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Journal Abstract Search

165 related items for PubMed ID: 2752669

  • 1. [A female case of carnitine palmitoyltransferase deficiency].
    Taniwaki T, Kira J, Kitaguchi T, Goto I, Sugiyama N.
    Rinsho Shinkeigaku; 1989 Mar; 29(3):382-4. PubMed ID: 2752669
    [Abstract] [Full Text] [Related]

  • 2. Carnitine palmitoyltransferase deficiency: a common cause of recurrent myoglobinuria.
    Sadeh M, Gutman A.
    Isr J Med Sci; 1990 Sep; 26(9):510-5. PubMed ID: 2228562
    [Abstract] [Full Text] [Related]

  • 3. Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: clinical, biochemical, and genetic features of adult-onset cases.
    Kilfoyle D, Hutchinson D, Potter H, George P.
    N Z Med J; 2005 Feb 25; 118(1210):U1320. PubMed ID: 15776096
    [Abstract] [Full Text] [Related]

  • 4. [Muscular carnitine-palmityl-transferase deficiency].
    Rumpf KW, Kaiser H, Goebel HH, Wagner HA, Ullmann B, DiMauro S, Scheler F.
    Dtsch Med Wochenschr; 1983 Jul 08; 108(27):1058-61. PubMed ID: 6861647
    [Abstract] [Full Text] [Related]

  • 5. [Myoglobinuria and carnitine palmitoyltransferase deficiency. Diagnostic procedure and differential diagnosis].
    Kiechl S, Kohlendorfer U, Paetzke I, Sperl W, Rainer J, Willeit J.
    Wien Klin Wochenschr; 1994 Jul 08; 106(6):174-7. PubMed ID: 8197749
    [Abstract] [Full Text] [Related]

  • 6. Biochemical and physiologic consequences of carnitine palmityltransferase deficiency.
    Carroll JE, Brooke MH, DeVivo DC, Kaiser KK, Hagberg JM.
    Muscle Nerve; 1978 Jul 08; 1(2):103-10. PubMed ID: 750917
    [Abstract] [Full Text] [Related]

  • 7. [Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].
    Meunier J, Perrot D, Bret M, Pissere-Meunier J, Bouletreau P, Pasquier J, Carrier H, Berthillier G.
    Nouv Presse Med; 1982 Sep 25; 11(37):2767-71. PubMed ID: 7145668
    [Abstract] [Full Text] [Related]

  • 8. [Intolerance to exercise caused by carnitine palmitoyltransferase deficiency].
    Desnuelle C, Pellissier JF, de Barsy T, Serratrice G.
    Rev Neurol (Paris); 1990 Sep 25; 146(3):231-4. PubMed ID: 2184487
    [Abstract] [Full Text] [Related]

  • 9. [Lipid metabolism disorder in skeletal musculature (carnitine palmitoyltransferase deficiency) and paroxysmal myoglobinuria].
    Aver'ianov IuN, Aleksandrovskaia TN, Kal'nova LI, Morozova EA, Shaldaeva VV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1980 Sep 25; 80(11):1623-8. PubMed ID: 6935889
    [Abstract] [Full Text] [Related]

  • 10. Selective carnitine palmitoyltransferase deficiency in fibroblasts from a patient with muscle CPT deficiency.
    Pula TP, Max SR, Zielke HR, Chacon M, Baab P, Gumbinas M, Reed WD.
    Ann Neurol; 1981 Aug 25; 10(2):196-8. PubMed ID: 7283405
    [Abstract] [Full Text] [Related]

  • 11. Metabolic causes of myoglobinuria.
    Tonin P, Lewis P, Servidei S, DiMauro S.
    Ann Neurol; 1990 Feb 25; 27(2):181-5. PubMed ID: 2156480
    [Abstract] [Full Text] [Related]

  • 12. Partial deficiency of muscle carnitine palmitoyltransferase with normal ketone production.
    Hostetler KY, Hoppel CL, Romine JS, Sipe JC, Gross SR, Higginbottom PA.
    N Engl J Med; 1978 Mar 09; 298(10):553-7. PubMed ID: 272487
    [No Abstract] [Full Text] [Related]

  • 13. [Recurrent myoglobinuria caused by carnitine-palmityl-transferase deficiency].
    Pamies-Andreu E, Sánchez-Román J, Bautista J, Segura DI.
    Rev Clin Esp; 1987 May 09; 180(8):462-3. PubMed ID: 3616029
    [No Abstract] [Full Text] [Related]

  • 14. Identification of novel mutations in Spanish patients with muscle carnitine palmitoyltransferase II deficiency.
    Martín MA, Rubio JC, del Hoyo P, García A, Bustos F, Campos Y, Cabello A, Culebras JM, Arenas J.
    Hum Mutat; 2000 Jun 09; 15(6):579-80. PubMed ID: 10862092
    [Abstract] [Full Text] [Related]

  • 15. [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 Jun 09; 28(3):229-34. PubMed ID: 7329599
    [No Abstract] [Full Text] [Related]

  • 16. Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.
    Ionasescu V, Hug G, Hoppel C.
    J Neurol Neurosurg Psychiatry; 1980 Aug 09; 43(8):679-82. PubMed ID: 7431028
    [Abstract] [Full Text] [Related]

  • 17. [Muscle carnitine deficiency associated with myalgia and rhabdomyolysis following exercise].
    Miyajima H, Sakamoto M, Takahashi Y, Mizoguchi K, Nishimura Y.
    Rinsho Shinkeigaku; 1989 Jan 09; 29(1):93-7. PubMed ID: 2743689
    [Abstract] [Full Text] [Related]

  • 18. Muscle carnitine palmitoyltransferase II deficiency: clinical and molecular genetic features and diagnostic aspects.
    Deschauer M, Wieser T, Zierz S.
    Arch Neurol; 2005 Jan 09; 62(1):37-41. PubMed ID: 15642848
    [Abstract] [Full Text] [Related]

  • 19. [Type II carnitine palmitoyl transferase deficiency complicated by acute respiratory failure].
    Joutel A, Moulonguet A, Demaugre F, Janowski M, Lacroix-Jousselin C, Said G.
    Rev Neurol (Paris); 1993 Jan 09; 149(12):797-9. PubMed ID: 7997741
    [Abstract] [Full Text] [Related]

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