Detalhe da pesquisa
1.
Broadening the phenotype of the TWNK gene associated Perrault syndrome.
BMC Med Genet
; 20(1): 198, 2019 12 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31852434
2.
Genetic, clinical and imaging implications of a noncompaction phenotype population with preserved ejection fraction.
Front Cardiovasc Med
; 11: 1337378, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38380180
3.
Does dermatitis herpetiformis result in bone loss as coeliac disease does? A cross sectional study.
Rev Esp Enferm Dig
; 105(4): 187-93, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23859446
4.
[Prevalence of gastric polypoid lesions at an endoscopic facility]. / A gyomor polypoid képleteinek gyakorisága egy endoszkópos centrumban.
Orv Hetil
; 154(20): 770-4, 2013 May 19.
Artigo
em Húngaro
| MEDLINE | ID: mdl-23666023
5.
[Vitamin D level in Hungarian patients with inflammatory bowel diseases]. / D-vitamin-szint mérése hazai gyulladásos bélbetegekben.
Orv Hetil
; 154(46): 1821-8, 2013 Nov 17.
Artigo
em Húngaro
| MEDLINE | ID: mdl-24212042
6.
[Current therapeutic and familial implications of the genetic background of prostate cancer]. / A prosztatarák genetikai hátterének aktuális terápiás és familiáris vonatkozásai.
Magy Onkol
; 67(2): 154-160, 2023 Jun 13.
Artigo
em Húngaro
| MEDLINE | ID: mdl-37314077
7.
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries.
Neurol Genet
; 7(1): e536, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33376799
8.
Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
Orphanet J Rare Dis
; 15(1): 290, 2020 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33059708
9.
Implementation of personalized medicine in Central-Eastern Europe: pitfalls and potentials based on citizen's attitude.
EPMA J
; 9(1): 103-112, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29515690