| Development of Guidelines on Defining and Monitoring Progression of ATTRv Amyloidosis Using the Delphi Technique |
|
2023 |
| Eplontersen in Hereditary ATTR-polyneuropathy: Week 66 Final Analysis of the Phase 3 NEURO-TTRansform Study |
|
2023 |
| Open-label extension study of patisiran, an investigational siRNA agent for familial amyloid polyneuropathy |
|
2015 |
| Evaluation of modifications of NIS+ 7 score in oligonucleotide trials in TTR FAP |
|
2015 |
| Early intervention with tafamidis provides long-term benefit in delaying neurological progression in patients with transthyretin familial amyloid polyneuropathy |
|
2015 |
| Analysis of transthyretin familial amyloid polyneuropathy disease progression in symptomatic V30M patients treated with tafamidis or liver tarnsplantation compared to untreated patients: an analysis from the transthyretin amyloidosis outcomes survey (THAOS) registry |
|
2015 |
| Identification of a new variant of TTR involved in familial amyloid cardiomyopathy (FAC) in Brazil:from the patient to the protein |
|
2015 |
| Early intervention with tafamidis provides long-term benefit in delaying neurological progression in patients with transthyretin familial amyloid polyneuropathy |
|
2015 |
| The phenotypical expression of an European inherithed TTR amyloidosis in Brazil. |
|
2015 |
| Bseline demographics of Brazilian Patients in THAOS |
|
2012 |
| The transthyretin amyloidosis outcomes survey |
|
2012 |
| Long-term effects of tafamidis for the treatment of transthyretin familial amyloidotic polyneuropathy |
|
2012 |
| Description of neuropathic symptoms reported by ATTR patients in THAOS: the Transthyretin Amyloidosis Outcomes Survey |
|
2012 |
| Nerve conduction, neurologic assessment, and quality of life in symptomatic patients enrolled in THAOS: the Transthyretin Amyloidosis Outcomes Survey |
|
2012 |
| Follow-up of transthyretin amyloidosis patients with liver transplants or receiving tafamidis treatment as documented in THAOS: the Transthyretin Amyloidosis Outcomes Survey |
|
2012 |
| Demographics and Neurologic Function in Early-and Late ? Onset Symptomatic Patients in the Transthyretin Amyloidosis Outcomes Survey (THAOS). |
|
2011 |
| Early-Treatment Effects of Tafamiddis in Transthyretin Type Familial Amyloid Polyneuropathy. |
|
2011 |
| Tafamidis and nerve fiber function in transthyretin-type familial amyloid polyneuropathy |
|
2011 |
| Nerve Conduction in symptomatic patients in the transthyretin amyloidosis outcomes survey |
|
2011 |
| Baseline nutritional status in symptomatic patients in the Transthyretin Amyloidosis Outcomes Survey (THAOS). |
|
2011 |
| ATTR transplantation consensus pannel 2009 |
|
2010 |
| Tafamidis (FX-1006 A): a first-in-class disease- modifying therapy for transthyretin familial amyloid |
|
2010 |
| Sustainability of response to tafamidis, a diseasemodifying therapy for transthyretin type familial amyloid polyneuropathy |
|
2010 |
| Initial findings from the transthyretin amyloidosis outcomes survey (THAOS) - A Global Web-based Registry |
|
2010 |
| A landmark clinical trial of a novel small molecule transthyretin (TTR) stabiliser Fx-1006 A, in patients with TTR amyloid polyneuropathy: a phase II/III, randomised, doulble blind, placebo-controled study |
|
2009 |
| A landmark clinical trial of a novel small molecule transthyretin (TTR) stabiliser Fx-1006 A, in patients with TTR amyloid polyneuropathy: a phase II/III, randomised, doulble blind, placebo-controled study |
|
2008 |
| Correlation of clinical outcomes and disease burden in patients with transthyretin (TTR) amyloid polyneuropathy: study FX-005 a landmark clinical trial of Fx-1006 A, a novel small molecule TTR stabiliser |
|
2008 |
