References analysis of the Wikipedia article "Batten disease" in the English version

doi.org

Hobert JA, Dawson G (October 2006). "Neuronal ceroid lipofuscinoses therapeutic strategies: past, present and future". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762 (10): 945–53. doi:10.1016/j.bbadis.2006.08.004. PMID 17049436.

Rakheja D, Narayan SB, Bennett MJ (September 2007). "Juvenile neuronal ceroid-lipofuscinosis (Batten disease): a brief review and update". Current Molecular Medicine. 7 (6): 603–8. doi:10.2174/156652407781695729. PMID 17896996.

Cooper JD (June 2008). "Moving towards therapies for juvenile Batten disease?". Experimental Neurology. 211 (2): 329–31. doi:10.1016/j.expneurol.2008.02.016. PMID 18400221. S2CID 32126291.

Ostergaard, JR (2016). "Juvenile neuronal ceroid lipofuscinosis (Batten disease): current insights". Degenerative Neurological and Neuromuscular Disease. 6: 73–83. doi:10.2147/DNND.S111967. PMC 6053093. PMID 30050370.

Cialone J, Adams H, Augustine EF, et al. (May 2012). "Females experience a more severe disease course in Batten disease". Journal of Inherited Metabolic Disease. 35 (3): 549–55. doi:10.1007/s10545-011-9421-6. PMC 3320704. PMID 22167274.

Jill M. Weimer; Elizabeth Kriscenski-Perry; Yasser Elshatory; David A. Pearce (2002). "The Neuronal Ceroid Lipofuscinoses: Mutations in Different Proteins Result in Similar Disease". NeuroMolecular Medicine. 1 (2): 111–124. doi:10.1385/nmm:1:2:111. PMID 12025857. S2CID 33921126.

Jalanko, Anu; Braulke, Thomas (2009). "Neuronal ceroid lipofuscinoses". Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1793 (4): 697–709. doi:10.1016/j.bbamcr.2008.11.004. PMID 19084560.

Simonati, A; Williams, RE (2022). "Neuronal Ceroid Lipofuscinosis: The Multifaceted Approach to the Clinical Issues, an Overview". Frontiers in Neurology. 13: 811686. doi:10.3389/fneur.2022.811686. PMC 8961688. PMID 35359645.

Bozorg, S; Ramirez-Montealegre, D; Chung, M; Pearce, DA (July 2009). "Juvenile neuronal ceroid lipofuscinosis (JNCL) and the eye". Survey of Ophthalmology. 54 (4): 463–71. doi:10.1016/j.survophthal.2009.04.007. PMC 4139962. PMID 19539834.

Kim, Jinkuk; Hu, Chunguang; Moufawad El Achkar, Christelle; Black, Lauren E.; Douville, Julie; Larson, Austin; Pendergast, Mary K.; Goldkind, Sara F.; Lee, Eunjung A.; Kuniholm, Ashley; Soucy, Aubrie; Vaze, Jai; Belur, Nandkishore R.; Fredriksen, Kristina; Stojkovska, Iva; Tsytsykova, Alla; Armant, Myriam; Didonato, Renata L.; Choi, Jaejoon; Cornelissen, Laura; Pereira, Luis M.; Augustine, Erika F.; Genetti, Casie A.; Dies, Kira; Barton, Brenda; Williams, Lucinda; Goodlett, Benjamin D.; Riley, Bobbie L.; Pasternak, Amy; et al. (2019). "Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease". New England Journal of Medicine. 381 (17): 1644–1652. doi:10.1056/NEJMoa1813279. PMC 6961983. PMID 31597037.

Kim, J; Hu, C; Moufawad El Achkar, C; Black, LE; Douville, J; Larson, A; Pendergast, MK; Goldkind, SF; Lee, EA; Kuniholm, A; Soucy, A; Vaze, J; Belur, NR; Fredriksen, K; Stojkovska, I; Tsytsykova, A; Armant, M; DiDonato, RL; Choi, J; Cornelissen, L; Pereira, LM; Augustine, EF; Genetti, CA; Dies, K; Barton, B; Williams, L; Goodlett, BD; Riley, BL; Pasternak, A; Berry, ER; Pflock, KA; Chu, S; Reed, C; Tyndall, K; Agrawal, PB; Beggs, AH; Grant, PE; Urion, DK; Snyder, RO; Waisbren, SE; Poduri, A; Park, PJ; Patterson, A; Biffi, A; Mazzulli, JR; Bodamer, O; Berde, CB; Yu, TW (24 October 2019). "Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease". The New England Journal of Medicine. 381 (17): 1644–1652. doi:10.1056/NEJMoa1813279. PMC 6961983. PMID 31597037. S2CID 204030052.

