Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.

Case Medical Research ◽

10.31525/ct1-nct03990727 ◽

2019 ◽

Author(s):

Keyword(s):

Retinitis Pigmentosa

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Doppler -- Sonography of the A.ciliares breves in Patients with Low Tension Glaucoma and with Retinitis Pigmentosa

European Journal of Ultrasound ◽

10.1016/s0929-8266(97)87283-7 ◽

1997 ◽

Vol 6 ◽

pp. S42-S43

Author(s):

V Klingmueller

Keyword(s):

Retinitis Pigmentosa ◽

Doppler Sonography ◽

Low Tension Glaucoma ◽

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A Dermatoglyphics Study of Retinitis Pigmentosa– A Case Study

PARIPEX-INDIAN JOURNAL OF RESEARCH ◽

10.15373/22501991/may2014/2 ◽

2012 ◽

Vol 3 (5) ◽

pp. 5-6

Author(s):

Dr. Chandan Kumar Sinha ◽

◽

Amminabhavi Nazia Banu Nurahmad ◽

Yogita Mallu Kattimani

Keyword(s):

Retinitis Pigmentosa

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Amplitude and Latency of Electroretinographical Peaks as a tool to Predict the Extent of Retinal Degeneration in Retinitis Pigmentosa Patients

http://www.fortunejournals.com/journal-of-ophthalmology-and-research-home-fjor.php ◽

10.26502/fjor.2644-00240024 ◽

2020 ◽

Vol 03 (03) ◽

Author(s):

Maryam Naser ◽

Seyed Mohammad Masoud Shushtarian

Keyword(s):

Retinitis Pigmentosa ◽

Retinal Degeneration

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Case of Unilateral retinitis pigmentosa

Oftalmologicheskii Zhurnal ◽

10.31288/oftalmolzh20141119121 ◽

2014 ◽

Vol 47 (1) ◽

pp. 119-121

Author(s):

A. Zborovskaya ◽

◽

A. Dorokhova ◽

L. Uvarenko ◽

A. Kurilyuk ◽

...

Keyword(s):

Retinitis Pigmentosa

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Orphan designation: Adenovirus-associated viral vector serotype 5 containing the human RPGR gene, Treatment of retinitis pigmentosa

Case Medical Research ◽

10.31525/cmr-12e1a9d ◽

2019 ◽

Author(s):

Keyword(s):

Retinitis Pigmentosa ◽

Viral Vector ◽

Orphan Designation ◽

Gene Treatment ◽

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Retinitis Pigmentosa Clinical Measures and Repeatability Testing of Potential Outcome Measures

Case Medical Research ◽

10.31525/ct1-nct03845218 ◽

2000 ◽

Author(s):

Keyword(s):

Retinitis Pigmentosa ◽

Outcome Measures ◽

Potential Outcome ◽

Clinical Measures

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A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene

Case Medical Research ◽

10.31525/ct1-nct04123626 ◽

2019 ◽

Author(s):

Keyword(s):

Retinitis Pigmentosa ◽

Autosomal Dominant ◽

Autosomal Dominant Retinitis Pigmentosa

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Management of Retinitis Pigmentosa by Mesenchymal Stem Cells by Wharton's Jelly Derived Mesenchymal Stem Cells

Case Medical Research ◽

10.31525/ct1-nct04224207 ◽

2020 ◽

Author(s):

Keyword(s):

Mesenchymal Stem Cells ◽

Retinitis Pigmentosa ◽

Wharton’S Jelly ◽

Wharton's Jelly

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Management of Retinitis Pigmentosa Via Electromagnetic Stimulation and Platelet Rich Plasma

Case Medical Research ◽

10.31525/ct1-nct04252534 ◽

2020 ◽

Author(s):

Keyword(s):

Retinitis Pigmentosa ◽

Platelet Rich Plasma ◽

Electromagnetic Stimulation

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Faculty Opinions recommendation of A rhodopsin mutant linked to autosomal dominant retinitis pigmentosa is prone to aggregate and interacts with the ubiquitin proteasome system.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1008543.108057 ◽

2002 ◽

Author(s):

David Bessant

Keyword(s):

Retinitis Pigmentosa ◽

Autosomal Dominant ◽

Ubiquitin Proteasome System ◽

Autosomal Dominant Retinitis Pigmentosa ◽

Ubiquitin Proteasome

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