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Results: 1 to 20 of 23

1.

A diet-induced mouse model for glutaric aciduria type I.

Zinnanti WJ, Lazovic J, Wolpert EB, Antonetti DA, Smith MB, Connor JR, Woontner M, Goodman SI, Cheng KC.

Brain. 2006 Apr;129(Pt 4):899-910. Epub 2006 Jan 30.

PMID:
16446282
[PubMed - indexed for MEDLINE]
Free Article
2.

The unsolved puzzle of neuropathogenesis in glutaric aciduria type I.

Jafari P, Braissant O, Bonafé L, Ballhausen D.

Mol Genet Metab. 2011 Dec;104(4):425-37. doi: 10.1016/j.ymgme.2011.08.027. Epub 2011 Sep 2. Review.

PMID:
21944461
[PubMed - indexed for MEDLINE]
3.

Glutaric acidemia type 1.

Hedlund GL, Longo N, Pasquali M.

Am J Med Genet C Semin Med Genet. 2006 May 15;142C(2):86-94. Review.

PMID:
16602100
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Vascular dysfunction as an additional pathomechanism in glutaric aciduria type I.

Mühlhausen C, Ergün S, Strauss KA, Koeller DM, Crnic L, Woontner M, Goodman SI, Ullrich K, Braulke T.

J Inherit Metab Dis. 2004;27(6):829-34. Review.

PMID:
15505389
[PubMed - indexed for MEDLINE]
5.

[Neuroradiologic findings of glutaric aciduria type I].

de Luis E, Larrache J, García-Eulate R, García JN, Zubieta JL.

Rev Med Univ Navarra. 2007 Jul-Sep;51(3):9-12. Review. Spanish.

PMID:
18183780
[PubMed - indexed for MEDLINE]
6.

Nutrition support for glutaric acidemia type I.

Yannicelli S, Rohr F, Warman ML.

J Am Diet Assoc. 1994 Feb;94(2):183-8,191; quiz 189-90. Review.

PMID:
8300996
[PubMed - indexed for MEDLINE]
7.

Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency.

Kölker S, Koeller DM, Okun JG, Hoffmann GF.

Ann Neurol. 2004 Jan;55(1):7-12. Review.

PMID:
14705106
[PubMed - indexed for MEDLINE]
8.

[L-2-hydroxyglutaric aciduria].

Terada N.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):392-4. Review. Japanese. No abstract available.

PMID:
9590079
[PubMed - indexed for MEDLINE]
9.

Striatal degeneration and spongy myelinopathy in glutaric acidemia.

Soffer D, Amir N, Elpeleg ON, Gomori JM, Shalev RS, Gottschalk-Sabag S.

J Neurol Sci. 1992 Feb;107(2):199-204. Review.

PMID:
1564518
[PubMed - indexed for MEDLINE]
10.

Glutaric aciduria type I and kynurenine pathway metabolites: a modified hypothesis.

Varadkar S, Surtees R.

J Inherit Metab Dis. 2004;27(6):835-42. Review.

PMID:
15505390
[PubMed - indexed for MEDLINE]
11.

Clinical and MRI findings in a case of D-2-hydroxyglutaric aciduria.

Sugita K, Kakinuma H, Okajima Y, Ogawa A, Watanabe H, Niimi H.

Brain Dev. 1995 Mar-Apr;17(2):139-41; discussion 144-5. Review.

PMID:
7625550
[PubMed - indexed for MEDLINE]
12.

Membrane translocation of glutaric acid and its derivatives.

Mühlhausen C, Burckhardt BC, Hagos Y, Burckhardt G, Keyser B, Lukacs Z, Ullrich K, Braulke T.

J Inherit Metab Dis. 2008 Apr;31(2):188-93. doi: 10.1007/s10545-008-0825-x. Epub 2008 Apr 4. Review.

PMID:
18404412
[PubMed - indexed for MEDLINE]
13.

Neonatal screening for glutaric aciduria type I: strategies to proceed.

Lindner M, Ho S, Fang-Hoffmann J, Hoffmann GF, Kölker S.

J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):378-82. Review.

PMID:
16763905
[PubMed - indexed for MEDLINE]
14.

Glutaric aciduria types I and II.

Gordon N.

Brain Dev. 2006 Apr;28(3):136-40. Epub 2005 Dec 20. Review.

PMID:
16368216
[PubMed - indexed for MEDLINE]
15.

Facial anomalies in D-2-hydroxyglutaric aciduria.

Amiel J, de Lonlay P, Francannet C, Picard A, Bruel H, Rabier D, Le Merrer M, Verhoeven N, Jakobs C, Lyonnet S, Munnich A.

Am J Med Genet. 1999 Sep 10;86(2):124-9. Review.

PMID:
10449646
[PubMed - indexed for MEDLINE]
16.

L: -2-Hydroxyglutaric aciduria, a disorder of metabolite repair.

Van Schaftingen E, Rzem R, Veiga-da-Cunha M.

J Inherit Metab Dis. 2009 Apr;32(2):135-42. doi: 10.1007/s10545-008-1042-3. Epub 2008 Nov 21. Review.

PMID:
19020988
[PubMed - indexed for MEDLINE]
17.

[Lysinuric protein intolerance and other cationic aminoacidurias].

Oyanagi K, Nagao M.

Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):562-4. Review. Japanese. No abstract available.

PMID:
9645134
[PubMed - indexed for MEDLINE]
18.

[3-Methylglutaconyl-CoA hydratase deficiency].

Yoshida I.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):288-91. Review. Japanese. No abstract available.

PMID:
9590049
[PubMed - indexed for MEDLINE]
19.

[Aciduria, glutaric (type 2)].

Yamaguchi S.

Ryoikibetsu Shokogun Shirizu. 2001;(33):108-10. Review. Japanese. No abstract available.

PMID:
11462354
[PubMed - indexed for MEDLINE]
20.

[Saccharopinuria (a variant form of familial hyperlysinemia)].

Higashino K.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):191-4. Review. Japanese. No abstract available.

PMID:
9590025
[PubMed - indexed for MEDLINE]

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