BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 7781210)

  • 1. [Clinical and biochemical analysis of 27 patients with myoglobinuria of unknown causes].
    Tsurui S; Sugie H; Ito M; Igarashi Y
    Rinsho Shinkeigaku; 1995 Jan; 35(1):24-8. PubMed ID: 7781210
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

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

  • 4. Recurrent childhood myoglobinuria.
    Tein I; DiMauro S; DeVivo DC
    Adv Pediatr; 1990; 37():77-117. PubMed ID: 2264536
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Biochemical analysis using biopsied muscle in 72 patients with metabolic myopathies].
    Sugie H; Tsurui S; Sugie Y; Suzuki M; Miyamoto R
    Rinsho Shinkeigaku; 1989 May; 29(5):584-7. PubMed ID: 2791407
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Exercise-induced muscular weakness, myalgia and contractures. I. A clinical review].
    Mattle H; Jerusalem F
    Schweiz Med Wochenschr; 1977 Apr; 107(13):428-36. PubMed ID: 139680
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Metabolic myopathies: evaluation by graded exercise testing.
    Elliot DL; Buist NR; Goldberg L; Kennaway NG; Powell BR; Kuehl KS
    Medicine (Baltimore); 1989 May; 68(3):163-72. PubMed ID: 2716515
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fuel utilization in subjects with carnitine palmitoyltransferase 2 gene mutations.
    Ørngreen MC; Dunø M; Ejstrup R; Christensen E; Schwartz M; Sacchetti M; Vissing J
    Ann Neurol; 2005 Jan; 57(1):60-6. PubMed ID: 15622536
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. 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]  

  • 14. Trifunctional enzyme deficiency: adult presentation of a usually fatal beta-oxidation defect.
    Schaefer J; Jackson S; Dick DJ; Turnbull DM
    Ann Neurol; 1996 Oct; 40(4):597-602. PubMed ID: 8871579
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Lipidic myopathies].
    Muñoz-Blanco JL
    Rev Neurol; 1998 Apr; 26 Suppl 1():S72-80. PubMed ID: 9810593
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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; 106(6):174-7. PubMed ID: 8197749
    [TBL] [Abstract][Full Text] [Related]  

  • 17. In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: limited diagnostic use of 1-13C fatty acid breath test using bolus technique.
    Jakobs C; Kneer J; Martin D; Boulloche J; Brivet M; Poll-The BT; Saudubray JM
    Eur J Pediatr; 1997 Aug; 156 Suppl 1():S78-82. PubMed ID: 9266222
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Metabolic myopathies: update 2009.
    van Adel BA; Tarnopolsky MA
    J Clin Neuromuscul Dis; 2009 Mar; 10(3):97-121. PubMed ID: 19258857
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 7.