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Sociocultural Pressures, Internalization, and Body Esteem in Congenitally Blind, Late-Blind, and Sighted Men and Women.
- Published in:
- Journal of Visual Impairment & Blindness, 2024, v. 118, n. 2, p. 73, doi. 10.1177/0145482X241235167
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- Publication type:
- Article
Dendrimers for gene delivery - a potential approach for ocular therapy?
- Published in:
- Journal of Pharmacy & Pharmacology, 2014, v. 66, n. 4, p. 542, doi. 10.1111/jphp.12104
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- Publication type:
- Article
AAV8(Y733F)-mediated gene therapy in a Spata7 knockout mouse model of Leber congenital amaurosis and retinitis pigmentosa.
- Published in:
- Gene Therapy, 2015, v. 22, n. 8, p. 619, doi. 10.1038/gt.2015.42
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- Publication type:
- Article
RPE65 gene therapy slows cone loss in Rpe65-deficient dogs.
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- Gene Therapy, 2013, v. 20, n. 5, p. 545, doi. 10.1038/gt.2012.63
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- Publication type:
- Article
Physiological and tissue-specific vectors for treatment of inherited diseases.
- Published in:
- Gene Therapy, 2011, v. 18, n. 2, p. 117, doi. 10.1038/gt.2010.138
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- Publication type:
- Article
HTRA1 Overexpression Induces the Exudative Form of Age-related Macular Degeneration.
- Published in:
- Journal of Stem Cells, 2015, v. 10, n. 3, p. 193
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- Publication type:
- Article
SOCIAL-EMOTIONAL DEVELOPMENT IN CHILDREN AND YOUTH WHO ARE DEAFBLIND.
- Published in:
- American Annals of the Deaf, 2016, v. 161, n. 4, p. 444, doi. 10.1353/aad.2016.0036
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- Publication type:
- Article
EARLY IDENTIFICATION OF INFANTS AND TODDLERS WITH DEAFBLINDNESS.
- Published in:
- American Annals of the Deaf, 2016, v. 161, n. 4, p. 412, doi. 10.1353/aad.2016.0034
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- Publication type:
- Article
Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome.
- Published in:
- Journal of Clinical Research in Pediatric Endocrinology, 2023, v. 15, n. 3, p. 318, doi. 10.4274/jcrpe.galenos.2021.2021.0186
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- Publication type:
- Article
Functional and structural changes throughout the auditory system following congenital and early-onset deafness: implications for hearing restoration.
- Published in:
- Frontiers in Systems Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnsys.2013.00092
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- Publication type:
- Article
Negative Electroretinogram in the Differential Diagnosis of Malingering of Night Blindness in the Military.
- Published in:
- Military Medicine, 2007, v. 172, n. 4, p. 402, doi. 10.7205/MILMED.172.4.402
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- Publication type:
- Article
Chemosensory Function in Congenitally Blind or Deaf Teenagers.
- Published in:
- Chemosensory Perception, 2016, v. 9, n. 1, p. 8, doi. 10.1007/s12078-015-9199-2
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- Publication type:
- Article
Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma.
- Published in:
- 2016
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- Publication type:
- journal article
Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis.
- Published in:
- 2016
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- Publication type:
- journal article
Species-Dependent Splice Recognition of a Cryptic Exon Resulting from a Recurrent Intronic CEP290 Mutation that Causes Congenital Blindness.
- Published in:
- International Journal of Molecular Sciences, 2015, v. 16, n. 3, p. 5285, doi. 10.3390/ijms16035285
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- Publication type:
- Article
The Relevance of Object Size to the Recognizability of Drawings by Individuals with Congenital Blindness.
- Published in:
- Journal of Visual Impairment & Blindness, 2019, v. 113, n. 3, p. 295, doi. 10.1177/0145482X19860015
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- Publication type:
- Article
Interaction of Dual Sensory Loss, Cognitive Function, and Communication in People Who Are Congenitally Deaf-Blind.
- Published in:
- Journal of Visual Impairment & Blindness, 2010, v. 104, n. 11, p. 719, doi. 10.1177/0145482X1010401108
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- Publication type:
- Article
The Role of Sound in Encouraging Infants with Congenital Blindness to Reach for Objects.
- Published in:
- Journal of Visual Impairment & Blindness, 2010, v. 104, n. 8, p. 478, doi. 10.1177/0145482X1010400804
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- Publication type:
- Article
Tactile Functioning in Children Who Are Blind: A Clinical Perspective.
- Published in:
- Journal of Visual Impairment & Blindness, 2010, v. 104, n. 1, p. 43, doi. 10.1177/0145482X1010400108
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- Publication type:
- Article
Divergent Development of Verbal Skills in Children Who Are Blind or Sighted.
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- Journal of Visual Impairment & Blindness, 2007, v. 101, n. 12, p. 749, doi. 10.1177/0145482X0710101205
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- Publication type:
- Article
Comparing the Effects of Congenital and Late Visual Impairments on Visuospatial Mental Abilities.
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- Journal of Visual Impairment & Blindness, 2007, v. 101, n. 5, p. 278, doi. 10.1177/0145482X0710100503
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- Publication type:
- Article
Impact of a Communication Intervention Model on Teachers' Practice with Children Who Are Congenitally Deaf-Blind.
- Published in:
- Journal of Visual Impairment & Blindness, 2002, v. 96, n. 3, p. 154, doi. 10.1177/0145482x0209600304
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- Publication type:
- Article
The Effect of Extended Acoustic Training on Spatial Updating in Adults Who Are Congenitally Blind.
