References analysis of the Wikipedia article "Spongy degeneration of the central nervous system" in the English version

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Baslow MH, Guilfoyle DN (April 2013). "Canavan disease, a rare early-onset human spongiform leukodystrophy: insights into its genesis and possible clinical interventions". Biochimie. 95 (4): 946–56. doi:10.1016/j.biochi.2012.10.023. PMID 23151389.

Namboodiri AM, Peethambaran A, Mathew R, Sambhu PA, Hershfield J, Moffett JR, Madhavarao CN (June 2006). "Canavan disease and the role of N-acetylaspartate in myelin synthesis". Molecular and Cellular Endocrinology. 252 (1–2): 216–23. doi:10.1016/j.mce.2006.03.016. PMID 16647192. S2CID 12255670.

Feigenbaum A, Moore R, Clarke J, Hewson S, Chitayat D, Ray PN, Stockley TL (January 2004). "Canavan disease: carrier-frequency determination in the Ashkenazi Jewish population and development of a novel molecular diagnostic assay". American Journal of Medical Genetics. Part A. 124A (2): 142–7. doi:10.1002/ajmg.a.20334. PMID 14699612. S2CID 25981659.

Matalon RM, Michals-Matalon K (March 2000). "Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings". Frontiers in Bioscience. 5: D307-11. doi:10.2741/matalon. PMID 10704428.

Madhavarao CN, Arun P, Moffett JR, Szucs S, Surendran S, Matalon R, et al. (April 2005). "Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease". Proceedings of the National Academy of Sciences of the United States of America. 102 (14): 5221–6. Bibcode:2005PNAS..102.5221M. doi:10.1073/pnas.0409184102. PMC 555036. PMID 15784740.

Surendran S, Michals-Matalon K, Quast MJ, Tyring SK, Wei J, Ezell EL, Matalon R (March 2006). "Canavan disease: a monogenic trait with complex genomic interaction". Molecular Genetics and Metabolism. 80 (1–2): 74–80. doi:10.1016/j.ymgme.2003.08.015. PMID 14567959.

Ahmed SS, Gao G (2014). Zschocke J, Baumgartner M, Morava E, Patterson M (eds.). "Making the White Matter Matters: Progress in Understanding Canavan's Disease and Therapeutic Interventions Through Eight Decades". JIMD Reports. 19. Berlin, Heidelberg: Springer Berlin Heidelberg: 11–22. doi:10.1007/8904_2014_356. ISBN 978-3-662-46189-1. PMC 4501231. PMID 25604619.

Matalon R, Michals K, Kaul R (October 1995). "Canavan disease: from spongy degeneration to molecular analysis". The Journal of Pediatrics. 127 (4): 511–7. doi:10.1016/S0022-3476(95)70105-2. PMID 7562269.

Adachi M, Schneck L, Cara J, Volk BW (September 1973). "Spongy degeneration of the central nervous system (van Bogaert and Bertrand type; Canavan's disease). A review". Human Pathology. 4 (3): 331–47. doi:10.1016/s0046-8177(73)80098-x. PMID 4593851.

Kantor B, McCown T, Leone P, Gray SJ (2014-01-01). Clinical Applications Involving CNS Gene Transfer. Advances in Genetics. Vol. 87. pp. 71–124. doi:10.1016/B978-0-12-800149-3.00002-0. ISBN 9780128001493. PMC 4518844. PMID 25311921.

Traeger EC, Rapin I (March 1998). "The clinical course of Canavan disease". Pediatric Neurology. 18 (3): 207–12. doi:10.1016/s0887-8994(97)00185-9. PMID 9568915.

Zeuthen T (2000). "Molecular water pumps". Reviews of Physiology, Biochemistry and Pharmacology. 141. Berlin, Heidelberg: Springer Berlin Heidelberg: 97–151. doi:10.1007/bfb0119578. ISBN 978-3-540-66627-1. PMID 10916424.

Wang J, Leone P, Wu G, Francis JS, Li H, Jain MR, et al. (January 2009). "Myelin lipid abnormalities in the aspartoacylase-deficient tremor rat". Neurochemical Research. 34 (1): 138–48. doi:10.1007/s11064-008-9726-5. PMC 4640699. PMID 18478328.

