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.
43. 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]
44. Spongy degeneration of the central nervous system (van Bogaert-Bertrand type?) in a newborn infant. A light and electron microscopic study. Towfighi J; Friedman Z; Maisels MJ Acta Neuropathol; 1977 Mar; 37(3):267-70. PubMed ID: 855648 [TBL] [Abstract][Full Text] [Related]
46. Strategies for evaluating the child with suspected neurodegenerative disease. Menkes JH Monatsschr Kinderheilkd; 1989 May; 137(5):254-6. PubMed ID: 2661995 [No Abstract] [Full Text] [Related]
47. N-acetylaspartic aciduria due to aspartoacylase deficiency--a new aetiology of childhood leukodystrophy. Hagenfeldt L; Bollgren I; Venizelos N J Inherit Metab Dis; 1987; 10(2):135-41. PubMed ID: 3116332 [TBL] [Abstract][Full Text] [Related]
48. Ultrastructural examination of the axillary skin biopsy in the diagnosis of metabolic diseases. Abramovich CM; Prayson RA; McMahon JT; Cohen BH Hum Pathol; 2001 Jun; 32(6):649-55. PubMed ID: 11431721 [TBL] [Abstract][Full Text] [Related]
49. Aspartoacylase deficiency and Canavan disease in Saudi Arabia. Ozand PT; Gascon GG; Dhalla M Am J Med Genet; 1990 Feb; 35(2):266-8. PubMed ID: 2309767 [TBL] [Abstract][Full Text] [Related]
50. van der Knaap's leukoencephalopathy: report of five new cases with emphasis on diffusion-weighted MRI findings. Gelal F; Callí C; Apaydín M; Erdem G Neuroradiology; 2002 Jul; 44(7):625-30. PubMed ID: 12136366 [TBL] [Abstract][Full Text] [Related]
51. Canavan disease and the role of N-acetylaspartate in myelin synthesis. Namboodiri AM; Peethambaran A; Mathew R; Sambhu PA; Hershfield J; Moffett JR; Madhavarao CN Mol Cell Endocrinol; 2006 Jun; 252(1-2):216-23. PubMed ID: 16647192 [TBL] [Abstract][Full Text] [Related]
52. [Infantile neuro-axonal dystrophy and Hallervorden-Spatz disease. Electro-clinical and anatomo-pathological and differential diagnostic aspects]. Radermecker J; Martin JJ Bull Acad R Med Belg; 1972 Jul; 12(7):459-502. PubMed ID: 4662801 [No Abstract] [Full Text] [Related]
53. Familial idiocy with spongy degeneration of the central nervous system of van Bogaert--Bertrand type. ZU RHEIN GM; EICHMAN PL; PULETTI F Neurology; 1960 Nov; 10():998-1006. PubMed ID: 13788842 [No Abstract] [Full Text] [Related]
54. Canavan disease: findings in four new cases. Michelakakis H; Giouroukos S; Divry P; Katsarou E; Rolland MO; Skardoutsou A J Inherit Metab Dis; 1991; 14(2):267-8. PubMed ID: 1886410 [No Abstract] [Full Text] [Related]
55. Brain biopsies for neurodegenerative disease in children. MacGregor DL; Humphrey RP; Armstrong DL; Becker LE J Pediatr; 1978 Jun; 92(6):903-5. PubMed ID: 660354 [TBL] [Abstract][Full Text] [Related]
56. [Indicative constellation of symptoms in Canavan-van Bogaert-Bertrand disease]. Kotlarek F; Schütz E; Zeumer H Rofo; 1982 Nov; 137(5):608-10. PubMed ID: 6217138 [No Abstract] [Full Text] [Related]
57. Sudden infant death syndrome: organic acid profiles in cerebrospinal fluid from 47 children and the occurrence of N-acetylaspartic acid. Divry P; Vianey-Liaud C; Jakobs C; ten-Brink HJ; Dutruge J; Gilly R J Inherit Metab Dis; 1990; 13(3):330-2. PubMed ID: 2122095 [No Abstract] [Full Text] [Related]
58. SPONGY DEGENERATION OF THE BRAIN. CROME L Dev Med Child Neurol; 1965 Jun; 7():322-3. PubMed ID: 14343234 [No Abstract] [Full Text] [Related]
59. Familial spongy degeneration of the brain. Mahloudji M; Daneshbod K; Karjoo M Arch Neurol; 1970 Apr; 22(4):294-8. PubMed ID: 5417637 [No Abstract] [Full Text] [Related]