- Published in:
- Journal of Visual Impairment & Blindness, 1999, v. 93, n. 7, p. 405, doi. 10.1177/0145482x9909300703
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- Publication type:
- Article
Body experiences of persons who are congenitally blind: A phenomenological-psychological study.
- Published in:
- Journal of Visual Impairment & Blindness, 1997, v. 91, n. 2, p. 151, doi. 10.1177/0145482x9709100208
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- Publication type:
- Article
The Effect of Visual Impairment on the Strength of Children's Hip and Knee Extensors.
- Published in:
- Journal of Visual Impairment & Blindness, 1997, v. 91, n. 1, p. 40, doi. 10.1177/0145482x9709100107
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- Publication type:
- Article
Object Permanence, Reaching, and Locomotion in Infants Who Are Blind.
- Published in:
- Journal of Visual Impairment & Blindness, 1997, v. 91, n. 1, p. 25, doi. 10.1177/0145482x9709100105
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- Publication type:
- Article
Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 7, p. 385
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- Publication type:
- Article
Coat's like vasculopathy in leber congenital amaurosis secondary to homozygous mutations in CRB1: a case report and discussion of the management options.
- Published in:
- 2016
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- Publication type:
- Case Study
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract.
- Published in:
- BMC Research Notes, 2016, v. 9, p. 1, doi. 10.1186/s13104-016-1890-0
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- Publication type:
- Article
Corrigendum: Prevalence of increases in functional connectivity in visual, somatosensory and language areas in congenital blindness.
- Published in:
- 2015
- Publication type:
- Correction Notice
Prevalence of increases in functional connectivity in visual, somatosensory and language areas in congenital blindness.
- Published in:
- Frontiers in Neuroanatomy, 2015, v. 9, p. 1, doi. 10.3389/fnana.2015.00086
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- Publication type:
- Article
Teriparatide increases bone mineral density in a man with osteoporosis pseudoglioma.
- Published in:
- Journal of Bone & Mineral Research, 2011, v. 26, n. 12, p. 2823, doi. 10.1002/jbmr.530
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- Publication type:
- Article
Crossmodal Recruitment of the Ventral Visual Stream in Congenital Blindness.
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- Neural Plasticity, 2012, v. 2012, p. 1, doi. 10.1155/2012/304045
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- Publication type:
- Article
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.
- Published in:
- Nature Genetics, 2007, v. 39, n. 7, p. 889, doi. 10.1038/ng2066
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- Publication type:
- Article
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
- Published in:
- Nature Genetics, 2006, v. 38, n. 7, p. 755, doi. 10.1038/ng1824
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- Publication type:
- Article
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
- Published in:
- Nature Genetics, 2000, v. 26, n. 3, p. 319, doi. 10.1038/81619
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- Publication type:
- Article
The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein.
- Published in:
- Nature Genetics, 2000, v. 26, n. 3, p. 324, doi. 10.1038/81627
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- Publication type:
- Article
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.
- Published in:
- Nature Genetics, 2000, v. 24, n. 1, p. 79, doi. 10.1038/71732
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- Publication type:
- Article
Mitochondrial oxidative phosphorylation in autosomal dominant optic atrophy.
- Published in:
- BMC Biochemistry, 2008, v. 9, p. 1, doi. 10.1186/1471-2091-9-22
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- Publication type:
- Article
REPRESENTATION OF HAPTIC OBJECTS DURING MENTAL ROTATION IN CONGENITAL BLINDNESS.
- Published in:
- Perceptual & Motor Skills, 2014, v. 118, n. 2, p. 587, doi. 10.2466/15.22.PMS.118k20w0
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- Publication type:
- Article
Rhodopsin mutation G90D and a molecular mechanism for congenital night blindness.
- Published in:
- Nature, 1994, v. 367, n. 6464, p. 639, doi. 10.1038/367639a0
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- Publication type:
- Article
Multisystemic Increment of Cortical Thickness in Congenital Blind Children.
- Published in:
- Cerebral Cortex Communications, 2020, v. 1, n. 1, p. 1, doi. 10.1093/texcom/tgaa071
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- Publication type:
- Article
Genetic heterogeneity of day blindness in Alaskan Malamutes.
- Published in:
- Animal Genetics, 2006, v. 37, n. 4, p. 407, doi. 10.1111/j.1365-2052.2006.01484.x
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- Publication type:
- Article
It’s Habit-Forming.
- Published in:
- Braille Monitor, 2020, v. 63, n. 6, p. 418
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- Publication type:
- Article
Production of basic emotions by children with congenital blindness: Evidence for the embodiment of theory of mind.
- Published in:
- British Journal of Developmental Psychology, 2006, v. 24, n. 3, p. 507, doi. 10.1348/026151005X50663
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- Publication type:
- Article
The podalic proprioception channel to increase motor skills in blind children: Operational applications.
- Published in:
- Journal of Human Sport & Exercise, 2017, v. 12, n. 3, p. 753, doi. 10.14198/jhse.2017.123.19
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- Publication type:
- Article
Superior Orthonasal but Not Retronasal Olfactory Skills in Congenital Blindness.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122567
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- Publication type:
- Article
Grasping without Sight: Insights from the Congenitally Blind.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110175
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- Publication type:
- Article
Morphometric Changes of the Corpus Callosum in Congenital Blindness.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107871
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- Publication type:
- Article
Multivoxel Pattern Analysis Reveals Auditory Motion Information in MT+ of Both Congenitally Blind and Sighted Individuals.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0063198
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- Publication type:
- Article