โรคจอตามีสารสี (Thai Wikipedia)

Lim, Jennifer I; Chow, Clement C; Genead, Mohamed Ali; Akkara, John Davis; Epley, K David; Shah, Vinay A (2019-03-14). "Retinitis Pigmentosa". American Academy of Ophthalmology. เก็บจากแหล่งเดิมเมื่อ 2018-07-30.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)

abstractsonline.com

Wen, Rong; Luo, Lingyu; Huang, Dequang; Xia, Xin; Wang, Zhengying; Chen, Pingping; Li, Yiwen (2012-05-07). Mesencephalic Astrocyte-derived Neurotrophic Factor (MANF) Protects Rod and Cone Photoreceptors from Degeneration in Transgenic Rats Carrying the S334ter Rhodopsin Mutation. ARVO 2012.

archive.org

Dryja, Thaddeus P.; McGee, Terri L.; Reichel, Elias; Hahn, Lauri B.; Cowley, Glenn S.; Yandell, David W.; Sandberg, Michael A.; Berson, Eliot L. (1990). "A point mutation of the rhodopsin gene in one form of retinitis pigmentosa". Nature. 343 (6256): 364–6. Bibcode:1990Natur.343..364D. doi:10.1038/343364a0. PMID 2137202.
Berson, E. L.; Rosner, B; Sandberg, M. A.; Weigel-Difranco, C; Dryja, T. P. (1991). "Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine". American Journal of Ophthalmology. 111 (5): 614–23. doi:10.1016/s0002-9394(14)73708-0. PMID 2021172.

archive.today

"Nahrungsergänzungsmittel: ALLES, was du wissen musst!". คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2013-08-19. สืบค้นเมื่อ 2013-08-19. ^{[ต้องการอ้างอิงเต็มรูปแบบ]}

arvojournals.org

iovs.arvojournals.org

Wen, Rong; Luo, Lingyu; Huang, Dequang; Xia, Xin; Wang, Zhengying; Chen, Pingping; Li, Yiwen (March 2012). "Mesencephalic Astrocyte-derived Neurotrophic Factor (MANF) Protects Rod and Cone Photoreceptors from Degeneration in Transgenic Rats Carrying the S334ter Rhodopsin Mutation". Invest. Ophthalmol. Vis. Sci. 53 (14): 2581. สืบค้นเมื่อ 2016-08-07.

columbia.edu

newsroom.cumc.columbia.edu

"Two Treatments for Retinitis Pigmentosa Move Closer to Clinical Trials" (Press release). Columbia University Medical Center. 2012-12-20. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2018-06-27. สืบค้นเมื่อ 2016-08-07.

columbiaeye.org

"Retinitis Pigmentosa". เก็บจากแหล่งเดิมเมื่อ 2018-12-22.

doctorsomkiat.com

rpsiam.doctorsomkiat.com

นพ. สมเกียรติ อธิคมกุลชัย. "โรคอาร์พี". เก็บจากแหล่งเดิมเมื่อ 2018-11-07. สืบค้นเมื่อ 2014-06-03.

doi.org

Shintani, Kelly; Shechtman, Diana L.; Gurwood, Andrew S. (2009). "Review and update: Current treatment trends for patients with retinitis pigmentosa". Optometry. 80 (7): 384–401. doi:10.1016/j.optm.2008.01.026. PMID 19545852.
Soucy, E; Wang, Y; Nirenberg, S; Nathans, J; Meister, M (1998). "A Novel Signaling Pathway from Rod Photoreceptors to Ganglion Cells in Mammalian Retina". Neuron. 21 (3): 481–93. doi:10.1016/S0896-6273(00)80560-7. PMID 9768836.
Hartong, Dyonne T; Berson, Eliot L; Dryja, Thaddeus P (2006). "Retinitis pigmentosa". The Lancet. 368 (9549): 1795–1809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430.
Daiger, S P; Sullivan, L S; Bowne, S J (2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Farrar, GJ; Kenna, PF; Humphries, P (March 2002). "On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention". EMBO J. 21 (5): 857–64. doi:10.1093/emboj/21.5.857. PMC 125887. PMID 11867514.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Rivolta, C.; Sharon, D; Deangelis, M. M.; Dryja, T. P. (2002). "Retinitis pigmentosa and allied diseases: Numerous diseases, genes, and inheritance patterns". Human Molecular Genetics. 11 (10): 1219–27. doi:10.1093/hmg/11.10.1219. PMID 12015282.
Berson, Eliot L.; Rosner, B; Sandberg, M. A.; Dryja, T. P. (1991). "Ocular Findings in Patients with Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)". Archives of Ophthalmology. 109 (1): 92–101. doi:10.1001/archopht.1991.01080010094039. PMID 1987956.
Senin, Ivan I.; Bosch, Laia; Ramon, Eva; Zernii, Evgeni Yu.; Manyosa, Joan; Philippov, Pavel P.; Garriga, Pere (2006). "Ca2+/recoverin dependent regulation of phosphorylation of the rhodopsin mutant R135L associated with retinitis pigmentosa". Biochemical and Biophysical Research Communications. 349 (1): 345–52. doi:10.1016/j.bbrc.2006.08.048. PMID 16934219.
Dryja, Thaddeus P.; McGee, Terri L.; Reichel, Elias; Hahn, Lauri B.; Cowley, Glenn S.; Yandell, David W.; Sandberg, Michael A.; Berson, Eliot L. (1990). "A point mutation of the rhodopsin gene in one form of retinitis pigmentosa". Nature. 343 (6256): 364–6. Bibcode:1990Natur.343..364D. doi:10.1038/343364a0. PMID 2137202.
Dryja, Thaddeus P.; McGee, Terri L.; Hahn, Lauri B.; Cowley, Glenn S.; Olsson, Jane E.; Reichel, Elias; Sandberg, Michael A.; Berson, Eliot L. (1990). "Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa". New England Journal of Medicine. 323 (19): 1302–7. doi:10.1056/NEJM199011083231903. PMID 2215617.
Berson, E. L.; Rosner, B; Sandberg, M. A.; Weigel-Difranco, C; Dryja, T. P. (1991). "Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine". American Journal of Ophthalmology. 111 (5): 614–23. doi:10.1016/s0002-9394(14)73708-0. PMID 2021172.
Oh, Kean T.; Weleber, R. G.; Lotery, A; Oh, D. M.; Billingslea, A. M.; Stone, E. M. (2000). "Description of a New Mutation in Rhodopsin, Pro23Ala, and Comparison with Electroretinographic and Clinical Characteristics of the Pro23His Mutation". Archives of Ophthalmology. 118 (9): 1269–76. doi:10.1001/archopht.118.9.1269. PMID 10980774.
Bujakowska, K.; Maubaret, C.; Chakarova, C. F.; Tanimoto, N.; Beck, S. C.; Fahl, E.; Humphries, M. M.; Kenna, P. F.; Makarov, E.; Makarova, O.; Paquet-Durand, F.; Ekstrom, P. A.; Van Veen, T.; Leveillard, T.; Humphries, P.; Seeliger, M. W.; Bhattacharya, S. S. (2009). "Study of Gene-Targeted Mouse Models of Splicing Factor Gene Prpf31 Implicated in Human Autosomal Dominant Retinitis Pigmentosa (RP)". Investigative Ophthalmology & Visual Science. 50 (12): 5927–5933. doi:10.1167/iovs.08-3275. PMID 19578015.
Mendes, HF; van der Spuy, J; Chapple, JP; Cheetham, ME (April 2005). "Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy". Trends in Molecular Medicine. 11 (4): 177–185. doi:10.1016/j.molmed.2005.02.007. PMID 15823756.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Chang, S; Vaccarella, L; Olatunji, S; Cebulla, C; Christoforidis, J (2011). "Diagnostic Challenges in Retinitis Pigmentosa: Genotypic Multiplicity and Phenotypic Variability". Current Genomics. 12 (4): 267–75. doi:10.2174/138920211795860116. PMC 3131734. PMID 22131872.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Hartong, DT; Berson, EL; Dryja, TP (November 2006). "Retinitis pigmentosa". The Lancet. 368 (9549): 1795–1809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Rayapudi, S; Schwartz, SG; Wang, X; Chavis, P (2013). "Vitamin A and fish oils for retinitis pigmentosa". Cochrane Database Syst Rev. 12 (12): CD008428. doi:10.1002/14651858.CD008428.pub2. PMC 4259575. PMID 24357340.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Lok, Corie (2014). "Curing blindness: Vision quest". Nature News & Comment. 513 (7517): 160–162. doi:10.1038/513160a. PMID 25209781.
Berson, Eliot L.; Rosner, B; Sandberg, M. A.; Hayes, K. C.; Nicholson, B. W.; Weigel-Difranco, C; Willett, W (1993). "A Randomized Trial of Vitamin a and Vitamin E Supplementation for Retinitis Pigmentosa". Archives of Ophthalmology. 111 (6): 761–72. doi:10.1001/archopht.1993.01090060049022. PMID 8512476.
Berson, Eliot L. (2007). "Long-term visual prognoses in patients with retinitis pigmentosa: The Ludwig von Sallmann lecture". Experimental Eye Research. 85 (1): 7–14. doi:10.1016/j.exer.2007.03.001. PMC 2892386. PMID 17531222.
Humayun, Mark S.; Dorn, Jessy D.; Da Cruz, Lyndon; Dagnelie, Gislin; Sahel, José-Alain; Stanga, Paulo E.; Cideciyan, Artur V.; Duncan, Jacque L.; Eliott, Dean; Filley, Eugene; Ho, Allen C.; Santos, Arturo; Safran, Avinoam B.; Arditi, Aries; Del Priore, Lucian V.; Greenberg, Robert J.; Argus Ii Study, Group (2012). "Interim Results from the International Trial of Second Sight's Visual Prosthesis". Ophthalmology. 119 (4): 779–88. doi:10.1016/j.ophtha.2011.09.028. PMC 3319859. PMID 22244176.
Stingl, K; Bartz-Schmidt, KU; Besch, D; Braun, A; Bruckmann, A; Gekeler, F; Greppmaier, U; Hipp, S; Hörtdörfer, G; Kernstock, C; Koitschev, A; Kusnyerik, A; Sachs, H; Schatz, A; Stingl, KT; Peters, T; Wilhelm, B; Zrenner, E (2013). "Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS". Proc. Biol. Sci. 280 (1757): 20130077. doi:10.1098/rspb.2013.0077. PMC 3619489. PMID 23427175.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Bainbridge, James W.B.; Smith, Alexander J.; Barker, Susie S.; Robbie, Scott; Henderson, Robert; Balaggan, Kamaljit; Viswanathan, Ananth; Holder, Graham E.; Stockman, Andrew; Tyler, Nick; Petersen-Jones, Simon; Bhattacharya, Shomi S.; Thrasher, Adrian J.; Fitzke, Fred W.; Carter, Barrie J.; Rubin, Gary S.; Moore, Anthony T.; Ali, Robin R. (2008). "Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis". New England Journal of Medicine. 358 (21): 2231–9. CiteSeerX 10.1.1.574.4003. doi:10.1056/NEJMoa0802268. PMID 18441371.
Maguire, AM; High, KA; Auricchio, A และคณะ (November 2009). "Age-dependent effects of RPE65 gene therapy for Lebers congenital amaurosis: a phase 1 dose-escalation trial". The Lancet. 374 (9701): 1597–1605. doi:10.1016/S0140-6736(09)61836-5. PMC 4492302. PMID 19854499.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Mezer, E; Babul-Hirji, R; Wise, R; Chipman, M; Dasilva, L; Rowell, M; Thackray, R; Shuman, C. T.; Levin, A. V. (2007). "Attitudes regarding predictive testing for retinitis pigmentosa". Ophthalmic Genet. 28 (1): 9–15. doi:10.1080/13816810701199423. PMID 17454742.
Parmeggiani, F (2011). "Clinics, Epidemiology and Genetics of Retinitis Pigmentosa". Current Genomics. 12 (4): 236–7. doi:10.2174/138920211795860080. PMC 3131730. PMID 22131868.
Hamel, Christian (2006). "Retinitis pigmentosa". Orphanet Journal of Rare Diseases. 1: 40. doi:10.1186/1750-1172-1-40. PMC 1621055. PMID 17032466.
Prokisch, Holger; Hartig, Monika; Hellinger, Rosa; Meitinger, Thomas; Rosenberg, Thomas (2007). "IOVS - A Population-Based Epidemiological and Genetic Study of X-Linked Retinitis Pigmentosa". Investigative Ophthalmology & Visual Science. 48 (9): 4012–8. doi:10.1167/iovs.07-0071. PMID 17724181.
Haim, Marianne (2002). "The epidemiology of retinitis pigmentosa in Denmark". Acta Ophthalmologica Scandinavica. 80: 1–34. doi:10.1046/j.1395-3907.2002.00001.x.
MacLaren, R. E.; Pearson, R. A.; MacNeil, A.; Douglas, R. H.; Salt, T. E.; Akimoto, M.; Swaroop, A.; Sowden, J. C.; Ali, R. R. (2006). "Retinal repair by transplantation of photoreceptor precursors". Nature. 444 (7116): 203–7. Bibcode:2006Natur.444..203M. doi:10.1038/nature05161. PMID 17093405.
Sato, Shigeru; Omori, Yoshihiro; Katoh, Kimiko; Kondo, Mineo; Kanagawa, Motoi; Miyata, Kentaro; Funabiki, Kazuo; Koyasu, Toshiyuki; Kajimura, Naoko; Miyoshi, Tomomitsu; Sawai, Hajime; Kobayashi, Kazuhiro; Tani, Akiko; Toda, Tatsushi; Usukura, Jiro; Tano, Yasuo; Fujikado, Takashi; Furukawa, Takahisa (2008). "Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation". Nature Neuroscience. 11 (8): 923–31. doi:10.1038/nn.2160. PMID 18641643.
Barragán, L; Borrego, S; Abd El-Aziz, MM; El-Ashry, MF; Antiñolo, G (January 2008). "Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs". Annals of Human Genetics. 72 (Pt 1): 26–34. doi:10.1111/j.1469-1809.2007.00393.x. PMID 17803723.
Busskamp, V.; Duebel, J.; Balya, D.; Fradot, M.; Viney, T. J.; Siegert, S.; Groner, A. C.; Cabuy, E.; Forster, V.; Seeliger, M.; Biel, M.; Humphries, P.; Paques, M.; Mohand-Said, S.; Trono, D.; Deisseroth, K.; Sahel, J. A.; Picaud, S.; Roska, B. (2010). "Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa" (PDF). Science. 329 (5990): 413–7. Bibcode:2010Sci...329..413B. doi:10.1126/science.1190897. PMID 20576849.
Tochitsky, Ivan; Polosukhina, Aleksandra; Degtyar, Vadim E.; Gallerani, Nicholas; Smith, Caleb M.; Friedman, Aaron; Van Gelder, Russell N.; Trauner, Dirk; Kaufer, Daniela; Kramer, Richard H. (2014). "Restoring Visual Function to Blind Mice with a Photoswitch that Exploits Electrophysiological Remodeling of Retinal Ganglion Cells". Neuron. 81 (4): 800–13. doi:10.1016/j.neuron.2014.01.003. PMC 3933823. PMID 24559673.
Bakondi, Benjamin; Lv, Wenjian; Lu, Bin; Jones, Melissa K.; Tsai, Yuchun; Kim, Kevin J.; Levy, Rachelle; Akhtar, Aslam Abbasi; Breunig, Joshua J.; Svendsen, Clive N.; Wang, Shaomei (2016). "Molecular Therapy - Abstract of article: In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa". Molecular Therapy. 24 (3): 556–563. doi:10.1038/mt.2015.220. PMC 4786918. PMID 26666451.

