Jose Ronaldo Lima de Carvalho Selected Research

Stargardt disease 4

12/2019

Compound heterozygous novel frameshift variants in the PROM1 gene result in Leber congenital amaurosis.

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Jose Ronaldo Lima de Carvalho Research Topics

Disease

3	Retinal Dystrophies 01/2022 - 12/2019
2	Atrophy 01/2022 - 12/2019
2	Retinitis Pigmentosa (Pigmentary Retinopathy) 01/2022 - 01/2020
2	Retinal Degeneration 01/2022 - 01/2020
2	Macular Degeneration (Age-Related Maculopathy) 10/2020 - 12/2019
1	Obesity 03/2022
1	Vitamin A Deficiency 03/2022
1	Cone Dystrophy 01/2022
1	Disease Progression 10/2020
1	Macular Edema 10/2020
1	Hypercholesterolemia 01/2020
1	Thromboembolism 01/2020
1	Protein S Deficiency (Deficiency, Protein S) 01/2020
1	Crisponi syndrome 12/2019
1	Stargardt disease 4 12/2019
1	Cone-Rod Dystrophy 12 12/2019
1	Retinitis Pigmentosa 41 12/2019
1	Retinoblastoma (Glioblastoma, Retinal) 12/2019

Drug/Important Bio-Agent (IBA)

8	Retinaldehyde (Retinal)IBA 01/2022 - 12/2019
2	Proteins (Proteins, Gene)FDA Link 01/2020 - 12/2019
1	tyrosyltubulin ligaseIBA 01/2022
1	Vitamin A (Retinol)FDA LinkGeneric 01/2022
1	Biomarkers (Surrogate Marker)IBA 10/2020
1	Atorvastatin (Lipitor)FDA Link 01/2020
1	Carrier Proteins (Binding Protein)IBA 01/2020
1	Aspirin (Acetylsalicylic Acid)FDA LinkGeneric 01/2020
1	Thrombin FDA Link 01/2020
1	AC133 AntigenIBA 12/2019
1	AcidsIBA 12/2019
1	Glycoproteins (Glycoprotein)IBA 12/2019

Therapy/Procedure

1	Bariatric Surgery 03/2022