Spange S, Wagner T, Heinzel T, Krämer OH (January 2009). "Acetylation of non-histone proteins modulates cellular signalling at multiple levels". The International Journal of Biochemistry & Cell Biology. 41 (1): 185–98. doi:10.1016/j.biocel.2008.08.027. PMID 18804549.

Kumar S, Biancotti JC, Matalon R, de Vellis J (November 2009). "Lack of aspartoacylase activity disrupts survival and differentiation of neural progenitors and oligodendrocytes in a mouse model of Canavan disease". Journal of Neuroscience Research. 87 (15): 3415–27. doi:10.1002/jnr.22233. PMID 19739253. S2CID 44554774.

Francis JS, Strande L, Markov V, Leone P (September 2012). "Aspartoacylase supports oxidative energy metabolism during myelination". Journal of Cerebral Blood Flow and Metabolism. 32 (9): 1725–36. doi:10.1038/jcbfm.2012.66. PMC 3434629. PMID 22617649.

Pederzolli CD, Mescka CP, Scapin F, Rockenbach FJ, Sgaravatti AM, Sgarbi MB, et al. (August 2007). "N-acetylaspartic acid promotes oxidative stress in cerebral cortex of rats". International Journal of Developmental Neuroscience. 25 (5): 317–24. doi:10.1016/j.ijdevneu.2007.04.002. PMID 17604935. S2CID 41719397.

Sreenivasan P, Purushothaman KK (January 2013). "Radiological clue to diagnosis of Canavan disease". Indian Journal of Pediatrics. 80 (1): 75–7. doi:10.1007/s12098-012-0794-9. PMID 22660905. S2CID 35979708.

Hoshino H, Kubota M (August 2014). "Canavan disease: clinical features and recent advances in research". Pediatrics International. 56 (4): 477–83. doi:10.1111/ped.12422. PMID 24977939. S2CID 206261733.

Hunt A, Burne R (January 1995). "Medical and nursing problems of children with neurodegenerative disease". Palliative Medicine. 9 (1): 19–26. doi:10.1177/026921639500900104. PMID 7719515. S2CID 20328927.

Bakewell J (August 2007). "Choosing support equipment in children's therapy". International Journal of Therapy and Rehabilitation. 14 (8): 379–381. doi:10.12968/ijtr.2007.14.8.24358. ISSN 1741-1645.

Roscoe RB, Elliott C, Zarros A, Baillie GS (July 2016). "Non-genetic therapeutic approaches to Canavan disease" (PDF). Journal of the Neurological Sciences. 366: 116–124. doi:10.1016/j.jns.2016.05.012. PMID 27288788. S2CID 329155.

Surendran S, Bhatnagar M (June 2011). "Upregulation of N-acetylaspartic acid induces oxidative stress to contribute in disease pathophysiology". The International Journal of Neuroscience. 121 (6): 305–9. doi:10.3109/00207454.2011.558225. PMID 21348802. S2CID 5406213.

Matsunaga S, Kishi T, Annas P, Basun H, Hampel H, Iwata N (2015). "Lithium as a Treatment for Alzheimer's Disease: A Systematic Review and Meta-Analysis". Journal of Alzheimer's Disease. 48 (2): 403–10. doi:10.3233/JAD-150437. PMID 26402004.

Lienhard U, Sass J (2011-01-01). "Canavan Disease: A Neurometabolic Disease Caused By Aspartoacylase Deficiency". Journal of Pediatric Sciences. 3 (1): 1–11. doi:10.17334/jps.44686 (inactive 1 November 2024).{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)

Naso MF, Tomkowicz B, Perry WL, Strohl WR (August 2017). "Adeno-Associated Virus (AAV) as a Vector for Gene Therapy". BioDrugs. 31 (4): 317–334. doi:10.1007/s40259-017-0234-5. PMC 5548848. PMID 28669112.

Wang D, Tai PW, Gao G (May 2019). "Adeno-associated virus vector as a platform for gene therapy delivery". Nature Reviews. Drug Discovery. 18 (5): 358–378. doi:10.1038/s41573-019-0012-9. PMC 6927556. PMID 30710128.

Liu D, Zhu M, Zhang Y, Diao Y (January 2021). "Crossing the blood-brain barrier with AAV vectors". Metabolic Brain Disease. 36 (1): 45–52. doi:10.1007/s11011-020-00630-2. ISSN 0885-7490. PMID 33201426. S2CID 226986888.

