Carlos Salgado

ORCID: 0000-0002-5819-5221
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About
Contact & Profiles
Research Areas
  • Retinal and Macular Surgery
  • Intraocular Surgery and Lenses
  • Vascular Malformations Diagnosis and Treatment
  • Acute Ischemic Stroke Management
  • Inflammatory Bowel Disease
  • Erythrocyte Function and Pathophysiology
  • Glaucoma and retinal disorders
  • Multiple Myeloma Research and Treatments
  • Hemoglobinopathies and Related Disorders
  • Venous Thromboembolism Diagnosis and Management
  • Neurological Complications and Syndromes
  • Pregnancy and preeclampsia studies
  • Musculoskeletal synovial abnormalities and treatments
  • Transcranial Magnetic Stimulation Studies
  • Cardiovascular Issues in Pregnancy
  • Drug-Induced Adverse Reactions
  • Ocular Diseases and Behçet’s Syndrome
  • Connective tissue disorders research
  • Cardiac Imaging and Diagnostics
  • Blood properties and coagulation
  • Child Abuse and Related Trauma
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Autoimmune and Inflammatory Disorders
  • Systemic Lupus Erythematosus Research
  • Bone Tumor Diagnosis and Treatments

Stanford Health Care
2022

University of Atlántico
2021

University Hospital Complex Of Vigo
2015

Complexo Hospitalario Universitario A Coruña
2015

Complejo Asistencial Universitario de Palencia
2010

Introdução: O plasmocitoma solitário é uma doença maligna caracterizada pela proliferação monoclonal e neoplásica de plasmócitos. Pode apresentar-se como ósseo (limitado a um local no esqueleto axial) ou extramedular (maioritariamente limitado aos tecidos moles). É rara (cerca 5% das doenças malignas células plasmáticas) afeta com maior frequência homens mais 40 anos atinge comumente as vértebras, sendo muito raro na maxila. seu diagnóstico, segundo os critérios da International Myeloma...

10.24873/j.rpemd.2024.12.1257 article PT cc-by-nc-nd Revista Portuguesa de Estomatologia Medicina Dentária e Cirurgia Maxilofacial 2024-12-30

Objective: To describe the development of retinal pigment epithelium (RPE) atrophy after uncomplicated pars plana vitrectomy (PPV) with epiretinal membrane (ERM) and/or internal limiting (ILM) peeling in 2 patients. Cases description: Case 1: A 79-years-old female diagnosis a full-thickness macular hole her right eye (OD) best corrected visual acuity (BCVA) of: 20/100 and left (OS): 20/70. After surgery she developed large RPE hyperplasia presented hand movement that did not improve pinhole....

10.22336/rjo.2022.16 article EN Romanian Journal of Ophthalmology 2022-03-31

Purpose: To present a clinical case and surgical technique for management of optic disk pit (ODP) maculopathy. Methods: Surgical video lens sparring pars plana vitrectomy, autologous scleral flap insertion gas tamponade. Results: After 1 year follow-up visual acuity was restored to 20/25, retinal serous detachment schisis were resolved the remained in (ODP). Conclusion: In this case, treatment with vitrectomy tamponade maculopathy provided satisfactory anatomical functional results.

10.1177/1120672120948731 article EN European Journal of Ophthalmology 2020-08-13

Background: The purpose of this study was to describe anatomical and visual outcomes after scleral buckling, pars plana vitrectomy, the use silicone oil as a tamponade in management retinal detachment associated with giant tears (GRT). Material methods: A retrospective descriptive chart review conducted for cases an initial presentation rhegmatogenous detachments GRT. Patients underwent surgical by single surgeon had follow-ups at least 12 months. Results: We included 32 eyes patients. All...

10.5603/oj.2022.0003 article EN cc-by-nc-nd Ophthalmology Journal 2022-03-17

We present the clinical case of an 8-years-old male patient with a genetic diagnosis Stickler syndrome type 1 and management associated vitreoretinal complications. The had antecedent no light perception in his left eye secondary to retinal detachment treated another health centre. He consulted history blunt trauma head unremarkable anterior segment fundus exam. Scleral indentation showed lesions be right eye. recommended follow-up every six months. did not come controls. was three years...

10.5603/oj.2021.0019 article EN cc-by-nc-nd Ophthalmology Journal 2021-01-25

We present the clinical case of a 28-year-old female patient with diagnosis Behçet’s disease and unilateral relapsing ocular involvement in systemic management infliximab. Optical coherence tomography angiography swept-source technology (DRI OCT Triton Plus™, Topcon Corporation, Tokyo, Japan) revealed asymmetric compromise between both eyes. Decreased foveal vascular density, asymmetrical avascular zone enlargement at superficial deep capillary plexuses, focal areas hypoperfusion plexus...

10.5603/oj.2021.0027 article EN cc-by-nc-nd Ophthalmology Journal 2021-01-25
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