fda.gov

"FDA approves first retinal implant for adults with rare genetic eye disease". คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2013-07-27.
Commissioner, Office of the. "Press Announcements - FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss". www.fda.gov (ภาษาอังกฤษ). เก็บจากแหล่งเดิมเมื่อ 2019-03-12. สืบค้นเมื่อ 2019-01-16.
"FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss". FDA. 2017-12-19. เก็บจากแหล่งเดิมเมื่อ 2019-03-12.

harvard.edu

ui.adsabs.harvard.edu

Dryja, Thaddeus P.; McGee, Terri L.; Reichel, Elias; Hahn, Lauri B.; Cowley, Glenn S.; Yandell, David W.; Sandberg, Michael A.; Berson, Eliot L. (1990). "A point mutation of the rhodopsin gene in one form of retinitis pigmentosa". Nature. 343 (6256): 364–6. Bibcode:1990Natur.343..364D. doi:10.1038/343364a0. PMID 2137202.
MacLaren, R. E.; Pearson, R. A.; MacNeil, A.; Douglas, R. H.; Salt, T. E.; Akimoto, M.; Swaroop, A.; Sowden, J. C.; Ali, R. R. (2006). "Retinal repair by transplantation of photoreceptor precursors". Nature. 444 (7116): 203–7. Bibcode:2006Natur.444..203M. doi:10.1038/nature05161. PMID 17093405.
Busskamp, V.; Duebel, J.; Balya, D.; Fradot, M.; Viney, T. J.; Siegert, S.; Groner, A. C.; Cabuy, E.; Forster, V.; Seeliger, M.; Biel, M.; Humphries, P.; Paques, M.; Mohand-Said, S.; Trono, D.; Deisseroth, K.; Sahel, J. A.; Picaud, S.; Roska, B. (2010). "Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa" (PDF). Science. 329 (5990): 413–7. Bibcode:2010Sci...329..413B. doi:10.1126/science.1190897. PMID 20576849.

