Detalhe da pesquisa
1.
A Particular SORL1 Micro-haplotype May Prevent Severe Liver Disease in a French Cohort of Alpha 1-Antitrypsin-deficient Children.
J Pediatr Gastroenterol Nutr
; 73(3): e68-e72, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33720088
2.
Liver disease related to alpha1-antitrypsin deficiency in French children: The DEFI-ALPHA cohort.
Liver Int
; 39(6): 1136-1146, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30589493
3.
Efficacy of two vitamin E formulations in patients with abetalipoproteinemia and chylomicron retention disease.
J Lipid Res
; 59(9): 1640-1648, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30021760
4.
SERPINA1 and MAN1B1 polymorphisms are not linked to severe liver disease in a French cohort of alpha-1 antitrypsin deficiency children.
Liver Int
; 37(11): 1608-1611, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28887821
5.
Screening of Wilson's disease in a psychiatric population: difficulties and pitfalls. A preliminary study.
Ann Gen Psychiatry
; 16: 19, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28392828
6.
Undernourished patients do not have increased risk of severe COVID-19 outcomes.
Clin Nutr Open Sci
; 44: 9-14, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35378830
7.
A prospective case-control pilot study to evaluate bone microarchitecture in children and teenagers on long-term parenteral nutrition using HR-pQCT.
Sci Rep
; 11(1): 9151, 2021 04 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-33911128
8.
Assessment of liver fibrosis by transient elastography (Fibroscan®) in patients with A1AT deficiency.
Clin Res Hepatol Gastroenterol
; 43(1): 77-81, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30612958
9.
Mechanisms by which atrial fibrillation-associated mutations in the S1 domain of KCNQ1 slow deactivation of IKs channels.
J Physiol
; 586(17): 4179-91, 2008 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18599533
10.
Childhood/adult-onset lysosomal acid lipase deficiency: A serious metabolic and vascular phenotype beyond liver disease-four new pediatric cases.
J Clin Lipidol
; 11(1): 167-177.e3, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391883
11.
ERAD defects and the HFE-H63D variant are associated with increased risk of liver damages in Alpha 1-Antitrypsin Deficiency.
PLoS One
; 12(6): e0179369, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28617828
12.
Prevention of implantable defibrillator shocks by cognitive behavioral therapy: a pilot trial.
Am Heart J
; 151(1): 191, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16368316
13.
Establishment of reference values of α-tocopherol in plasma, red blood cells and adipose tissue in healthy children to improve the management of chylomicron retention disease, a rare genetic hypocholesterolemia.
Orphanet J Rare Dis
; 11(1): 114, 2016 08 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27520363
14.
Dramatic increase of central venous catheter-related infections associated with a high turnover of the nursing team.
Clin Nutr
; 35(2): 446-452, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25886708
15.
Quantitative study of nerves of the human left atrium.
Heart Rhythm
; 2(5): 518-22, 2005 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-15840477
16.
Incorrect evaluation of the frequency of malnutrition and of its screening in hospitalized children by health care professionals.
J Eval Clin Pract
; 21(5): 958-62, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26202860
17.
Toward personal eHealth in cardiology. Results from the EPI-MEDICS telemedicine project.
J Electrocardiol
; 38(4 Suppl): 100-6, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16226083