| Penetrance estimation and haplotype analysis of TTR val 30 met mutation of Brazilian families with familial amyloidotic polyneuropathy type I |
|
2007 |
| Ten-year experience with liver transplantation for familial amyloidotic polyneuropathy type I in Rio de Janeiro/Brazil |
|
2007 |
| Liver transplantation for familial amyloidotic polyneuropathy |
|
2007 |
| Penetrance estimation of TTR val30met mutation in Brazilian families with familial amyloidotic polyneuropathy using a survival analysis approach |
|
2006 |
| Discordant expression of familial amyloid neuropathy in a pair of monozygotic brazilian twis |
|
2006 |
| Assisted thiraciscopic cervical thymectomy for myasthenia gravis a 3 years experience at Clementino Fraga Filho University Hospital |
|
2006 |
| Perfil dos pacientes com miastenia gravis de um hospital universitário federal do rio de janeiro |
|
2006 |
| Discordant expression of familial amyloid polyneuropathy in a pair of monozygotic Brasilian twins |
|
2006 |
| Difference of penetrance in transthyretin amyloid neuropathies across families from european and brazilian origin |
|
2006 |
| Non-paraneoplastic Lambert-Eaton myasthenic syndrome with severe gastrointestinal dysfunction. Case report |
|
2005 |
| Initial results of video-assisted thoracoscopia cervical thymectomy for myasthenia gravis at Clementino Fraga Filho University Hospital |
|
2004 |
| Electroneuromyography study before and after liver transplantation in Brazilian familial amyloidotic polyneuropathy type I patients |
|
2004 |
| Polineuropatia do doente crítico no centro de terapia intensiva da UFRJ |
|
2002 |
| Liver transplantation for familial amyloidotic polyneuropathy. Clinical and eletroneuromyography study |
|
2001 |
| Liver transplantation for familial amyloidotic polyneuropathy. Clinical and electroneromyography study |
|
2001 |
| Estudo clínico e eletroneuromiográfico em pacientes em tratamento com talidomida |
|
2000 |
| Transplante hepático em pacientes em polineuropatias amiloidótica familiar. Estudo clínico e eletroneuromiográfico |
|
2000 |
| Síndrome de Eaton Lambert com ausência de anticorpos anti canal de cálcio |
|
2000 |
| Estudo eletroneuromiográfico em pacientes críticos noc entro de terapia intensiva do HUCFF |
|
2000 |
| Disautonomia idiopática |
|
2000 |
| Lesão da ponta anterior da medula e hipertiroidismo. Relato de dois casos |
|
2000 |
| Neuropatia atáxica sensitiva após raquianestesia |
|
2000 |
| Miosite por corpos de inclusão |
|
1999 |
| Miosite eosinofílica. Relato de caso |
|
1999 |
| Citopatia mitocondrial. Relato de caso |
|
1999 |
| Avaliação evolutiva de pacientes com polineuropatia amiloidótica familiar submetidos a transplante de fígado |
|
1999 |
| Polineuropatia amiloidótica familiar PAF. Estudo clínico e eletroneuromiográfia pré e pós transplante hepático |
|
1998 |
| Acometimento cardíaco ne polineuropatia amiloidpotica familiar tipo I |
|
1998 |
| Electroneuromyography and somatosensory evoked potentials in HTLV-I associated myelopathy |
|
1998 |
| Familial amyloidotic polyneuropathy. Clinical profile and elestroneuromyography before and after liver transplantion |
|
1998 |
| Electrneuromyography (ENMG) and somatosensory evoked potentials (EP) in HTLV-I associated myelopathy |
|
1998 |
| Familial amyloidotic polyneuropathy (FAP) clinical profile and electroneuromyography before and after liver transplantation |
|
1998 |
| PAF - tipo I. Estudo clínico e eletroneuromiográfico pré e pós transplante hepático |
|
1997 |
| ENMG e PESS na mielopatia pelo HTLV -I |
|
1997 |
| Avaliação clínica e por ENMG antes e pós transplante hepático em apcientes com PAF tipo I |
|
1997 |
| Polineuropatia amiloidótica. relato de caso |
|
1996 |
| Polineuropatia amiloidótica familiar tipo I PAF. Estuido clínico e eletroneuromiográfico (ENMG) pré e pós transplante hepático |