inserm.fr

hal.inserm.fr

Busskamp, V.; Duebel, J.; Balya, D.; Fradot, M.; Viney, T. J.; Siegert, S.; Groner, A. C.; Cabuy, E.; Forster, V.; Seeliger, M.; Biel, M.; Humphries, P.; Paques, M.; Mohand-Said, S.; Trono, D.; Deisseroth, K.; Sahel, J. A.; Picaud, S.; Roska, B. (2010). "Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa" (PDF). Science. 329 (5990): 413–7. Bibcode:2010Sci...329..413B. doi:10.1126/science.1190897. PMID 20576849.

intechopen.com

cdn.intechopen.com

Gundogan, Fatih Cakir; Tas, Ahmet; Sobaci, Gungor (2011). Belusic, Gregor (บ.ก.). Electroretinogram in Hereditary Retinal Disorders (PDF). Electroretinograms. Turkey: In Tech. ISBN 978-953-307-383-5. เก็บ (PDF)จากแหล่งเดิมเมื่อ 2017-11-17.

inventorspot.com

Levenstein, Steve (2008-07-24). "Lightning-Fast Vision Protein Named After Pikachu". InventorSpot.com. Halcyon Solutions. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2017-07-11. สืบค้นเมื่อ 2014-06-12.

jkscience.org

Sharma, Yog Raj; Reddy, P Raja Rami; Singh, Deependra V (2004). "Retinitis Pigmentosa and Allied Disorders (Review Article)" (PDF). JK SCIENCE. 6 (3): 115–120. สืบค้นเมื่อ 5 มิถุนายน 2557. {{cite journal}}: ตรวจสอบค่าวันที่ใน: |accessdate= (help)CS1 maint: uses authors parameter (ลิงก์)

mda.org

"Diseases - MM - Types Of Overview". Muscular Dystrophy Association. 2015-12-18. เก็บจากแหล่งเดิมเมื่อ 2018-01-17.

