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23. Reliable prenatal diagnosis of Canavan disease by measuring N-acetylaspartate in amniotic fluid using liquid chromatography tandem mass spectrometry. Al-Dirbashi OY; Kurdi W; Imtiaz F; Ahmad AM; Al-Sayed M; Tulbah M; Al-Nemer M; Rashed MS Prenat Diagn; 2009 May; 29(5):477-80. PubMed ID: 19235826 [TBL] [Abstract][Full Text] [Related]
25. Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings. Matalon RM; Michals-Matalon K Front Biosci; 2000 Mar; 5():D307-11. PubMed ID: 10704428 [TBL] [Abstract][Full Text] [Related]
26. A case of Canavan disease with microcephaly. Gowda VK; Bhat MD; Srinivasan VM; Prasad C; Benakappa A; Faruq M Brain Dev; 2016 Sep; 38(8):759-62. PubMed ID: 26992473 [TBL] [Abstract][Full Text] [Related]
27. [A case of Canavan-Van Bogaert-Bertrand leukodystrophy]. Mikhaĭlova SV; Zakharova EIu; Bukina AM; Il'ina ES; Pokrovskaia AIa; Fedoniuk ID; Bembeeva RTs; Petrukhin AS Zh Nevrol Psikhiatr Im S S Korsakova; 2004; 104(4):50-4. PubMed ID: 15270300 [No Abstract] [Full Text] [Related]
28. Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease. McPhee SW; Francis J; Janson CG; Serikawa T; Hyland K; Ong EO; Raghavan SS; Freese A; Leone P Brain Res Mol Brain Res; 2005 Apr; 135(1-2):112-21. PubMed ID: 15857674 [TBL] [Abstract][Full Text] [Related]
29. Canavan disease: studies on the knockout mouse. Matalon R; Michals-Matalon K; Surendran S; Tyring SK Adv Exp Med Biol; 2006; 576():77-93; discussion 361-3. PubMed ID: 16802706 [TBL] [Abstract][Full Text] [Related]
30. Protracted course of N-acetylaspartic aciduria in two non-Jewish siblings: identical clinical and magnetic resonance imaging findings. Zafeiriou DI; Kleijer WJ; Maroupoulos G; Anastasiou AL; Augoustidou-Savvopoulou P; Papadopoulou F; Kontopoulos EE; Fagan E; Payne S Brain Dev; 1999 Apr; 21(3):205-8. PubMed ID: 10372908 [TBL] [Abstract][Full Text] [Related]
31. The impact of structural biology on neurobiology. Viola RE Proc Natl Acad Sci U S A; 2007 Jan; 104(2):399-400. PubMed ID: 17213329 [No Abstract] [Full Text] [Related]
32. The spectrum of mutations of the aspartoacylase gene in Canavan disease in non-Jewish patients. Elpeleg ON; Shaag A J Inherit Metab Dis; 1999 Jun; 22(4):531-4. PubMed ID: 10407784 [TBL] [Abstract][Full Text] [Related]
34. Canavan disease: a white matter disorder. Kumar S; Mattan NS; de Vellis J Ment Retard Dev Disabil Res Rev; 2006; 12(2):157-65. PubMed ID: 16807907 [TBL] [Abstract][Full Text] [Related]
35. Canavan disease. Analysis of the nature of the metabolic lesions responsible for development of the observed clinical symptoms. Baslow MH; Resnik TR J Mol Neurosci; 1997 Oct; 9(2):109-25. PubMed ID: 9407392 [TBL] [Abstract][Full Text] [Related]
36. Molecular basis of Canavan's disease: from human to mouse. Surendran S; Matalon KM; Tyring SK; Matalon R J Child Neurol; 2003 Sep; 18(9):604-10. PubMed ID: 14572138 [TBL] [Abstract][Full Text] [Related]
37. Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease. Kaul R; Gao GP; Balamurugan K; Matalon R Nat Genet; 1993 Oct; 5(2):118-23. PubMed ID: 8252036 [TBL] [Abstract][Full Text] [Related]
38. N-Acetylaspartate Synthase Deficiency Corrects the Myelin Phenotype in a Canavan Disease Mouse Model But Does Not Affect Survival Time. Maier H; Wang-Eckhardt L; Hartmann D; Gieselmann V; Eckhardt M J Neurosci; 2015 Oct; 35(43):14501-16. PubMed ID: 26511242 [TBL] [Abstract][Full Text] [Related]
39. A benign polymorphism in the aspartoacylase gene may cause misinterpretation of Canavan gene testing. Propheta O; Magal N; Shohat M; Eyal N; Navot N; Horowitz M Eur J Hum Genet; 1998; 6(6):635-7. PubMed ID: 9887384 [TBL] [Abstract][Full Text] [Related]