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Journal Abstract Search
108 related items for PubMed ID: 11710318
1. [Canavan disease]. Harting I, Seitz A. Rofo; 2001 Oct; 173(10):M275-6. PubMed ID: 11710318 [No Abstract] [Full Text] [Related]
2. [Canavan disease or N-acetyl aspartic aciduria: a case report]. Boughamoura L, Chaabane F, Tilouche S, Chabchoub I, Kabachi N, Tlili K, Yacoub M, Essoussi AS. Arch Pediatr; 2007 Feb; 14(2):173-6. PubMed ID: 17196380 [Abstract] [Full Text] [Related]
4. Canavan disease: a review of recent developments. Gordon N. Eur J Paediatr Neurol; 2001 Feb; 5(2):65-9. PubMed ID: 11589315 [Abstract] [Full Text] [Related]
5. Atypical MRI findings in Canavan disease: a patient with a mild course. Yalcinkaya C, Benbir G, Salomons GS, Karaarslan E, Rolland MO, Jakobs C, van der Knaap MS. Neuropediatrics; 2005 Oct; 36(5):336-9. PubMed ID: 16217711 [Abstract] [Full Text] [Related]
6. Early diagnosis of Canavan syndrome: how can we get there? De Bernardo G, Giordano M, Sordino D, Buono S. BMJ Case Rep; 2015 Aug 05; 2015():. PubMed ID: 26245283 [Abstract] [Full Text] [Related]
7. 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 05; 21(3):205-8. PubMed ID: 10372908 [Abstract] [Full Text] [Related]
8. Novel splice site mutation of aspartoacylase gene in a Turkish patient with Canavan disease. Rady PL, Penzien JM, Vargas T, Tyring SK, Matalon R. Eur J Paediatr Neurol; 2000 Apr 05; 4(1):27-30. PubMed ID: 10701101 [Abstract] [Full Text] [Related]
10. [Megalencephaly with dystonia revealing Canavan disease]. Maaloul I, Fourati H, Wali M, Chabchoub I, Kamoun T, Mnif Z, Kaabachi N, Hachicha M. Arch Pediatr; 2013 Jul 05; 20(7):783-6. PubMed ID: 23727372 [Abstract] [Full Text] [Related]
11. Natural history of Canavan disease revealed by proton magnetic resonance spectroscopy (1H-MRS) and diffusion-weighted MRI. Janson CG, McPhee SW, Francis J, Shera D, Assadi M, Freese A, Hurh P, Haselgrove J, Wang DJ, Bilaniuk L, Leone P. Neuropediatrics; 2006 Aug 05; 37(4):209-21. PubMed ID: 17177147 [Abstract] [Full Text] [Related]
14. Homozygosity for mutation G212A of the gene for aspartoacylase is associated with atypical form of Canavan's disease. Velinov M, Zellers N, Styles J, Wisniewski K. Clin Genet; 2008 Mar 05; 73(3):288-9. PubMed ID: 18070137 [No Abstract] [Full Text] [Related]