nih.gov

pubmed.ncbi.nlm.nih.gov

Shintani, Kelly; Shechtman, Diana L.; Gurwood, Andrew S. (2009). "Review and update: Current treatment trends for patients with retinitis pigmentosa". Optometry. 80 (7): 384–401. doi:10.1016/j.optm.2008.01.026. PMID 19545852.
Soucy, E; Wang, Y; Nirenberg, S; Nathans, J; Meister, M (1998). "A Novel Signaling Pathway from Rod Photoreceptors to Ganglion Cells in Mammalian Retina". Neuron. 21 (3): 481–93. doi:10.1016/S0896-6273(00)80560-7. PMID 9768836.
Hartong, Dyonne T; Berson, Eliot L; Dryja, Thaddeus P (2006). "Retinitis pigmentosa". The Lancet. 368 (9549): 1795–1809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430.
Daiger, S P; Sullivan, L S; Bowne, S J (2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Farrar, GJ; Kenna, PF; Humphries, P (March 2002). "On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention". EMBO J. 21 (5): 857–64. doi:10.1093/emboj/21.5.857. PMC 125887. PMID 11867514.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Rivolta, C.; Sharon, D; Deangelis, M. M.; Dryja, T. P. (2002). "Retinitis pigmentosa and allied diseases: Numerous diseases, genes, and inheritance patterns". Human Molecular Genetics. 11 (10): 1219–27. doi:10.1093/hmg/11.10.1219. PMID 12015282.
Berson, Eliot L.; Rosner, B; Sandberg, M. A.; Dryja, T. P. (1991). "Ocular Findings in Patients with Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)". Archives of Ophthalmology. 109 (1): 92–101. doi:10.1001/archopht.1991.01080010094039. PMID 1987956.
Senin, Ivan I.; Bosch, Laia; Ramon, Eva; Zernii, Evgeni Yu.; Manyosa, Joan; Philippov, Pavel P.; Garriga, Pere (2006). "Ca2+/recoverin dependent regulation of phosphorylation of the rhodopsin mutant R135L associated with retinitis pigmentosa". Biochemical and Biophysical Research Communications. 349 (1): 345–52. doi:10.1016/j.bbrc.2006.08.048. PMID 16934219.
Dryja, Thaddeus P.; McGee, Terri L.; Reichel, Elias; Hahn, Lauri B.; Cowley, Glenn S.; Yandell, David W.; Sandberg, Michael A.; Berson, Eliot L. (1990). "A point mutation of the rhodopsin gene in one form of retinitis pigmentosa". Nature. 343 (6256): 364–6. Bibcode:1990Natur.343..364D. doi:10.1038/343364a0. PMID 2137202.
Dryja, Thaddeus P.; McGee, Terri L.; Hahn, Lauri B.; Cowley, Glenn S.; Olsson, Jane E.; Reichel, Elias; Sandberg, Michael A.; Berson, Eliot L. (1990). "Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa". New England Journal of Medicine. 323 (19): 1302–7. doi:10.1056/NEJM199011083231903. PMID 2215617.
Berson, E. L.; Rosner, B; Sandberg, M. A.; Weigel-Difranco, C; Dryja, T. P. (1991). "Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine". American Journal of Ophthalmology. 111 (5): 614–23. doi:10.1016/s0002-9394(14)73708-0. PMID 2021172.
Inglehearn, C. F.; Bashir, R; Lester, D. H.; Jay, M; Bird, A. C.; Bhattacharya, S. S. (1991). "A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa". American Journal of Human Genetics. 48 (1): 26–30. PMC 1682750. PMID 1985460.
Oh, Kean T.; Weleber, R. G.; Lotery, A; Oh, D. M.; Billingslea, A. M.; Stone, E. M. (2000). "Description of a New Mutation in Rhodopsin, Pro23Ala, and Comparison with Electroretinographic and Clinical Characteristics of the Pro23His Mutation". Archives of Ophthalmology. 118 (9): 1269–76. doi:10.1001/archopht.118.9.1269. PMID 10980774.
Bujakowska, K.; Maubaret, C.; Chakarova, C. F.; Tanimoto, N.; Beck, S. C.; Fahl, E.; Humphries, M. M.; Kenna, P. F.; Makarov, E.; Makarova, O.; Paquet-Durand, F.; Ekstrom, P. A.; Van Veen, T.; Leveillard, T.; Humphries, P.; Seeliger, M. W.; Bhattacharya, S. S. (2009). "Study of Gene-Targeted Mouse Models of Splicing Factor Gene Prpf31 Implicated in Human Autosomal Dominant Retinitis Pigmentosa (RP)". Investigative Ophthalmology & Visual Science. 50 (12): 5927–5933. doi:10.1167/iovs.08-3275. PMID 19578015.
Mendes, HF; van der Spuy, J; Chapple, JP; Cheetham, ME (April 2005). "Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy". Trends in Molecular Medicine. 11 (4): 177–185. doi:10.1016/j.molmed.2005.02.007. PMID 15823756.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Chang, S; Vaccarella, L; Olatunji, S; Cebulla, C; Christoforidis, J (2011). "Diagnostic Challenges in Retinitis Pigmentosa: Genotypic Multiplicity and Phenotypic Variability". Current Genomics. 12 (4): 267–75. doi:10.2174/138920211795860116. PMC 3131734. PMID 22131872.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Hartong, DT; Berson, EL; Dryja, TP (November 2006). "Retinitis pigmentosa". The Lancet. 368 (9549): 1795–1809. doi:10.1016/S0140-6736(06)69740-7. PMID 17113430.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Rayapudi, S; Schwartz, SG; Wang, X; Chavis, P (2013). "Vitamin A and fish oils for retinitis pigmentosa". Cochrane Database Syst Rev. 12 (12): CD008428. doi:10.1002/14651858.CD008428.pub2. PMC 4259575. PMID 24357340.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Lok, Corie (2014). "Curing blindness: Vision quest". Nature News & Comment. 513 (7517): 160–162. doi:10.1038/513160a. PMID 25209781.
Berson, Eliot L.; Rosner, B; Sandberg, M. A.; Hayes, K. C.; Nicholson, B. W.; Weigel-Difranco, C; Willett, W (1993). "A Randomized Trial of Vitamin a and Vitamin E Supplementation for Retinitis Pigmentosa". Archives of Ophthalmology. 111 (6): 761–72. doi:10.1001/archopht.1993.01090060049022. PMID 8512476.
