Sandra García

ORCID: 0000-0002-1605-827X
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About
Contact & Profiles
Research Areas
  • Genetic and rare skin diseases.
  • Skin and Cellular Biology Research
  • Medical research and treatments
  • Autoimmune Bullous Skin Diseases
  • Cancer and Skin Lesions
  • melanin and skin pigmentation
  • Medicine and Dermatology Studies History
  • Health and Lifestyle Studies
  • Hedgehog Signaling Pathway Studies
  • Tumors and Oncological Cases
  • Dermatological and Skeletal Disorders
  • Nail Diseases and Treatments
  • Dermatologic Treatments and Research
  • Drug-Induced Adverse Reactions
  • Obesity, Physical Activity, Diet
  • Cutaneous Melanoma Detection and Management
  • Oral Health Pathology and Treatment
  • Oral and gingival health research
  • Skin Diseases and Diabetes
  • Vasculitis and related conditions
  • Inflammatory Myopathies and Dermatomyositis
  • Cutaneous lymphoproliferative disorders research
  • Urticaria and Related Conditions
  • Health and Medical Education
  • Atherosclerosis and Cardiovascular Diseases

Pontificia Universidad Javeriana
2024-2025

Saint Göran Hospital
2024

Hospital Posadas
2002-2022

Instituto de Efectividad Clínica y Sanitaria
2021

Clínica Santa María
2013

To describe the epidemiology, clinical features, and classification of uveitis in a large cohort Colombian patients.

10.1007/s00417-024-06422-z article EN cc-by Graefe s Archive for Clinical and Experimental Ophthalmology 2024-03-06

Actinomyces meyeri cutaneous actinomycosis is a very rare disease. It often results from contiguous dissemination of an underlying focus. We report case pulmonary actinomicosis with secondary involvement which led to the diagnosis. A 51-year-old man presented indurated, erythematous plaque on his right chest wall. He had been diagnosed pneumoniae one month prior ago and received antibiotic treatment but symptoms persisted. Fibrobroncoscopy was normal bronchoalveolar lavage samples were...

10.1111/j.1365-4632.2009.03798.x article EN International Journal of Dermatology 2009-01-19

Abstract Giant congenital melanocytic nevi (GCMN) are rare and occur in about one out of every 200 000–500 000 births. Their importance resides the aesthetic alteration they produce possibility malignant transformation or their association with central nervous system as a distinctive syndrome: neurocutaneous melanoblastosis nevomatosis, due to fact that lesions produced by infiltration nevus cells. We present here patient combination GCMN an outstanding lipomatosis located on same area.

10.1046/j.1468-3083.2002.00569.x article EN Journal of the European Academy of Dermatology and Venereology 2002-07-01

La queratosis folicular invertida es un tumor anexial benigno infrecuente derivado del epitelio de la vaina radicular externa folículo piloso. Predomina en el sexo masculino y tiene mayor incidencia quinta década vida. Se presenta como una lesión solitaria, localizada principalmente rostro (labio superior mejilla). Es rosado tipo pápula, firme e hiperqueratósico, tamaño variable asintomático. Su diagnóstico se basa histopatología tratamiento elección exéresis quirúrgica. Presentamos serie...

10.47196/da.v30i1.2393 article ES cc-by-nc-nd Dermatología Argentina 2024-02-06

Gene expression profiles are used for decision making in the adjuvant setting of hormone receptor-positive, HER2-negative (HR+/HER2-) breast cancer. Previous studies have reported algorithms to optimize use RS/Oncotype Dx. However, no such efforts focused on ROR/Prosigna. In addition, there is data adherence testing guidelines. Postmenopausal women with resected HR+/HER2- and node-negative cancer that had undergone ROR/Prosigna four Swedish regions between March 2020 2022 were included...

10.1016/j.esmoop.2024.103124 article EN cc-by-nc-nd ESMO Open 2024-05-01
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