Results 161 to 170 of about 61,429 (293)
Fibroblast Transcriptomics in Molecular Diagnostics of a Comprehensive Dystonia Cohort
Objective Genomic sequencing leaves >50% of dystonia‐affected individuals without a diagnosis. Where DNA‐oriented approaches remain insufficient, integrating multiomics is essential to advance genome interpretation. Herein, we incorporated RNA sequencing (RNA‐seq) data from 167 patients with dystonia across a range of ages and presentations. Methods We
Alice Saparov +42 more
wiley +1 more source
Images in Medicine: Recognizing Hereditary Hemorrhagic Telangiectasia Through Mucocutaneous Findings and Its Management Challenges. [PDF]
Khodzandi S +4 more
europepmc +1 more source
Outcome of Inverted Internal Limiting Membrane Flap Technique in Full- Thickness Macular Hole Secondary to Macular Telangiectasia Type 2. [PDF]
Alshehri MS, Alharthi RA, Alqahtani FS.
europepmc +1 more source
ABSTRACT Hemolacria is a rare condition characterized by bloody tears. Its etiology is often multifactorial, but functional/psychosomatic mechanisms have been proposed when organic causes are excluded. A 48‐year‐old woman with a history of multiple traumatic brain injuries (coma in 2008, car accident in 2017) presented with refractory generalized ...
Roghayeh Mohammadi, Ahmad Alipour
wiley +1 more source
Therapeutic effect of faricimab in macular telangiectasia type 1 and Coats' disease: case series. [PDF]
Park HY, Joo K, Woo SJ.
europepmc +1 more source
ABSTRACT The combination of Endolift laser therapy and injectable platelet‐rich fibrin (i‐PRF) is an emerging strategy in aesthetic medicine, but the optimal scheduling of these modalities remains unexplored. This case report highlights a novel treatment schedule combining i‐PRF and Endolift laser therapy, resulting in noticeable short‐term facial ...
Mohammad Ali Nilforoushzadeh +3 more
wiley +1 more source
Osteolysis After Interphalangeal Joint Arthrodesis in Systemic Sclerosis: A Case Series. [PDF]
Mathias KR +3 more
europepmc +1 more source
ABSTRACT Myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) is an autoimmune disorder characterized by demyelination of the central nervous system. It can impact the optic nerves, spinal cord, brain parenchyma, and brainstem, resulting in various clinical presentations such as acute disseminated encephalomyelitis (ADEM), optic ...
Yuxian Shi +5 more
wiley +1 more source
Severe Transfusion-Dependent Anemia in Hereditary Hemorrhagic Telangiectasia: A Critical Case of Gastrointestinal Bleeding and Pulmonary Arteriovenous Malformation. [PDF]
Shetty M, Awale MS, Gangula S, Patri JR.
europepmc +1 more source

