Detalles de la búsqueda
1.
Urinary cell cycle arrest biomarkers and chitinase 3-like protein 1 (CHI3L1) to detect acute kidney injury in the critically ill: a post hoc laboratory analysis on the FINNAKI cohort.
Crit Care
; 24(1): 144, 2020 04 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32276601
2.
Survey by TEDDY European Network of Excellence for Paediatric Clinical Research demonstrates potential for Europe-wide trials.
Acta Paediatr
; 109(3): 607-612, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31532836
3.
Urinary chitinase 3-like protein 1 for early diagnosis of acute kidney injury: a prospective cohort study in adult critically ill patients.
Crit Care
; 20: 38, 2016 Feb 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-26864834
4.
Development and performance of the c4c national clinical trial networks for optimizing pediatric trial facilitation.
Front Pediatr
; 11: 1302272, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38188909
5.
Potential of Urine Biomarkers CHI3L1, NGAL, TIMP-2, IGFBP7, and Combinations as Complementary Diagnostic Tools for Acute Kidney Injury after Pediatric Cardiac Surgery: A Prospective Cohort Study.
Diagnostics (Basel)
; 13(6)2023 Mar 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-36980354
6.
Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene.
Am J Med Genet A
; 143A(24): 3144-9, 2007 Dec 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-18000903
7.
Diagnosis of cardiac surgery-associated acute kidney injury: differential roles of creatinine, chitinase 3-like protein 1 and neutrophil gelatinase-associated lipocalin: a prospective cohort study.
Ann Intensive Care
; 7(1): 24, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28251598
8.
The molecular basis of classic Ehlers-Danlos syndrome: a comprehensive study of biochemical and molecular findings in 48 unrelated patients.
Hum Mutat
; 25(1): 28-37, 2005 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-15580559
9.
Update of the UMD-FBN1 mutation database and creation of an FBN1 polymorphism database.
Hum Mutat
; 22(3): 199-208, 2003 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-12938084
10.
Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene.
J Invest Dermatol
; 123(4): 656-63, 2004 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-15373769
11.
Functional mannose-binding lectin haplotype variants are associated with Alzheimer's disease.
J Alzheimers Dis
; 35(1): 121-7, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23348713
12.
Role of mannose-binding lectin (MBL2) genotyping in predicting the risk of recurrent otitis media (rOM).
Adv Exp Med Biol
; 586: 281-90, 2006.
Artículo
en Inglés
| MEDLINE | ID: mdl-16893079
13.
Gene polymorphisms of Toll-like and related recognition receptors in relation to the vaginal carriage of Gardnerella vaginalis and Atopobium vaginae.
J Reprod Immunol
; 79(2): 163-73, 2009 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-19200604
14.
An interstitial deletion of chromosome 7 at band q21: a case report and review.
Am J Med Genet A
; 134A(1): 12-23, 2005 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-15732063
15.
Mannose-binding lectin: laying the stepping stones from clinical research to personalized medicine.
Per Med
; 1(1): 35-52, 2004 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29793226
16.
Discordance between phenotypic appearance and genotypic findings in a familial case of classical Ehlers-Danlos syndrome.
Am J Med Genet A
; 128A(4): 436-8, 2004 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-15264295
Resultados
1 -
16
de 16
1
Próxima >
>>