Search details
1.
Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial.
Mol Genet Metab
; 127(1): 86-94, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30987917
2.
Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?
Pediatr Nephrol
; 33(11): 2095-2101, 2018 11.
Article
in English
| MEDLINE | ID: mdl-29987457
3.
[Guidelines for diagnosis, monitoring and treatment of Fabry disease]. / Guía para el diagnóstico, seguimiento y tratamiento de la enfermedad de Fabry.
Medicina (B Aires)
; 73(5): 482-94, 2013.
Article
in Spanish
| MEDLINE | ID: mdl-24152410
4.
Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes.
JIMD Rep
; 58(1): 104-113, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-33728253
5.
A few challenges in mucopolysaccharidosis type I. / Algunos desafíos en mucopolisacaridosis tipo I.
Arch Argent Pediatr
; 119(3): e193-e201, 2021 06.
Article
in English, Spanish
| MEDLINE | ID: mdl-34033424
6.
New recommendations for the care of patients with mucopolysaccharidosis type I. / Nuevas recomendaciones para el cuidado de los pacientes con mucopolisacaridosis tipo I.
Arch Argent Pediatr
; 119(2): e121-e128, 2021 04.
Article
in English, Spanish
| MEDLINE | ID: mdl-33749201
7.
Enzyme replacement therapy interruption in patients with Mucopolysaccharidoses: Recommendations for distinct scenarios in Latin America.
Mol Genet Metab Rep
; 23: 100572, 2020 Jun.
Article
in English
| MEDLINE | ID: mdl-32140416
8.
Infantile-onset Pompe disease: Diagnosis and management. / Enfermedad de Pompe infantil: Diagnóstico y tratamiento.
Arch Argent Pediatr
; 117(4): 271-278, 2019 08 01.
Article
in English, Spanish
| MEDLINE | ID: mdl-31339275
9.
Consenso de expertos sobre recomendaciones basadas en evidencia para el diagnóstico, tratamiento y seguimiento de enfermedad de Fabry en pediatría / Expert Consensus on Evidence-Based Recommendations for the Diagnosis, Treatment, and Follow-Up of Fabry Disease in Pediatric Patients / Consenso de especialistas colombianos sobre recomendações baseadas em evidências para o diagnóstico, tratamento e acompanhamento da doença de Fabry em pediatria
Rev. cienc. salud (Bogotá)
; 21(3): [1-24], 20230901.
Article
in Spanish
| LILACS | ID: biblio-1512799
10.
Liver disease and dyslipidemia as a manifestation of lysosomal acid lipase deficiency (LAL-D). Clinical and diagnostic aspects, and a new treatment. An update. / Enfermedad hepática y dislipemia como manifestación de deficiencia de lipasa acida lisosomal (LAL-D). Aspectos clínicos, diagnósticos y nuevo tratamiento. Actualización.
Arch Argent Pediatr
; 115(3): 287-293, 2017 06 01.
Article
in English, Spanish
| MEDLINE | ID: mdl-28504497
11.
Nuevas recomendaciones para el cuidado de los pacientes con mucopolisacaridosis tipo I / New recommendations for the care of patients with mucopolysaccharidosis type I
Arch. argent. pediatr
; 119(2): e121-e128, abril 2021. tab
Article
in English, Spanish
| BINACIS, LILACS | ID: biblio-1151878
12.
Algunos desafíos en mucopolisacaridosis tipo I / A few challenges in mucopolysaccharidosis type I
Arch. argent. pediatr
; 119(3): e193-e201, Junio 2021. tab, ilus
Article
in English, Spanish
| LILACS, BINACIS | ID: biblio-1223310
13.
[Morquio disease (Mucopolysaccharidosis type IV-A): clinical aspects, diagnosis and new treatment with enzyme replacement therapy]. / Enfermedad de Morquio (mucopolisacaridosis IV-A): aspectos clínicos, diagnósticos y nuevo tratamiento con terapia de reemplazo enzimático.
Arch Argent Pediatr
; 113(4): 359-64, 2015 Aug.
Article
in Spanish
| MEDLINE | ID: mdl-26172013
14.
Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial.
PLoS One
; 10(5): e0124987, 2015.
Article
in English
| MEDLINE | ID: mdl-25955246
15.
Enfermedad de Pompe infantil: Diagnóstico y tratamiento / Infantile-onset Pompe disease: Diagnosis and management
Arch. argent. pediatr
; 117(4): 271-278, ago. 2019. tab
Article
in English, Spanish
| LILACS, BINACIS | ID: biblio-1054936
16.
Recommendations for Assessment and Management of Health-Related Quality of Life in Patients with Mucopolysaccharidoses in Latin America
J. inborn errors metab. screen
; 7: e20190004, 2019. tab
Article
in English
|
LILACS-Express
| ID: biblio-1090974
17.
[Lymphatic malformations: percutaneus treatment with bleomycin]. / Malformaciones linfáticas: tratamiento percutáneo con bleomicina.
Arch Argent Pediatr
; 109(5): 417-22, 2011 10.
Article
in Spanish
| MEDLINE | ID: mdl-22042072
18.
Guía para el diagnóstico, seguimiento y tratamiento de la enfermedad de Fabry / Guidelines for diagnosis, monitoring and treatment of Fabry disease
Medicina (B.Aires)
; 73(5): 482-494, oct. 2013. ilus, tab
Article
in Spanish
| LILACS | ID: lil-708540
19.
Malformaciones linfáticas: tratamiento percutáneo con bleomicina / Lymphatic malformations: percutaneus treatment with bleomycin
Arch. argent. pediatr
; 109(5): 417-422, sept.-oct. 2011. ilus, tab
Article
in Spanish
| LILACS | ID: lil-633201
20.
Hemangiomas / Hemangiomas
Rev. Hosp. Niños B.Aires
; 52(238): 472-489, nov. 2010. ilus, graf
Article
in Spanish
| LILACS | ID: lil-667068