544 related articles for article (PubMed ID: 17940249)
1. Magnetic resonance imaging and magnetic resonance spectroscopy in isolated sulfite oxidase deficiency.
Hoffmann C; Ben-Zeev B; Anikster Y; Nissenkorn A; Brand N; Kuint J; Kushnir T
J Child Neurol; 2007 Oct; 22(10):1214-21. PubMed ID: 17940249
[TBL] [Abstract][Full Text] [Related]
2. Isolated sulfite oxidase deficiency: mutation analysis and DNA-based prenatal diagnosis.
Johnson JL; Rajagopalan KV; Renier WO; Van der Burgt I; Ruitenbeek W
Prenat Diagn; 2002 May; 22(5):433-6. PubMed ID: 12001203
[TBL] [Abstract][Full Text] [Related]
3. Isolated sulfite oxidase deficiency.
Rupar CA; Gillett J; Gordon BA; Ramsay DA; Johnson JL; Garrett RM; Rajagopalan KV; Jung JH; Bacheyie GS; Sellers AR
Neuropediatrics; 1996 Dec; 27(6):299-304. PubMed ID: 9050047
[TBL] [Abstract][Full Text] [Related]
4. Neurological findings in aminoacylase 1 deficiency.
Sass JO; Olbrich H; Mohr V; Hart C; Woldseth B; Krywawych S; Bjurulf B; Lakhani PK; Buchdahl RM; Omran H
Neurology; 2007 Jun; 68(24):2151-3. PubMed ID: 17562838
[No Abstract] [Full Text] [Related]
5. Isolated sulfite oxidase deficiency: a case report with a novel mutation and review of the literature.
Tan WH; Eichler FS; Hoda S; Lee MS; Baris H; Hanley CA; Grant PE; Krishnamoorthy KS; Shih VE
Pediatrics; 2005 Sep; 116(3):757-66. PubMed ID: 16140720
[TBL] [Abstract][Full Text] [Related]
6. An inborn error of metabolism presenting as hypoxic-ischemic insult.
Eyaid WM; Al-Nouri DM; Rashed MS; Al-Rifai MT; Al-Wakeel AS
Pediatr Neurol; 2005 Feb; 32(2):134-6. PubMed ID: 15664777
[TBL] [Abstract][Full Text] [Related]
7. Isolated sulfite oxidase deficiency: review of two cases in one family.
Edwards MC; Johnson JL; Marriage B; Graf TN; Coyne KE; Rajagopalan KV; MacDonald IM
Ophthalmology; 1999 Oct; 106(10):1957-61. PubMed ID: 10519592
[TBL] [Abstract][Full Text] [Related]
8. DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.
Lam CW; Li CK; Lai CK; Tong SF; Chan KY; Ng GS; Yuen YP; Cheng AW; Chan YW
Mol Genet Metab; 2002 Jan; 75(1):91-5. PubMed ID: 11825068
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation in neonatal isolated sulphite oxidase deficiency.
Lee HF; Mak BS; Chi CS; Tsai CR; Chen CH; Shu SG
Neuropediatrics; 2002 Aug; 33(4):174-9. PubMed ID: 12368985
[TBL] [Abstract][Full Text] [Related]
10. Proton magnetic resonance spectroscopy and diffusion-weighted imaging in isolated sulfite oxidase deficiency.
Eichler F; Tan WH; Shih VE; Grant PE; Krishnamoorthy K
J Child Neurol; 2006 Sep; 21(9):801-5. PubMed ID: 16970890
[TBL] [Abstract][Full Text] [Related]
11. A mild form of infantile isolated sulphite oxidase deficiency.
Barbot C; Martins E; Vilarinho L; Dorche C; Cardoso ML
Neuropediatrics; 1995 Dec; 26(6):322-4. PubMed ID: 8719749
[TBL] [Abstract][Full Text] [Related]
12. [Isolated sulfite oxidase deficiency].
Matsuishi T; Wada N; Isakai T; Togo A
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):189-91. PubMed ID: 9645040
[No Abstract] [Full Text] [Related]
13. Magnetic resonance imaging of the brain in glutaric acidemia type I: a review of the literature and a report of four new cases with attention to the basal ganglia and imaging technique.
Desai NK; Runge VM; Crisp DE; Crisp MB; Naul LG
Invest Radiol; 2003 Aug; 38(8):489-96. PubMed ID: 12874515
[TBL] [Abstract][Full Text] [Related]
14. Isolated sulfite oxidase deficiency: MR imaging features.
Dublin AB; Hald JK; Wootton-Gorges SL
AJNR Am J Neuroradiol; 2002 Mar; 23(3):484-5. PubMed ID: 11901024
[TBL] [Abstract][Full Text] [Related]
15. MRI and 1H-MRS findings in early-onset cobalamin C/D defect.
Longo D; Fariello G; Dionisi-Vici C; Cannatà V; Boenzi S; Genovese E; Deodato F
Neuropediatrics; 2005 Dec; 36(6):366-72. PubMed ID: 16429376
[TBL] [Abstract][Full Text] [Related]
16. Advances in magnetic resonance neuroimaging techniques in the evaluation of neonatal encephalopathy.
Panigrahy A; Blüml S
Top Magn Reson Imaging; 2007 Feb; 18(1):3-29. PubMed ID: 17607141
[TBL] [Abstract][Full Text] [Related]
17. [Sulfite oxidase deficiency presenting as Leigh syndrome].
Amiel J; Gagey V; Rabier D; Dorche C; Bonnefont JP; Dufier JL; Saudubray JM; Rey J; Munnich A
Arch Pediatr; 1994 Nov; 1(11):1023-7. PubMed ID: 7834040
[TBL] [Abstract][Full Text] [Related]
18. Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency.
Strauss KA; Lazovic J; Wintermark M; Morton DH
Brain; 2007 Jul; 130(Pt 7):1905-20. PubMed ID: 17478444
[TBL] [Abstract][Full Text] [Related]
19. Sulphite oxidase deficiency--a report of two siblings.
Goh A; Lim KW
Singapore Med J; 1997 Sep; 38(9):391-4. PubMed ID: 9407766
[TBL] [Abstract][Full Text] [Related]
20. Cerebral white matter involvement in children with mitochondrial encephalopathies.
Moroni I; Bugiani M; Bizzi A; Castelli G; Lamantea E; Uziel G
Neuropediatrics; 2002 Apr; 33(2):79-85. PubMed ID: 12075488
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
