Detalhe da pesquisa
1.
[The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. / A késoi kezdetu Pompe-kórban szenvedok enzimpótló kezelésének hosszú távú követése.
Ideggyogy Sz
; 73(05-06): 151-159, 2020 05 30.
Artigo
em Húngaro
| MEDLINE | ID: mdl-32579304
2.
Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries.
Orphanet J Rare Dis
; 17(1): 190, 2022 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35538504
3.
The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers.
Orphanet J Rare Dis
; 17(1): 136, 2022 03 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35331284
4.
[Clinical manifestations, course and outcome of enzyme replacement therapy in Hungarian patients with Pompe's disease]. / Pompe-kór fenotípusvariációi, kórlefolyása és az enzimpótló kezelés eredményei: hazai tapasztalatok.
Orv Hetil
; 152(39): 1569-75, 2011 Sep 25.
Artigo
em Húngaro
| MEDLINE | ID: mdl-21920843
5.
Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease.
Life (Basel)
; 11(6)2021 May 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34072668
6.
[Cartilage-hair hypoplasia]. / Porc-haj hypoplasia.
Orv Hetil
; 149(5): 209-17, 2008 Feb 03.
Artigo
em Húngaro
| MEDLINE | ID: mdl-18218588
7.
Applicability results of a nonlinear model-based robust blood glucose control algorithm.
J Diabetes Sci Technol
; 7(3): 708-16, 2013 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23759404
8.
Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.
Orphanet J Rare Dis
; 6: 72, 2011 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22059643
9.
Differences in the laboratory parameters of obese and healthy Hungarian children and their use in automatic classification.
Annu Int Conf IEEE Eng Med Biol Soc
; 2010: 3883-6, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21097074
10.
No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome.
Am J Med Genet A
; 121A(1): 82-4, 2003 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12900909