Berson, Eliot L. (2007). "Long-term visual prognoses in patients with retinitis pigmentosa: The Ludwig von Sallmann lecture". Experimental Eye Research. 85 (1): 7–14. doi:10.1016/j.exer.2007.03.001. PMC 2892386. PMID 17531222.
Humayun, Mark S.; Dorn, Jessy D.; Da Cruz, Lyndon; Dagnelie, Gislin; Sahel, José-Alain; Stanga, Paulo E.; Cideciyan, Artur V.; Duncan, Jacque L.; Eliott, Dean; Filley, Eugene; Ho, Allen C.; Santos, Arturo; Safran, Avinoam B.; Arditi, Aries; Del Priore, Lucian V.; Greenberg, Robert J.; Argus Ii Study, Group (2012). "Interim Results from the International Trial of Second Sight's Visual Prosthesis". Ophthalmology. 119 (4): 779–88. doi:10.1016/j.ophtha.2011.09.028. PMC 3319859. PMID 22244176.
Fernandes, RA; Diniz, B; Ribeiro, R; Humayun, M (2012-06-25). "Artificial vision through neuronal stimulation". Neuroscience letters. 519 (2): 122–8. PMID 22342306.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Stingl, K; Bartz-Schmidt, KU; Besch, D; Braun, A; Bruckmann, A; Gekeler, F; Greppmaier, U; Hipp, S; Hörtdörfer, G; Kernstock, C; Koitschev, A; Kusnyerik, A; Sachs, H; Schatz, A; Stingl, KT; Peters, T; Wilhelm, B; Zrenner, E (2013). "Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS". Proc. Biol. Sci. 280 (1757): 20130077. doi:10.1098/rspb.2013.0077. PMC 3619489. PMID 23427175.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Bainbridge, James W.B.; Smith, Alexander J.; Barker, Susie S.; Robbie, Scott; Henderson, Robert; Balaggan, Kamaljit; Viswanathan, Ananth; Holder, Graham E.; Stockman, Andrew; Tyler, Nick; Petersen-Jones, Simon; Bhattacharya, Shomi S.; Thrasher, Adrian J.; Fitzke, Fred W.; Carter, Barrie J.; Rubin, Gary S.; Moore, Anthony T.; Ali, Robin R. (2008). "Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis". New England Journal of Medicine. 358 (21): 2231–9. CiteSeerX 10.1.1.574.4003. doi:10.1056/NEJMoa0802268. PMID 18441371.
Maguire, AM; High, KA; Auricchio, A และคณะ (November 2009). "Age-dependent effects of RPE65 gene therapy for Lebers congenital amaurosis: a phase 1 dose-escalation trial". The Lancet. 374 (9701): 1597–1605. doi:10.1016/S0140-6736(09)61836-5. PMC 4492302. PMID 19854499.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Mezer, E; Babul-Hirji, R; Wise, R; Chipman, M; Dasilva, L; Rowell, M; Thackray, R; Shuman, C. T.; Levin, A. V. (2007). "Attitudes regarding predictive testing for retinitis pigmentosa". Ophthalmic Genet. 28 (1): 9–15. doi:10.1080/13816810701199423. PMID 17454742.
Parmeggiani, F (2011). "Clinics, Epidemiology and Genetics of Retinitis Pigmentosa". Current Genomics. 12 (4): 236–7. doi:10.2174/138920211795860080. PMC 3131730. PMID 22131868.
Hamel, Christian (2006). "Retinitis pigmentosa". Orphanet Journal of Rare Diseases. 1: 40. doi:10.1186/1750-1172-1-40. PMC 1621055. PMID 17032466.
Prokisch, Holger; Hartig, Monika; Hellinger, Rosa; Meitinger, Thomas; Rosenberg, Thomas (2007). "IOVS - A Population-Based Epidemiological and Genetic Study of X-Linked Retinitis Pigmentosa". Investigative Ophthalmology & Visual Science. 48 (9): 4012–8. doi:10.1167/iovs.07-0071. PMID 17724181.
MacLaren, R. E.; Pearson, R. A.; MacNeil, A.; Douglas, R. H.; Salt, T. E.; Akimoto, M.; Swaroop, A.; Sowden, J. C.; Ali, R. R. (2006). "Retinal repair by transplantation of photoreceptor precursors". Nature. 444 (7116): 203–7. Bibcode:2006Natur.444..203M. doi:10.1038/nature05161. PMID 17093405.
Sato, Shigeru; Omori, Yoshihiro; Katoh, Kimiko; Kondo, Mineo; Kanagawa, Motoi; Miyata, Kentaro; Funabiki, Kazuo; Koyasu, Toshiyuki; Kajimura, Naoko; Miyoshi, Tomomitsu; Sawai, Hajime; Kobayashi, Kazuhiro; Tani, Akiko; Toda, Tatsushi; Usukura, Jiro; Tano, Yasuo; Fujikado, Takashi; Furukawa, Takahisa (2008). "Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation". Nature Neuroscience. 11 (8): 923–31. doi:10.1038/nn.2160. PMID 18641643.
Barragán, L; Borrego, S; Abd El-Aziz, MM; El-Ashry, MF; Antiñolo, G (January 2008). "Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs". Annals of Human Genetics. 72 (Pt 1): 26–34. doi:10.1111/j.1469-1809.2007.00393.x. PMID 17803723.
Busskamp, V.; Duebel, J.; Balya, D.; Fradot, M.; Viney, T. J.; Siegert, S.; Groner, A. C.; Cabuy, E.; Forster, V.; Seeliger, M.; Biel, M.; Humphries, P.; Paques, M.; Mohand-Said, S.; Trono, D.; Deisseroth, K.; Sahel, J. A.; Picaud, S.; Roska, B. (2010). "Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa" (PDF). Science. 329 (5990): 413–7. Bibcode:2010Sci...329..413B. doi:10.1126/science.1190897. PMID 20576849.
Tochitsky, Ivan; Polosukhina, Aleksandra; Degtyar, Vadim E.; Gallerani, Nicholas; Smith, Caleb M.; Friedman, Aaron; Van Gelder, Russell N.; Trauner, Dirk; Kaufer, Daniela; Kramer, Richard H. (2014). "Restoring Visual Function to Blind Mice with a Photoswitch that Exploits Electrophysiological Remodeling of Retinal Ganglion Cells". Neuron. 81 (4): 800–13. doi:10.1016/j.neuron.2014.01.003. PMC 3933823. PMID 24559673.
Bakondi, Benjamin; Lv, Wenjian; Lu, Bin; Jones, Melissa K.; Tsai, Yuchun; Kim, Kevin J.; Levy, Rachelle; Akhtar, Aslam Abbasi; Breunig, Joshua J.; Svendsen, Clive N.; Wang, Shaomei (2016). "Molecular Therapy - Abstract of article: In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa". Molecular Therapy. 24 (3): 556–563. doi:10.1038/mt.2015.220. PMC 4786918. PMID 26666451.

