Psychopathological Dimensions in Portuguese Subjects with Transthyretin Familial Amyloid Polyneuropathy
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Psychopathological Dimensions in Portuguese Subjects with Transthyretin Familial Amyloid Polyneuropathy ; volume:2 ; number:3 ; year:2017
Biomedicine hub ; 2, Heft 3 (2017)
- Urheber
-
Lopes, Alice
Fonseca, Isabel
Sousa, Alexandra
Branco, Margarida
Rodrigues, Carla
Coelho, Teresa
Sequeiros, Jorge
Freitas, Paula
- DOI
-
10.1159/000485118
- URN
-
urn:nbn:de:101:1-2018013115236
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:45 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Lopes, Alice
- Fonseca, Isabel
- Sousa, Alexandra
- Branco, Margarida
- Rodrigues, Carla
- Coelho, Teresa
- Sequeiros, Jorge
- Freitas, Paula
Ähnliche Objekte (12)
Vasculopathy in transthyretin Val30Met familial amyloid polyneuropathy
Ocular manifestations of transthyretin-related familial amyloid polyneuropathy
Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
Patient-specific induced pluripotent stem cell-based modelling of transthyretin-related Familial Amyloidotic Polyneuropathy
Specific ophtalmologic changes in late onset familial amyloid polyneuropathy (FAP) portuguese patients
Positive real-world effectiveness of tafamidis for delaying disease progression in transthyretin familial amyloid polyneuropathy
Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llàtzer Hospital descriptive study
Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease
Familial amyloidotic polyneuropathy associated with the transthyretin CYS 114 gene in a Russian pair of monozygotic twins
Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm
Familial amyloidotic polyneuropathy in Crete, Greece
Vasculopathy in transthyretin Val30Met familial amyloid polyneuropathy
Ocular manifestations of transthyretin-related familial amyloid polyneuropathy
Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
Patient-specific induced pluripotent stem cell-based modelling of transthyretin-related Familial Amyloidotic Polyneuropathy
Specific ophtalmologic changes in late onset familial amyloid polyneuropathy (FAP) portuguese patients
Positive real-world effectiveness of tafamidis for delaying disease progression in transthyretin familial amyloid polyneuropathy
Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llàtzer Hospital descriptive study
Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease
Familial amyloidotic polyneuropathy associated with the transthyretin CYS 114 gene in a Russian pair of monozygotic twins
Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm
Familial amyloidotic polyneuropathy in Crete, Greece
Vasculopathy in transthyretin Val30Met familial amyloid polyneuropathy
Ocular manifestations of transthyretin-related familial amyloid polyneuropathy
Brazilian consensus for diagnosis, management and treatment of transthyretin familial amyloid polyneuropathy
Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy
Patient-specific induced pluripotent stem cell-based modelling of transthyretin-related Familial Amyloidotic Polyneuropathy
Specific ophtalmologic changes in late onset familial amyloid polyneuropathy (FAP) portuguese patients
Positive real-world effectiveness of tafamidis for delaying disease progression in transthyretin familial amyloid polyneuropathy
Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llàtzer Hospital descriptive study
Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease
Familial amyloidotic polyneuropathy associated with the transthyretin CYS 114 gene in a Russian pair of monozygotic twins
Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm