Literature DB >> 12485190

Genetic landmarks through philately: Luís Morquio 1867-1935.

A E Chudley1, C Chakravorty.   

Abstract

Morquio syndrome, also known as Mucopolysaccharidosis Type IV, is well known to pediatricians and geneticists, although it is rare. Many do not know much about the physician who first described this lysosomal disorder. In this brief review, the person and the disease are described, along with philatelic illustrations that have been issued to honor this famous Latin American medical hero.

Entities:  

Mesh:

Year:  2002        PMID: 12485190     DOI: 10.1034/j.1399-0004.2002.620603.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Clinical outcomes in elderly patients with Morquio a syndrome receiving enzyme replacement therapy - experience in a Colombian center.

Authors:  Andrés Felipe Erazo-Narváez; Juan Manuel Muñoz-Vidal; Guillermo Hernando Rodríguez-Vélez; María Amparo Acosta-Aragón
Journal:  Mol Genet Metab Rep       Date:  2020-12-02

2.  Elosulfase alfa for mucopolysaccharidosis type IVA: Real-world experience in 7 patients from the Spanish Morquio-A early access program.

Authors:  Guillem Pintos-Morell; Javier Blasco-Alonso; María L Couce; Luís G Gutiérrez-Solana; Encarna Guillén-Navarro; Mar O'Callaghan; Mireia Del Toro
Journal:  Mol Genet Metab Rep       Date:  2018-04-05
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.