Detalhe da pesquisa
1.
Novel de novo large deletion in cystic fibrosis transmembrane conductance regulator gene results in a severe cystic fibrosis phenotype.
J Pediatr
; 159(2): 343-6.e1, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21663921
2.
Analysis of CFTR, SPINK1, PRSS1 and AAT mutations in children with acute or chronic pancreatitis.
J Pediatr Gastroenterol Nutr
; 43(3): 299-306, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16954950
3.
Is there evidence for correct diagnosis in cystic fibrosis registries?
J Cyst Fibros
; 13(3): 275-80, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24274930
4.
[Genetic risk markers of low bone mineral density in cystic fibrosis children]. / Genetyczne markery ryzyka wystapienia obnizonej gestosci mineralnej tkanki kostnej u dzieci z mukowiscydoza.
Med Wieku Rozwoj
; 14(4): 334-43, 2010.
Artigo
em Polonês
| MEDLINE | ID: mdl-21462477
5.
[On the way to gene therapy in cystic fibrosis]. / Na drodze do terapii genowej mukowiscydozy.
Med Wieku Rozwoj
; 10(1 Pt 2): 247-74, 2006.
Artigo
em Polonês
| MEDLINE | ID: mdl-17028392
6.
[Genetic markers in the pathogenesis of osteopenia and osteoporosis in cystic fibrosis]. / Genetyczne markery osteopenii i osteoporozy w mukowiscydozie.
Med Wieku Rozwoj
; 10(1 Pt 2): 275-87, 2006.
Artigo
em Polonês
| MEDLINE | ID: mdl-17028393