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La ricerca find articoli where soggetti phrase all words 'RETINITIS-PIGMENTOSA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 1263 riferimenti
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    1. Thompson, DA; McHenry, CL; Li, Y; Richards, JE; Othman, MI; Schwinger, E; Vollrath, D; Jacobson, SG; Gal, A
      Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome2, with homoallelism for mutations in RPE65 or MERTK, respectively

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Petit, C
      Usher syndrome: From genetics to pathogenesis

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    3. Liang, FQ; Aleman, TS; Dejneka, NS; Dudus, L; Fisher, KJ; Maguire, AM; Jacobson, SG; Bennett, J
      Long-term protection of retinal structure but not function using RAAV.CNTFin animal models of retinitis pigmentosa

      MOLECULAR THERAPY
    4. Green, ES; Rendahl, KG; Zhou, SZ; Ladner, M; Coyne, M; Srivastava, R; Manning, WC; Flannery, JG
      Two animal models of retinal degeneration are rescued by recombinant adeno-associated virus-mediated production of FGF-5 and FGF-18

      MOLECULAR THERAPY
    5. Liang, FQ; Dejneka, NS; Cohen, DR; Krasnoperova, NV; Lem, J; Maguire, AM; Dudus, L; Fisher, KJ; Bennett, J
      AAV-mediated delivery of ciliary neurotrophic factor prolongs photoreceptor survival in the rhodopsin knockout mouse

      MOLECULAR THERAPY
    6. Chapple, JP; Grayson, C; Hardcastle, AJ; Saliba, RS; van der Spuy, J; Cheetham, ME
      Unfolding retinal dystrophies: a role for molecular chaperones?

      TRENDS IN MOLECULAR MEDICINE
    7. Baehr, W; Chen, CK
      RP11 and RP13: unexpected gene loci

      TRENDS IN MOLECULAR MEDICINE
    8. Hiraoka, M; Trese, MT; Shastry, BS
      Evaluation of RP2 and RP3 genes in an X-linked RP family manifesting loss of central vision and preserved peripheral function

      JOURNAL OF HUMAN GENETICS
    9. Eksandh, L; Ekstrom, U; Abrahamson, M; Bauer, B; Andreasson, S
      Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    10. Gjorloff, K; Bruun, A; Ghosh, R
      Cone photoreceptors in laminated retinal transplants

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    11. Lund, RD; Kwan, ASL; Keegan, DJ; Sauve, Y; Coffey, PJ; Lawrence, JM
      Cell transplantation as a treatment for retinal disease

      PROGRESS IN RETINAL AND EYE RESEARCH
    12. Mohand-Said, S; Hicks, D; Leveillard, T; Picaud, S; Porto, F; Sahel, JA
      Rod-cone interactions: Developmental and clinical significance

      PROGRESS IN RETINAL AND EYE RESEARCH
    13. Takashima, H; Boerkoel, CF; Lupski, JR
      Screening for mutations in a genetically heterogeneous disorder: DHPLC versus DNA sequence for mutation detection in multiple genes causing Charcot-Marie-Tooth neuropathy

      GENETICS IN MEDICINE
    14. Karakousis, PC; John, SK; Behling, KC; Surace, EM; Smith, JE; Hendrickson, A; Tang, WX; Bennett, J; Milam, AH
      Localization of pigment epithelium derived factor (PEDF) in developing andadult human ocular tissues

      MOLECULAR VISION
    15. Wu, J; Trogadis, J; Bremner, R
      Rod and cone degeneration in the rd mouse is p53 independent

      MOLECULAR VISION
    16. Hartman, SJ; Menon, I; Haug-Collet, K; Colley, NJ
      Expression of rhodopsin and arrestin during the light-dark cycle in Drosophila

      MOLECULAR VISION
    17. Hooks, JJ; Tso, MOM; Detrick, B
      Retinopathies associated with antiretinal antibodies

      CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY
    18. Rivolta, C; Berson, EL; Dryja, TP
      Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX

      HUMAN MUTATION
    19. Miano, MG; Testa, F; Filippini, F; Trujillo, M; Conte, I; Lanzara, C; Millan, JM; De Bernardo, C; Grammatico, B; Mangino, M; Torrente, I; Carrozzo, R; Simonelli, F; Rinaldi, E; Ventruto, V; D'Urso, M; Ayuso, C; Ciccodicola, A
      Identification of novel RP2 mutations in a subset of X-linked Retinitis Pigmentosa families and prediction of new domains

