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Journal Abstract Search

134 related items for PubMed ID: 11596365

  • 1. [Mitochondrial diseases with recurrent myoglobinuria].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001; (36):183-5. PubMed ID: 11596365
    [No Abstract] [Full Text] [Related]

  • 2. Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy.
    Tein I, De Vivo DC, Hale DE, Clarke JT, Zinman H, Laxer R, Shore A, DiMauro S.
    Ann Neurol; 1991 Sep; 30(3):415-9. PubMed ID: 1835339
    [Abstract] [Full Text] [Related]

  • 3. Recurrent myoglobinuria as a presenting manifestation of very long chain acyl coenzyme A dehydrogenase deficiency.
    Straussberg R, Harel L, Varsano I, Elpeleg ON, Shamir R, Amir J.
    Pediatrics; 1997 Jun; 99(6):894-6. PubMed ID: 9164788
    [No Abstract] [Full Text] [Related]

  • 4. [Recurrent myoglobinuria in a girl due to carnitine palmitoyltransferase deficiency].
    Carrasco Marina LL, Ramos Lizana J, Vázquez López M, Garrote de Marcos JM, Arregui Sierra A, Bornstein B, Arenas J.
    An Esp Pediatr; 1996 Jan; 44(1):67-9. PubMed ID: 8849066
    [No Abstract] [Full Text] [Related]

  • 5. [Coenzyme Q10 deficiency].
    Imataka G, Yamanouchi H.
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():462-5. PubMed ID: 12013914
    [No Abstract] [Full Text] [Related]

  • 6. [Fatal infantile mitochondrial disease].
    Murakami N.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr; (36):173-5. PubMed ID: 11596361
    [No Abstract] [Full Text] [Related]

  • 7. [Recurrent myoglobinuria caused by carnitine-palmityl-transferase deficiency].
    Pamies-Andreu E, Sánchez-Román J, Bautista J, Segura DI.
    Rev Clin Esp; 1987 May; 180(8):462-3. PubMed ID: 3616029
    [No Abstract] [Full Text] [Related]

  • 8. Exercise intolerance and the mitochondrial respiratory chain.
    DiMauro S.
    Ital J Neurol Sci; 1999 Dec; 20(6):387-93. PubMed ID: 10937858
    [Abstract] [Full Text] [Related]

  • 9. [Acute recurrent renal insufficiency in a patient with atraumatic rhabdomyolysis caused by carnitine-palmitoyltransferase deficiency].
    Castiglione A, Cornelio F, Vendemia F, Rimoldi M, Sinico R, Baroni M, D'Amico G.
    Minerva Nefrol; 1981 Dec; 28(3):229-34. PubMed ID: 7329599
    [No Abstract] [Full Text] [Related]

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  • 11. [Pure mitochondrial myopathy].
    Murakami N, Sakuta R.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec; (36):186-9. PubMed ID: 11596366
    [No Abstract] [Full Text] [Related]

  • 12. Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Enns GM, Bennett MJ, Hoppel CL, Goodman SI, Weisiger K, Ohnstad C, Golabi M, Packman S.
    J Pediatr; 2000 Feb; 136(2):251-4. PubMed ID: 10657835
    [Abstract] [Full Text] [Related]

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  • 14. Respiratory chain deficiency presenting as recurrent myoglobinuria in childhood.
    de Lonlay-Debeney P, Edery P, Cormier-Daire V, Parfait B, Chrétien D, Rötig A, Romero N, Saudubray JM, Munnich A, Rustin P.
    Neuropediatrics; 1999 Feb; 30(1):42-4. PubMed ID: 10222461
    [Abstract] [Full Text] [Related]

  • 15. Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects.
    Divry P, Vianey-Saban C, Mathieu M.
    J Inherit Metab Dis; 1999 May; 22(3):286-8. PubMed ID: 10384388
    [No Abstract] [Full Text] [Related]

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  • 17. Very-long-chain acyl-coenzyme A dehydrogenase deficiency--a new cause of myoglobinuric acute renal failure.
    Cairns AP, O'Donoghue PM, Patterson VH, Brown JH.
    Nephrol Dial Transplant; 2000 Aug; 15(8):1232-4. PubMed ID: 10910451
    [No Abstract] [Full Text] [Related]

  • 18. Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria.
    Minetti C, Garavaglia B, Bado M, Invernizzi F, Bruno C, Rimoldi M, Pons R, Taroni F, Cordone G.
    Neuromuscul Disord; 1998 Feb; 8(1):3-6. PubMed ID: 9565984
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