ncbi.nlm.nih.gov

O'Neal, Teri B; Luther, Euil E (2018-12-20). "Retinitis Pigmentosa". StatPearls Publishing LLC. เก็บจากแหล่งเดิมเมื่อ 2019-04-16.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)
Daiger, S P; Sullivan, L S; Bowne, S J (2013). "Genes and mutations causing retinitis pigmentosa". Clinical Genetics. 84 (2): 132–41. doi:10.1111/cge.12203. PMC 3856531. PMID 23701314.
Farrar, GJ; Kenna, PF; Humphries, P (March 2002). "On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention". EMBO J. 21 (5): 857–64. doi:10.1093/emboj/21.5.857. PMC 125887. PMID 11867514.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Online 'Mendelian Inheritance in Man' (OMIM) RETINITIS PIGMENTOSA; RP -268000
Inglehearn, C. F.; Bashir, R; Lester, D. H.; Jay, M; Bird, A. C.; Bhattacharya, S. S. (1991). "A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa". American Journal of Human Genetics. 48 (1): 26–30. PMC 1682750. PMID 1985460.
Fahim, Abigail T (1993). "Nonsyndromic Retinitis Pigmentosa Overview". Retinitis Pigmentosa Overview. University of Washington, Seattle.
Chang, S; Vaccarella, L; Olatunji, S; Cebulla, C; Christoforidis, J (2011). "Diagnostic Challenges in Retinitis Pigmentosa: Genotypic Multiplicity and Phenotypic Variability". Current Genomics. 12 (4): 267–75. doi:10.2174/138920211795860116. PMC 3131734. PMID 22131872.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Rayapudi, S; Schwartz, SG; Wang, X; Chavis, P (2013). "Vitamin A and fish oils for retinitis pigmentosa". Cochrane Database Syst Rev. 12 (12): CD008428. doi:10.1002/14651858.CD008428.pub2. PMC 4259575. PMID 24357340.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Berson, Eliot L. (2007). "Long-term visual prognoses in patients with retinitis pigmentosa: The Ludwig von Sallmann lecture". Experimental Eye Research. 85 (1): 7–14. doi:10.1016/j.exer.2007.03.001. PMC 2892386. PMID 17531222.
Humayun, Mark S.; Dorn, Jessy D.; Da Cruz, Lyndon; Dagnelie, Gislin; Sahel, José-Alain; Stanga, Paulo E.; Cideciyan, Artur V.; Duncan, Jacque L.; Eliott, Dean; Filley, Eugene; Ho, Allen C.; Santos, Arturo; Safran, Avinoam B.; Arditi, Aries; Del Priore, Lucian V.; Greenberg, Robert J.; Argus Ii Study, Group (2012). "Interim Results from the International Trial of Second Sight's Visual Prosthesis". Ophthalmology. 119 (4): 779–88. doi:10.1016/j.ophtha.2011.09.028. PMC 3319859. PMID 22244176.
Stingl, K; Bartz-Schmidt, KU; Besch, D; Braun, A; Bruckmann, A; Gekeler, F; Greppmaier, U; Hipp, S; Hörtdörfer, G; Kernstock, C; Koitschev, A; Kusnyerik, A; Sachs, H; Schatz, A; Stingl, KT; Peters, T; Wilhelm, B; Zrenner, E (2013). "Artificial vision with wirelessly powered subretinal electronic implant alpha-IMS". Proc. Biol. Sci. 280 (1757): 20130077. doi:10.1098/rspb.2013.0077. PMC 3619489. PMID 23427175.{{cite journal}}: CS1 maint: multiple names: authors list (ลิงก์)
Maguire, AM; High, KA; Auricchio, A และคณะ (November 2009). "Age-dependent effects of RPE65 gene therapy for Lebers congenital amaurosis: a phase 1 dose-escalation trial". The Lancet. 374 (9701): 1597–1605. doi:10.1016/S0140-6736(09)61836-5. PMC 4492302. PMID 19854499.{{cite journal}}: CS1 maint: uses authors parameter (ลิงก์)
Parmeggiani, F (2011). "Clinics, Epidemiology and Genetics of Retinitis Pigmentosa". Current Genomics. 12 (4): 236–7. doi:10.2174/138920211795860080. PMC 3131730. PMID 22131868.
Hamel, Christian (2006). "Retinitis pigmentosa". Orphanet Journal of Rare Diseases. 1: 40. doi:10.1186/1750-1172-1-40. PMC 1621055. PMID 17032466.
Tochitsky, Ivan; Polosukhina, Aleksandra; Degtyar, Vadim E.; Gallerani, Nicholas; Smith, Caleb M.; Friedman, Aaron; Van Gelder, Russell N.; Trauner, Dirk; Kaufer, Daniela; Kramer, Richard H. (2014). "Restoring Visual Function to Blind Mice with a Photoswitch that Exploits Electrophysiological Remodeling of Retinal Ganglion Cells". Neuron. 81 (4): 800–13. doi:10.1016/j.neuron.2014.01.003. PMC 3933823. PMID 24559673.
Bakondi, Benjamin; Lv, Wenjian; Lu, Bin; Jones, Melissa K.; Tsai, Yuchun; Kim, Kevin J.; Levy, Rachelle; Akhtar, Aslam Abbasi; Breunig, Joshua J.; Svendsen, Clive N.; Wang, Shaomei (2016). "Molecular Therapy - Abstract of article: In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa". Molecular Therapy. 24 (3): 556–563. doi:10.1038/mt.2015.220. PMC 4786918. PMID 26666451.

nei.nih.gov

"Facts About Retinitis Pigmentosa". National Eye Institute (ภาษาอังกฤษ). May 2014. เก็บจากแหล่งเดิมเมื่อ 2019-03-07. สืบค้นเมื่อ 2017-12-02.

ghr.nlm.nih.gov

"Retinitis pigmentosa". NIH, US National Library of Medicine. เก็บจากแหล่งเดิมเมื่อ 2019-02-06. สืบค้นเมื่อ 2019-04-06.

nytimes.com

Belluck, Pam (2013-02-15). "Device Offers Partial Vision for the Blind". New York Times. เก็บจากแหล่งเดิมเมื่อ 2019-04-12.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)
"Well". The New York Times.^{[ลิงก์เสีย]}

psu.edu

citeseerx.ist.psu.edu

Bainbridge, James W.B.; Smith, Alexander J.; Barker, Susie S.; Robbie, Scott; Henderson, Robert; Balaggan, Kamaljit; Viswanathan, Ananth; Holder, Graham E.; Stockman, Andrew; Tyler, Nick; Petersen-Jones, Simon; Bhattacharya, Shomi S.; Thrasher, Adrian J.; Fitzke, Fred W.; Carter, Barrie J.; Rubin, Gary S.; Moore, Anthony T.; Ali, Robin R. (2008). "Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis". New England Journal of Medicine. 358 (21): 2231–9. CiteSeerX 10.1.1.574.4003. doi:10.1056/NEJMoa0802268. PMID 18441371.

reuters.com

"Spark's price for Luxturna blindness gene therapy too high: ICER". Reuters. 2018-01-13. เก็บจากแหล่งเดิมเมื่อ 2018-12-05.

rpfightingblindness.org.uk

"Usher Syndrome". เก็บจากแหล่งเดิมเมื่อ 2016-08-17.
"Bardet-Biedl (Laurence Moon)". คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2016-08-17.

rush.edu

"Ophthalmologists Implant Five Patients with Artificial Silicon Retina Microchip To Treat Vision Loss from Retinitis Pigmentosa" (Press release). Rush University Medical Center. 2005-01-31. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2005-02-08. สืบค้นเมื่อ 2007-06-16.

sciencedaily.com

"'First Bionic Eye' Retinal Chip for Blind". Science Daily. 2013-06-29. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2019-02-27. สืบค้นเมื่อ 2013-06-30.
"Gene editing technique improves vision in rats with inherited blindness: Data show the new 'CRISPR/Cas9' system potentially can be used to prevent retinal damage in a type of retinitis pigmentosa". Science Daily. 2016-01-08. สืบค้นเมื่อ 2016-01-15.

stemcellsfreak.com

"Experiments show retinitis pigmentosa is treatable". Stem Cells Freak. 2012-12-22. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2018-12-13.

technologyreview.com

"A Second Artificial Retina Option for the E.U." Technology Review. 2013-07-03.
Bourzac, Katherine. "A blind woman in Texas is first person to undergo optogenetic therapy, which could let her see again if successful". technologyreview.com.

