppl; 1981; 7():283-6. PubMed ID: 6939253
    [No Abstract]   [Full Text] [Related]  

  • 4. [Neuromuscular mitochondriopathy. A morphological expression of disorders of the energy metabolism (author's transl)].
    Walter GF
    Veroff Pathol; 1981; 117():1-111. PubMed ID: 6210998
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial neuromuscular disease with "myotubes".
    Meyers KR; Golomb HM; Hansen JL; McKusick VA
    Clin Genet; 1974; 5(4):327-37. PubMed ID: 4136736
    [No Abstract]   [Full Text] [Related]  

  • 6. Nemaline myopathy and a mitochondrial neuromuscular disorder in one family.
    Shapira YA; Yarom R; Blank A
    Neuropediatrics; 1981 May; 12(2):152-65. PubMed ID: 6267500
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV.
    Mizusawa H; Watanabe M; Kanazawa I; Nakanishi T; Kobayashi M; Tanaka M; Suzuki H; Nishikimi M; Ozawa T
    J Neurol Sci; 1988 Sep; 86(2-3):171-84. PubMed ID: 2851645
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A familial mitochondrial myopathy with central defect in neural transmission.
    Barron SA; Heffner RR; Zwirecki R
    Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial encephalomyopathies.
    DiMauro S; Bonilla E; Lombes A; Shanske S; Minetti C; Moraes CT
    Neurol Clin; 1990 Aug; 8(3):483-506. PubMed ID: 2170831
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial centronuclear myopathy: a clinical and pathological study.
    Reske-Nielsen E; Hein-Sørensen O; Vorre P
    Acta Neurol Scand; 1987 Aug; 76(2):115-22. PubMed ID: 3673497
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Familial neural mitochondrial deafness].
    Marangos N; Mausolf A
    HNO; 1990 Sep; 38(9):322-5. PubMed ID: 2262349
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [2 cases of mitochondrial encephalomyopathy].
    Parisi L; Mariorenzi R; Renato Valente GO; Caramia M; Palmieri G; Amabile G
    Riv Neurol; 1988; 58(3):110-5. PubMed ID: 3175460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothers.
    Marbini A; Gemignani F; Saccardi F; Rimoldi M
    J Neurol; 1989 Oct; 236(7):418-20. PubMed ID: 2809644
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuromuscular disorders with abnormal muscle mitochondria.
    Kamieniecka Z; Schmalbruch H
    Int Rev Cytol; 1980; 65():321-57. PubMed ID: 6993406
    [No Abstract]   [Full Text] [Related]  

  • 15. Familial nemaline myopathy.
    Scarlato G; Pellegrini G; Moggio M; Meola G; Cordone G; Minetti C; Lester A
    Neuropediatrics; 1982 Nov; 13(4):211-5. PubMed ID: 6296713
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Myopathy with pathological features of both centronuclear myopathy and multicore disease.
    Fitzsimons RB; McLeod JG
    J Neurol Sci; 1982 Dec; 57(2-3):395-405. PubMed ID: 7161626
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Concentric laminated bodies in muscle pathology.
    Gambarelli D; Hassoun J; Pellissier JF; Berard M; Toga M
    Pathol Eur; 1974; 9(4):289-96. PubMed ID: 4457782
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Recent diagnostic and pathogenetic aspects of neuromuscular diseases].
    Gullotta F
    Pathologica; 1985; 77(1048):121-31. PubMed ID: 3909086
    [No Abstract]   [Full Text] [Related]  

  • 19. Psychiatric disturbance in mitochondrial encephalomyopathy.
    Suzuki T; Koizumi J; Shiraishi H; Ofuku K; Sasaki M; Hori T; Oskoshi N
    J Neurol Neurosurg Psychiatry; 1989 Jul; 52(7):920-2. PubMed ID: 2769294
    [No Abstract]   [Full Text] [Related]  

  • 20. Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees.
    Bethlem J; Wijngaarden GK
    Brain; 1976 Mar; 99(1):91-100. PubMed ID: 963533
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.