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Treatment of Macular Degeneration with Sildenafil: Results of a Two-Year Trial.
- Published in:
- Ophthalmologica, 2018, v. 240, n. 1, p. 45, doi. 10.1159/000486105
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- Publication type:
- Article
Clinical exome sequencing for inherited retinal degenerations at a tertiary care center.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13026-2
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- Publication type:
- Article
A lymphatic-absorbed multi-targeted kinase inhibitor for myelofibrosis therapy.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32486-8
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- Publication type:
- Article
Cross-Gender Brand Extensions: Effects of Gender of the Brand, Gender of Consumer, and Product Type on Evaluation of Cross-Gender Extensions.
- Published in:
- Advances in Consumer Research, 2006, v. 33, n. 1, p. 67
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- Publication type:
- Article
The Effect of Obesity on Acetaminophen Pharmacokinetics in Man.
- Published in:
- 1981
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- Publication type:
- Other
Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy.
- Published in:
- 2017
- By:
- Publication type:
- journal article
IER5, a DNA damage response gene, is required for Notch-mediated induction of squamous cell differentiation.
- Published in:
- eLife, 2020, p. 1, doi. 10.7554/eLife.58081
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- Publication type:
- Article
Phenotypic expansion and progression of <italic>SPATA7</italic>-associated retinitis pigmentosa.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Rapid resolution of retinoschisis with acetazolamide.
- Published in:
- Documenta Ophthalmologica, 2015, v. 131, n. 1, p. 63, doi. 10.1007/s10633-015-9496-8
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- Publication type:
- Article
Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene.
- Published in:
- Documenta Ophthalmologica, 2014, v. 128, n. 1, p. 59, doi. 10.1007/s10633-013-9420-z
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- Publication type:
- Article
ERG amplification is a secondary recurrent driver event in myeloid malignancy with complex karyotype and TP53 mutations.
- Published in:
- Genes, Chromosomes & Cancer, 2022, v. 61, n. 7, p. 399, doi. 10.1002/gcc.23027
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- Publication type:
- Article
Quantitative MRI reveals heterogeneous impacts of treatment on diseased bone marrow in a mouse model of myelofibrosis.
- Published in:
- Magnetic Resonance in Medicine, 2024, v. 91, n. 6, p. 2568, doi. 10.1002/mrm.30016
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- Publication type:
- Article
Central Microscotoma: A Rare Presentation of Epiretinal Membranes.
- Published in:
- 2015
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- Publication type:
- journal article
Early structural anomalies observed by high-resolution imaging in two related cases of autosomal-dominant retinitis pigmentosa.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Photoreceptor cells as a source of fundus autofluorescence in recessive Stargardt disease.
- Published in:
- Journal of Neuroscience Research, 2019, v. 97, n. 1, p. 98, doi. 10.1002/jnr.24252
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- Publication type:
- Article
Complex inheritance of ABCA4 disease: four mutations in a family with multiple macular phenotypes.
- Published in:
- Human Genetics, 2016, v. 135, n. 1, p. 9, doi. 10.1007/s00439-015-1605-y
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- Publication type:
- Article
GATA1 Is a Sensitive and Specific Nuclear Marker for Erythroid and Megakaryocytic Lineages.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Reevaluating the Association of Sex With ABCA4 Alleles in Patients With Stargardt Disease.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Quantitative Autofluorescence Intensities in Acute Zonal Occult Outer Retinopathy vs Healthy Eyes.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Complication of Autologous Stem Cell Transplantation in Retinitis Pigmentosa.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Quantitative Autofluorescence as a Clinical Tool for Expedited Differential Diagnosis of Retinal Degeneration.
- Published in:
- JAMA Ophthalmology, 2015, v. 133, n. 2, p. 219, doi. 10.1001/jamaophthalmol.2014.4507
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- Publication type:
- Article
Novel Compound Heterozygous Mutations Resulting in Cone Dystrophy With Supernormal Rod Response.
- Published in:
- JAMA Ophthalmology, 2013, v. 131, n. 11, p. 1482, doi. 10.1001/jamaophthalmol.2013.4681
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- Publication type:
- Article
Challenges in the Management of HIV and Hepatitis C Virus Co-infection.
