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2003 31
2004 33
2005 36
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2007 34
2008 30
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2010 36
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1,189 results
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Canavan Disease.
Matalon R, Delgado L, Michals-Matalon K. Matalon R, et al. 1999 Sep 16 [updated 2018 Sep 13]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 1999 Sep 16 [updated 2018 Sep 13]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301412 Free Books & Documents. Review.
Surveillance: Neonatal/infantile Canavan disease. Follow up every six months to evaluate developmental status and evidence of any new problems. Mild/juvenile Canavan disease. Annual routine follow up by a pediatric neurologist or a developmental pediatrician is indi …
Surveillance: Neonatal/infantile Canavan disease. Follow up every six months to evaluate developmental status and evidence of any new …
Canavan Disease as a Model for Gene Therapy-Mediated Myelin Repair.
Lotun A, Gessler DJ, Gao G. Lotun A, et al. Front Cell Neurosci. 2021 Apr 23;15:661928. doi: 10.3389/fncel.2021.661928. eCollection 2021. Front Cell Neurosci. 2021. PMID: 33967698 Free PMC article. Review.
Given the significance of myelin formation in the developing brain, myelin repair in a time-dependent fashion is critical in restoring homeostatic functionality to the CNS of patients diagnosed with white matter disorders. Using Canavan Disease (CD) as a leukodystrophy mod …
Given the significance of myelin formation in the developing brain, myelin repair in a time-dependent fashion is critical in restoring homeo …
Canavan Disease.
Bokhari MR, Samanta D, Bokhari SRA. Bokhari MR, et al. 2022 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. 2022 Jul 4. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. PMID: 28613566 Free Books & Documents.
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary disorder that begins in infancy. ...
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, is a rare, progressive, and fatal neurological hereditary d …
[Mild Canavan disease in a child].
Zhou J, Ding CH, Zhuo XW, Ren XT, Zhang WH, Gong S. Zhou J, et al. Zhonghua Er Ke Za Zhi. 2019 Dec 2;57(12):961-963. doi: 10.3760/cma.j.issn.0578-1310.2019.12.014. Zhonghua Er Ke Za Zhi. 2019. PMID: 31795566 Chinese.
Canavan disease: an Arab scenario.
Zayed H. Zayed H. Gene. 2015 Apr 10;560(1):9-14. doi: 10.1016/j.gene.2015.02.009. Epub 2015 Feb 7. Gene. 2015. PMID: 25668701 Review.
The autosomal recessive Canavan disease (CD) is a neurological disorder that begins in infancy. ...
The autosomal recessive Canavan disease (CD) is a neurological disorder that begins in infancy. ...
Pathophysiology and Treatment of Canavan Disease.
Pleasure D, Guo F, Chechneva O, Bannerman P, McDonough J, Burns T, Wang Y, Hull V. Pleasure D, et al. Neurochem Res. 2020 Mar;45(3):561-565. doi: 10.1007/s11064-018-2693-6. Epub 2018 Dec 8. Neurochem Res. 2020. PMID: 30535831 No abstract available.
Non-genetic therapeutic approaches to Canavan disease.
Roscoe RB, Elliott C, Zarros A, Baillie GS. Roscoe RB, et al. J Neurol Sci. 2016 Jul 15;366:116-124. doi: 10.1016/j.jns.2016.05.012. Epub 2016 May 10. J Neurol Sci. 2016. PMID: 27288788 Review.
Canavan disease (CD) is a rare leukodystrophy characterized by diffuse spongiform white matter degeneration, dysmyelination and intramyelinic oedema with consequent impairment of psychomotor development and early death. ...
Canavan disease (CD) is a rare leukodystrophy characterized by diffuse spongiform white matter degeneration, dysmyelination and intra …
Canavan Disease: Clinical and Laboratory Profile from Southern Part of India.
Gowda VK, Bharathi NK, Bettaiah J, Bhat M, Shivappa SK. Gowda VK, et al. Ann Indian Acad Neurol. 2021 May-Jun;24(3):347-350. doi: 10.4103/aian.AIAN_386_20. Epub 2020 Dec 1. Ann Indian Acad Neurol. 2021. PMID: 34446995 Free PMC article.
BACKGROUND: Canavan disease (CD) is an autosomal recessively inherited leukodystrophy. ...
BACKGROUND: Canavan disease (CD) is an autosomal recessively inherited leukodystrophy. ...
[Canavan disease (aspartoacylase deficiency)].
Kobayashi K, Sakuragawa N. Kobayashi K, et al. Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):385-8. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590077 Review. Japanese. No abstract available.
Canavan disease: from spongy degeneration to molecular analysis.
Matalon R, Michals K, Kaul R. Matalon R, et al. J Pediatr. 1995 Oct;127(4):511-7. doi: 10.1016/s0022-3476(95)70105-2. J Pediatr. 1995. PMID: 7562269 Review.
Establishing the basic defect in Canavan disease has led to reliable biochemical methods for the diagnosis of this disease. The isolation of the gene and identification of mutations causing Canavan disease have led to the possibility of using DNA methods for the dia …
Establishing the basic defect in Canavan disease has led to reliable biochemical methods for the diagnosis of this disease. The isola …
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