Cargando…

Need leads to change: Transition to home infusion in Pompe disease in Brazil in the COVID-19 pandemic

Detalles Bibliográficos
Autores principales:	Horovitz, Dafne Dain Gandelman, Barth, Anneliese Lopes, Alves, Welton Correia, Llerena, Juan Clinton
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Academic Press 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7849464/ http://dx.doi.org/10.1016/j.ymgme.2020.12.107

Ejemplares similares

Transition to home infusion in Pompe disease in Brazil: Safety of the regimen during the COVID-19 pandemic and thereafter
por: Horovitz, Dafne D.G., et al.
Publicado: (2023)

Respiratory manifestations in late-onset Pompe disease: a case series conducted in Brazil
por: Sixel, Bruna de Souza, et al.
Publicado: (2017)

Otolaryngologists and the Early Diagnosis of Mucopolysaccharidoses: A Cross-Sectional Study
por: Torres, Danielle de Araujo, et al.
Publicado: (2019)

Laryngeal, Tracheal, and Bronchial Disease in the Mucopolysaccharidoses: Endoscopic Study
por: Pires de Mello, Paulo, et al.
Publicado: (2020)

Genetics and genomics in Brazil: a promising future
por: Passos-Bueno, Maria Rita, et al.
Publicado: (2014)

Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes
por: Politei, Juan, et al.
Publicado: (2021)

Alternative laronidase dose regimen for patients with mucopolysaccharidosis I: a multinational, retrospective, chart review case series
por: Horovitz, Dafne Dain Gandelman, et al.
Publicado: (2016)

Mucopolysaccharidosis VII in Brazil: natural history and clinical findings
por: Giugliani, Roberto, et al.
Publicado: (2021)

Home-Based Infusion of Alglucosidase Alfa Can Safely be Implemented in Adults with Late-Onset Pompe Disease: Lessons Learned from 18,380 Infusions
por: Ditters, Imke A. M., et al.
Publicado: (2023)

A Systematic Review and Meta-Analysis of Enzyme Replacement Therapy in Late-Onset Pompe Disease
por: Dornelles, Alícia Dorneles, et al.
Publicado: (2021)

Mucopolysaccharidosis Type I
por: Kubaski, Francyne, et al.
Publicado: (2020)

Neurological Phenotypes of IRF2BPL Gene Variants: A Report of Four Novel Variants
por: Horovitz, Dafne Dain Gandelman, et al.
Publicado: (2023)

GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry
por: Reuser, Arnold J. J., et al.
Publicado: (2019)

Walking delay as leading symptom in late-onset Pompe disease
por: Gökce, S, et al.
Publicado: (2013)

Pompes turbomoleculaires
por: Versolatto, B
Publicado: (1982)

Characteristics of Pompe disease in China: a report from the Pompe registry
por: Zhao, Yuying, et al.
Publicado: (2019)

The humanistic burden of Pompe disease: are there still unmet needs? A systematic review
por: Schoser, Benedikt, et al.
Publicado: (2017)

The Timely Needs for Infantile Onset Pompe Disease Newborn Screening—Practice in Taiwan
por: Chiang, Shu-Chuan, et al.
Publicado: (2020)

Raccords de pompes
por: Riboni, P
Publicado: (1976)

Pregnancy in Pompe disease
por: Plöckinger, Ursula
Publicado: (2013)

Familial Pompe Disease
por: Tecellioglu, Mehmet, et al.
Publicado: (2015)

The Pompe Registry: tracking Pompe disease symptoms in a broad patient population
por: Byrne, B, et al.
Publicado: (2008)

Early hematopoietic stem cell transplantation in a patient with severe mucopolysaccharidosis II: A 7 years follow-up
por: Barth, Anneliese L., et al.
Publicado: (2017)

Home-based enzyme replacement therapy in children and adults with Pompe disease; a prospective study
por: Ditters, Imke A. M., et al.
Publicado: (2023)

Telemonitoring of home infusion technology
por: Jutte, Sonja
Publicado: (2010)

Genetic counseling in Pompe disease
por: Taglia, Antonella, et al.
Publicado: (2011)

Hearing in adults with Pompe disease
por: van der Beek, Nadine A. M. E., et al.
Publicado: (2011)

Les pompes à chaleur
por: Veith, Heinz, et al.
Publicado: (1974)

Les pompes à chaleur
por: Dumon, Roger, et al.
Publicado: (1980)

Pompe 3500 1/s MSC
por: Versolatto, B
Publicado: (1978)

Pompe disease: the role of MRI
por: Fernández, C Pérez, et al.
Publicado: (2013)

Clinical features of Pompe disease
por: MANGANELLI, FIORE, et al.
Publicado: (2013)

Newborn Screening for Pompe Disease
por: Sawada, Takaaki, et al.
Publicado: (2020)

Enzyme replacement therapy for Mucopolysaccharidosis Type I among patients followed within the MPS Brazil Network
por: Dornelles, Alícia Dorneles, et al.
Publicado: (2014)

Pomp and circumstance : military march No. 1 in D Op. 39 No. 1
por: Elgar, Edward, 1857-1934
Publicado: (1958)

Effect of enzyme replacement therapy (ERT) added to Home Mechanical Ventilation (HMV) in Adult Pompe disease
por: Sayeed, Nadia, et al.
Publicado: (2015)

Positive Impact of Home ERT for Mucopolysaccharidoses and Pompe Disease: The Lesson Learnt from the COVID-19 Pandemic
por: Fiumara, Agata, et al.
Publicado: (2023)

Amorcer la pompe à réflexions
Publicado: (1998)

Grande pompe pour le LEP
Publicado: (1989)

Pompe disease diagnosis and management guideline
por: Kishnani, Priya S., et al.
Publicado: (2006)

Cannot write session to /tmp/vufind_sessions/sess_n0a5g645etunrkk2c7fainfjc3