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 *

133 related articles for article (PubMed ID: 750917)

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

  • 2. A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase.
    Bank WJ; DiMauro S; Bonilla E; Capuzzi DM; Rowland LP
    N Engl J Med; 1975 Feb; 292(9):443-9. PubMed ID: 123038
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 149(12):797-9. PubMed ID: 7997741
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 298(10):553-7. PubMed ID: 272487
    [No Abstract]   [Full Text] [Related]  

  • 7. Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.
    Bertorini T; Yeh YY; Trevisan C; Stadlan E; Sabesin S; DiMauro S
    Neurology; 1980 Mar; 30(3):263-71. PubMed ID: 7189025
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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; 80(11):1623-8. PubMed ID: 6935889
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Disorders of lipid metabolism in muscle.
    Di Mauro S; Trevisan C; Hays A
    Muscle Nerve; 1980; 3(5):369-88. PubMed ID: 7421873
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial combined deficiency of muscle carnitine and carnitine palmityl transferase (CPT).
    Skard Heier M; Dietrichson P; Landaas S
    Acta Neurol Scand; 1986 Dec; 74(6):479-85. PubMed ID: 3825503
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 118(1210):U1320. PubMed ID: 15776096
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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; 11(37):2767-71. PubMed ID: 7145668
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial deficiency of carnitine palmityltransferase: physiologic and biochemical consequences.
    Layzer RB; Havel RJ; McIlroy MB
    Neurology; 1980 Jun; 30(6):627-33. PubMed ID: 7189839
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. 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; 10(2):196-8. PubMed ID: 7283405
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. [Myopathy due to carnitine palmitoyltransferase deficiency. Report of 2 cases with enzymatic analyses on muscle tissue].
    Werneck LC; Boer CA; Papadimitriou A; Di Mauro S
    Arq Neuropsiquiatr; 1983 Dec; 41(4):377-84. PubMed ID: 6661102
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. Rhabdomyolysis and respiratory failure: rare presentation of carnitine palmityl-transferase II deficiency.
    Gentili A; Iannella E; Masciopinto F; Latrofa ME; Giuntoli L; Baroncini S
    Minerva Anestesiol; 2008 May; 74(5):205-8. PubMed ID: 18414363
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency.
    Stanley CA
    Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.