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 *

99 related articles for article (PubMed ID: 6726538)

  • 1. Congenital anomalies in glutaric aciduria type 2.
    Mitchell G; Saudubray JM; Gubler MC; Habib R; Ogier H; Frezal J; Boue J
    J Pediatr; 1984 Jun; 104(6):961-2. PubMed ID: 6726538
    [No Abstract]   [Full Text] [Related]  

  • 2. Late-onset type II glutaric aciduria with massive pericardial effusion associated with severe fatty liver.
    Hirose S; Hamamoto K; Yoshida I; Inokuchi T; Kogo T; Mitsudome A
    Acta Paediatr; 2000 Jul; 89(7):887-8. PubMed ID: 10943977
    [No Abstract]   [Full Text] [Related]  

  • 3. Glutaric aciduria type II: review of the phenotype and report of an unusual glomerulopathy.
    Wilson GN; de Chadarévian JP; Kaplan P; Loehr JP; Frerman FE; Goodman SI
    Am J Med Genet; 1989 Mar; 32(3):395-401. PubMed ID: 2658591
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe clinical course with recurrent hyperpyrexia in a patient with glutaric aciduria type I.
    Hauser SE; Boneh A
    Neuropediatrics; 1999 Feb; 30(1):51-2. PubMed ID: 10222465
    [No Abstract]   [Full Text] [Related]  

  • 5. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II. Morphology and pathogenesis.
    Böhm N; Uy J; Kiessling M; Lehnert W
    Eur J Pediatr; 1982 Sep; 139(1):60-5. PubMed ID: 7173260
    [No Abstract]   [Full Text] [Related]  

  • 6. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.
    Lehnert W; Wendel U; Lindenmaier S; Böhm N
    Eur J Pediatr; 1982 Sep; 139(1):56-9. PubMed ID: 7173259
    [No Abstract]   [Full Text] [Related]  

  • 7. Glutaric aciduria Type II.
    Sweetman L; Nyhan WL; Tauner DA; Merritt TA; Singh M
    J Pediatr; 1980 Jun; 96(6):1020-6. PubMed ID: 7373461
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Glutaric aciduria type I.
    Muranjan MM; Kantharia V; Bavdekar SB; Ursekar M
    Indian Pediatr; 2001 Oct; 38(10):1148-54. PubMed ID: 11677304
    [No Abstract]   [Full Text] [Related]  

  • 9. Glutaric aciduria. A "common" metabolic disorder?
    Kyllerman M; Steen G
    Arch Fr Pediatr; 1980 Apr; 37(4):279. PubMed ID: 7406647
    [No Abstract]   [Full Text] [Related]  

  • 10. Outcome of three cases of untreated maternal glutaric aciduria type I.
    Garcia P; Martins E; Diogo L; Rocha H; Marcão A; Gaspar E; Almeida M; Vaz C; Soares I; Barbot C; Vilarinho L
    Eur J Pediatr; 2008 May; 167(5):569-73. PubMed ID: 17661081
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Glutaric aciduria type II: multiple defects in isolated muscle mitochondria and deficient beta-oxidation in fibroblasts.
    Mooy PD; Giesberts MA; van Gelderen HH; Scholte HR; Luyt-Houwen IE; Przyrembel H; Blom W
    J Inherit Metab Dis; 1984; 7 Suppl 2():101-2. PubMed ID: 6434854
    [No Abstract]   [Full Text] [Related]  

  • 12. Glutaric aciduria type 1: a clinician's view of progress.
    Strauss KA
    Brain; 2005 Apr; 128(Pt 4):697-9. PubMed ID: 15788552
    [No Abstract]   [Full Text] [Related]  

  • 13. Glutaric aciduria type I: a neuroimaging diagnosis?
    Santos CC; Roach ES
    J Child Neurol; 2005 Jul; 20(7):588-90. PubMed ID: 16159525
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Glutaric aciduria type I diagnosed after poliovirus immunization: magnetic resonance findings.
    Alkan A; Baysal T; Yakinci C; Sigirci A; Kutlu R
    Pediatr Neurol; 2002 May; 26(5):405-7. PubMed ID: 12057806
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Abuse or metabolic disorder?
    Hoffmann GF; Naughten ER
    Arch Dis Child; 1998 Apr; 78(4):399. PubMed ID: 9623419
    [No Abstract]   [Full Text] [Related]  

  • 16. Riboflavin responsive glutaric aciduria type II.
    Gregersen N; Rhead W; Christensen E
    Prog Clin Biol Res; 1990; 321():477-94. PubMed ID: 2183240
    [No Abstract]   [Full Text] [Related]  

  • 17. Postnatal and antenatal laboratory diagnosis of glutaric aciduria II in a South African family.
    Henderson HE; Balla R; de Jong G; Piek CJ; Mienie LJ; Erasmus E
    S Afr Med J; 1987 May; 71(9):589-91. PubMed ID: 3576410
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder.
    Coude FX; Ogier H; Charpentier C; Thomassin G; Checoury A; Amedee-Manesme O; Saudubray JM; Frezal J
    Hum Genet; 1981; 59(3):263-5. PubMed ID: 7199025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. D-2-hydroxyglutaric aciduria in association with spondyloenchondromatosis.
    Talkhani IS; Saklatvala J; Dwyer J
    Skeletal Radiol; 2000 May; 29(5):289-92. PubMed ID: 10883451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nephrocalcinosis and medullary cysts in 3-methylglutaconic aciduria.
    Laube GF; Leonard JV; van't Hoff WG
    Pediatr Nephrol; 2003 Jul; 18(7):712-3. PubMed ID: 12750979
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.