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: 9475600)

  • 21. Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.
    Elias E; Gray RG; Poulton K; Green A
    J Hepatol; 1997 Feb; 26(2):433-6. PubMed ID: 9059968
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ethylmalonic Aciduria in an Infant with Neurological and Skin Presentation.
    Peake RWA; Rodan LH
    Clin Chem; 2017 Nov; 63(11):1771-1773. PubMed ID: 29089323
    [No Abstract]   [Full Text] [Related]  

  • 23. Congenital Brain and Spinal Cord Malformations and Their Associated Cutaneous Markers.
    Dias M; Partington M;
    Pediatrics; 2015 Oct; 136(4):e1105-19. PubMed ID: 26416933
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Pachygyria in Weaver syndrome.
    Freeman BM; Hoon AH; Breiter SN; Hamosh A
    Am J Med Genet; 1999 Oct; 86(4):395-7. PubMed ID: 10494098
    [No Abstract]   [Full Text] [Related]  

  • 25. Vertebral column and spinal cord malformation in children with exstrophy of the cloaca, with emphasis on their functional correlates.
    Weaver KB; Matthews H; Chegini S; King H; Shurtleff DB; McLaughlin JF
    Teratology; 1997 Apr; 55(4):241-8. PubMed ID: 9216041
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency.
    Lehnert W; Ruitenbeek W
    J Inherit Metab Dis; 1993; 16(3):557-9. PubMed ID: 7609451
    [No Abstract]   [Full Text] [Related]  

  • 27. Mild form of 3-methylglutaconic aciduria type IV and mutation in the TMEM70 genes.
    Stojanović V; Doronjski A
    J Pediatr Endocrinol Metab; 2013; 26(1-2):151-4. PubMed ID: 23382305
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Central nervous system malformations in the CHARGE association.
    Lin AE; Siebert JR; Graham JM
    Am J Med Genet; 1990 Nov; 37(3):304-10. PubMed ID: 2260555
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Methylmalonic aciduria. Study of its occurrence in clinical material].
    Kastrup KW
    Ugeskr Laeger; 1968 Jun; 130(25):1056-8. PubMed ID: 4302991
    [No Abstract]   [Full Text] [Related]  

  • 30. [Progress in pediatric neurology].
    Landrieu P
    Rev Neurol (Paris); 2000 Jul; 156(6-7):595-605. PubMed ID: 10891793
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Iniencephaly: a neuropathologic study.
    Aleksic S; Budzilovich G; Greco MA; Feigin I; Epstein F; Pearson J
    Clin Neuropathol; 1983; 2(2):55-61. PubMed ID: 6851297
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines.
    Rinaldo P; Welch RD; Previs SF; Schmidt-Sommerfeld E; Gargus JJ; O'Shea JJ; Zinn AB
    Pediatr Res; 1991 Sep; 30(3):216-21. PubMed ID: 1945558
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.
    Kang ES; Snodgrass PJ; Gerald PS
    Pediatr Res; 1972 Dec; 6(12):875-9. PubMed ID: 4643536
    [No Abstract]   [Full Text] [Related]  

  • 34. Relationship of cine phase-contrast magnetic resonance imaging with outcome after decompression for Chiari I malformations.
    McGirt MJ; Nimjee SM; Fuchs HE; George TM
    Neurosurgery; 2006 Jul; 59(1):140-6; discussion 140-6. PubMed ID: 16823310
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Interstitial deletion of the long arm of chromosome 1 (1q 25-32). Clinical and endocrine features with a long term follow-up.
    Maggio MC; Iachininoto R; Arena V; Liotta A
    Minerva Pediatr; 2003 Feb; 55(1):55-9, 59-61. PubMed ID: 12660627
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The use of neomycin in the treatment of methylmalonic aciduria.
    Snyderman SE; Sansaricq C; Norton P; Phansalkar SV
    Pediatrics; 1972 Dec; 50(6):925-7. PubMed ID: 4636459
    [No Abstract]   [Full Text] [Related]  

  • 37. Vertebral defects in patients with Peters plus syndrome and mutations in B3GALTL.
    Faletra F; Athanasakis E; Minen F; Fornasier F; Marchetti F; Gasparini P
    Ophthalmic Genet; 2011 Nov; 32(4):256-8. PubMed ID: 21671750
    [No Abstract]   [Full Text] [Related]  

  • 38. The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
    Amendt BA; Rhead WJ
    J Clin Invest; 1986 Jul; 78(1):205-13. PubMed ID: 3722376
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria.
    Coulombe JT; Shih VE; Levy HL
    Pediatrics; 1981 Jan; 67(1):26-31. PubMed ID: 7243433
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Syrinx location and size according to etiology: identification of Chiari-associated syrinx.
    Strahle J; Muraszko KM; Garton HJ; Smith BW; Starr J; Kapurch JR; Maher CO
    J Neurosurg Pediatr; 2015 Jul; 16(1):21-9. PubMed ID: 25837888
    [TBL] [Abstract][Full Text] [Related]  

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