Cargando…

How to test for a relative afferent pupillary defect (RAPD)

Mostrar otras versiones (1)

Detalles Bibliográficos
Autor principal:	Broadway, David C
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	International Centre for Eye Health 2016
Materias:	Relative Afferent Pupillary Defect
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365042/ https://www.ncbi.nlm.nih.gov/pubmed/28381906

Ejemplares similares

How to test for a relative afferent pupillary defect (RAPD)
por: Broadway, David C
Publicado: (2012)

Residential Institutions for Mental Defectives
Publicado: (1912)

Industrial Colonies for Mental Defectives
Publicado: (1912)

‘Kinesinopathies’: emerging role of the kinesin family member genes in birth defects
por: Kalantari, Silvia, et al.
Publicado: (2020)

Test–Retest Reliability of Virtual Reality Devices in Quantifying for Relative Afferent Pupillary Defect
por: Sarker, Prithul, et al.
Publicado: (2023)

Objective assessment of a relative afferent pupillary defect by B-mode ultrasound
por: Schmidt, Felix A., et al.
Publicado: (2018)

Detection of Relative Afferent Pupillary Defects Using Eye Tracking and a VR Headset
por: Bruegger, Dominik, et al.
Publicado: (2023)

ARF1-related disorder: phenotypic and molecular spectrum
por: de Sainte Agathe, Jean-Madeleine, et al.
Publicado: (2023)

Asymmetric Macular Structural Damage Is Associated With Relative Afferent Pupillary Defects in Patients With Glaucoma
por: Gracitelli, Carolina P. B., et al.
Publicado: (2016)

More sensitive correlation of afferent pupillary defect with ganglion cell complex
por: Besada, Eulogio, et al.
Publicado: (2018)

Cross-sectional pupillographic evaluation of relative afferent pupillary defect in age-related macular degeneration
por: Takayama, Kei, et al.
Publicado: (2016)

ARHGDIA: a novel gene implicated in nephrotic syndrome
por: Gupta, Indra Rani, et al.
Publicado: (2013)

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome
por: Hempel, Annmarie, et al.
Publicado: (2016)

Relative Afferent Pupillary Defects in Homonymous Visual Field Defects Caused by Stroke of the Occipital Lobe Using Pupillometer
por: Takizawa, Go, et al.
Publicado: (2017)

Diagnostic value of exome and whole genome sequencing in craniosynostosis
por: Miller, Kerry A, et al.
Publicado: (2017)

A specific mutation in TBL1XR1 causes Pierpont syndrome
por: Heinen, Charlotte A, et al.
Publicado: (2016)

Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder
por: Bedoyan, Jirair Krikor, et al.
Publicado: (2012)

Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
por: Schmidts, Miriam, et al.
Publicado: (2013)

X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
por: Kolvenbach, Caroline M, et al.
Publicado: (2023)

Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation
por: Jani, Priyam, et al.
Publicado: (2020)

FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly
por: Simonis, Nicolas, et al.
Publicado: (2013)

Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approach
por: Best, Sunayna, et al.
Publicado: (2022)

The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes
por: Waters, Aoife M, et al.
Publicado: (2015)

Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia
por: Samuels, Mark E, et al.
Publicado: (2013)

Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function
por: Tooze, Rebecca S, et al.
Publicado: (2023)

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel
por: Al-Hamed, Mohamed H, et al.
Publicado: (2016)

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)
por: Rad, Abolfazl, et al.
Publicado: (2019)

Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes
por: Roosing, Susanne, et al.
Publicado: (2016)

Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome
por: Bondy, Carolyn, et al.
Publicado: (2013)

Industrial Training and After-Care
Publicado: (1912)

The Royal Commission Report
Publicado: (1912)

Familial bilateral cryptorchidism is caused by recessive variants in RXFP2
por: Ayers, Katie, et al.
Publicado: (2019)

Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
por: Sarogni, Patrizia, et al.
Publicado: (2020)

DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypes
por: Marquez, Jonathan, et al.
Publicado: (2021)

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
por: Laquerriere, Annie, et al.
Publicado: (2022)

Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis
por: Smeland, Marie F., et al.
Publicado: (2023)

Biallelic NPR1 loss of function variants are responsible for neonatal systemic hypertension
por: Capri, Yline, et al.
Publicado: (2023)

Quantification of RAPD by an automated pupillometer in asymmetric glaucoma and its correlation with manual pupillary assessment
por: Pillai, Manju R, et al.
Publicado: (2019)

Correlation between relative afferent pupillary defect and visual field defects on Humphrey automated perimetry: A cross-sectional clinical trial
por: Witthayaweerasak, Juthamat, et al.
Publicado: (2022)

Association between a relative afferent pupillary defect using pupillography and inner retinal atrophy in optic nerve disease
por: Takizawa, Go, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_ui7e4jg56tv0lp5cq2va0nlrla