Amyloidosis
Mostrando 1-12 de 318 artigos, teses e dissertações.
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1. MALT lymphoma associated with laryngeal amyloidosis: case report
Brazilian Journal of Otorhinolaryngology. Publicado em: 2022
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2. Oral manifestations of systemic amyloidosis, an aid to diagnosis of multiple myeloma - report of two cases
Brazilian Journal of Otorhinolaryngology. Publicado em: 2022
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3. Ophthalmological manifestations of hereditary transthyretin amyloidosis
RESUMO A amiloidose familiar por transtirretina é a forma mais comum de amiloidose sistêmica hereditária mundialmente. A condição é secundária a mais de 100 mutações ponto diferentes no gene da transtirretina (18q12.1). Mutações levam a depósitos anormais de amilóide principalmente no coração e nos nervos periféricos. O envolvimento leptomen�
Arquivos Brasileiros de Oftalmologia. Publicado em: 2022
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4. Gene Silencing Therapeutics in Cardiology: A Review Article
Abstract Therapeutics that inhibit enzymes, receptors, ion channels, and cotransporters have long been the mainstay of cardiovascular medicine. Now, oligonucleotide therapeutics offer a modern variation on this paradigm of protein inhibition. Rather than target a protein, however, small interfering ribonucleic acids and antisense oligonucleotides target the
International Journal of Cardiovascular Sciences. Publicado em: 2022
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5. Hereditary transthyretin-mediated amyloidosis with polyneuropathy: baseline anthropometric, demographic and disease characteristics of patients from a reference center
RESUMO Antecedentes: Amiloidose hereditária por transtirretina (hATTR) com polineuropatia é uma doença rara, hereditária, multissistêmica, frequentemente fatal, causada por mutação no gene da transtirretina (TTR). Características dos pacientes ao diagnóstico, especialmente dados antropométricos, são raros na literatura, e são relevantes para def
Arquivos de Neuro-Psiquiatria. Publicado em: 2022
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6. Systemic amyloidosis manifestation in a patient with psoriatic arthritis
Abstract Systemic amyloidosis secondary to psoriatic arthritis is rare, and published data are based mainly on case reports and are associated with increased mortality. This is the report of a patient with long-term psoriatic arthritis and chronic sialadenitis, who showed an inadequate response to therapy. The diagnosis of secondary amyloidosis was attained
An. Bras. Dermatol.. Publicado em: 2021-06
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7. Clinical Profile of Patients with Head and Neck Amyloidosis: A Single-Institution Retrospective Chart Review
Abstract Introduction Isolated amyloidosis involving the head and neck is a rare entity. The pathophysiology of the localized disease appears to be distinct from that of the systemic counterpart. Systemic progression of the localized disease is unusual, and the prognosis of the localized form is excellent. Objective To describe the demographic and clinicop
Int. Arch. Otorhinolaryngol.. Publicado em: 2020-12
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8. Amyloidosis: the use of the Daratumumab
Resumo Em 2008, Satoshi Nakamoto, pseudônimo de uma pessoa desconhecida, lançou o “Bitcoin”, uma criptomoeda descentralizada, com o objetivo de contornar qualquer banco ou governo e retornar a um sistema monetário mais “austero” e controlado. Após o advento do Bitcoin, várias outras criptomoedas foram criadas, suscitando um debate sobre a capaci
Rev. Assoc. Med. Bras.. Publicado em: 2020-12
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9. Use of daratumumab in patients with amyloidosis
The Guidelines Project, an initiative of the Brazilian Medical Association, aims to combine information from the medical field in order to standardize producers to assist the reasoning and decision-making of doctors. The information provided through this project must be assessed and criticized by the physician responsible for the conduct that will be adopted
Rev. Assoc. Med. Bras.. Publicado em: 2020-11
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10. Cardiac amyloidosis: non-invasive diagnosis
RESUMO A amiloidose cardíaca é uma doença infiltrativa que exige um alto grau de suspeição clínica para o diagnóstico apropriado. O diagnóstico precoce e a definição do subtipo de amiloidose têm um papel fundamental para a terapêutica e prognóstico desta doença. Nesse contexto, o emprego de biomarcadores cardíacos como as troponinas e NT-proBN
Rev. Assoc. Med. Bras.. Publicado em: 2020-03
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11. Evaluation of the structure, autoimmunity, and functions of the thyroid gland in familial Mediterranean fever patients
ABSTRACT Objective Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disorder that is frequently seen in the eastern Mediterranean region. The thyroid gland can be affected in FMF patients through autoimmunity or amyloidosis. Here, we aimed to evaluate the structure and functions of the thyroid gland in addition to possible auto
Arch. Endocrinol. Metab.. Publicado em: 2020-02
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12. Insufficient iodine intake in pregnant women in different regions of the world: a systematic review
ABSTRACT Objective Familial Mediterranean fever (FMF) is an autosomal recessive autoinflammatory disorder that is frequently seen in the eastern Mediterranean region. The thyroid gland can be affected in FMF patients through autoimmunity or amyloidosis. Here, we aimed to evaluate the structure and functions of the thyroid gland in addition to possible auto
Arch. Endocrinol. Metab.. Publicado em: 2020-02