297 related articles for article (PubMed ID: 17196380)
1. [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
[TBL] [Abstract][Full Text] [Related]
2. [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; 20(7):783-6. PubMed ID: 23727372
[TBL] [Abstract][Full Text] [Related]
3. Use of localized proton nuclear magnetic resonance spectroscopy in Canavan's disease.
Aydinli N; Calişkan M; Calay M; Ozmen M
Turk J Pediatr; 1998; 40(4):549-57. PubMed ID: 10028864
[TBL] [Abstract][Full Text] [Related]
4. A mutation of aspartoacylase gene in a Turkish patient with Canavan disease.
Eke GH; Iscan A; Cece H; Calik M
Genet Couns; 2012; 23(1):9-12. PubMed ID: 22611636
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. [Canavan disease].
Harting I; Seitz A
Rofo; 2001 Oct; 173(10):M275-6. PubMed ID: 11710318
[No Abstract] [Full Text] [Related]
8. Canavan disease: a review of recent developments.
Gordon N
Eur J Paediatr Neurol; 2001; 5(2):65-9. PubMed ID: 11589315
[TBL] [Abstract][Full Text] [Related]
9. [Magnetic resonance tomography and localized proton spectroscopy in 2 siblings with Canavan's disease].
Engelbrecht V; Rassek M; Gärtner J; Kahn T; Mödder U
Rofo; 1995 Sep; 163(3):238-44. PubMed ID: 7548871
[TBL] [Abstract][Full Text] [Related]
10. Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease.
Matalon R; Michals K; Sebesta D; Deanching M; Gashkoff P; Casanova J
Am J Med Genet; 1988 Feb; 29(2):463-71. PubMed ID: 3354621
[TBL] [Abstract][Full Text] [Related]
11. [N-acetylaspartic aciduria. Clinical, biological and physiopathological study].
Gay C; Divry P; Macabeo V; Gilly R
Arch Fr Pediatr; 1991; 48(6):409-13. PubMed ID: 1929728
[TBL] [Abstract][Full Text] [Related]
12. N-acetylaspartic aciduria in Canavan disease: another proof in two infants.
Yalaz K; Topçu M; Topaloğlu H; Gürçay O; Ozcan OE; Onol B; Renda Y
Neuropediatrics; 1990 Aug; 21(3):140-2. PubMed ID: 2234319
[TBL] [Abstract][Full Text] [Related]
13. New T530C mutation in the aspartoacylase gene caused Canavan disease with no correlation between severity and N-acetylaspartate excretion.
Di Pietro V; Cavallari U; Amorini AM; Lazzarino G; Longo S; Poggiani C; Cavalli P; Tavazzi B
Clin Biochem; 2013 Dec; 46(18):1902-4. PubMed ID: 24036223
[TBL] [Abstract][Full Text] [Related]
14. Rapid and sensitive screening for and chemical diagnosis of Canavan disease by gas chromatography-mass spectrometry.
Inoue Y; Kuhara T
J Chromatogr B Analyt Technol Biomed Life Sci; 2004 Jun; 806(1):33-9. PubMed ID: 15149608
[TBL] [Abstract][Full Text] [Related]
15. Radiological clue to diagnosis of Canavan disease.
Sreenivasan P; Purushothaman KK
Indian J Pediatr; 2013 Jan; 80(1):75-7. PubMed ID: 22660905
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Spongy degeneration of the neuraxis (Canavan-van Bogaert disease) and N-acetylaspartic aciduria.
Echenne B; Divry P; Vianey-Liaud C
Neuropediatrics; 1989 May; 20(2):79-81. PubMed ID: 2739878
[TBL] [Abstract][Full Text] [Related]
18. Lithium citrate for Canavan disease.
Janson CG; Assadi M; Francis J; Bilaniuk L; Shera D; Leone P
Pediatr Neurol; 2005 Oct; 33(4):235-43. PubMed ID: 16194720
[TBL] [Abstract][Full Text] [Related]
19. Early diagnosis of Canavan syndrome: how can we get there?
De Bernardo G; Giordano M; Sordino D; Buono S
BMJ Case Rep; 2015 Aug; 2015():. PubMed ID: 26245283
[TBL] [Abstract][Full Text] [Related]
20. 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; 37(4):209-21. PubMed ID: 17177147
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
