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