TTR-FAP: liver transplant vs oral medication. How and when

por Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Vitreous Amyloidosis as the Presenting Symptom of Familial Amyloid Polyneuropathy TTR Val30Met in a Portuguese Patient

por Seca, Mariana, Ferreira, Natália, Coelho, Teresa
Publicado 2014

Specific ophtalmologic changes in late onset familial amyloid polyneuropathy (FAP) portuguese patients

por Ferreira, Natalia, Dias, David, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Patients with hereditary ATTR amyloidosis experience an increasing burden of illness as the disease progresses

por Adams, David, Amitay, Oved, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Corino de Andrade disease: mechanisms and impact on reproduction

por Lopes, Rita A, Coelho, Teresa, Barros, Alberto, Sousa, Mário
Publicado en JBRA Assist Reprod (2017)

Preliminary assessment of neuropathy progression in patients with hereditary ATTR amyloidosis after orthotopic liver transplantation (OLT)

por Adams, David, Buades, Juan, Suhr, Ole, Obici, Laura, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Advances in the treatment of hereditary transthyretin amyloidosis: A review

por Gertz, Morie A., Mauermann, Michelle L., Grogan, Martha, Coelho, Teresa
Publicado en Brain Behav (2019)

Specific ocular changes in TTR Met30-FAP after liver transplantation

por Ferreira, Natalia, Dias, David, Vilas-Boas, Carmen, Fonseca, Isabel, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Unravelling the epidemiology of late-onset and asymptomatic carriers of FAP ATTR V30M in a Portuguese population

por Lemos, Carolina, Coelho, Teresa, Alves-Ferreira, Miguel, Santos, Diana, Sequeiros, Jorge, Sousa, Alda
Publicado en Orphanet J Rare Dis (2015)

Transthyretin familial amyloid polyneuropathy impact on health-related quality of life

por Inês, Mónica, Coelho, Teresa, Conceição, Isabel, Ferreira, Lara, de Carvalho, Mamede, Costa, João
Publicado en Orphanet J Rare Dis (2015)

Health-related quality of life in hereditary transthyretin amyloidosis polyneuropathy: a prospective, observational study

por Inês, Mónica, Coelho, Teresa, Conceição, Isabel, Ferreira, Lara, de Carvalho, Mamede, Costa, João
Publicado en Orphanet J Rare Dis (2020)

Evaluation of Mortality During Long-Term Treatment with Tafamidis for Transthyretin Amyloidosis with Polyneuropathy: Clinical Trial Results up to 8.5 Years

por Merlini, Giampaolo, Coelho, Teresa, Waddington Cruz, Márcia, Li, Huihua, Stewart, Michelle, Ebede, Ben
Publicado en Neurol Ther (2020)

Psychopathological dimensions in familial amyloid polyneuropathy patients

por Lopes, Alice, Sousa, Alexandra, Fonseca, Isabel, Branco, Margarida, Rodrigues, Carla, Freitas, Paula, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Life paths of familial amiloidotic polyneuropathy patients: a descriptive study

por Lopes, Alice, Sousa, Alexandra, Fonseca, Isabel, Branco, Margarida, Rodrigues, Carla, Freitas, Paula, Coelho, Teresa
Publicado en Orphanet J Rare Dis (2015)

Epidemiology of transthyretin familial amyloid polyneuropathy in Portugal

por Inês, Mónica, Coelho, Teresa, Conceição, Isabel, Duarte-Ramos, Filipa, de Carvalho, Mamede, Costa, João
Publicado en Orphanet J Rare Dis (2015)

Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns...

por Parman, Yesim, Adams, David, Obici, Laura, Galán, Lucía, Guergueltcheva, Velina, Suhr, Ole B., Coelho, Teresa
Publicado en Curr Opin Neurol (2016)

Exonization of an Intronic LINE-1 Element Causing Becker Muscular Dystrophy as a Novel Mutational Mechanism in Dystrophin Gene

por Gonçalves, Ana, Oliveira, Jorge, Coelho, Teresa, Taipa, Ricardo, Melo-Pires, Manuel, Sousa, Mário, Santos, Rosário
Publicado en Genes (Basel) (2017)

A Narrative Review of the Role of Transthyretin in Health and Disease

por Liz, Marcia Almeida, Coelho, Teresa, Bellotti, Vittorio, Fernandez-Arias, Maria Isabel, Mallaina, Pablo, Obici, Laura
Publicado en Neurol Ther (2020)

Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis

por Obici, Laura, Kuks, Jan B., Buades, Juan, Adams, David, Suhr, Ole B., Coelho, Teresa, Kyriakides, Theodore
Publicado en Curr Opin Neurol (2016)

Life paths of patients with transthyretin-related familial amyloid polyneuropathy Val30Met: a descriptive study

por Lopes, Alice, Sousa, Alexandra, Fonseca, Isabel, Branco, Margarida, Rodrigues, Carla, Coelho, Teresa, Sequeiros, Jorge, Freitas, Paula
Publicado en J Community Genet (2017)