      HUMAN MUTATION
    20. Paloma, E; Martinez-Mir, A; Vilageliu, L; Gonzalez-Duarte, R; Balcells, S
      Spectrum ABCA4 (ABCR) gene mutations in Spanish patients with autosomal recessive macular dystrophies

      HUMAN MUTATION
    21. Sohocki, MM; Daiger, SP; Bowne, SJ; Rodriguez, JA; Northrup, H; Heckenlively, JR; Birch, DG; Mintz-Hittner, H; Ruiz, RS; Lewis, RA; Saperstein, DA; Sullivan, LS
      Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies

      HUMAN MUTATION
    22. Moritz, OL; Tam, BM; Hurd, LL; Peranen, J; Deretic, D; Papermaster, DS
      Mutant rab8 impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods

      MOLECULAR BIOLOGY OF THE CELL
    23. Li, L
      Zebrafish mutants: Behavioral genetic studies of visual system defects

      DEVELOPMENTAL DYNAMICS
    24. Jomary, C; Neal, MJ; Jones, SE
      Characterization of cell death pathways in murine retinal neurodegeneration implicates cytochrome c release, caspase activation, and bid cleavage

      MOLECULAR AND CELLULAR NEUROSCIENCE
    25. Soong, GP; Lovie-Kitchin, JE; Brown, B
      Does mobility performance of visually impaired adults improve immediately after orientation and mobility training?

      OPTOMETRY AND VISION SCIENCE
    26. Turano, KA; Geruschat, DR; Baker, FH; Stahl, JW; Shapiro, MD
      Direction of gaze while walking a simple route: Persons with normal visionand persons with retinitis pigmentosa

      OPTOMETRY AND VISION SCIENCE
    27. Haymes, SA; Johnston, AW; Heyes, AD
      A weighted version of the Melbourne low-vision ADL index: A measure of disability impact

      OPTOMETRY AND VISION SCIENCE
    28. Peli, E
      Vision multiplexing: an engineering approach to vision rehabilitation device development

      OPTOMETRY AND VISION SCIENCE
    29. Gerber, S; Perrault, I; Hanein, S; Barbet, F; Ducroq, D; Ghazi, I; Martin-Coignard, D; Leowski, C; Homfray, T; Dufier, JL; Munnich, A; Kaplan, J; Rozet, JM
      Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis

      EUROPEAN JOURNAL OF HUMAN GENETICS
    30. Shroyer, NF; Lewis, RA; Yatsenko, AN; Wensel, TG; Lupski, JR
      Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degeneration

      HUMAN MOLECULAR GENETICS
    31. Clarke, G; Lumsden, CJ; McInnes, RR
      Inherited neurodegenerative diseases: the one-hit model of neurodegeneration

      HUMAN MOLECULAR GENETICS
    32. Stone, EM; Sheffield, VC; Hageman, GS
      Molecular genetics of age-related macular degeneration

      HUMAN MOLECULAR GENETICS
    33. Toomes, C; Marchbank, NJ; Mackey, DA; Craig, JE; Newbury-Ecob, RA; Bennett, CP; Vize, CJ; Desai, SP; Black, GCM; Patel, N; Teimory, M; Markham, AF; Inglehearn, CF; Churchill, AJ
      Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy

      HUMAN MOLECULAR GENETICS
    34. Ikeda, A; Ikeda, S; Gridley, T; Nishina, PM; Naggert, JK
      Neural tube defects and neuroepithelial cell death in Tulp3 knockout mice

      HUMAN MOLECULAR GENETICS
    35. Schwahn, U; Paland, N; Techritz, S; Lenzner, S; Berger, W
      Mutations in the X-linked RP2 gene cause intracellular misrouting and lossof the protein

      HUMAN MOLECULAR GENETICS
    36. Verdugo, ME; Alling, J; Lazar, ES; del Cerro, M; Ray, J; Aguirre, G
      Posterior segment approach for subretinal transplantation or injection in the canine model

      CELL TRANSPLANTATION
    37. Gordo, MA; Recio, M; Sanchez-Barcelo, EJ
      Decreased sleep quality in patients suffering from retinitis pigmentosa

      JOURNAL OF SLEEP RESEARCH
    38. Jun, L; Frints, S; Duhamel, H; Herold, A; Abad-Rodrigues, J; Dotti, C; Izaurralde, E; Marynen, P; Froyen, G
      NXF5, a novel member of the nuclear RNA export factor family, is lost in amale patient with a syndromic form of mental retardation

