Cargando…

Lymphocyte infiltration in CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy

PURPOSE: To describe immunohistopathological findings in autosomal dominant neovascular inflammatory vitreoretinopathy (ADNIV). METHODS: An enucleated eye specimen from a patient with Stage V ADNIV was examined using standard histopathological methods and lymphocyte markers. RESULTS: A c.731T>C C...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mahajan, Vinit B, Lin, Jonathan H
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3704602/ https://www.ncbi.nlm.nih.gov/pubmed/23861576 http://dx.doi.org/10.2147/OPTH.S46450

Ejemplares similares

Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy
por: Rowell, Hannah A, et al.
Publicado: (2012)

T-cell infiltration in autosomal dominant neovascular inflammatory vitreoretinopathy
por: Mahajan, Vinit B., et al.
Publicado: (2010)

Secondary glaucoma in CAPN5-associated neovascular inflammatory vitreoretinopathy
por: Cham, Abdourahman, et al.
Publicado: (2016)

Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy
por: Velez, Gabriel, et al.
Publicado: (2019)

Surgical management of fibrotic encapsulation of the fluocinolone acetonide implant in CAPN5-associated proliferative vitreoretinopathy
por: Tlucek, Paul S, et al.
Publicado: (2013)

A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay
por: Velez, Gabriel, et al.
Publicado: (2018)

Structural Modeling of a Novel CAPN5 Mutation that Causes Uveitis and Neovascular Retinal Detachment
por: Bassuk, Alexander G., et al.
Publicado: (2015)

CAPN5 gene silencing by short hairpin RNA interference
por: Nelson, Nnamdi G, et al.
Publicado: (2014)

Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
por: Cerino, Mathieu, et al.
Publicado: (2020)

Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy
por: Nallamilli, Babi Ramesh Reddy, et al.
Publicado: (2020)

An anti-CAPN5 intracellular antibody acts as an inhibitor of CAPN5-mediated neuronal degeneration
por: Wang, Yan, et al.
Publicado: (2017)

Capn5 Expression in the Healthy and Regenerating Zebrafish Retina
por: Coomer, Cagney E., et al.
Publicado: (2018)

New COL6A6 Variant Causes Autosomal Dominant Retinitis Pigmentosa in a Four-Generation Family
por: Vaclavik, Veronika, et al.
Publicado: (2022)

Inflammatory and Fibrogenic Factors in Proliferative Vitreoretinopathy Development
por: Chaudhary, Rishika, et al.
Publicado: (2020)

Inflammatory mediators of proliferative vitreoretinopathy: hypothesis and review
por: Dai, Ying, et al.
Publicado: (2020)

Extensive Mongolian Spots with Autosomal Dominant Inheritance
por: Beeregowda, YC, et al.
Publicado: (2012)

Cleidocranial Dysplasia with Autosomal Dominant Inheritance Pattern
por: Bhargava, P, et al.
Publicado: (2014)

An SNX31 variant underlies dominant familial exudative vitreoretinopathy-like pathogenesis
por: Xu, Ningda, et al.
Publicado: (2023)

CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76
por: Garcia-Berlanga, Jesus Eduardo, et al.
Publicado: (2019)

Autosomal Dominant Inherited Cowden's Disease in a Family
por: Ha, Jun-Wook
Publicado: (2013)

Autosomal Dominant Centronuclear Myopathy with Unique Clinical Presentations
por: Lee, Jee-Young, et al.
Publicado: (2007)

Educational Case: Autosomal Dominant Polycystic Kidney Disease
por: Frazier, Ryan L., et al.
Publicado: (2020)

Atypical Autosomal-Dominant Inheritance of Familial Mediterranean Fever
por: Evans, Neil Shadbeh, et al.
Publicado: (2021)

Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa
por: Oh, Jin Kyun, et al.
Publicado: (2019)

CAPN6 in disease: An emerging therapeutic target (Review)
por: Chen, Lin, et al.
Publicado: (2020)

Autosomal dominant intellectual disability
por: Wieczorek, Dagmar
Publicado: (2018)

Autosomal dominant polycystic kidney
por: Gudadhe, Rugaved Raghavendra, et al.
Publicado: (2022)

Bilateral emphysematous pyelonephritis in autosomal dominant polycystic kidney disease
por: Lakshminarayana, G., et al.
Publicado: (2012)

An Unusual Cardiac Manifestation in Autosomal Dominant Polycystic Kidney Disease
por: Catapano, Fausta, et al.
Publicado: (2012)

Sacral radicular cysts in autosomal dominant polycystic kidney disease
por: Peces, Ramón, et al.
Publicado: (2009)

Autosomal dominant Hashimoto’s thyroiditis with a mutation in TNFAIP3
por: Hori, Tomohiro, et al.
Publicado: (2019)

Effectiveness of Open Fenestration for Autosomal Dominant Polycystic Liver Disease
por: Norcia, Luiz Fernando, et al.
Publicado: (2022)

Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures
por: Teleanu, Raluca Ioana, et al.
Publicado: (2023)

Familial Exudative Vitreoretinopathy
por: Sızmaz, Selçuk, et al.
Publicado: (2015)

MAPK8 and CAPN1 as potential biomarkers of intervertebral disc degeneration overlapping immune infiltration, autophagy, and ceRNA
por: Zhang, Yuxin, et al.
Publicado: (2023)

Fluoroscopy and CT Guided Translumbar Tunneled Dialysis Catheter for Hemodialysis Access Failure in a Case of Autosomal Dominant Polycystic Kidney Disease
por: Rathod, Krantikumar, et al.
Publicado: (2023)

Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report
por: Siavrienė, Evelina, et al.
Publicado: (2021)

Calpain-5 Mutations Cause Autoimmune Uveitis, Retinal Neovascularization, and Photoreceptor Degeneration
por: Mahajan, Vinit B., et al.
Publicado: (2012)

Limb Girdle Muscular Dystrophy due to Digenic Inheritance of DES and CAPN3 Mutations
por: Peddareddygari, Leema Reddy, et al.
Publicado: (2018)

Autosomal dominant transmission of transient neonatal lactic acidosis: a case report
por: Mardian, Emily B., et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_rs1vonktv4hf2f4nknhrhv5lj6