Detalhe da pesquisa
1.
The DNA methyltransferase inhibitor, guadecitabine, targets tumor-induced myelopoiesis and recovers T cell activity to slow tumor growth in combination with adoptive immunotherapy in a mouse model of breast cancer.
BMC Immunol
; 21(1): 8, 2020 02 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-32106810
2.
Liver transplantation for classical maple syrup urine disease: long-term follow-up.
J Pediatr Gastroenterol Nutr
; 59(5): 636-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24979318
3.
Recurrence of bile salt export pump deficiency after liver transplantation.
N Engl J Med
; 361(14): 1359-67, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19797282
4.
Seroprevalence and epidemiology of hepatitis B and C viruses in pregnant women in Spain. Risk factors for vertical transmission.
PLoS One
; 15(5): e0233528, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32437468
5.
Health-related quality of life in pre-adolescent liver transplant recipients with biliary atresia: A cross-sectional study.
Clin Res Hepatol Gastroenterol
; 43(4): 427-435, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30528863
6.
Efficacy and safety of valganciclovir in liver-transplanted children infected with Epstein-Barr virus.
Liver Transpl
; 14(8): 1185-93, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18668670
7.
Efficacy and safety of peginterferon-alpha2b and ribavirin combination therapy in children with chronic hepatitis C infection.
Pediatr Infect Dis J
; 27(2): 142-8, 2008 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18174875
8.
A new variant in PHKA2 is associated with glycogen storage disease type IXa.
Mol Genet Metab Rep
; 10: 52-55, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28116244
9.
Update on lysosomal acid lipase deficiency: Diagnosis, treatment and patient management. / Actualización en deficiencia de lipasa ácida lisosomal: diagnóstico, tratamiento y seguimiento de los pacientes.
Med Clin (Barc)
; 148(9): 429.e1-429.e10, 2017 May 10.
Artigo
em Inglês, Espanhol
| MEDLINE | ID: mdl-28285817
10.
Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1.
Hum Mol Genet
; 13(20): 2451-60, 2004 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-15317749