|
1996 |
| Miastenia Gravis. Experiência clínica e cirúrgica do HUCFF-UFRJ |
|
1996 |
| Painful legs and moving toes |
|
1996 |
| Inervação anômala da musculatura da mão pouco usual associada à Síndrome do Túnel de carpo bilateral |
|
1995 |
| Estudo clínico e eletrofisiológico em pacientes com a forma crônica da Doença de Chagas (DC) |
|
1995 |
| Electroneuromyography and somatosensory evoked potentials in tropical spastic paraparesis patients. |
|
1995 |
| Liver transplantation in FAP type I brazilian patients |
|
1995 |
| Eletroneuromyography and somatosensory evoked potentials in tropical spastic paraparesis patients |
|
1995 |
| Manifestações neuromusculares do hipotireoidismo primário |
|
1994 |
| Eletroneuromiografia em pacientes com hipoteoirdismo primário |
|
1993 |
| Eletroneuromiografia e potenciais evocados somatosensitivos em pacientes com mielopatia associado ao HTLV-I |
|
1993 |
| Myelopathy and HTLV-I. ENMG and SSEP study |
|
1993 |
| ENMG study in primary hypothyroidism |
|
1993 |
| Myelopathy and HTLV-I |
|
1993 |
| ENMG and SSEP study |
|
1993 |
| Mielopatoa assoaciada à infecção por HTLV-I |
|
1992 |
| Perfil das EMG realizados no laboratório de neurofisiologia clínica de HUCFF-UFRJ |
|
1992 |
| Neuro Behcet e Siringomieila |
|
1992 |
| Múltiplas compressões de nervos periféricos de causa indeterminada. Relato de caso |
|
1992 |
| Lesão do nervo mediano na fossa ante-cubital por punção arterial |
|
1992 |
| Estudo ENMG em pacientes com hipotireoidismo primário |
|
1992 |
| Cacinose associada a quadro neuromiopático. Relato de caso |
|
1992 |
| Estudo ENMG em paientes com hipotireoidismo primário |
|
1992 |
| FAP type I in black patients report on two brazilian families |
|
1992 |
| Neurohanseníase - Case report |
|
1992 |
| Familal amyloidotic polyneuropathy type I. A Case report |
|
1992 |
| Familial amyloidotic polyneuropathy type I - a case report |
|
1992 |
| Alterações eletroneuromiográficas associadas a infecção pelo HIV-I numa família brasileira |
|
1991 |
| Estudo eletroneuromiográfico em 10 pacientes com mielopatia associada ao HTLV-I |
|
1991 |
| Clinical Aspects in 191 patients from Rio de Janeiro - Brazil |
|
1991 |
| Neurological disorders associated with HTLV-I infection in a Brazilian family |
|
1991 |
| Myelopathy and HTLV-I electromyography study |
|
1991 |
| Familial amyloidotic polyneuropathy type I. Clinical aspects in 191 patients from Rio de Janeiro |
|
1991 |
| Familial amyloidotic polyneuropathy type I. Geographical distribution of 35 families |
|
1991 |
| Neurological disorders associated with HTLV-I infection in a Brazilian family |
|
1991 |
| Protocolo multidisciplinar de atendimento aos pacientes com FAP tipo I |
|
1990 |
| Relato de duas familias negras acometidas pelo PAF tipo I |
|
1990 |
| Distribuição geográfica em 35 famílias acometidas pelo PAF tipo I |
|
1990 |
| Análise retrospectiva de 35 pacientes timectomisados por miastenia gravis |
|
1990 |
| Análise dos aspectos clínicos de 50 pacientes acompanhados por miastenia gravis |
|
1990 |
| Análise dos aspectos clínicos em 161 pacientes com polineuropatia amiloidótica familiar tipo I - PAF tipo I |
|
1990 |
| Automutilação no curso da Doença de Dick |
|
1990 |
| Automutilação no curso da Doença de Pick |
|
1990 |
| Familial Amyloidotic Polyneuropathy of the portuguese type in RJ - Brazil. A study of the origin on geografic distribution in 22 families |
|
1989 |
| Familial amyloidotic polyneuropathy of the portuguese type in Rj-Brasil. Clinical features in 127 patientes from 22 familes |
|
1989 |
| Síndrome de Kearns-Sayer. Relato de caso com instalação rápida e ocumentação anatomopatológica |
|
1988 |
| Síndrome de Lowe. Relato de caso e revisão da literatura |
|
1988 |