      CURRENT BIOLOGY
    39. Liang, FQ; Aleman, TS; Yang, ZX; Cideciyan, AV; Jacobson, SG; Bennett, J
      Melatonin delays photoreceptor degeneration in the rds/rds mouse

      NEUROREPORT
    40. Goldsmith, P
      Modelling eye diseases in zebrafish

      NEUROREPORT
    41. Bessant, DAR; Ali, RR; Bhattacharya, SS
      Molecular genetics and prospects for therapy of the inherited retinal dystrophies

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    42. Kremers, J; Scholl, HPN
      Rod-/L-cone and rod-/M-cone interactions in electroretinograms at different temporal frequencies

      VISUAL NEUROSCIENCE
    43. Humphries, MM; Kiang, S; McNally, N; Donovan, MA; Sieving, P; Bush, RA; Machida, S; Cotter, T; Hobson, A; Farrar, J; Humphries, P; Kenna, P
      Comparative structural and functional analysis of photoreceptor neurons ofRho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background

      VISUAL NEUROSCIENCE
    44. Jamison, JA; Bush, RA; Lei, B; Sieving, PA
      Characterization of the rod photoresponse isolated from the dark-adapted primate ERG

      VISUAL NEUROSCIENCE
    45. Chowers, I; Banin, E; Merin, S; Cooper, M; Granot, E
      Long-term assessment of combined vitamin A and E treatment for the prevention of retinal degeneration in abetalipoproteinaemia and hypobetalipoproteinaemia patients

      EYE
    46. Ohashi, H; Yamakawa, R; Ohashi, H
      Retinal detachment associated with macular hole in a patient with high myopic Usher's syndrome

      EYE
    47. Seeliger, M; Biesalski, HK
      Vitamin-A metabolism and retinal degeneration

      OPHTHALMOLOGE
    48. Zrenner, E; Ruther, K
      Dosage of vitamin-A derivatives in hereditary retinal degeneration. Current recommendations

      OPHTHALMOLOGE
    49. Kohler, K; Hartmann, JA; Werts, D; Zrenner, E
      Retinal degeneration and biocompatibility of subretinal implants: a histological analysis

      OPHTHALMOLOGE
    50. Eckhorn, R; Stett, A; Schanze, T; Gekeler, F; Schwahn, H; Zrenner, E; Wilms, M; Eger, M; Hesse, L
      Physiological testing of function of retinal implants with animal models

      OPHTHALMOLOGE
    51. Reichel, MB; Schlichtenbrede, F; Paul, D; Wiedemann, P
      Retinal degeneration

      OPHTHALMOLOGE
    52. Palmowski, AM; Allgayer, R; Heinemann-Vernaleken, B; Scherer, V; Eich, W; Ruprecht, KW
      Multifocal electroretinography in segmental retinitis pigmentosa

      OPHTHALMOLOGE
    53. Feigl, B; Haas, A
      Multifocal ERG in central areolar choroidal dystrophy

      OPHTHALMOLOGE
    54. Uhlig, CE; Taneri, S; Benner, FP; Gerding, H
      Electrical stimulation of the visual system. From empirical approaches to the development of visual implants

      OPHTHALMOLOGE
    55. Fauser, S; Aslanukov, A; Roepman, R; Ferreira, PA
      Genomic organization, expression, and localization of murine Ran-binding protein 2 (RanBP2) gene

      MAMMALIAN GENOME
    56. Kalikin, LM; Bugeaud, EM; Palmbos, PL; Lyons, RH; Petty, EM
      Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag

      MAMMALIAN GENOME
    57. Richardson, D; Shires, M; Davison, AM
      Renal diagnosis without renal biopsy. Nephritis and sensorineural deafness

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    58. Hildebrandt, F; Omram, H
      New insights: nephronophthisis-medullary cystic kidney disease

      PEDIATRIC NEPHROLOGY
    59. Tamm, SA; Whitcup, SM; Gery, I; Wiggert, B; Nussenblatt, RB; Kaiser-Kupfer, MI
      Immune response to retinal antigens in patients with gyrate atrophy and other hereditary retinal dystrophies

      OCULAR IMMUNOLOGY AND INFLAMMATION
    60. Rice, DS; Nusinowitz, S; Azimi, AM; Martinez, A; Soriano, E; Curran, T
      The reelin pathway modulates the structure and function of retinal synaptic circuitry

