Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Andrés LOZANO-ARANGO"'
1
Akademický článek
Sobrecarga del cuidador de pacientes con atrofia muscular espinal
Autor: Maripaz Martínez-Jalilie, Andrés Lozano-Arango, Bernardita Suárez, Macarena Born, Javiera Jofré, Marie Diemer, Magdalena Castro, Claudia Castiglioni
Publikováno v: Revista Médica Clínica Las Condes, Vol 31, Iss 3, Pp 358-366 (2020)
Resumen: Introducción: La sobrecarga del cuidador ha sido ampliamente descrita en gerontología, pocos estudios la abordan en niños con enfermedades neuromusculares. El cuidado de pacientes con atrofia muscular espinal (AME), requiere atención con
Externí odkaz: https://doaj.org/article/975794b3b9474dbe9f93938f44dd1ca1
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2
Akademický článek
Atrofias musculares espinales no asociadas a SMN1
Autor: Claudia Castiglioni, Andrés Lozano-Arango
Publikováno v: Revista Médica Clínica Las Condes, Vol 29, Iss 6, Pp 643-653 (2018)
RESUMEN: Las atrofias musculares espinales no-5q son un conjunto de entidades hereditarias, clínica y genéticamente heterogéneas secundarias a compromiso de las células del asta anterior de la médula. No están asociadas a deleción del gen de s
Externí odkaz: https://doaj.org/article/b9764dbcd67648868ae8c4b7973bf1bb
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3
Akademický článek
Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
Autor: Karin ALVAREZ, Bernardita SUAREZ, María Angélica PALOMINO, Cecilia HERVIAS, Giancarlo CALCAGNO, Maripaz MARTÍNEZ-JALILIE, Andrés LOZANO-ARANGO, Susana LILLO, Mariana HARO, Fanny CORTÉS, Samuel PANTOJA, Andrés CHAHIN, Paulina ORELLANA, Jorge A BEVILACQUA, Enrico BERTINI, Claudia CASTIGLIONI
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 77, Iss 7, Pp 470-477
ABSTRACT Spinal muscular atrophy (SMA) has gained much attention in the last few years because of the approval of the first intrathecal treatment for this neurodegenerative disease. Latin America needs to develop the demographics of SMA, timely acces
Externí odkaz: https://doaj.org/article/c1d9e5aeaf8648dd84b111b702c69fe6
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4
Spontaneous symptomatic improvement in a pediatric patient with anti-3-hydroxy-3-methylglutraryl-coenzyme A reductase myopathy
Autor: Jorge A. Bevilacqua, Giancarlo Calcagno, Jorge Díaz, Ximena Ortega, Andrés Lozano-Arango, Claudia Castiglioni, Bernardita Suárez, Javiera Jofré
Publikováno v: Neuromuscular Disorders. 30:503-509
Immune-mediated necrotizing myopathy with antibodies against 3-hydroxy-3-methylglutaryl-coenzyme A reductase is a subgroup of idiopathic inflammatory myopathies mainly described in adults and requiring long term immunomodulatory therapy for remission
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::124bdb39b92aded1399aa7cdc910149c
https://doi.org/10.1016/j.nmd.2020.03.008
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5
Severe brain involvement in 5q spinal muscular atrophy type 0
Autor: Rodrigo de Holanda Mendonça, Antônio José da Rocha, Ivon Cuscó, Eduardo F. Tizzano, Leslie Domenici Kulikowski, Claudia Castiglioni, André Macedo Serafim da Silva, Ida Paramonov, Andrés Lozano-Arango, Astry B. Diaz, Edmar Zanoteli, Umbertina Conti Reed
Publikováno v: Annals of neurologyReferences. 86(3)
Spinal muscular atrophy (SMA) type 0 is the most severe form of SMA, associated with the SMN1 gene and manifesting at birth. Most patients die in the first weeks of life. In this work, we present 3 patients with SMA type 0 who survived >1 year and pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d4fa97055c8ee5744030e3d0a5e89cd
https://pubmed.ncbi.nlm.nih.gov/31502291
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6
Observations from a nationwide vigilance program in medical care for spinal muscular atrophy patients in Chile
Autor: Maripaz Martínez-Jalilie, Jorge A. Bevilacqua, Cecilia Hervias, Susana Lillo, Paulina Orellana, María Angélica Palomino, Giancarlo Calcagno, Claudia Castiglioni, Andrés Lozano-Arango, Bernardita Suárez, Karin Alvarez, Enrico Bertini, Fanny Cortés, Mariana Haro, Andrés Chahin, Samuel Pantoja
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 77, Iss 7, Pp 470-477
Arquivos de Neuro-Psiquiatria v.77 n.7 2019
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 77, Issue: 7, Pages: 470-477, Published: 29 JUL 2019
Spinal muscular atrophy (SMA) has gained much attention in the last few years because of the approval of the first intrathecal treatment for this neurodegenerative disease. Latin America needs to develop the demographics of SMA, timely access to diag
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e43d7c6d40af8b389ab56226df9bcf64
https://pubmed.ncbi.nlm.nih.gov/31365638
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7
Miopatías relacionadas a colágeno VI. Cuando sospecharlas, cómo identificarlas. Aporte de la resonancia magnética muscular
Autor: Cecilia Hervias, Giancarlo Calcagno, Andrés Lozano-Arango, Ximena Ortega, Diego Araneda, Claudia Castiglioni, Fanny Cortés, Bernardita Suárez
Publikováno v: Revista chilena de pediatría v.89 n.3 2018
SciELO Chile
CONICYT Chile
instacron:CONICYT
Resumen: Las miopatías secundarias a mutaciones en el colágeno VI (M-COLVI) son las más frecuentes en el hemisferio norte, afectando población adulta y pediátrica. No existen datos de su prevalencia en Latinoamérica. Se caracterizan por present
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d7081fcef4e288eef46092dd66bed4
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062018000300399
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8
[Collagen VI related myopathies. When to suspect, how to identify. The contribution of muscle magnetic resonance]
Autor: Bernardita, Suárez, Andrés, Lozano-Arango, Diego, Araneda, Fanny, Cortés, Cecilia, Hervias, Giancarlo, Calcagno, Ximena, Ortega, Claudia, Castiglioni
Publikováno v: Revista chilena de pediatria. 89(3)
Myopathies secondary to collagen VI mutations (COLVI-M) are the most frequent in the northern hemisphere, affecting the adult and pediatric population. There are no data on its prevalence in Latin America. They are characterized by a great clinical v
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::668b80d0a8d5e07240282579a7a2aedf
https://pubmed.ncbi.nlm.nih.gov/29999148
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