umich.edu

kellogg.umich.edu

Openshaw, Amanda (Feb 2008). Understanding Retinitis Pigmentosa (PDF). University of Michigan Kellogg Eye Center. คลังข้อมูลเก่าเก็บจากแหล่งเดิม (PDF)เมื่อ 2017-08-29. สืบค้นเมื่อ 2017-12-02.
"Understanding Retinitis Pigmentosa" (PDF). คลังข้อมูลเก่าเก็บจากแหล่งเดิม (PDF)เมื่อ 2017-03-29. สืบค้นเมื่อ 2015-03-16.

visionaware.org

"The Argus II Retinal Prosthesis ("Bionic Eye") Receives Medicare Approval". Visionware, American Printing House for the Blind. 2013-08-19. เก็บจากแหล่งเดิมเมื่อ 2018-12-31.

web.archive.org

"Facts About Retinitis Pigmentosa". National Eye Institute (ภาษาอังกฤษ). May 2014. เก็บจากแหล่งเดิมเมื่อ 2019-03-07. สืบค้นเมื่อ 2017-12-02.
นพ. สมเกียรติ อธิคมกุลชัย. "โรคอาร์พี". เก็บจากแหล่งเดิมเมื่อ 2018-11-07. สืบค้นเมื่อ 2014-06-03.
Openshaw, Amanda (Feb 2008). Understanding Retinitis Pigmentosa (PDF). University of Michigan Kellogg Eye Center. คลังข้อมูลเก่าเก็บจากแหล่งเดิม (PDF)เมื่อ 2017-08-29. สืบค้นเมื่อ 2017-12-02.
O'Neal, Teri B; Luther, Euil E (2018-12-20). "Retinitis Pigmentosa". StatPearls Publishing LLC. เก็บจากแหล่งเดิมเมื่อ 2019-04-16.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)
Lim, Jennifer I; Chow, Clement C; Genead, Mohamed Ali; Akkara, John Davis; Epley, K David; Shah, Vinay A (2019-03-14). "Retinitis Pigmentosa". American Academy of Ophthalmology. เก็บจากแหล่งเดิมเมื่อ 2018-07-30.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)
"Usher Syndrome". เก็บจากแหล่งเดิมเมื่อ 2016-08-17.
"Diseases - MM - Types Of Overview". Muscular Dystrophy Association. 2015-12-18. เก็บจากแหล่งเดิมเมื่อ 2018-01-17.
"Bardet-Biedl (Laurence Moon)". คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2016-08-17.
"Retinitis pigmentosa". NIH, US National Library of Medicine. เก็บจากแหล่งเดิมเมื่อ 2019-02-06. สืบค้นเมื่อ 2019-04-06.
"Understanding Retinitis Pigmentosa" (PDF). คลังข้อมูลเก่าเก็บจากแหล่งเดิม (PDF)เมื่อ 2017-03-29. สืบค้นเมื่อ 2015-03-16.
Gundogan, Fatih Cakir; Tas, Ahmet; Sobaci, Gungor (2011). Belusic, Gregor (บ.ก.). Electroretinogram in Hereditary Retinal Disorders (PDF). Electroretinograms. Turkey: In Tech. ISBN 978-953-307-383-5. เก็บ (PDF)จากแหล่งเดิมเมื่อ 2017-11-17.
"Retinitis Pigmentosa". เก็บจากแหล่งเดิมเมื่อ 2018-12-22.
"FDA approves first retinal implant for adults with rare genetic eye disease". คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2013-07-27.
"'First Bionic Eye' Retinal Chip for Blind". Science Daily. 2013-06-29. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2019-02-27. สืบค้นเมื่อ 2013-06-30.
"The Argus II Retinal Prosthesis ("Bionic Eye") Receives Medicare Approval". Visionware, American Printing House for the Blind. 2013-08-19. เก็บจากแหล่งเดิมเมื่อ 2018-12-31.
Belluck, Pam (2013-02-15). "Device Offers Partial Vision for the Blind". New York Times. เก็บจากแหล่งเดิมเมื่อ 2019-04-12.{{cite web}}: CS1 maint: uses authors parameter (ลิงก์)
Commissioner, Office of the. "Press Announcements - FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss". www.fda.gov (ภาษาอังกฤษ). เก็บจากแหล่งเดิมเมื่อ 2019-03-12. สืบค้นเมื่อ 2019-01-16.
"Spark's price for Luxturna blindness gene therapy too high: ICER". Reuters. 2018-01-13. เก็บจากแหล่งเดิมเมื่อ 2018-12-05.
"Ophthalmologists Implant Five Patients with Artificial Silicon Retina Microchip To Treat Vision Loss from Retinitis Pigmentosa" (Press release). Rush University Medical Center. 2005-01-31. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2005-02-08. สืบค้นเมื่อ 2007-06-16.
Levenstein, Steve (2008-07-24). "Lightning-Fast Vision Protein Named After Pikachu". InventorSpot.com. Halcyon Solutions. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2017-07-11. สืบค้นเมื่อ 2014-06-12.
"Experiments show retinitis pigmentosa is treatable". Stem Cells Freak. 2012-12-22. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2018-12-13.
"Two Treatments for Retinitis Pigmentosa Move Closer to Clinical Trials" (Press release). Columbia University Medical Center. 2012-12-20. คลังข้อมูลเก่าเก็บจากแหล่งเดิมเมื่อ 2018-06-27. สืบค้นเมื่อ 2016-08-07.
"FDA approves novel gene therapy to treat patients with a rare form of inherited vision loss". FDA. 2017-12-19. เก็บจากแหล่งเดิมเมื่อ 2019-03-12.

wiley.com

onlinelibrary.wiley.com

Haim, Marianne (2002). "The epidemiology of retinitis pigmentosa in Denmark". Acta Ophthalmologica Scandinavica. 80: 1–34. doi:10.1046/j.1395-3907.2002.00001.x.