Detalles de la búsqueda
1.
Cerebral Palsy Heterogeneity: Clinical Characteristics and Diagnostic Significance from a Large Sample Analysis.
Neuroepidemiology
; 2024 Apr 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-38636464
2.
[Analysis of NOVA2 gene variant in a child with Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(2): 213-216, 2023 Feb 10.
Artículo
en Zh
| MEDLINE | ID: mdl-36709943
3.
[Analysis of CYP2U1 gene variants in a child with Hereditary spastic paraplegia type 56].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(5): 577-581, 2023 May 10.
Artículo
en Zh
| MEDLINE | ID: mdl-37102293
4.
[Clinical features and genetic analysis of a child with EAST/SeSAME syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 40(7): 838-841, 2023 Jul 10.
Artículo
en Zh
| MEDLINE | ID: mdl-37368386
5.
[Clinical and genetic analyses of Joubert syndrome in children]. / å¿ç«¥Joubert综åå¾ä¸´åºåéä¼ å¦åæ.
Zhongguo Dang Dai Er Ke Za Zhi
; 25(5): 497-501, 2023 May 15.
Artículo
en Zh
| MEDLINE | ID: mdl-37272176
6.
Identification of a 5 bp duplicate in the AP1S2 gene of an individual with X-linked intellectual disability.
Neurogenetics
; 23(3): 179-185, 2022 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35391588
7.
[Analysis of GCH1 gene variant in a consanguineous Chinese pedigree affected with tetrahydrobiopterin deficiency].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 39(7): 713-717, 2022 Jul 10.
Artículo
en Zh
| MEDLINE | ID: mdl-35810427
8.
[Effect of rehabilitation treatment based on the ICF-CY Core Sets on activities of daily living in children with cerebral palsy: a prospective randomized controlled study].
Zhongguo Dang Dai Er Ke Za Zhi
; 23(6): 608-612, 2021 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-34130783
9.
[Autosomal dominant intellectual disability-40 caused by a de novo mutation of the CHAMP1 gene: a case report].
Zhongguo Dang Dai Er Ke Za Zhi
; 22(10): 1131-1134, 2020 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-33059813
10.
[Clinical effectiveness of Subjective Global Nutritional Assessment in hospitalized children with cerebral palsy].
Zhongguo Dang Dai Er Ke Za Zhi
; 22(11): 1188-1192, 2020 Nov.
Artículo
en Zh
| MEDLINE | ID: mdl-33172553
11.
Role of Hypoxia-Inducible Factors 1α (HIF1α) in SH-SY5Y Cell Autophagy Induced by Oxygen-Glucose Deprivation.
Med Sci Monit
; 24: 2758-2766, 2018 May 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-29724989
12.
[Effect of suspension exercise training on motor and balance functions in children with spastic cerebral palsy].
Zhongguo Dang Dai Er Ke Za Zhi
; 20(6): 465-469, 2018 Jun.
Artículo
en Zh
| MEDLINE | ID: mdl-29972120
13.
[Prospective study of ketogenic diet in treatment of children with global developmental delay].
Zhongguo Dang Dai Er Ke Za Zhi
; 19(10): 1038-1043, 2017 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-29046197
14.
Ketogenic diet effects on neurobehavioral development of children with intractable epilepsy: A prospective study.
Epilepsy Behav
; 55: 87-91, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26773676
15.
[Effect of botulinum toxin A injection in the treatment of gastrocnemius spasticity in children aged 9-36 months with cerebral palsy: a prospective study].
Zhongguo Dang Dai Er Ke Za Zhi
; 18(2): 123-9, 2016 Feb.
Artículo
en Zh
| MEDLINE | ID: mdl-26903058
16.
The association of apolipoprotein E gene polymorphisms with cerebral palsy in Chinese infants.
Mol Genet Genomics
; 289(3): 411-6, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24522486
17.
The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsy.
J Neuroinflammation
; 11: 100, 2014 Jun 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-24903966
18.
[Therapeutic effects of different doses of botulinum toxin A injection on tiptoe deformation in children with cerebral palsy].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(7): 720-4, 2014 Jul.
Artículo
en Zh
| MEDLINE | ID: mdl-25008880
19.
[Therapeutic effect of ketogenic diet for refractory epilepsy in children: a prospective observational study].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(5): 513-7, 2014 May.
Artículo
en Zh
| MEDLINE | ID: mdl-24857003
20.
Autosomal recessive intellectual disability caused by compound heterozygous variants of the EEF1D gene in a Chinese family.
Mol Genet Genomic Med
; 12(1): e2333, 2024 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-38083972