Detalles de la búsqueda
1.
[Psychomotor retardation and intermitent convulsions for 8 months in an infant].
Zhongguo Dang Dai Er Ke Za Zhi
; 18(1): 67-71, 2016 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-26781416
2.
Dopamine-melanin nanofilms for biomimetic structural coloration.
Biomacromolecules
; 16(2): 660-6, 2015 Feb 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-25587771
3.
[Acute brainstem encephalitis and myelitis in a girl with isolated methylmalonic aciduria due to MUT gene defect].
Zhongguo Dang Dai Er Ke Za Zhi
; 17(10): 1103-6, 2015 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-26483233
4.
[A Chinese boy with methylmalonic aciduria cblB type and a novel mutation in the MMAB gene].
Zhongguo Dang Dai Er Ke Za Zhi
; 17(2): 172-5, 2015 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-25760844
5.
[Clinical and ATP7A gene analysis of three infants with Menkes disease and prenatal diagnosis for a fetus at risk].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(6): 624-8, 2014 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-24927440
6.
[Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(1): 62-6, 2014 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-24461181
7.
[A boy with Fabry disease with the onset at the age of four].
Beijing Da Xue Xue Bao Yi Xue Ban
; 45(2): 307-11, 2013 Apr 18.
Artículo
en Zh
| MEDLINE | ID: mdl-23591357
8.
[Advances in clinical and molecular genetics studies on argininemia].
Zhongguo Dang Dai Er Ke Za Zhi
; 15(11): 954-9, 2013 Nov.
Artículo
en Zh
| MEDLINE | ID: mdl-24229587
9.
[Intrahepatic cholestasis due to mitochondrial respiratory chain complex I deficiency in a Chinese boy].
Zhongguo Dang Dai Er Ke Za Zhi
; 14(4): 241-6, 2012 Apr.
Artículo
en Zh
| MEDLINE | ID: mdl-22537948
10.
[Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene].
Zhongguo Dang Dai Er Ke Za Zhi
; 14(8): 561-6, 2012 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-22898272
11.
[Leucodystrophy induced by late onset 3-hydroxy-3-methylglutaric aciduria].
Zhongguo Dang Dai Er Ke Za Zhi
; 13(5): 392-5, 2011 May.
Artículo
en Zh
| MEDLINE | ID: mdl-21575345
12.
[Leigh syndrome due to mitochondrial respiratory chain complex II deficiency].
Zhongguo Dang Dai Er Ke Za Zhi
; 13(7): 569-72, 2011 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-21752325
13.
[Skin lesions induced by malnutrition in an infant with methylmalonic aciduria and homocysteic acidemia].
Zhongguo Dang Dai Er Ke Za Zhi
; 14(3): 233-4, 2012 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-22433417
14.
Facile and Scalable Synthesis Method for High-Quality Few-Layer Graphene through Solution-Based Exfoliation of Graphite.
ACS Appl Mater Interfaces
; 9(5): 4548-4557, 2017 Feb 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28094493
15.
Prenatal diagnosis of citrullinemia type 1: a Chinese family with a novel mutation of the ASS1 gene.
Brain Dev
; 36(3): 264-7, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23611581
16.
Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy.
Brain Dev
; 36(5): 394-8, 2014 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-23849264
17.
Five novel mutations in ARG1 gene in Chinese patients of argininemia.
Pediatr Neurol
; 49(2): 119-23, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23859858
18.
[Clinical, biochemical and genetic analysis of the mitochondrial disorders presenting with cardiac damage].
Zhonghua Er Ke Za Zhi
; 51(12): 909-14, 2013 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-24495761
19.
Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency.
Mitochondrial DNA
; 24(1): 67-73, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-22947169
20.
Heterogeneity of six children and their mothers with mitochondrial DNA 3243 A>G mutation.
Mitochondrial DNA
; 24(3): 297-302, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23360351