- Published in:
- Drugs, 2004, v. 64, n. 7, p. 693, doi. 10.2165/00003495-200464070-00002
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- Publication type:
- Article
Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho<sup>D190N</sup> mutation.
- Published in:
- Cellular & Molecular Life Sciences, 2019, v. 76, n. 18, p. 3657, doi. 10.1007/s00018-019-03090-9
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- Publication type:
- Article
Patients and animal models of CNGβ1-deficient retinitis pigmentosa support gene augmentation approach.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Pure erythroid leukemia.
- Published in:
- Clinical Case Reports, 2020, v. 8, n. 11, p. 2286, doi. 10.1002/ccr3.3056
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- Publication type:
- Article
Structural requirements of SIRPα binding to CD47.
- Published in:
- FASEB Journal, 2007, v. 21, n. 5, p. A132, doi. 10.1096/fasebj.21.5.a132
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- Publication type:
- Article
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt disease.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 14, p. 1293, doi. 10.1093/hmg/ddab122
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- Publication type:
- Article
New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5774, doi. 10.1093/hmg/ddu291
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- Publication type:
- Article
Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T‐ALL like mutations.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 11, p. 1358, doi. 10.1002/ajh.25256
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- Publication type:
- Article
Display Characteristics and Their Impact on Digital Pathology: A Current Review of Pathologists' Future "Microscope".
- Published in:
- International Archives of Integrated Medicine, 2020, v. 7, n. 8, p. 1, doi. 10.4103/jpi.jpi_38_20
- By:
- Publication type:
- Article
A mutation in CRX causing pigmented paravenous retinochoroidal atrophy.
- Published in:
- European Journal of Ophthalmology, 2022, v. 32, n. 1, p. NP235, doi. 10.1177/1120672120957599
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- Publication type:
- Article
Stem Cell Therapies in Retinal Disorders.
- Published in:
- Cells (2073-4409), 2017, v. 6, n. 1, p. 4, doi. 10.3390/cells6010004
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- Publication type:
- Article
Diagnostic Considerations in the Evaluation of Large B-Cells on Lymph Node Cytology Specimens.
- Published in:
- Acta Cytologica, 2021, v. 65, n. 1, p. 105, doi. 10.1159/000510322
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- Publication type:
- Article
Genetic and Clinical Analysis of ABCA4-Associated Disease in African American Patients.
- Published in:
- Human Mutation, 2014, v. 35, n. 10, p. 1187, doi. 10.1002/humu.22626
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- Publication type:
- Article
The diagnostic challenges and clinical course of a myeloid/lymphoid neoplasm with eosinophilia and ZBTB20-JAK2 gene fusion presenting as B-lymphoblastic leukemia.
- Published in:
- Cold Spring Harbor Molecular Case Studies, 2020, v. 6, n. 2, p. 1, doi. 10.1101/mcs.a004937
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- Publication type:
- Article
Hyperautofluorescent Dots are Characteristic in Ceramide Kinase Like-associated Retinal Degeneration.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-37578-4
- By:
- Publication type:
- Article
Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 3, p. 1, doi. 10.1371/journal.pgen.1010129
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- Publication type:
- Article
Recessive Stargardt disease phenocopying hydroxychloroquine retinopathy.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2016, v. 254, n. 5, p. 865, doi. 10.1007/s00417-015-3142-8
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- Publication type:
- Article
Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2013, v. 251, n. 10, p. 2299, doi. 10.1007/s00417-013-2296-5
- By:
- Publication type:
- Article
Display Characteristics and Their Impact on Digital Pathology: A Current Review of Pathologists' Future "Microscope".
- Published in:
- Journal of Pathology Informatics, 2020, v. 11, p. 1, doi. 10.4103/jpi.jpi_38_20
- By:
- Publication type:
- Article
Display Characteristics and Their Impact on Digital Pathology: A Current Review of Pathologists' Future "Microscope".
- Published in:
- Journal of Pathology Informatics, 2020, v. 11, p. 1, doi. 10.4103/jpi.jpi_38_20
- By:
- Publication type:
- Article
Display Characteristics and Their Impact on Digital Pathology: A Current Review of Pathologists' Future "Microscope".
- Published in:
- Journal of Pathology Informatics, 2020, v. 11, p. 1, doi. 10.4103/jpi.jpi_38_20
- By:
- Publication type:
- Article