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.
154 related articles for article (PubMed ID: 18330844)
1. Conversion of a normal MRI into an MRI showing a cystic leukoencephalopathy is not a known feature of vanishing white matter. van der Knaap MS; Schiffmann R; Scheper GC Neuropediatrics; 2007 Oct; 38(5):264. PubMed ID: 18330844 [No Abstract] [Full Text] [Related]
2. Nonprogressive familial leukoencephalopathy with porencephalic cyst and focal seizures. Blumkin L; Watemberg N; Lev D; Malinger G; Luckman Y; Ben-Zeev B; Lerman-Sagie T J Child Neurol; 2006 Feb; 21(2):145-8. PubMed ID: 16566879 [TBL] [Abstract][Full Text] [Related]
3. Vanishing white matter disease: the first reported chinese patient. Wong SS; Luk DC; Wong VC; Scheper GC; van der Knaap MS J Child Neurol; 2008 Jun; 23(6):710-4. PubMed ID: 18539998 [TBL] [Abstract][Full Text] [Related]
4. Megalencephalic leukoencephalopathy with subcortical cysts. Hari Krishnan K; Leema Pauline C; Kumaresan G; Vasantha Mallika TK Indian Pediatr; 2005 Jan; 42(1):60-3. PubMed ID: 15695862 [TBL] [Abstract][Full Text] [Related]
5. Megalencephalic leukoencephalopathy with subcortical cysts. Juneja M; Sharma S Indian J Pediatr; 2005 Feb; 72(2):179-80. PubMed ID: 15758546 [No Abstract] [Full Text] [Related]
6. The spectrum of mutations for the diagnosis of vanishing white matter disease. Scali O; Di Perri C; Federico A Neurol Sci; 2006 Sep; 27(4):271-7. PubMed ID: 16998732 [TBL] [Abstract][Full Text] [Related]
7. The latest on leukodystrophies. Schiffmann R; van der Knaap MS Curr Opin Neurol; 2004 Apr; 17(2):187-92. PubMed ID: 15021247 [TBL] [Abstract][Full Text] [Related]
8. Where has all the white matter gone? Unraveling the mysteries of leukoencephalopathies. Kaye EM; Moser H Neurology; 2004 May; 62(9):1464-5. PubMed ID: 15136665 [No Abstract] [Full Text] [Related]
10. Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up. Bektaş G; Yeşil G; Özkan MU; Yıldız EP; Uzunhan TA; Çalışkan M Clin Neurol Neurosurg; 2018 Aug; 171():190-193. PubMed ID: 29933199 [TBL] [Abstract][Full Text] [Related]
11. Dominant form of vanishing white matter-like leukoencephalopathy. Labauge P; Fogli A; Castelnovo G; Le Bayon A; Horzinski L; Nicoli F; Cozzone P; Pagès M; Briere C; Marty-Double C; Delhaume O; Gelot A; Boespflug-Tanguy O; Rodriguez D Ann Neurol; 2005 Oct; 58(4):634-9. PubMed ID: 16047349 [TBL] [Abstract][Full Text] [Related]
12. Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families. Passemard S; Gelot A; Fogli A; N'Guyen S; Barnerias C; Niel F; Doummar D; Arbues AS; Mignot C; de Villemeur TB; Ponsot G; Boespflug-Tanguy O; Rodriguez D Neurology; 2007 Jul; 69(4):400-2. PubMed ID: 17646634 [No Abstract] [Full Text] [Related]
13. Novel mutation in EIF2B gene in a case of adult-onset leukoencephalopathy with vanishing white matter. Matsui M; Mizutani K; Ohtake H; Miki Y; Ishizu K; Fukuyama H; Shimohata T; Onodera O; Nishizawa M; Takayama Y; Shibasaki H Eur Neurol; 2007; 57(1):57-8. PubMed ID: 17119336 [No Abstract] [Full Text] [Related]
14. Infantile onset Vanishing White Matter disease associated with a novel EIF2B5 variant, remarkably long life span, severe epilepsy, and hypopituitarism. Woody AL; Hsieh DT; McIver HK; Thomas LP; Rohena L Am J Med Genet A; 2015 Apr; 167A(4):826-30. PubMed ID: 25758335 [TBL] [Abstract][Full Text] [Related]
15. Leukoencephalopathy with vanishing white matter due to homozygous EIF2B2 gene mutation. First Polish cases. Mierzewska H; van der Knaap MS; Scheper GC; Jurkiewicz E; Schmidt-Sidor B; Szymańska K Folia Neuropathol; 2006; 44(2):144-8. PubMed ID: 16823698 [TBL] [Abstract][Full Text] [Related]
16. Adult-onset vanishing white matter leukoencephalopathy presenting as psychosis. Denier C; Orgibet A; Roffi F; Jouvent E; Buhl C; Niel F; Boespflug-Tanguy O; Said G; Ducreux D Neurology; 2007 May; 68(18):1538-9. PubMed ID: 17470759 [No Abstract] [Full Text] [Related]
17. A mouse model for eukaryotic translation initiation factor 2B-leucodystrophy reveals abnormal development of brain white matter. Geva M; Cabilly Y; Assaf Y; Mindroul N; Marom L; Raini G; Pinchasi D; Elroy-Stein O Brain; 2010 Aug; 133(Pt 8):2448-61. PubMed ID: 20826436 [TBL] [Abstract][Full Text] [Related]
18. Natural history of adult-onset eIF2B-related disorders: a multi-centric survey of 16 cases. Labauge P; Horzinski L; Ayrignac X; Blanc P; Vukusic S; Rodriguez D; Mauguiere F; Peter L; Goizet C; Bouhour F; Denier C; Confavreux C; Obadia M; Blanc F; de Sèze J; Fogli A; Boespflug-Tanguy O Brain; 2009 Aug; 132(Pt 8):2161-9. PubMed ID: 19625339 [TBL] [Abstract][Full Text] [Related]
19. Genotype-phenotype correlation in vanishing white matter disease. van der Lei HD; van Berkel CG; van Wieringen WN; Brenner C; Feigenbaum A; Mercimek-Mahmutoglu S; Philippart M; Tatli B; Wassmer E; Scheper GC; van der Knaap MS Neurology; 2010 Oct; 75(17):1555-9. PubMed ID: 20975056 [TBL] [Abstract][Full Text] [Related]
20. [Leukoencephalopathy with vanishing white matter: a clinical case of adult onset]. Pato Pato A; Lorenzo González JR; Cimas Hernando I; Rodríguez-Constenla I Neurologia; 2009 Sep; 24(7):504-5. PubMed ID: 21469262 [No Abstract] [Full Text] [Related] [Next] [New Search]