Esteban Uribe-Bojanini

ORCID: 0000-0003-3465-9180
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About
Contact & Profiles
Research Areas
  • Diverticular Disease and Complications
  • Infectious Diseases and Tuberculosis
  • Diagnosis and treatment of tuberculosis
  • Nonmelanoma Skin Cancer Studies
  • Vitamin K Research Studies
  • Hedgehog Signaling Pathway Studies
  • Lymphoma Diagnosis and Treatment
  • Cutaneous lymphoproliferative disorders research
  • Hormonal Regulation and Hypertension
  • Thermal Regulation in Medicine
  • Diet and metabolism studies
  • Mitochondrial Function and Pathology
  • Genetic and rare skin diseases.
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Organ Transplantation Techniques and Outcomes
  • T-cell and Retrovirus Studies
  • Enzyme function and inhibition
  • DNA Repair Mechanisms
  • Genetic Neurodegenerative Diseases
  • Cutaneous Melanoma Detection and Management
  • Infectious Diseases and Mycology
  • Vascular Malformations and Hemangiomas

Clínica CES
2016-2017

University of Miami
2012

Universidad de Antioquia
1961

We report the case of a woman with history hypertension and hyperlipidemia presenting recurrent episodes consistent clinically cerebrovascular accidents (CVA), MRI changes suggestive ischemia versus vasculitis as their cause. No anatomical neurological, rheumatic, cardioembolic, or arteriosclerotic etiologies could be determined by extensive workup. Incidentally, patient was found to have prolonged activated Partial Thromboplastin Time (aPTT) normal Prothrombin (PT); further testing revealed...

10.1155/2012/723204 article EN cc-by Case Reports in Hematology 2012-01-01

Several genetic disorders caused by defective nucleotide excision repair that affect the skin and nervous system have been described, including Xeroderma Pigmentosum (XP), De Sanctis-Cacchione syndrome (DSC), Cockayne syndrome, Trichothiodystrophy. Cutaneous photosensitivity with an increased risk of malignancy is a common feature these disorders, but clinical manifestations commonly overlap syndromes. genes found to be altered in pathologies, we lack more genotype-phenotype correlations...

10.1155/2017/7162737 article EN cc-by Case Reports in Medicine 2017-01-01

Becker’s nevus syndrome is part of the epidermal syndromes and has been described with a phenotype that includes nevus, ipsilateral breast hypoplasia, variable skeletal malformations. It more frequent in males than females (5 : 1) but relevant females. The diagnosis clinically based skin lesion must be present no other numbered criteria have established, being possibility higher. Regarding treatment use antiandrogen medication demonstrated adequate clinical response dose 50 mg/day spironolactone.

10.1155/2016/3856518 article EN cc-by Case Reports in Pediatrics 2016-01-01

La medición del cortisol total en sangre ha sido parte fundamental el estudio eje hipotálamo-hipófisis-adrenal y de sus alteraciones, tales como síndrome Cushing la insuficiencia adrenal. El circula plasma su mayoría unido a proteínas, pero fracción libre es biológicamente activa se puede medir sangre, orina saliva. secreción no homogénea durante día, por contrario, está regida un ritmo circadiano, que vez, ver afectado diferentes estresores físicos psicológicos. Por esta razón, cuenta con...

10.36384/01232576.74 article ES Medicina y Laboratorio 2016-03-01
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