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 *

68 related articles for article (PubMed ID: 1182012)

  • 1. [Proceedings: Paroxysmal, idiopathic and familial myoglobinuria].
    Nuyts JP; Bombart E; Deconinck B; Maeker B
    Arch Fr Pediatr; 1975 May; 32(5):495. PubMed ID: 1182012
    [No Abstract]   [Full Text] [Related]  

  • 2. [Paroxysmal idiopathic myoglobinuria].
    Mensi E; Bini P
    Minerva Nipiol; 1968; 18():Suppl 6:347+. PubMed ID: 4910415
    [No Abstract]   [Full Text] [Related]  

  • 3. [Biochemical and electron optical studies in a case of idiopathic paroxysmal myoglobinuria].
    Lechner K; Moser K; Stockinger L
    Beitr Pathol Anat; 1966 Aug; 134(1):65-83. PubMed ID: 5990972
    [No Abstract]   [Full Text] [Related]  

  • 4. [Idiopathic paroxysmal myoglobulinuria].
    Mallet R; Ribierre M; Labrune B; Reyrole L
    Bull Mem Soc Med Hop Paris; 1965 Apr; 116(8):785-801. PubMed ID: 5835634
    [No Abstract]   [Full Text] [Related]  

  • 5. [A case of familial paroxysmal myoglobinuria. Possible pathogenetic interpretation].
    Pirrelli A
    Minerva Med; 1966 Jul; 57(59):2627-34. PubMed ID: 5942383
    [No Abstract]   [Full Text] [Related]  

  • 6. [Case of idiopathic paroxysmal myoglobinuria].
    Akamatsu H; Irie Y; Tsuji M; Matsubara T
    Saishin Igaku; 1971 May; 26(5):980-8. PubMed ID: 5560173
    [No Abstract]   [Full Text] [Related]  

  • 7. Idiopathic muscle necrosis with apparent myoglobinuria in Macaca arctoides.
    Seibold HR; Roberts JA; Wolf RH
    Lab Anim Sci; 1971 Apr; 21(2):242-6. PubMed ID: 4325698
    [No Abstract]   [Full Text] [Related]  

  • 8. [Further contribution to the knowledge of human myoglobinuria].
    Vallarino G; Merlini M; Farina MG
    Minerva Pediatr; 1969 Mar; 21(10):417-25. PubMed ID: 5777644
    [No Abstract]   [Full Text] [Related]  

  • 9. Familial paroxysmal rhabdomyolysis in children. A myoglobinuric syndrome.
    Favara BE; Vawter GF; Wagner R; Kevy S; Porter EG
    Am J Med; 1967 Feb; 42(2):196-207. PubMed ID: 6018531
    [No Abstract]   [Full Text] [Related]  

  • 10. [Creatininphosphokinase isoenzymes in anaesthesia-induced myoglobinuria (AIM) (author's transl)].
    Bernhardt D; Hörder MH
    Anaesthesist; 1981 Mar; 30(3):131-3. PubMed ID: 7224141
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Morphological study of somatic muscles in alimentary-toxic paroxysmal myoglobinuria].
    Nepomniashchikh LM; Bakarev MA
    Biull Eksp Biol Med; 1996 Feb; 121(2):228-33. PubMed ID: 9026138
    [No Abstract]   [Full Text] [Related]  

  • 12. [Myoglobinuria and familial hematuria with dominant autosomal transmission: mitochondrial disorder or basal lamina disorder?].
    Martin-Du Pan RC; Martin-Du Pan R; Bottani A; Morris M; Bordier B; Myers P; Junod A; Favre H
    Rev Med Suisse Romande; 1996 Sep; 116(9):735-41. PubMed ID: 8966475
    [No Abstract]   [Full Text] [Related]  

  • 13. Necrosis and regeneration of muscle in paroxysmal idiopathic myoglobinuria: electron microscopic observations.
    Schutta HS; Kelly AM; Zacks SI
    Brain; 1969 Mar; 92(1):191-202. PubMed ID: 5774027
    [No Abstract]   [Full Text] [Related]  

  • 14. [Laboratory diagnosis of primary idiopathic myoglobinuria].
    Kal'nova LI; Aver'ianov IuN
    Lab Delo; 1981; (2):81-4. PubMed ID: 6163920
    [No Abstract]   [Full Text] [Related]  

  • 15. [Idiopathic paroxysmal rhabdomyolysis or essential myoglobinuria (Meyer-Betz disease)].
    Michel M
    Pediatrie; 1967 Sep; 22(6):743-6. PubMed ID: 5621103
    [No Abstract]   [Full Text] [Related]  

  • 16. [Familial parocystic rhabdomyolysis in children].
    Rev Clin Esp; 1968 Jun; 109(6):536-9. PubMed ID: 5719728
    [No Abstract]   [Full Text] [Related]  

  • 17. Familial myoglobinuria. A study of muscle and kidney pathophysiology in three brothers.
    Christensen TE; Saxtrup O; Hansen TI; Kristensen BH; Beck BL; Plesner T; Krogh IM; Andersen V; Strandgaard S
    Dan Med Bull; 1983 Mar; 30(2):112-5. PubMed ID: 6851679
    [No Abstract]   [Full Text] [Related]  

  • 18. Mitochondrial DNA deletions in inherited recurrent myoglobinuria.
    Ohno K; Tanaka M; Sahashi K; Ibi T; Sato W; Yamamoto T; Takahashi A; Ozawa T
    Ann Neurol; 1991 Apr; 29(4):364-9. PubMed ID: 1929207
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Paroxysmal myoglobinuria. Biochemical study and morphologic study by electron microscope].
    Casenave C; Lamagnere JP; Laugier J; Jobard P; Mouray H; Grenier
    Arch Fr Pediatr; 1972 May; 29(5):539-49. PubMed ID: 4655649
    [No Abstract]   [Full Text] [Related]  

  • 20. Idiopathic rhabdomyolysis in children.
    Ghatak NR; Erenberg G; Hirano A; Golden GS
    J Neurol Sci; 1973 Nov; 20(3):253-68. PubMed ID: 4762944
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.