Detalles de la búsqueda
1.
Homozygous familial hypobetalipoproteinemia caused by APOB gene variations: a case report and review of literature / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 70-75, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970239
2.
Infant glycogen storage disease type Ⅳ: a clinicopathological and genetic characteristics analysis of five cases / 中华病理学杂志
Chinese Journal of Pathology
; (12): 1255-1260, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-1012402
3.
Characteristics of plasma Epstein-Barr virus DNA in children with primary infection / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 245-249, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970275
4.
Liver transplantation for the treatment of acute liver failure in 3 cases with NBAS gene deficiency and literature review / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 66-69, 2023.
Artículo
en Zh
| WPRIM | ID: wpr-970238
5.
Analysis of 6 cases with hepatocerebral mitochondrial DNA depletion syndrome and literature review / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 457-461, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-935720
6.
Clinicopathological features of hepatic fibrinogen storage disease in children / 中华病理学杂志
Chinese Journal of Pathology
; (12): 326-331, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-935534
7.
Significance of V444A polymorphism of ABCB11 gene in neonatal cholestasis / 中华实用儿科临床杂志
Chinese Journal of Applied Clinical Pediatrics
; (24): 92-94, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-732923
8.
Mutation analysis of FAH gene in patients with tyrosinemia type 1 / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 302-307, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-359750
9.
Characteristics of the plasma amino acid spectrum of neonatal intrahepatic cholestasis caused by citrin deficiency / 中华肝脏病杂志
Chinese Journal of Hepatology
; (12): 934-939, 2013.
Artículo
en Zh
| WPRIM | ID: wpr-252295
10.
Personal experience in pediatric emergency medicine training in Canada and China / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 3747-3749, 2012.
Artículo
en Inglés
| WPRIM | ID: wpr-256654
11.
A new frame-shifting mutation of UGT1A1 gene causes type I Crigler-Najjar syndrome / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 4109-4111, 2011.
Artículo
en Inglés
| WPRIM | ID: wpr-273914
12.
Clinical characteristics of autoimmune hepatitis in 11 children / 中华儿科杂志
Chinese Journal of Pediatrics
; (12): 758-763, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-231245
13.
The reassessment of the diagnostic value of 24-hour urinary copper excretion in children with Wilson's disease / 中华肝脏病杂志
Chinese Journal of Hepatology
; (12): 49-53, 2010.
Artículo
en Zh
| WPRIM | ID: wpr-247602
14.
Clinical features of hepatolenticular degeneration in children / 中华肝脏病杂志
Chinese Journal of Hepatology
; (12): 224-226, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-332278
15.
SLC25A13 gene mutations in Chinese infants with intrahepatic cholestasis and abnormal blood amino acids / 中华肝脏病杂志
Chinese Journal of Hepatology
; (12): 445-448, 2008.
Artículo
en Zh
| WPRIM | ID: wpr-332208
16.
Relationship between interleukin-12B gene + 1188 polymorphism and the susceptibility to hepatitis B virus intrauterine infection / 中华传染病杂志
Chinese Journal of Infectious Diseases
; (12)2007.
Artículo
en Zh
| WPRIM | ID: wpr-679876
17.
ABCB11 Gene Variation and Cholestatic Diseases / 实用儿科临床杂志
Journal of Applied Clinical Pediatrics
; (24)2006.
Artículo
en Zh
| WPRIM | ID: wpr-640108
18.
Study on the S region gene mutation of hepatitis B virus during prevention of HBV transmission in uterus with hepatitis B immunoglobulin / 中华流行病学杂志
Chinese Journal of Epidemiology
; (12): 522-525, 2006.
Artículo
en Zh
| WPRIM | ID: wpr-233912
19.
Relationship between cytokine gene polymorphism and susceptibility to hepatitis B virus intrauterine infection / 中华流行病学杂志
Chinese Journal of Epidemiology
; (12): 236-239, 2005.
Artículo
en Zh
| WPRIM | ID: wpr-232099
20.
Relationship between cytokines gene polymorphism and susceptibility to hepatitis B virus intrauterine infection / 中华医学杂志(英文版)
Chinese Medical Journal
; (24): 1604-1609, 2005.
Artículo
en Inglés
| WPRIM | ID: wpr-320726