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: 8283368)

  • 21. Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis.
    Tein I; Christodoulou J; Donner E; McInnes RR
    J Pediatr; 1994 Jun; 124(6):938-40. PubMed ID: 8201482
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.
    Yang BZ; Ding JH; Dewese T; Roe D; He G; Wilkinson J; Day DW; Demaugre F; Rabier D; Brivet M; Roe C
    Mol Genet Metab; 1998 Aug; 64(4):229-36. PubMed ID: 9758712
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pathophysiological approach to carnitine palmitoyltransferase II deficiencies.
    Demaugre F; Bonnefont JP; Brivet M; Cepanec C; Pollitt RJ; Priestley BL; Saudubray JM; Leroux JP
    Prog Clin Biol Res; 1992; 375():301-8. PubMed ID: 1438375
    [No Abstract]   [Full Text] [Related]  

  • 24. 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]  

  • 25. Genetics of carnitine palmitoyltransferase II deficiencies.
    Wieser T; Deschauer M; Zierz S
    Adv Exp Med Biol; 1999; 466():339-45. PubMed ID: 10709661
    [No Abstract]   [Full Text] [Related]  

  • 26. Partial muscle carnitine palmitoyltransferase-A deficiency. Rhabdomyolysis associated with transiently decreased muscle carnitine content after ibuprofen therapy.
    Ross NS; Hoppel CL
    JAMA; 1987 Jan; 257(1):62-5. PubMed ID: 3783904
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutations.
    Vladutiu GD; Quackenbush EJ; Hainline BE; Albers S; Smail DS; Bennett MJ
    J Pediatr; 2002 Nov; 141(5):734-6. PubMed ID: 12410208
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Lipid storage myopathies--carnitine deficiency, carnitine palmitoyltransferase deficiency, pyruvate decarboxylase deficiency].
    Itagaki Y; Nishitani H
    Nihon Rinsho; 1990 Jul; 48(7):1510-6. PubMed ID: 2402068
    [No Abstract]   [Full Text] [Related]  

  • 30. [Rhabdomyolysis caused by carnitine palmitoyltransferase deficiency].
    Weber M; Goebel HH; Wandel E; Gerken G; DiMauro S; Köhler H
    Med Klin (Munich); 1987 Apr; 82(7-8):297-9. PubMed ID: 3587175
    [No Abstract]   [Full Text] [Related]  

  • 31. [Clinical aspects of disorders of lipid metabolism in humans. II. Carnitine palmitoyltransferase deficiency].
    Czyzewski K
    Neurol Neurochir Pol; 1988; 22(6):548-52. PubMed ID: 3077435
    [No Abstract]   [Full Text] [Related]  

  • 32. [Carnitine in normal subjects and in pathology].
    Odièvre M
    Arch Fr Pediatr; 1984 Dec; 41(10):721-6. PubMed ID: 6398040
    [No Abstract]   [Full Text] [Related]  

  • 33. [Carnitine palmitoyltransferase deficiency (I, II)].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 2001; (33):320-3. PubMed ID: 11462457
    [No Abstract]   [Full Text] [Related]  

  • 34. Reversible asphyxial status in a newborn due to neonatal form of carnitine palmitoyltransferase II deficiency.
    Brucknerova I; Bzduch V; Behulova D; Ferianec V; Dubovicky M; Ujhazy E; Mach M
    Neuro Endocrinol Lett; 2008 Oct; 29(5):627-30. PubMed ID: 18987586
    [TBL] [Abstract][Full Text] [Related]  

  • 35. No carnitine palmitoyltransferase deficiency in skeletal muscle in 18 malignant hyperthermia susceptible individuals.
    Wieser T; Kraft B; Kress HG
    Neuromuscul Disord; 2008 Jun; 18(6):471-4. PubMed ID: 18430572
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Noninvasive evaluation of adult onset myopathy from carnitine palmitoyl transferase II deficiency using proton magnetic resonance spectroscopy.
    Videen JS; Haseler LJ; Karpinski NC; Terkeltaub RA
    J Rheumatol; 1999 Aug; 26(8):1757-63. PubMed ID: 10451074
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Deficiency of carnitine palmitoyltransferase I.
    Bonnefont JP; Haas R; Wolff J; Thuy LP; Buchta R; Carroll JE; Saudubray JM; Demaugre F; Nyhan WL
    J Child Neurol; 1989 Jul; 4(3):198-203. PubMed ID: 2768784
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A case of carnitine palmitoyltransferase II deficiency in human skeletal muscle.
    Singh R; Shepherd IM; Derrick JP; Ramsay RR; Sherratt HS; Turnbull DM
    FEBS Lett; 1988 Dec; 241(1-2):126-30. PubMed ID: 3197828
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
    Demaugre F; Bonnefont JP; Colonna M; Cepanec C; Leroux JP; Saudubray JM
    J Clin Invest; 1991 Mar; 87(3):859-64. PubMed ID: 1999498
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Carnitine palmitoyltransferase II (CPT II) deficiency: genotype-phenotype analysis of 50 patients.
    Joshi PR; Deschauer M; Zierz S
    J Neurol Sci; 2014 Mar; 338(1-2):107-11. PubMed ID: 24398345
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.