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Late-onset postoperative angioedema triggered by angiotensin-converting enzyme inhibitor: An emergent airway forethought

Revista espanola de anestesiologia y reanimacion, 2023, Vol.70 (9), p.536-539

2023

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Idiopathic pleuroparenchymal fibroelastosis with suggestive biopsy of pulmonary carcinoma - Case report

Revista portuguesa de pneumologia, 2017, Vol.23 (2), p.111-113

2017

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Solitary endobronchial papilloma: a case report

Revista portuguesa de pneumologia, 2015, Vol.21 (1), p.49-50

2015

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Bronchial mucous gland adenoma: A rare tumor

Revista portuguesa de pneumologia, 2017, Vol.23 (4), p.241-242

2017

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Beyond a pleural effusion: Primary pleuropulmonary sarcomas and the challenge of diagnosis

Revista portuguesa de pneumologia, 2016, Vol.22 (5), p.298-299

2016

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Congenital Zika syndrome phenotype in a child born in Brazil in December 2011

Clinical case reports, 2018, Vol.6 (11), p.2053-2056

2018

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Severe glomerulonephritis and encephalopathy associated with parvovirus B19 infection mimicking systemic lupus erythematosus

Scandinavian journal of rheumatology, 2012, Vol.41 (1), p.79-81

2012

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Renal cell carcinoma in the context of tuberous sclerosis: report of a paediatric case with intra-operative cytology, histology, immunohistochemistry and molecular cytogenetics

Cytopathology : official journal of the British Society for Clinical Cytology, 2014, Vol.25 (1), p.57-59

2014

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Endoscopic sclerotherapy for upper gastrointestinal bleeding due to Mallory-Weiss syndrome

The American journal of gastroenterology, 1995, Vol.90 (8), p.1364-1365

1995

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Thoracoscopic enucleation of a leiomyoma of the upper thoracic esophagus

Diseases of the Esophagus, 2003, Vol.16 (4), p.339-341

2003

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Chronic monocytic leukemia

American journal of clinical pathology, 1978, Vol.69 (6), p.648-649

1978

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Renal-cell carcinoma: cytologic diagnosis in a child

Diagnostic cytopathology, 1999, Vol.21 (5), p.362-362

1999

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Inflammatory pseudotumor of the spleen in a child

Medical and pediatric oncology, 2001, Vol.37 (1), p.77-78

2001

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Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome

Epigenetics, 2023, Vol.18 (1)

2023

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Eleven hours of hypothermic oxygenated machine perfusion (HOPE) for complex liver retransplantation: A case report

Artificial organs, 2023, Vol.47 (8), p.1413-1415

2023

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The potential role for topical imiquimod in the treatment of chronic mucocutaneous candidiasis caused by gain-of-function mutation in STAT1: A case-report

Dermatologic therapy, 2021, Vol.34 (5), p.e15043-e15043

2021

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Silent Intruder: Unusual Presentation of Neurocysticercosis in an HIV-Infected Patient from the Far Northern Brazilian Amazon

Medicina (Kaunas, Lithuania), 2024, Vol.60 (3)

2024

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Thyroid and Breast Cancer in 2 Sisters With Monoallelic Mutations in the Ataxia Telangiectasia Mutated (ATM) Gene

Journal of the Endocrine Society, 2022, Vol.6 (4), p.bvac026-bvac026

2022

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Is kinesiophobia related to fear of falling, dizziness disability, and migraine disability in patients with migraine?

Physiotherapy Theory and Practice, 2022, Vol.38 (13), p.2727-2735

2022

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Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication

Cytogenetic and genome research, 2021, Vol.161 (3-4), p.160-166

2021

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Increase in the incidence of chronic critical disease in a University Hospital over eight years

Medicina intensiva, 2021, Vol.45 (7), p.e22-e24

2021

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COVID-19 in a temporal relation to the onset of multiple sclerosis

Multiple sclerosis and related disorders, 2021, Vol.50, p.102863-102863

2021

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Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families

International journal of molecular sciences, 2023, Vol.24 (15)

2023

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Cardiac disease in the Spix Macaw (Cyanopsitta spixii): two cases

Australian veterinary journal, 2021, Vol.99 (9), p.402-407

2021

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Spondyloepimetaphyseal dysplasia with elevated plasma lysosomal enzymes caused by homozygous variant in MBTPS1

American journal of medical genetics. Part A, 2020, Vol.182 (7), p.1796-1800

2020

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Late-onset postoperative angioedema triggered by angiotensin-converting enzyme inhibitor: An emergent airway forethought

Idiopathic pleuroparenchymal fibroelastosis with suggestive biopsy of pulmonary carcinoma - Case report

Solitary endobronchial papilloma: a case report

Bronchial mucous gland adenoma: A rare tumor

Beyond a pleural effusion: Primary pleuropulmonary sarcomas and the challenge of diagnosis

Congenital Zika syndrome phenotype in a child born in Brazil in December 2011

Severe glomerulonephritis and encephalopathy associated with parvovirus B19 infection mimicking systemic lupus erythematosus

Renal cell carcinoma in the context of tuberous sclerosis: report of a paediatric case with intra-operative cytology, histology, immunohistochemistry and molecular cytogenetics

Endoscopic sclerotherapy for upper gastrointestinal bleeding due to Mallory-Weiss syndrome

Thoracoscopic enucleation of a leiomyoma of the upper thoracic esophagus

Chronic monocytic leukemia

Renal-cell carcinoma: cytologic diagnosis in a child

Inflammatory pseudotumor of the spleen in a child

Contribution of miR-124 rs531564 polymorphism to the occurrence of congenital Zika syndrome

Eleven hours of hypothermic oxygenated machine perfusion (HOPE) for complex liver retransplantation: A case report

The potential role for topical imiquimod in the treatment of chronic mucocutaneous candidiasis caused by gain-of-function mutation in STAT1: A case-report

Silent Intruder: Unusual Presentation of Neurocysticercosis in an HIV-Infected Patient from the Far Northern Brazilian Amazon

Thyroid and Breast Cancer in 2 Sisters With Monoallelic Mutations in the Ataxia Telangiectasia Mutated (ATM) Gene

Is kinesiophobia related to fear of falling, dizziness disability, and migraine disability in patients with migraine?

Clinical Features of de novo Pure 16q21q24.1 Chromosome Duplication

Increase in the incidence of chronic critical disease in a University Hospital over eight years

COVID-19 in a temporal relation to the onset of multiple sclerosis

Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families

Cardiac disease in the Spix Macaw (Cyanopsitta spixii): two cases

Spondyloepimetaphyseal dysplasia with elevated plasma lysosomal enzymes caused by homozygous variant in MBTPS1

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