      NEURON
    61. Saari, JC; Nawrot, M; Kennedy, BN; Garwin, GG; Hurley, JB; Huang, J; Possin, DE; Crabb, JW
      Visual cycle impairment in cellular retinaldehyde binding protein (CRALBP)knockout mice results in delayed dark adaptation

      NEURON
    62. Uechi, T; Tanaka, T; Kenmochi, N
      A complete map of the human ribosomal protein genes: Assignment of 80 genes to the cytogenetic map and implications for human disorders

      GENOMICS
    63. Swaiman, KF
      Hallervorden-Spatz syndrome

      PEDIATRIC NEUROLOGY
    64. Scholl, HPN; Langrova, H; Weber, BHF; Zrenner, E; Apfelstedt-Sylla, E
      Clinical electrophysiology of two rod pathways: normative values and clinical application

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    65. Cursiefen, C; Holbach, LM; Schlotzer-Schrehardt, U; Naumann, GOH
      Persisting retinal ganglion cell axons in blind atrophic human eyes

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    66. Bolanos-Jimenez, F; Bordais, A; Behra, M; Strahle, U; Mornet, D; Sahel, J; Rendon, A
      Molecular cloning and characterization of dystrophin and Dp71, two products of the Duchenne Muscular Dystrophy gene, in zebrafish

      GENE
    67. Heikenwalder, MF; Koritschoner, NP; Pajer, P; Chaboissier, MC; Kurz, SM; Briegel, KJ; Bartunek, P; Zenke, M
      Molecular cloning, expression and regulation of the avian tubby-like protein 1 (tulp1) gene

      GENE
    68. Rana, BK; Shiina, T; Insel, PA
      Genetic variations and polymorphisms of G protein-coupled receptors: Functional and therapeutic implications

      ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY
    69. Fumagalli, A; Ferrari, M; Soriani, N; Gessi, A; Foglieni, B; Martina, E; Manitto, MP; Brancato, R; Dean, M; Allikmets, R; Cremonesi, L
      Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients

      HUMAN GENETICS
    70. Yatsenko, AN; Shroyer, NF; Lewis, RA; Lupski, JR
      Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4)

      HUMAN GENETICS
    71. Stevenson, VL; Hardie, RJ
      Acanthocytosis and neurological disorders

      JOURNAL OF NEUROLOGY
    72. Lu, C; Peng, YW; Shang, J; Pawlyk, BS; Yu, F; Li, T
      The mammalian retinal degeneration B2 gene is not required for photoreceptor function and survival

      NEUROSCIENCE
    73. Sauve, Y; Girman, SV; Wang, S; Lawrence, JM; Lund, RD
      Progressive visual sensitivity loss in the Royal College of Surgeons rat: Perimetric study in the superior colliculus

      NEUROSCIENCE
    74. Lichanska, AM; McGibbon, D; Silvestri, G; Hughes, AE
      A physical and expression map of the D17S1810-D17S1353 region spanning thecentral areolar choroidal dystrophy locus

      CYTOGENETICS AND CELL GENETICS
    75. Aparicio, JM; Belanger-Quintana, A; Suarez, L; Mayo, D; Benitez, J; Diaz, M; Escobar, H
      Ataxia with isolated vitamin E deficiency: Case report and review of the literature

      JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
    76. Osborne, NN; Chidlow, G; Wood, JPM; Schmidt, KG; Casson, R; Melena, J
      Expectations in the treatment of retinal diseases: Neuroprotection

      CURRENT EYE RESEARCH
    77. Weiss, ER; Ducceschi, MH; Horner, TJ; Li, AM; Craft, CM; Osawa, S
      Species-specific differences in expression of G-protein-coupled receptor kinase (GRK) 7 and GRK1 in mammalian cone photoreceptor cells: Implications for cone cell phototransduction

      JOURNAL OF NEUROSCIENCE
    78. Doerre, G; Malicki, J
      A mutation of early photoreceptor development, mikre oko, reveals cell-cell interactions involved in the survival and differentiation of zebrafish photoreceptors

      JOURNAL OF NEUROSCIENCE
    79. Sieving, PA; Fowler, ML; Bush, RA; Machida, S; Calvert, PD; Green, DG; Makino, CL; McHenry, CL
      Constitutive "light" adaptation in rods from G90D rhodopsin: A mechanism for human congenital nightblindness without rod cell loss