Worgall S, Sondhi D, Hackett NR, et al. (May 2008). "Treatment of late infantile neuronal ceroid lipofuscinosis by CNS administration of a serotype 2 adeno-associated virus expressing CLN2 cDNA". Human Gene Therapy. 19 (5): 463–74. CiteSeerX 10.1.1.553.872. doi:10.1089/hum.2008.022. PMID 18473686.

Kovács, Attila D.; Pearce, David A. (2008-01-01). "Attenuation of AMPA receptor activity improves motor skills in a mouse model of juvenile Batten disease". Experimental Neurology. The Role of α-synuclein in the Pathogenesis of Parkinson's Disease / Gene Therapy for Parkinson's. 209 (1): 288–291. doi:10.1016/j.expneurol.2007.09.012. PMC 4418195. PMID 17963751.

Selden, NR; Al-Uzri, A; Huhn, SL; Koch, TK; Sikora, DM; Nguyen-Driver, MD; Guillaume, DJ; Koh, JL; Gultekin, SH; Anderson, JC; Vogel, H; Sutcliffe, TL; Jacobs, Y; Steiner, RD (June 2013). "Central nervous system stem cell transplantation for children with neuronal ceroid lipofuscinosis". Journal of Neurosurgery. Pediatrics. 11 (6): 643–52. doi:10.3171/2013.3.PEDS12397. PMID 23581634.

Augustine, EF; Beck, CA; Adams, HR; Defendorf, S; Vierhile, A; Timm, D; Weimer, JM; Mink, JW; Marshall, FJ (2019). "Short-Term Administration of Mycophenolate Is Well-Tolerated in CLN3 Disease (Juvenile Neuronal Ceroid Lipofuscinosis)". JIMD Reports. 43: 117–124. doi:10.1007/8904_2018_113. ISBN 978-3-662-58613-6. PMC 6323012. PMID 29923092.

Sondhi, Dolan; Kaminsky, Stephen M.; Hackett, Neil R.; Pagovich, Odelya E.; Rosenberg, Jonathan B.; De, Bishnu P.; Chen, Alvin; Van de Graaf, Benjamin; Mezey, Jason G.; Mammen, Grace W.; Mancenido, Denesy; Xu, Fang; Kosofsky, Barry; Yohay, Kaleb; Worgall, Stefan; Kaner, Robert J.; Souwedaine, Mark; Greenwald, Bruce M.; Kaplitt, Michael; Dyke, Jonathan P.; Ballon, Douglas J.; Heier, Linda A.; Kiss, Szilard; Crystal, Ronald G. (2 December 2020). "Slowing late infantile Batten disease by direct brain parenchymal administration of a rh.10 adeno-associated virus expressing CLN2". Science Translational Medicine. 12 (572): eabb5413. doi:10.1126/scitranslmed.abb5413. ISSN 1946-6234. PMC 8056991. PMID 33268510.

Haney, Matthew J.; Klyachko, Natalia L.; Harrison, Emily B.; Zhao, Yuling; Kabanov, Alexander V.; Batrakova, Elena V. (June 2019). "TPP1 Delivery to Lysosomes with Extracellular Vesicles and their Enhanced Brain Distribution in the Animal Model of Batten Disease". Advanced Healthcare Materials. 8 (11): 1801271. doi:10.1002/adhm.201801271. ISSN 2192-2640. PMC 6584948. PMID 30997751.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cooper JD (June 2008). "Moving towards therapies for juvenile Batten disease?". Experimental Neurology. 211 (2): 329–31. doi:10.1016/j.expneurol.2008.02.016. PMID 18400221. S2CID 32126291.

Mole, Sara E.; Williams, Ruth E. (1993). "Neuronal Ceroid-Lipofuscinoses – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY". GeneReviews. University of Washington, Seattle. PMID 20301601.

ncbi.nlm.nih.gov

ninds.nih.gov

psu.edu

citeseerx.ist.psu.edu

semanticscholar.org

api.semanticscholar.org

Cooper JD (June 2008). "Moving towards therapies for juvenile Batten disease?". Experimental Neurology. 211 (2): 329–31. doi:10.1016/j.expneurol.2008.02.016. PMID 18400221. S2CID 32126291.

worldcat.org

Batten disease (English Wikipedia)

books.google.com

clinicaltrials.gov

doi.org

ghostarchive.org

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

ninds.nih.gov

noahshope.com

otago.ac.nz

portlandtribune.com

progress.org.uk

psu.edu

citeseerx.ist.psu.edu

semanticscholar.org

api.semanticscholar.org

wbur.org

web.archive.org

whonamedit.com

worldcat.org

youtube.com