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 *

107 related articles for article (PubMed ID: 6685833)

  • 1. Idiopathic recurrent myoglobinuria and persistent weakness.
    Bermils C; Tassin S; Brucher JM; de Barsy T
    Neurology; 1983 Dec; 33(12):1613-5. PubMed ID: 6685833
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Acute alcoholic myopathy, rhabdomyolysis and acute renal failure: a case report.
    Singh S; Sharma A; Sharma S; Sud A; Wanchu A; Bambery P
    Neurol India; 2000 Mar; 48(1):84-5. PubMed ID: 10751822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pseudometabolic presentation of dystrophinopathy due to a missense mutation.
    Veerapandiyan A; Shashi V; Jiang YH; Gallentine WB; Schoch K; Smith EC
    Muscle Nerve; 2010 Dec; 42(6):975-9. PubMed ID: 21104870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Necrotizing vacuolar myopathy presenting with recurrent myoglobinuria.
    Nandhagopal R; Al-Asmi A; Arunodaya GR; Jacob PC; Al-Azri F; Harper C
    Int J Neurosci; 2010 Dec; 120(12):784-6. PubMed ID: 20942590
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Idiopathic rhabdomyolysis.
    Savage DC; Forbes M; Pearce GW
    Arch Dis Child; 1971 Oct; 46(249):594-607. PubMed ID: 4107384
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A fatal case of acute polymyositis with persistent myoglobinuria and progressive renal failure.
    Misra A; Singh RR; Kapoor SK; Kumar A; Malaviya AN
    J Assoc Physicians India; 1988 Feb; 36(2):153-4. PubMed ID: 3182644
    [No Abstract]   [Full Text] [Related]  

  • 7. Enhydrina schistosa (Elapidae: Hydrophiinae) the most dangerous sea snake in Sri Lanka: three case studies of severe envenoming.
    Kularatne SA; Hettiarachchi R; Dalpathadu J; Mendis AS; Appuhamy PD; Zoysa HD; Maduwage K; Weerasinghe VS; de Silva A
    Toxicon; 2014 Jan; 77():78-86. PubMed ID: 24239658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Rhabdomyolysis and myoglobinuria].
    Lindner A; Zierz S
    Nervenarzt; 2003 Jun; 74(6):505-15. PubMed ID: 12799789
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An adolescent girl with Meyer-Betz syndrome.
    Kasap B; Soylu A; Türkmen M; Kavukcu S
    Clin Rheumatol; 2006 Nov; 25(6):904-6. PubMed ID: 16328090
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent myoglobinuria and HIV seropositivity: incidental or pathogenic association?
    Younger DS; Hays AP; Uncini A; Lange DJ; Lovelace RE; DiMauro S
    Muscle Nerve; 1989 Oct; 12(10):842-3. PubMed ID: 2608081
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Metabolic Myoglobinuria.
    Barca E; Emmanuele V; DiMauro SB
    Curr Neurol Neurosci Rep; 2015 Oct; 15(10):69. PubMed ID: 26319173
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myoglobinuria.
    David WS
    Neurol Clin; 2000 Feb; 18(1):215-43. PubMed ID: 10658177
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Acute rhabdomyolysis, myoglobinuria and renal insufficiency caused by ethanol: review of the literature and description of a clinical case with fatal outcome].
    Piazza I; Girardi A
    G Clin Med; 1989 Nov; 70(11):661-9. PubMed ID: 2599288
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low succinate dehydrogenase (SDH) activity in a patient with a hereditary myopathy with paroxysmal myoglobinuria.
    Linderholm H; Essén-Gustavsson B; Thornell LE
    J Intern Med; 1990 Jul; 228(1):43-52. PubMed ID: 2384736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Idiopathic recurrent rhabdomyolysis with myoglobinuria. Case report, with diagnostic recommendations and demonstration of unusual heme compounds in the urine.
    KOSSMANN RJ; CAMP WA; ENGLE RL
    Am J Med; 1963 Apr; 34():554-64. PubMed ID: 14035019
    [No Abstract]   [Full Text] [Related]  

  • 16. Mitochondrial trifunctional protein deficiency associated with recurrent myoglobinuria in adolescence.
    Miyajima H; Orii KE; Shindo Y; Hashimoto T; Shinka T; Kuhara T; Matsumoto I; Shimizu H; Kaneko E
    Neurology; 1997 Sep; 49(3):833-7. PubMed ID: 9305349
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Non-traumatic acute rhabdomyolysis.
    Taly AB; Nair KP; Arunodaya GR; Das S; Christopher R; Mohan C; Swamy HS
    Neurol India; 1999 Mar; 47(1):51-4. PubMed ID: 10339709
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Myoglobinuria and the kidney].
    Shigematsu H
    Rinsho Byori; 1991 Feb; 39(2):148-55. PubMed ID: 2041212
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Carnitine palmitoyltransferase type 2 deficiency: novel mutation in a Native South American family with whole-body muscle magnetic resonance imaging findings: two case reports.
    Avila-Smirnow D; Boutron A; Beytía-Reyes MLÁ; Contreras-Olea O; Caicedo-Feijoo A; Gejman-Enríquez R; Escobar-Henríquez R; Förster-Mujica J
    J Med Case Rep; 2018 Aug; 12(1):249. PubMed ID: 30149802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rhabdomyolysis with cardiac and respiratory involvement.
    Wynne JW; Goslen JB; Ballinger WE
    South Med J; 1977 Sep; 70(9):1125-7, 1130. PubMed ID: 897741
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.