      JOURNAL OF NEUROSCIENCE
    80. Pierce, EA
      Pathways to photoreceptor cell death in inherited retinal degenerations

      BIOESSAYS
    81. Rumen, F; Souied, E; Oubraham, H; Coscas, G; Soubrane, G
      Optical coherence tomography used for following up macular edema during the course of retinis pigmentosa

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    82. Souied, E; Kaplan, J; Coscas, G; Soubrane, G
      Genetic of AMD

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    83. Sakamoto, T; Ikeda, Y; Yonemitsu, Y
      Gene targeting to the retina

      ADVANCED DRUG DELIVERY REVIEWS
    84. Driessen, CAGG; Janssen, BPM; Winkens, HJ; Kuhlmann, LD; Van Vugt, AHM; Pinckers, AJLG; Deutman, AF; Janssen, JJM
      Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus

      OPHTHALMOLOGY
    85. Syed, N; Smith, JE; John, SK; Seabra, MC; Aguirre, GD; Milam, AH
      Evaluation of retinal photoreceptors and pigment epithelium in a female carrier of choroideremia

      OPHTHALMOLOGY
    86. Megarbane, A; Waked, N; Chouery, E; Moglabey, YB; Saliba, N; Mornet, E; Serre, JL; Slim, R
      Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers

      AMERICAN JOURNAL OF MEDICAL GENETICS
    87. Yokoyama, A; Maruiwa, F; Hayakawa, M; Kanai, A; Vervoort, R; Wright, AF; Yamada, K; Niikawa, N; Naoi, N
      Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa

      AMERICAN JOURNAL OF MEDICAL GENETICS
    88. Hedera, P; Gorski, JL
      Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: Possible familial RHYNS syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    89. Hagstrom, SA; Adamian, M; Scimeca, M; Pawlyk, BS; Yue, GH; Li, TS
      A role for the tubby-like protein 1 in rhodopsin transport

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    90. Anderson, RE; Maude, MB; Bok, D
      Low docosahexaenoic acid levels in rod outer segment membranes of mice with rds/peripherin and P216L peripherin mutations

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    91. Jacobson, SG; Cideciyan, AV; Wright, E; Wright, AF
      Phenotypic marker for early disease detection in dominant late-onset retinal degeneration

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    92. Webster, AR; Heon, E; Lotery, AJ; Vandenburgh, K; Casavant, TL; Oh, KT; Beck, G; Fishman, GA; Lam, BL; Levin, A; Heckenlively, JR; Jacobson, SG; Weleber, RG; Sheffield, VC; Stone, EM
      An analysis of allelic variation in the ABCA4 gene

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    93. Rozet, JM; Perrault, I; Gerber, S; Hanein, S; Barbet, F; Ducroq, D; Souied, E; Munnich, A; Kaplan, J
      Complete abolition of the retinal-specific guanylyl cyclase (retGC-1) catalytic ability consistently leads to leber congenital amaurosis (LCA)

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    94. Haymes, SA; Johnston, AW; Heyes, AD
      The development of the Melbourne Low-Vision ADL Index: A measure of visiondisability

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    95. Kondo, M; Miyake, Y; Kondo, N; Tanikawa, A; Suzuki, S; Horiguchi, M; Terasaki, H
      Multifocal ERG findings in complete type congenital stationary night blindness

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    96. Scholl, HPN; Kremers, J; Vonthein, R; White, K; Weber, BHF
      L- and M-cone-driven electroretinograms in Stargardt's macular dystrophy-fundus flavimaculatus

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    97. Nilsson, SFE; Maepea, O; Alm, A; Narfstrom, K
      Ocular blood flow and retinal metabolism in Abyssinian cats with hereditary retinal degeneration

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    98. Machida, S; Chaudhry, P; Shinohara, T; Singh, DP; Reddy, VN; Chylack, LT; Sieving, PA; Bush, RA
      Lens epithelium-derived growth factor promotes photoreceptor survival in light-damaged and RCS rats

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    99. Tan, E; Wang, Q; Quiambao, AB; Xu, XP; Qtaishat, NM; Peachey, NS; Lem, J; Fliesler, SJ; Pepperberg, DR; Naash, M; Al-Ubaidi, MR
      The relationship between opsin overexpression and photoreceptor degeneration

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    100. Medeiros, NE; Curcio, CA
      Preservation of ganglion cell layer neurons in age-related macular degeneration

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 13/08/20 alle ore 02:30:21