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

Journal Abstract Search


136 related items for PubMed ID: 9377513

  • 1. Glutaric aciduria type I: a serious pitfall if diagnosed too late.
    Pfluger T, Weil S, Muntau A, Willemsen UF, Hahn K.
    Eur Radiol; 1997; 7(8):1264-6. PubMed ID: 9377513
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)].
    Lawrenz-Wolf B, Herberg KP, Hoffmann GF, Hunneman DH, Lehnert W, Hanefeld F.
    Klin Padiatr; 1993; 205(1):23-9. PubMed ID: 8445849
    [Abstract] [Full Text] [Related]

  • 8. Two cases of glutaric aciduria type 1: clinical and neuropathological findings.
    Kimura S, Hara M, Nezu A, Osaka H, Yamazaki S, Saitoh K.
    J Neurol Sci; 1994 May; 123(1-2):38-43. PubMed ID: 8064319
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds.
    Amir N, Elpeleg ON, Shalev RS, Christensen E.
    J Pediatr; 1989 Jun; 114(6):983-9. PubMed ID: 2723913
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Dystonia and dyskinesia in glutaric aciduria type I: clinical heterogeneity and therapeutic considerations.
    Kyllerman M, Skjeldal OH, Lundberg M, Holme I, Jellum E, von Döbeln U, Fossen A, Carlsson G.
    Mov Disord; 1994 Jan; 9(1):22-30. PubMed ID: 8139602
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)].
    Hayasaka K, Ikeda H.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan; (18 Pt 1):332-5. PubMed ID: 9590060
    [No Abstract] [Full Text] [Related]

  • 17. Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
    Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Müller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E.
    Neuropediatrics; 1996 Jun; 27(3):115-23. PubMed ID: 8837070
    [Abstract] [Full Text] [Related]

  • 18. First trimester prenatal exclusion of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type 1).
    Christensen E.
    J Inherit Metab Dis; 1989 Jun; 12 Suppl 2():277-9. PubMed ID: 2512425
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. 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]


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