Chen W, Hu Y, Ju D (August 2020). "Gene therapy for neurodegenerative disorders: advances, insights and prospects". Acta Pharmaceutica Sinica B. 10 (8): 1347–1359. doi:10.1016/j.apsb.2020.01.015. PMC 7488363. PMID 32963936.

Bass NE, Debrosse SD (2014-01-01). "Canavan's Disease". Encyclopedia of the Neurological Sciences. Academic Press. pp. 577–579. doi:10.1016/B978-0-12-385157-4.00088-9. ISBN 9780123851581.

Globus JH, Strauss I (1928-12-01). "Progressive Degenerative Subcortical Encephalopathy". Archives of Neurology & Psychiatry. 20 (6): 1190–1228. doi:10.1001/archneurpsyc.1928.02210180041003. ISSN 0096-6754.

Klugmann, Matthias; Leichtlein, Claudia B. (2006). "Clinical Trials of Gene Therapy for Canavan Disease – I. The Nosology of Canavan Disease". In Kaplitt, Michael G.; During, Matthew J. (eds.). Gene Therapy of the Central Nervous System. pp. 303–316. doi:10.1016/B978-012397632-1/50024-1. ISBN 978-0-12-397632-1.

Bertorini, Tulio E.; Perez, Angel (2014). "Neurologic complications of disorders of the adrenal glands". In Biller, José; Ferro, José M. (eds.). Handbook of Clinical Neurology: Neurologic Aspects of Systemic Disease Part II. Vol. 120. pp. 749–771. doi:10.1016/B978-0-7020-4087-0.00050-4. ISBN 9780702040870. PMID 24365350.

Canavan MM (February 1931). "Schilder's encephalitis periaxialis diffusa: Report of a case in a child aged sixteen and one-half months". Archives of Neurology & Psychiatry. 25 (2): 299–308. doi:10.1001/archneurpsyc.1931.02230020085005.

Adachi M (1967). "Studies on Spongy Degeneration of the Central Nervous System (Van Bogaert–Bertrand Type)". Inborn Disorders of Sphingolipid Metabolism. Elsevier. pp. 129–147. doi:10.1016/b978-1-4831-9855-2.50013-7. ISBN 978-1-4831-9855-2.

Eiselsberg F (1937-06-01). "Über frühkindliche familiäre diffuse Hirnsklerose". Zeitschrift für Kinderheilkunde (in German). 58 (6): 702–725. doi:10.1007/BF02249721. ISSN 1432-1076. S2CID 31242183.

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pubmed.ncbi.nlm.nih.gov

Bokhari MR, Samanta D, Bokhari SR (2021). Canavan Disease. Treasure Island (FL): StatPearls Publishing. PMID 28613566. {{cite book}}: |work= ignored (help)

Matalon R, Delgado L, Michals-Matalon K (1993). Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, Amemiya A (eds.). Canavan Disease. Seattle (WA): University of Washington, Seattle. PMID 20301412. {{cite book}}: |work= ignored (help)

Traeger EC, Rapin I (March 1998). "The clinical course of Canavan disease". Pediatric Neurology. 18 (3): 207–12. doi:10.1016/s0887-8994(97)00185-9. PMID 9568915.

Chuang YC (March 2010). "Mitochondrial dysfunction and oxidative stress in seizure-induced neuronal cell death". Acta Neurologica Taiwanica. 19 (1): 3–15. PMID 20711885.

Kaul R, Gao GP, Aloya M, Balamurugan K, Petrosky A, Michals K, Matalon R (July 1994). "Canavan disease: mutations among Jewish and non-Jewish patients". American Journal of Human Genetics. 55 (1): 34–41. PMC 1918221. PMID 8023850.

Poser, CM; Goutières, F; Carpentier, MA; Aicardi, J (January 1986). "Schilder's myelinoclastic diffuse sclerosis". Pediatrics. 77 (1): 107–112. PMID 3940347. Erratum in: Pediatrics. 78(1): 138, (July 1986). The term "Schilder's disease" has been used to describe conditions as disparate as adrenoleukodystrophy, myelinoclastic diffuse sclerosis... The eponymic designation should be reserved for instances of myelinoclastic diffuse sclerosis that correspond to the case described by Schilder in 1912.

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Spongy degeneration of the central nervous system (English Wikipedia)

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