A5022130568- Glaucoma and retinal disorders
- Hemoglobinopathies and Related Disorders
- Cerebral Venous Sinus Thrombosis
- Retinal and Optic Conditions
- Intraocular Surgery and Lenses
- Retinal Diseases and Treatments
- Corneal surgery and disorders
- Cerebrovascular and genetic disorders
- Sympathectomy and Hyperhidrosis Treatments
- Ocular Diseases and Behçet’s Syndrome
- Retinal Imaging and Analysis
- Retinal and Macular Surgery
- Cardiovascular Conditions and Treatments
- Vasculitis and related conditions
- Pulmonary Hypertension Research and Treatments
- Ophthalmology and Eye Disorders
- Blood transfusion and management
- Neurosurgical Procedures and Complications
- Chromatin Remodeling and Cancer
- Neurological disorders and treatments
- Congenital Anomalies and Fetal Surgery
- Ophthalmology and Visual Impairment Studies
- Reconstructive Facial Surgery Techniques
- Optical Coherence Tomography Applications
- Healthcare Systems and Practices
Délégation Paris 5
2013-2019
Université Paris Cité
2013-2019
Assistance Publique – Hôpitaux de Paris
2013-2019
Hôpital Avicenne
2018
Sorbonne Paris Cité
2017
Hôpital Necker-Enfants Malades
2015-2017
Bicêtre Hospital
2012-2017
Institut Necker Enfants Malades
2017
Fondation de Rothschild
2016
HIA du Val-de-Grâce à Paris
2012-2015
Temporal macular involvement in sickle cell disease can now easily be detected by optical coherence tomography (OCT). However, while recent studies have demonstrated its high prevalence, little is known about potential consequences on visual function.To assess the function of patients with no symptoms despite temporal atrophy.This retrospective case series included data collection and explorations made a single referral center for 2016. Three exhibiting preserved acuity but showing retinal...
ARID1B mutations in Coffin–Siris syndrome are a cause of intellectual disability (0.5–1%), with various degrees autism and agenesis the corpus callosum (10%). Little is known regarding cognitive motor consequences humans no link has been made between anomalies visuospatial neuromotor dysfunctions. We have investigated phenotype eight patients mutations. A paramedian sagittal section brain MRI was selected, measured anteroposterior length, genu trunk width. Spearman’s rank order coefficients...
Purpose Cytomegalovirus retinitis in children is poor known and his management remains controversial. The objective of this study to provide a precise clinical description set treatment protocol for better these patients. Methods Retrospective including all children's eyes with primary immune deficiency (PID) patients CMV confirmed by PCR on aqueous humor. consisted of: an anti‐viral intravitreal injection (IVT) associated general treatment. endpoint was the good response defined...
Introduction The recent rise of OCT showed that asymptomatic atrophy the median temporal raphe retina (ATR) was a frequent occurrence in sickle cell disease (SCD). However, prevalence, mechanisms and significance ATR is not known, especially paediatric field. Methods SCD-children prospectively underwent fundus examination an macula retina. Atrophy MTR quantified on thickness maps. Data from brain imaging were collected SS-type SCD children. Results Eighty-one children studied; 64.2%...