Detalhe da pesquisa
1.
Fluid management in children with volume depletion.
Pediatr Nephrol
; 39(2): 423-434, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37452205
2.
Sustainability of biologic treatment in paediatric patients with Crohn's disease: population-based registry analysis.
Pediatr Res
; 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38012309
3.
Practical recommendations for the management of children after kidney and liver transplantation.
Cas Lek Cesk
; 161(7-8): 296-302, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36868838
4.
The role of endoscopy in non-oncologic gastrointestinal disorders in pediatric patients.
Cesk Patol
; 58(2): 100-106, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35882544
5.
The Accuracy of a Home-performed Faecal Calprotectin Test in Paediatric Patients With Inflammatory Bowel Disease.
J Pediatr Gastroenterol Nutr
; 69(1): 75-81, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30908389
6.
Correction to: Fecal calprotectin is not a clinically useful marker for the prediction of the early nonresponse to exclusive enteral nutrition in pediatric patients with Crohn disease.
Eur J Pediatr
; 177(11): 1695, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30280223
7.
Fecal calprotectin is not a clinically useful marker for the prediction of the early nonresponse to exclusive enteral nutrition in pediatric patients with Crohn disease.
Eur J Pediatr
; 177(11): 1685-1693, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30128744
8.
Current views on the diagnosis and management of hypokalaemia in children.
Acta Paediatr
; 105(7): 762-72, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26972906
9.
Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations.
Pediatr Diabetes
; 12(3 Pt 2): 266-9, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21214702
10.
Is It Useful to Monitor Thiopurine Metabolites in Pediatric Patients with Crohn's Disease on Combination Therapy? A Multicenter Prospective Observational Study.
Paediatr Drugs
; 23(2): 183-194, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33709340
11.
Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation in NEUROD1.
Pediatr Diabetes
; 9(4 Pt 2): 367-72, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18331410
12.
Pilot newborn screening project for cystic fibrosis in the Czech Republic: defining role of the delay in its symptomatic diagnosis and influence of ultrasound-based prenatal diagnosis on the incidence of the disease.
J Cyst Fibros
; 8(3): 224-7, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19208501