Ana Francisca Junqueira Ribeiro Pereira

ORCID: 0000-0003-1161-8810
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About
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Research Areas
  • Cutaneous Melanoma Detection and Management
  • Sexual function and dysfunction studies
  • Lung Cancer Treatments and Mutations
  • Vascular anomalies and interventions
  • Sexual Differentiation and Disorders
  • Lung Cancer Diagnosis and Treatment
  • Diverticular Disease and Complications
  • Autoimmune and Inflammatory Disorders Research
  • Renal and Vascular Pathologies
  • Skin Protection and Aging
  • Hormonal and reproductive studies
  • Prenatal Screening and Diagnostics
  • Research on Leishmaniasis Studies
  • Financial Literacy, Pension, Retirement Analysis
  • Gestational Diabetes Research and Management
  • Autoimmune and Inflammatory Disorders
  • Nonmelanoma Skin Cancer Studies
  • Hair Growth and Disorders
  • Inflammasome and immune disorders
  • Central Venous Catheters and Hemodialysis
  • Autoimmune Bullous Skin Diseases
  • Bacterial Infections and Vaccines
  • Actinomycetales infections and treatment

Hospital das Clínicas da Universidade Federal de Minas Gerais
2013-2020

Hospital de Santa Maria
2019

Universidade Federal de Minas Gerais
2010-2013

Prefeitura Municipal de Belo Horizonte
2010

Finasteride is a 5α-reductase enzyme inhibitor that has been approved for the treatment of male androgenic alopecia since 1997. Over time, it considered safe and well-tolerated drug with rare reversible side effects. Recently there have reports adverse drug-related reactions persisted at least three months after discontinuation this drug, term post-finasteride syndrome arose. It includes persistent sexual, neuropsychiatric, physical symptoms. Studies to date cannot refute or confirm as...

10.1016/j.abd.2020.02.001 article EN cc-by Anais Brasileiros de Dermatologia 2020-03-25

BACKGROUND: The incidence of melanoma has been steadily rising in past decades. Although it accounts for only 3% all skin cancers, is responsible 75% deaths. OBJECTIVE: to describe the epidemiological aspects a university hospital setting over period 20 years. METHODS: A total 166 patients were analyzed between January 1990 and 2010 clinical histological variables correlations them. 5% level significance was adopted. RESULTS: majority Caucasians (74%), females (61%), with mean age at...

10.1590/abd1806-4841.20131855 article EN cc-by-nc Anais Brasileiros de Dermatologia 2013-06-01

Muckle-Wells syndrome is a rare autosomal dominant disease that belongs to group of hereditary febrile syndromes. It characterized by recurrent and self-limited episodes fever, urticaria, arthralgia, myalgia conjunctivitis since childhood, which are related exposure cold temperatures. Lately, progressive sensorineural hearing loss occurs. Amyloidosis the main complication can be found in about 25% cases. has been demonstrated there an association with mutations NLRP3 gene, codifies...

10.1590/s0365-05962010000600022 article EN cc-by Anais Brasileiros de Dermatologia 2010-12-01

Bilateral deep vein thrombosis (DVT) should prompt investigation for pro-thrombotic conditions and the exclusion of vascular compromise due to intrinsic extrinsic factors. The authors present case a 47-year-old man admitted with bilateral DVT diagnosed inferior vena cava (IVC) infra-renal segment agenesis, discuss management this rare condition.Bilateral in young otherwise healthy individuals aetiology risk factors life-long treatment anticoagulation therapy is required.Although rare,...

10.12890/2019_001063 article EN cc-by-nc-nd European Journal of Case Reports in Internal Medicine 2019-03-15

Nocardiosis is a rare infection in immunocompetent patients. Nocardia spp. an uncommon cause of prostate abscesses and responsible for only 1-2% brain abscess. Hematogenous dissemination can occur, presentation more than two locations required to determine disseminated nocardiosis. The microbiological diagnosis this agent still challenge due the complexity its identification regular laboratories. An early adequate treatment with effective antibiotics are critical treating entity. We report...

10.14740/jmc3673 article EN Journal of Medical Cases 2021-01-01
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