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Brain & Development
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March 24, 2018
Early risk factors for mortality in children with seizure and/or impaired consciousness accompanied by fever without known etiology
Kazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development
|
February 26, 2018
Development of a new screening tool for neuromotor development in children aged two - the neuromotor 5 min exam 2-year-old version (N5E2)
Sayaka Aoki, Keiji Hashimoto, Hidetoshi Mezawa, et al.
Brain & Development
|
June 7, 2022
Geniospasm: A systematic review on natural history, prognosis, and treatment
Lip-Yuen Teng, Dianah Abd Hadi, Poorani Anandakrishnan, et al.
Brain & Development
|
January 11, 2021
HPeV3-associated acute encephalitis/encephalopathy among Japanese infants
Yuichi Abe, Takuro Ohno, Hiroshi Matsumoto, et al.
Brain & Development
|
June 6, 2021
Head titubation and irritability as early symptoms of Joubert syndrome with a homozygous NPHP1 variant
Yoshie Sakurai, Tatsuya Watanabe, Yuki Abe, et al.
Brain & Development
|
June 7, 2021
Hemiplegic migraine type 2 caused by a novel variant within the P-type ATPase motif in ATP1A2 concomitant with a CACNA1A variant
Tomoya Kubota, Shin Nabatame, Ruka Sato, et al.
Brain & Development
|
June 2, 2021
A retrospective analysis of memantine use in a pediatric neurology clinic
Sarah Bouhadoun, Chantal Poulin, Saoussen Berrahmoune, et al.
Brain & Development
|
January 1, 1988
Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
M Nakajima, S Ishii, T Mito, et al.
Brain & Development
|
January 1, 1988
Use of erythromycin to inhibit carbamazepine metabolism in children with partial complex seizures
P Curatolo, O Bruni, R Cusmai
Brain & Development
|
November 16, 2020
Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability
Chupong Ittiwut, Sathida Poonmaksatit, Ponghatai Boonsimma, et al.
Page
of 517
Search research articles
Search
Showing results (841-850 of 5,166) with videos related to
Sort By:
Page
of 517
Brain & Development
|
March 24, 2018
Early risk factors for mortality in children with seizure and/or impaired consciousness accompanied by fever without known etiology
Kazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development
|
February 26, 2018
Development of a new screening tool for neuromotor development in children aged two - the neuromotor 5 min exam 2-year-old version (N5E2)
Sayaka Aoki, Keiji Hashimoto, Hidetoshi Mezawa, et al.
Brain & Development
|
June 7, 2022
Geniospasm: A systematic review on natural history, prognosis, and treatment
Lip-Yuen Teng, Dianah Abd Hadi, Poorani Anandakrishnan, et al.
Brain & Development
|
January 11, 2021
HPeV3-associated acute encephalitis/encephalopathy among Japanese infants
Yuichi Abe, Takuro Ohno, Hiroshi Matsumoto, et al.
Brain & Development
|
June 6, 2021
Head titubation and irritability as early symptoms of Joubert syndrome with a homozygous NPHP1 variant
Yoshie Sakurai, Tatsuya Watanabe, Yuki Abe, et al.
Brain & Development
|
June 7, 2021
Hemiplegic migraine type 2 caused by a novel variant within the P-type ATPase motif in ATP1A2 concomitant with a CACNA1A variant
Tomoya Kubota, Shin Nabatame, Ruka Sato, et al.
Brain & Development
|
June 2, 2021
A retrospective analysis of memantine use in a pediatric neurology clinic
Sarah Bouhadoun, Chantal Poulin, Saoussen Berrahmoune, et al.
Brain & Development
|
January 1, 1988
Clinical, biochemical and ultrastructural study on the pathogenesis of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
M Nakajima, S Ishii, T Mito, et al.
Brain & Development
|
January 1, 1988
Use of erythromycin to inhibit carbamazepine metabolism in children with partial complex seizures
P Curatolo, O Bruni, R Cusmai
Brain & Development
|
November 16, 2020
Novel de novo mutation substantiates ATP6V0C as a gene causing epilepsy with intellectual disability
Chupong Ittiwut, Sathida Poonmaksatit, Ponghatai Boonsimma, et al.
Page
of 517