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1.
[Vogt-Koyanagi-Harada syndrome in the setting of vemurafenib therapy for metastatic melanoma: a case report].
Zhonghua Yan Ke Za Zhi
; 58(11): 925-928, 2022 Nov 11.
Artículo
en Zh
| MEDLINE | ID: mdl-36348532
2.
[Clinical features of anti-myelin oligodendrocyte glycoprotein antibody-associated diseases in children with cortical encephalitis].
Zhonghua Yi Xue Za Zhi
; 100(25): 1952-1955, 2020 Jul 07.
Artículo
en Zh
| MEDLINE | ID: mdl-32629595
3.
[Preliminary study on reading speed test with IReST for normally-sighted young Chinese readers].
Zhonghua Yan Ke Za Zhi
; 54(2): 120-124, 2018 Feb 11.
Artículo
en Zh
| MEDLINE | ID: mdl-29429297
4.
[Clinical and prognostic analysis of opsoclonus-myoclonus-ataxia syndrome in children].
Zhonghua Er Ke Za Zhi
; 62(3): 256-261, 2024 Mar 02.
Artículo
en Zh
| MEDLINE | ID: mdl-38378288
5.
[Pediatric autoimmune encephalitis associated with anti-glutamic acid decarboxylase 65 antibody: two cases report and literature review].
Zhonghua Er Ke Za Zhi
; 59(1): 47-52, 2021 Jan 02.
Artículo
en Zh
| MEDLINE | ID: mdl-33397004
6.
[Clinical characteristics and gene analysis of SYNGAP1-related epilepsy in children].
Zhonghua Er Ke Za Zhi
; 59(12): 1059-1064, 2021 Dec 02.
Artículo
en Zh
| MEDLINE | ID: mdl-34856666
7.
[Clinical observation on the overlapping syndrome of myelin oligodendrocyte glycoprotein antibody and anti-N-methyl-D aspartate receptor in children].
Zhonghua Er Ke Za Zhi
; 58(7): 581-585, 2020 Jul 02.
Artículo
en Zh
| MEDLINE | ID: mdl-32605343
8.
[Phenotype and genotype of twelve Chinese children with mitochondrial DNA depletion syndromes].
Zhonghua Er Ke Za Zhi
; 57(3): 211-216, 2019 Mar 02.
Artículo
en Zh
| MEDLINE | ID: mdl-30818899
9.
[Phenotypic and genotypic characteristics of fever-induced paroxysmal weakness and encephalopathy caused by ATP1A3 pathogenic variants].
Zhonghua Er Ke Za Zhi
; 57(7): 543-547, 2019 Jul 02.
Artículo
en Zh
| MEDLINE | ID: mdl-31269555
10.
[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].
Zhonghua Er Ke Za Zhi
; 57(11): 844-851, 2019 Nov 02.
Artículo
en Zh
| MEDLINE | ID: mdl-31665838
11.
DUHOCAMIS: a dual hollow cathode ion source for metal ion beams.
Rev Sci Instrum
; 79(2 Pt 2): 02B315, 2008 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-18315181
12.
[Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation].
Zhonghua Er Ke Za Zhi
; 56(11): 818-823, 2018 Nov 02.
Artículo
en Zh
| MEDLINE | ID: mdl-30392205
13.
[Clinical features and diagnosis of childhood leukoencephalopathy with cerebral calcifications and cysts in four cases].
Zhonghua Er Ke Za Zhi
; 56(7): 539-544, 2018 Jul 02.
Artículo
en Zh
| MEDLINE | ID: mdl-29996189
14.
[A case report of hereditary sensory and autonomic neuropathy type â ¦].
Zhonghua Er Ke Za Zhi
; 59(1): 56-58, 2021 Jan 02.
Artículo
en Zh
| MEDLINE | ID: mdl-33397006
15.
[Allogeneic hematopoietic stem cell transplantation in a case of Krabbe disease].
Zhonghua Er Ke Za Zhi
; 58(5): 420-422, 2020 May 02.
Artículo
en Zh
| MEDLINE | ID: mdl-32392961
16.
[Pediatric stress-induced epileptic ataxia syndrome caused by ADPRHL2 gene variation].
Zhonghua Er Ke Za Zhi
; 58(6): 503-505, 2020 Jun 02.
Artículo
en Zh
| MEDLINE | ID: mdl-32521964
17.
[Mild Canavan disease in a child].
Zhonghua Er Ke Za Zhi
; 57(12): 961-963, 2019 12 02.
Artículo
en Zh
| MEDLINE | ID: mdl-31795566
18.
[KMT2B variants responsible for children dystonia 28: report of two cases].
Zhonghua Er Ke Za Zhi
; 57(7): 564-566, 2019 07 02.
Artículo
en Zh
| MEDLINE | ID: mdl-31269560
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