Cargando…

A narrative review and expert recommendations on the assessment of the clinical manifestations, follow-up, and management of post-OLT patients with ATTRv amyloidosis

Orthotopic liver transplantation (OLT) was the first treatment able to modify the natural course of hereditary transthyretin (ATTRv) amyloidosis, which is a rare and fatal disorder caused by the accumulation of misfolded transthyretin (TTR) variants in different organs and tissues and which leads to...

Descripción completa

Detalles Bibliográficos
Autores principales:	Casasnovas, Carlos, Lladó, Laura, Borrachero, Cristina, Pérez-Santamaría, Patricia Valentina, Muñoz-Beamud, Francisco, Losada-López, Inés Asunción, Baliellas-Comellas, Maria Carme, González-Moreno, Juan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467168/ https://www.ncbi.nlm.nih.gov/pubmed/37655225 http://dx.doi.org/10.1177/17562864231191590

Ejemplares similares

The Olt.
Publicado: (1964)

Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects
por: Russo, Massimo, et al.
Publicado: (2020)

Current Evidence Supporting the Role of Immune Response in ATTRv Amyloidosis
por: Plantone, Domenico, et al.
Publicado: (2023)

The patient journey toward a diagnosis of hereditary transthyretin (ATTRv) amyloidosis
por: Vera-Llonch, Montserrat, et al.
Publicado: (2021)

Urinary Transthyretin as a Biomarker in ATTRv Val50Met Amyloidosis
por: Matsushita, Hiroaki, et al.
Publicado: (2022)

Drug and Gene Therapy for Treating Variant Transthyretin Amyloidosis (ATTRv) Neuropathy
por: Dardiotis, Efthimios, et al.
Publicado: (2023)

Variant Transthyretin Amyloidosis (ATTRv) in Hungary: First Data on Epidemiology and Clinical Features
por: Pozsonyi, Zoltán, et al.
Publicado: (2021)

Ocular findings in patients with acquired ATTRv amyloidosis following domino liver transplantation
por: Kitahara, Junya, et al.
Publicado: (2023)

Disease risk estimates in V30M variant transthyretin amyloidosis (A-ATTRv) from Mallorca
por: Cisneros-Barroso, E., et al.
Publicado: (2023)

Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy
por: Magliano, Lorenza, et al.
Publicado: (2021)

Preliminary assessment of neuropathy progression in patients with hereditary ATTR amyloidosis after orthotopic liver transplantation (OLT)
por: Adams, David, et al.
Publicado: (2015)

The Clinical and Economic Burden of Newly Diagnosed Hereditary Transthyretin (ATTRv) Amyloidosis: A Retrospective Analysis of Claims Data
por: Reddy, Sheila R., et al.
Publicado: (2020)

Use of Drugs for ATTRv Amyloidosis in the Real World: How Therapy Is Changing Survival in a Non-Endemic Area
por: Russo, Massimo, et al.
Publicado: (2021)

Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy
por: Di Stefano, Vincenzo, et al.
Publicado: (2023)

Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy
por: Nedkova-Hristova, Velina, et al.
Publicado: (2022)

Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen
por: Coelho, Teresa, et al.
Publicado: (2022)

Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy
por: Adams, David, et al.
Publicado: (2020)

A Descriptive Analysis of ATTR Amyloidosis in Spain from the Transthyretin Amyloidosis Outcomes Survey
por: González-Moreno, Juan, et al.
Publicado: (2021)

Prevalence estimation of ATTRv in China based on genetic databases
por: Yongsheng, Zheng, et al.
Publicado: (2023)

Patisiran Enhances Muscle Mass after Nine Months of Treatment in ATTRv Amyloidosis: A Study with Bioelectrical Impedance Analysis and Handgrip Strength
por: Di Stefano, Vincenzo, et al.
Publicado: (2022)

Trajectories of Kidney Function in Patients with ATTRv Treated with Gene Silencers
por: Luigetti, Marco, et al.
Publicado: (2022)

Hereditary Transthyretin Amyloidosis with Polyneuropathy: Monitoring and Management
por: Vélez-Santamaría, Valentina, et al.
Publicado: (2022)

Case Report: Hereditary transthyretin (ATTRv) amyloidosis: The p.G103R mutation of the transthyretin gene in a Han Chinese family is associated with vitreous hemorrhage
por: Shen, Junhui, et al.
Publicado: (2022)

Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner
por: Gertz, Morie, et al.
Publicado: (2020)

The Etiology, Incidence, and Impact of Preservation Fluid Contamination during Liver Transplantation
por: Oriol, Isabel, et al.
Publicado: (2016)

Deterioration after Liver Transplantation and Transthyretin Stabilizer Administration in a Patient with ATTRv Amyloidosis with a Leu58Arg (p.Leu78Arg) TTR Variant
por: Hikishima, Sadao, et al.
Publicado: (2022)

Predictors of renal recovery in patients with pre-orthotopic liver transplant (OLT) renal dysfunction
por: Iglesias, Jose, et al.
Publicado: (2013)

Agrometeorological drought in the Romanian plain within the sector delimited by the valleys of the Olt and Buzău Rivers
por: Murărescu, Ovidiu, et al.
Publicado: (2014)

1317. Pharmacokinetics (PK) of Ampicillin-Sulbactam (SAM) during Orthotopic Liver Transplantation (OLT)
por: Lasko, Maxwell J, et al.
Publicado: (2020)

Accumulation and ecotoxicological risk assessment of heavy metals in surface sediments of the Olt River, Romania
por: Iordache, Andreea Maria, et al.
Publicado: (2022)

Dexamethasone and OLT1177 Cooperate in the Reduction of Melanoma Growth by Inhibiting STAT3 Functions
por: Dinarello, Alberto, et al.
Publicado: (2023)

Patisiran treatment in patients with hereditary transthyretin‐mediated amyloidosis with polyneuropathy after liver transplantation
por: Schmidt, Hartmut H., et al.
Publicado: (2022)

A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report
por: Thimm, Andreas, et al.
Publicado: (2022)

Successful Pregnancies in Two Orthotopic Liver Transplant (OLT) Recipients in Iran; Two Case Reports
por: Tayebi, Zahra, et al.
Publicado: (2009)

ATTRv in Lazio-Italy: A High-Prevalence Region in a Non-Endemic Country
por: Luigetti, Marco, et al.
Publicado: (2021)

Cutaneous amyloid is a biomarker in early ATTRv neuropathy and progresses across disease stages
por: Freeman, Roy, et al.
Publicado: (2022)

Ocular Morpho-Functional Evaluation in ATTRv Pre-Symptomatic Carriers: A Case Series
por: Maceroni, Martina, et al.
Publicado: (2023)

Study of the parent-of-origin effect in monogenic diseases with variable age of onset. Application on ATTRv
por: Alarcon, Flora, et al.
Publicado: (2023)

Efficacy and Safety of Delayed Prolonged-Release Tacrolimus Initiation in De Novo Hepatitis C Virus-Negative Orthotopic Liver Transplant Recipients: A Single-Center, Single-Arm, Prospective Study
por: Lladó, Laura, et al.
Publicado: (2019)

Facial Paralysis as Initial Manifestation of Light-chain Amyloidosis
por: Martins, André M, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_h1ooh7jhn5kdkm7sjufk986lpf