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 *

150 related articles for article (PubMed ID: 1065164)

  • 1. [McArdle's disease (a familial case)].
    Shevchenko AM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1976; 76(5):655-9. PubMed ID: 1065164
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical features, diagnosis and treatment of McArdle's glycogenosis].
    Lobzin VS; Saĭkova LA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(3):342-5. PubMed ID: 6586038
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mcardle's disease. A case report.
    Dirik E; Taşkin F; Eroğlu Y; Büyükgebiz B; Selamzade M; Cevik NT
    Turk J Pediatr; 1996; 38(3):355-9. PubMed ID: 8827906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [McArdle's metabolic myopathy].
    Shutov AA; Bessonov AV; Sidorov VV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(10):1485-90. PubMed ID: 4530582
    [No Abstract]   [Full Text] [Related]  

  • 5. [Late diagnosis of a McArdle disease's case (type V glycogenosis)].
    Flavier S; Rolland MO; Eude M; Fédou C; Brun JF; Maire I; Mercier J; Raynaud E
    Ann Biol Clin (Paris); 2007; 65(5):550-4. PubMed ID: 17913675
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Apropos of a further case of absence of phosphorylase in the striated muscle (McArdle's disease)].
    Delwaide PJ; Reznik M; Lemaire R; Lelièvre P; Bonnet F
    Rev Neurol (Paris); 1967 Feb; 116(2):119-40. PubMed ID: 5230980
    [No Abstract]   [Full Text] [Related]  

  • 7. [Glycogenosis (molecular mechanism of muscle glycogenosis)].
    Tarui S; Mineo I; Nakajima H; Kono N
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):637-42. PubMed ID: 3270875
    [No Abstract]   [Full Text] [Related]  

  • 8. McArdle's disease in two generations: autosomal recessive transmission with manifesting heterozygote.
    Schmidt B; Servidei S; Gabbai AA; Silva AC; de Sousa Bulle de Oliveira A; DiMauro S
    Neurology; 1987 Sep; 37(9):1558-61. PubMed ID: 3476861
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [McArdle's disease in adults: clinical and genetic study].
    Olmos JM; Zarrabeitia MT; Valero MC; Figols J; Matorras P; Riancho JA
    Med Clin (Barc); 1997 Nov; 109(19):753-5. PubMed ID: 9470186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Variable presentation of the clinical phenotype of McArdle's disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene.
    Paradas C; Fernandez-Cadenas I; Gallardo E; Lligé D; Arenas J; Illa I; Andreu AL
    Neurosci Lett; 2005 Dec; 391(1-2):28-31. PubMed ID: 16154688
    [TBL] [Abstract][Full Text] [Related]  

  • 11. McArdle disease in a Druze family.
    Sarova-Pinhas I; Sadeh M
    Isr J Med Sci; 1989 Feb; 25(2):64-8. PubMed ID: 2703328
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [McArdle's disease without typical symptoms].
    Watanabe M; Matsubara E; Amari M; Okamoto K; Hirai S
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1247-51. PubMed ID: 2085931
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [McArdle's disease. Apropos of a case].
    Yuste JR; Beloqui O; De la Peña A; Rodríguez-Rosado R; Monreal JI; Prósper F; Prieto J
    Rev Med Univ Navarra; 1998; 42(1):29-33. PubMed ID: 10420954
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exercise intolerance in patients with McArdle's disease or mitochondrial myopathies.
    Chaussain M; Camus F; Defoligny C; Eymard B; Fardeau M
    Eur J Med; 1992 Dec; 1(8):457-63. PubMed ID: 1341204
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [McArdle's disease].
    Löfberg M; Junes M; Seppänen H; Rautakorpi I; Paetau A; Härkönen M; Somer H
    Duodecim; 1993; 109(19):1676-82. PubMed ID: 7736987
    [No Abstract]   [Full Text] [Related]  

  • 16. [McArdle's disease: a case report].
    Levy JA; Gagioti SM; Cavalieri MJ; Pereira JR
    Arq Neuropsiquiatr; 1980 Dec; 38(4):411-4. PubMed ID: 6937160
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [McArdle's disease and dystrophia myotonica].
    Vedeler CA; Gilhus NE; Nyland H; Mørk S
    Tidsskr Nor Laegeforen; 1987 Mar; 107(8):736-8. PubMed ID: 3472368
    [No Abstract]   [Full Text] [Related]  

  • 18. [McArdle's disease: therapeutic use of depot-glucagon].
    Schmid R; Wiethölter H
    Dtsch Med Wochenschr; 1982 Nov; 107(47):1809-11. PubMed ID: 6958445
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myopathy in McArdle's syndrome. Improvement with a high-protein diet.
    Slonim AE; Goans PJ
    N Engl J Med; 1985 Feb; 312(6):355-9. PubMed ID: 3855499
    [No Abstract]   [Full Text] [Related]  

  • 20. Peripheral nerve and vasculature involvement in myophosphorylase deficiency (McArdle's disease).
    Byard RW; Lach B; Preston DN
    Pathology; 1991 Jan; 23(1):62-5. PubMed ID: 2062570
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.