Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mucopolisacaridosis VI"'
Autor:
Bárbara Bernardo Figueirêdo, Paulo Magalhães, Breno Azevedo, Maria Lucila Cavalcanti, Maria Emília Melo, Cinthia Vasconcelos
Publikováno v:
Fisioterapia e Pesquisa, Volume: 28, Issue: 1, Pages: 117-123, Published: 18 JUN 2021
Fisioterapia e Pesquisa, Vol 28, Iss 1, Pp 117-123 (2021)
Fisioterapia e Pesquisa v.28 n.1 2021
Fisioterapia e Pesquisa
Universidade de São Paulo (USP)
instacron:USP
Fisioterapia e Pesquisa, Vol 28, Iss 1, Pp 117-123 (2021)
Fisioterapia e Pesquisa v.28 n.1 2021
Fisioterapia e Pesquisa
Universidade de São Paulo (USP)
instacron:USP
To evaluate knee and ankle disorders during functional gait assessment in individuals with Mucopolysaccharidosis type VI (MPS VI). 19 subjects were included in this cross-sectional study and allocated in three groups according to age: Children Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64f9036ddf643c836c082948a4dd1088
https://doi.org/10.1590/1809-2950/21003228012021
https://doi.org/10.1590/1809-2950/21003228012021
Publikováno v:
Research, Society and Development; Vol. 10 No. 3; e1810313036
Research, Society and Development; Vol. 10 Núm. 3; e1810313036
Research, Society and Development; v. 10 n. 3; e1810313036
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 10 Núm. 3; e1810313036
Research, Society and Development; v. 10 n. 3; e1810313036
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Introduction: Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome is a rare, hereditary metabolic disease, known as a lysosomal deposit disease where patients have progressive deformities. There is a need to understand how the center of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::d4cbb8793c72d41d36ccbc980882dc9d
https://rsdjournal.org/index.php/rsd/article/view/13036
https://rsdjournal.org/index.php/rsd/article/view/13036
Autor:
Gómez Ruíz, Alba Milena
Introducción: La mucopolisacaridosis (MPS) se define como una familia de 7 enfermedades por almacenamiento lisosómico que consisten en errores innatos del metabolismo, secundarios a defectos enzimáticos que producen un acúmulo lisosomal de divers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1326::84c15270e839cb66274603190983b891
http://bdigital.unal.edu.co/61081/
http://bdigital.unal.edu.co/61081/
Publikováno v:
Colombia Médica : CM
Repositorio Digital Univalle
Universidad del Valle
instacron:Universidad del Valle
Repositorio Digital Univalle
Universidad del Valle
instacron:Universidad del Valle
Mucopolysaccharidosis type VI or Maroteaux Lamy syndrome is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B, the clinical features include short stature, hepatosplenomegaly, dysostosis multiplex, stiff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::777a7a6c554a688caa60809e07d59168
https://doi.org/10.25100/cm.v45i2.1441
https://doi.org/10.25100/cm.v45i2.1441
Publikováno v:
Colombia Médica, Volume: 45, Issue: 2, Pages: 85-88, Published: APR 2014
La mucopolisacaridosis tipo VI o síndrome de Maroteaux Lamy es una enfermedad de depósito lisosomal autosómica recesiva que resulta de una deficiencia de la enzima arilsulfatasa B, las características clínicas incluyen talla baja, hepatoesplenom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______618::6af5aa1849360535e86a0e9b531d7f5b
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S1657-95342014000200008&lng=en&tlng=en
http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S1657-95342014000200008&lng=en&tlng=en
Publikováno v:
Repositorio ICESI
Universidad ICESI
instacron:Universidad ICESI
Universidad ICESI
instacron:Universidad ICESI
Mucopolysaccharidosis type VI or Maroteaux Lamy syndrome is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B, the clinical features include short stature, hepatosplenomegaly, dysostosis multiplex, stiff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c2cdc1360fdfeadcd6a467741717b5b8
https://hdl.handle.net/10906/81901
https://hdl.handle.net/10906/81901
Autor:
Politei, Juan a, ⁎, Schenone, Andrea B. a, Blanco, Mariana a, Calzone, Cesar b, Negri, Pablo b, Gardella, Javier b, Szlago, Marina a
Publikováno v:
In Neurología Argentina January-March 2014 6(1):40-43