Detalhe da pesquisa
1.
Expanding the phenotype of DNAJC30-associated Leigh syndrome.
Clin Genet
; 102(5): 438-443, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35861300
2.
Coincidence of PTPN22 c.1858CC and FCRL3 -169CC genotypes as a biomarker of preserved residual ß-cell function in children with type 1 diabetes.
Pediatr Diabetes
; 18(8): 696-705, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27615679
3.
The PURPLE N study: objective and perceived nutritional status in children and adolescents with cerebral palsy.
Disabil Rehabil
; 44(22): 6668-6675, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34473588
4.
Difficulties or mistakes in diagnosing type 1 diabetes in children?--demographic factors influencing delayed diagnosis.
Pediatr Diabetes
; 10(8): 542-9, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19496971
5.
[Pathological daytime sleepiness in an 11-year old girl receiving growth hormone treatment previously cured from craniopharyngioma]. / Napady patologicznej sennosci dziennej u 11-letniej dziewczynki leczonej ludzkim rekombinowanym hormonem wzrostu po zakonczonym leczeniu z powodu czaszkogardlaka.
Pediatr Endocrinol Diabetes Metab
; 18(4): 158-62, 2012.
Artigo
em Polonês
| MEDLINE | ID: mdl-23739621
6.
Comparing the effect of hydroxyethyl starch 130/0.4 with balanced crystalloid solution on mortality and kidney failure in patients with severe sepsis (6S--Scandinavian Starch for Severe Sepsis/Septic Shock trial): study protocol, design and rationale for a double-blinded, randomised clinical trial.
Trials
; 12: 24, 2011 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21269526
7.
Difficulties or mistakes in diagnosing type 1 diabetes mellitus in children? The consequences of delayed diagnosis.
Pediatr Endocrinol Diabetes Metab
; 14(1): 7-12, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18577340