Works matching IS 25742272 AND DT 2022 AND VI 6 AND IP 1

Results: 11

Instruction for Authors.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 55, doi. 10.1002/ped4.12319
Publication type:
Article
Collaborative studies of U.S.–China neurologists on acute motor axonal neuropathy.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 1, doi. 10.1002/ped4.12316
By:
- Lv, Junlan;
- Zhaori, Getu
Publication type:
Article
Independent temporal lobe epilepsy in patients with tuberous sclerosis complex.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 23, doi. 10.1002/ped4.12315
By:
- Liu, Tinghong;
- Ding, Jing;
- Zhang, Shaohui;
- Wang, Yangshuo;
- Xu, Jinshan;
- Yuan, Liu;
- Zhai, Feng;
- Zhang, Guojun;
- Liang, Shuli
Publication type:
Article
RNA sequencing role and application in clinical diagnostic.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 29, doi. 10.1002/ped4.12314
By:
- Peymani, Fatemeh;
- Farzeen, Aiman;
- Prokisch, Holger
Publication type:
Article
Current role of surgery for tuberous sclerosis complex‐associated epilepsy.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 16, doi. 10.1002/ped4.12312
By:
- Specchio, Nicola;
- Pavia, Giusy Carfi;
- de Palma, Luca;
- De Benedictis, Alessandro;
- Pepi, Chiara;
- Conti, Marta;
- Marras, Carlo Efisio;
- Vigevano, Federico;
- Curatolo, Paolo
Publication type:
Article
Abnormal gait and hypoglycorrhachia in a toddler with seizures.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 47, doi. 10.1002/ped4.12311
By:
- Angeli, Maria;
- Vergadi, Eleni;
- Niotakis, Georgios;
- Raissaki, Maria;
- Galanakis, Emmanouil
Publication type:
Article
Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 5, doi. 10.1002/ped4.12310
By:
- Zhang, Weihua;
- Li, Jiuwei;
- Zhuo, Xiuwei;
- Zhou, Ji;
- Feng, Weixing;
- Gong, Shuai;
- Ren, Xiaotun;
- Ding, Changhong;
- Han, Tongli;
- Fang, Fang
Publication type:
Article
The role of epigenetics in childhood autoimmune diseases with hematological manifestations.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 36, doi. 10.1002/ped4.12309
By:
- Gkoutsias, Athanasios;
- Makis, Alexandros
Publication type:
Article
Characteristics of infantile convulsions and choreoathetosis syndrome caused by PRRT2 mutation.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 11, doi. 10.1002/ped4.12308
By:
- Deng, Yaxian;
- Xu, Juanyu;
- Yao, Chunmei;
- Wang, Lei;
- Dong, Xiaohuan;
- Zhao, Chengsong
Publication type:
Article
Staging surgery for intraventricular bilateral giant Rosai–Dorfman disease in children.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. 50, doi. 10.1002/ped4.12306
By:
- Zhang, Jiyin;
- Li, Dapeng;
- Cheng, Ran;
- Zhang, Nan;
- Ni, Xin;
- Ge, Ming
Publication type:
Article
MEMBER LIST OF THE FIRST EDITORIAL BOARD OF PEDIATRIC INVESTIGATION.
Published in:
Pediatric Investigation, 2022, v. 6, n. 1, p. i, doi. 10.1002/ped4.12271
Publication type:
Article