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: 8815169)

  • 21. [Rhabdomyolysis in carnitine palmitoyltransferase II deficiency: developments in pathophysiology, diagnosis and therapy].
    Imoberdorf R; Krähenbühl S; Krapf R
    Schweiz Med Wochenschr; 1998 Jun; 128(25):1024-9. PubMed ID: 9691338
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Muscular carnitine palmitoyltransferase II deficiency in infancy.
    Hurvitz H; Klar A; Korn-Lubetzki I; Wanders RJ; Elpeleg ON
    Pediatr Neurol; 2000 Feb; 22(2):148-50. PubMed ID: 10738923
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency.
    Corti S; Bordoni A; Ronchi D; Musumeci O; Aguennouz M; Toscano A; Lamperti C; Bresolin N; Comi GP
    J Neurol Sci; 2008 Mar; 266(1-2):97-103. PubMed ID: 17936304
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel mutations associated with carnitine palmitoyltransferase II deficiency.
    Taggart RT; Smail D; Apolito C; Vladutiu GD
    Hum Mutat; 1999; 13(3):210-20. PubMed ID: 10090476
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Myoglobinuria due to a deficiency of carnitine palmitoyltransferase II. A clinical case report].
    Venturini E; Pupeschi L
    Recenti Prog Med; 1994 May; 85(5):282-3. PubMed ID: 8023007
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Carnitine palmitoyltransferase deficiency in a college athlete: a case report and literature review.
    Faigel HC
    J Am Coll Health; 1995 Sep; 44(2):51-4. PubMed ID: 7593992
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: studies with malonyl-CoA suggest absence of only CPT-II.
    Trevisan CP; Angelini C; Freddo L; Isaya G; Martinuzzi A
    Neurology; 1984 Mar; 34(3):353-6. PubMed ID: 6538275
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Carnitine palmitoyl transferase II deficiency in an adolescent presenting with rhabdomyolysis and acute renal failure.
    Topçu Y; Bayram E; Karaoğlu P; Yiş U; Bayram M; Kurul SH
    Pediatr Emerg Care; 2014 May; 30(5):343-4. PubMed ID: 24786990
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene.
    Vladutiu GD; Bennett MJ; Smail D; Wong LJ; Taggart RT; Lindsley HB
    Mol Genet Metab; 2000 Jun; 70(2):134-41. PubMed ID: 10873395
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. An ignored cause of red urine in children: rhabdomyolysis due to carnitine palmitoyltransferase II (CPT-II) deficiency.
    Melek E; Bulut FD; Atmış B; Yılmaz BŞ; Bayazıt AK; Mungan NÖ
    J Pediatr Endocrinol Metab; 2017 Feb; 30(2):237-239. PubMed ID: 28085674
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A novel mutation identified in carnitine palmitoyltransferase II deficiency.
    Yang BZ; Ding JH; Roe D; Dewese T; Day DW; Roe CR
    Mol Genet Metab; 1998 Feb; 63(2):110-5. PubMed ID: 9562964
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Adult-onset carnitine palmitoyl transferase II (CPT II) deficiency presenting with rhabdomyolysis and acute kidney injury.
    Akar HT; Yıldız Y; Mutluay R; Tekin E; Tokatlı A
    CEN Case Rep; 2024 Apr; 13(2):81-85. PubMed ID: 37341884
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Regulatory properties of a mutant carnitine palmitoyltransferase in human skeletal muscle.
    Zierz S; Engel AG
    Eur J Biochem; 1985 May; 149(1):207-14. PubMed ID: 3996401
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical Features.
    Lehmann D; Motlagh L; Robaa D; Zierz S
    Int J Mol Sci; 2017 Jan; 18(1):. PubMed ID: 28054946
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Carnitine palmitoyltransferase deficiency in a patient with severe psychomotor retardation].
    Suzuki H; Hirayama Y; Hirano S; Takahashi R; Nonaka I; Sugie H; Sugiyama N
    No To Hattatsu; 1991 Jan; 23(1):93-7. PubMed ID: 1995000
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Molecular analysis of a patient with carnitine palmitoyltransferase II deficiency].
    Akanuma J; Wataya K; Matubara Y; Yamamoto T; Kira J; Narisawa K
    Rinsho Shinkeigaku; 1997 Jun; 37(6):532-5. PubMed ID: 9366186
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
    Herman J; Nadler HL
    J Pediatr; 1977 Aug; 91(2):247-50. PubMed ID: 874682
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.