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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

139 related items for PubMed ID: 6823975

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. Argininosuccinate synthetase activity in cultured skin fibroblasts of citrullinemic patients.
    Saheki T, Ueda A, Iizima K, Yamada N, Kobayashi K, Takahashi K, Katsunuma T.
    Clin Chim Acta; 1982 Jan 05; 118(1):93-7. PubMed ID: 7053910
    [Abstract] [Full Text] [Related]

  • 43. Genetic variations in proteins of the amniotic fluid.
    Roychoudhury A, Talukder G, Sharma A.
    Obstet Gynecol Surv; 1978 Oct 05; 33(10):627-40. PubMed ID: 368692
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45. Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia.
    Kobayashi K, Jackson MJ, Tick DB, O'Brien WE, Beaudet AL.
    J Biol Chem; 1990 Jul 05; 265(19):11361-7. PubMed ID: 2358466
    [Abstract] [Full Text] [Related]

  • 46. Prospective management of a child with neonatal citrullinemia.
    Melnyk AR, Matalon R, Henry BW, Zeller WP, Lange C.
    J Pediatr; 1993 Jan 05; 122(1):96-8. PubMed ID: 8419623
    [Abstract] [Full Text] [Related]

  • 47. Prenatal diagnosis of inborn errors of metabolism.
    Matalon R.
    Int J Gynaecol Obstet; 1976 Jan 05; 14(4):301-7. PubMed ID: 15886
    [Abstract] [Full Text] [Related]

  • 48. Episodic Tourette's syndrome in a patient with citrullinemia.
    Drury I, Mellinger JF, Michels VV.
    Ann Neurol; 1986 Jun 05; 19(6):612. PubMed ID: 3460517
    [No Abstract] [Full Text] [Related]

  • 49. Kinetic analysis of argininosuccinate synthetase in a variant form of citrullinaemia.
    Akaboshi I, Endo F, Matsuda I, Saheki T.
    J Inherit Metab Dis; 1983 Jun 05; 6(1):36-9. PubMed ID: 6408307
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52. Molecular definition of bovine argininosuccinate synthetase deficiency.
    Dennis JA, Healy PJ, Beaudet AL, O'Brien WE.
    Proc Natl Acad Sci U S A; 1989 Oct 05; 86(20):7947-51. PubMed ID: 2813370
    [Abstract] [Full Text] [Related]

  • 53. Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid.
    Jakobs C, Sweetman L, Wadman SK, Duran M, Saudubray JM, Nyhan WL.
    Eur J Pediatr; 1984 Jan 05; 141(3):153-7. PubMed ID: 6698061
    [Abstract] [Full Text] [Related]

  • 54. Antenatal diagnosis of glutaric acidemia.
    Goodman SI, Gallegos DA, Pullin CJ, Halpern B, Truscott RJ, Wise G, Wilcken B, Ryan ED, Whelen DT.
    Am J Hum Genet; 1980 Sep 05; 32(5):695-9. PubMed ID: 6893520
    [Abstract] [Full Text] [Related]

  • 55. Acute neonatal and benign citrullinaemia in one sibship.
    Burgess EA, Oberholzer VG, Semmens JM, Stern J.
    Arch Dis Child; 1978 Feb 05; 53(2):179-82. PubMed ID: 646426
    [Abstract] [Full Text] [Related]

  • 56. Fetal tissue amino acid concentrations in argininosuccinic aciduria and in "maternal homocystinuria".
    Rassin DK, Fleisher LD, Muir A, Desnick RJ, Gaull GE.
    Clin Chim Acta; 1979 Jun 01; 94(2):101-8. PubMed ID: 455723
    [Abstract] [Full Text] [Related]

  • 57. Citrullinemia, report of a case, with studies on antenatal diagnosis.
    Roerdink FH, Gouw WL, Okken A, van der Blij JF, Luit-de Haan G, Hommes FA, Huisjes HJ.
    Pediatr Res; 1973 Nov 01; 7(11):863-9. PubMed ID: 4749002
    [No Abstract] [Full Text] [Related]

  • 58. Messenger RNA coding for argininosuccinate synthetase in citrullinemia.
    Kobayashi K, Saheki T, Imamura Y, Noda T, Inoue I, Matuo S, Hagihara S, Nomiyama H, Jinno Y, Shimada K.
    Am J Hum Genet; 1986 May 01; 38(5):667-80. PubMed ID: 3459354
    [Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60. Prenatal diagnosis of hereditary tyrosinemia by determination of fumarylacetoacetase in cultured amniotic fluid cells.
    Kvittingen EA, Steinmann B, Gitzelmann R, Leonard JV, Andria G, Børresen AL, Mossman J, Micara G, Lindblad B.
    Pediatr Res; 1985 Apr 01; 19(4):334-7. PubMed ID: 4000758
    [Abstract] [Full Text] [Related]

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