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Your search keyword '"Amiloidose Familiar/genética"' showing total 3 results
Start Over Descriptor "Amiloidose Familiar/genética"
3 results on '"Amiloidose Familiar/genética"'

1. Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)

Author

Nunes, Nágela S. V., Carvalho, João Paulo Moreira, Costa, Fernanda Salomão, Nacif, Marcelo Souto, Dominato, Joelma, Mesquita, Claudio Tinoco, and Mesquita, Evandro Tinoco

Subjects
Cardiomyopathies/diagnosis, Amyloid Neuropathies, Familial, Neuropatias Amiloides Familiares, Prevalence, Amiloidose Familiar/genética, Amyloidosis, Familial/genetics, Síncope, Diagnostic, Imaging/methods, Cardiomiopatias/diagnóstico, Syncope, Prevalência, Diagnóstico por Imagem/métodos
Published
2019

2. Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)

Author

Nágela S. V. Nunes, João Paulo Moreira Carvalho, Fernanda Salomão Costa, Marcelo Souto Nacif, Joelma Dominato, Claudio Tinoco Mesquita, and Evandro Tinoco Mesquita

Subjects
síncope, amiloidose familiar/genética, neuropatias amiloides familiares, cardiomiopatias/diagnóstico, diagnóstico por imagem/métodos, prevalência., Diseases of the circulatory (Cardiovascular) system, RC666-701
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3. Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile)

Author

Nágela S. V. Nunes, João Paulo Moreira Carvalho, Fernanda Salomão Costa, Marcelo Souto Nacif, Joelma Dominato, Claudio Tinoco Mesquita, and Evandro Tinoco Mesquita

Subjects
lcsh:Diseases of the circulatory (Cardiovascular) system, síncope, neuropatias amiloides familiares, lcsh:RC666-701, prevalência, amiloidose familiar/genética, diagnóstico por imagem/métodos, cardiomiopatias/diagnóstico

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