Editorial Board
(Source: Brain and Development)
Source: Brain and Development - August 18, 2022 Category: Neurology Source Type: research

Announcements
(Source: Brain and Development)
Source: Brain and Development - August 18, 2022 Category: Neurology Source Type: research

Cover
(Source: Brain and Development)
Source: Brain and Development - August 18, 2022 Category: Neurology Source Type: research

Contents
(Source: Brain and Development)
Source: Brain and Development - August 18, 2022 Category: Neurology Source Type: research

Effectiveness of the internet based parent education program on applied behavior analysis for parents of children with autism spectrum disorder
In this study, a short-term, internet based on-demand PE program was conducted for parents of children with ASD to acquire knowledge of ABA and basic teaching techniques. (Source: Brain and Development)
Source: Brain and Development - August 18, 2022 Category: Neurology Authors: Masahiko Inoue, Aika Tatumi, Toshiki Fukuzaki Source Type: research

A first case of childhood chronic inflammatory demyelinating polyneuropathy associated with alopecia universalis
Chronic inflammatory demyelinating polyneuropathy (CIDP) is an acquired demyelinating disease of the peripheral nervous system with unknown etiology. Alopecia universalis, an advanced form of alopecia areata (AA), is a condition characterized by complete hair loss. Here we report the first case of childhood CIDP associated with AA who was successfully treated with a combination of intravenous immunoglobulin (IVIg) and corticosteroids. (Source: Brain and Development)
Source: Brain and Development - August 12, 2022 Category: Neurology Authors: Yukimune Okubo, Takuya Miyabayashi, Ryo Sato, Wakaba Endo, Takehiko Inui, Noriko Togashi, Kazuhiro Haginoya Tags: Case Report Source Type: research

A nationwide survey of monocarboxylate transporter 8 deficiency in Japan: Its incidence, clinical course, MRI and laboratory findings
Monocarboxylate transporter 8 (MCT8) deficiency is an X-linked recessive developmental disorder characterized by initially marked truncal hypotonia, later athetotic posturing, and severe intellectual disability caused by mutations in SLC16A2, which is responsible for the transport of triiodothyronine (T3) into neurons. We conducted a nationwide survey of patients with MCT8 deficiency to clarify their current status. (Source: Brain and Development)
Source: Brain and Development - August 6, 2022 Category: Neurology Authors: Masaya Kubota, Akiko Yakuwa, Hiroshi Terashima, Hideki Hoshino Tags: Original article Source Type: research

Call for abstracts for oral and poster presentations
(Source: Brain and Development)
Source: Brain and Development - August 5, 2022 Category: Neurology Source Type: research

Editorial Board
(Source: Brain and Development)
Source: Brain and Development - August 3, 2022 Category: Neurology Source Type: research

Call_for_Papers_The_65th_Annual_Meeting_of_JSCN_draft_final
(Source: Brain and Development)
Source: Brain and Development - August 3, 2022 Category: Neurology Source Type: research

Cover
(Source: Brain and Development)
Source: Brain and Development - August 3, 2022 Category: Neurology Source Type: research

Contents
(Source: Brain and Development)
Source: Brain and Development - August 3, 2022 Category: Neurology Source Type: research

A case of ALG11-congenital disorders of glycosylation diagnosed by post-mortem whole exome sequencing
Congenital disorders of glycosylation (CDG) are inherited inborn errors of metabolism due to abnormal protein and lipid glycosylation that present with multi-systemic manifestations. The heterogeneity of CDG poses a serious diagnostic challenge; therefore, whole-exome sequencing (WES), which plays an increasingly important role in the molecular diagnosis of CDG, is used for examining patients with CDG. (Source: Brain and Development)
Source: Brain and Development - July 27, 2022 Category: Neurology Authors: Yuto Arai, Tohru Okanishi, Sotaro Kanai, Tetsuya Okazaki, Eriko Koshimizu, Satoko Miyatake, Yukinori Maeoka, Ayataka Fujimoto, Naomichi Matsumoto, Yoshihiro Maegaki Tags: Case Report Source Type: research

Guillain-Barr é syndrome in children – High occurrence of Miller Fisher syndrome in East Asian region
Guillain-Barr é syndrome (GBS) is a rare acquired immune-mediated polyneuropathy. Updated population-based data concerning paediatric GBS is needed. (Source: Brain and Development)
Source: Brain and Development - July 26, 2022 Category: Neurology Authors: Annie Ting Gee Chiu, Ricky Wing Ki Chan, Maggie Lo Yee Yau, Angus Chi Lap Yuen, Alva King Fai Lam, Shirley Wai Yin Lau, Alan Ming Chung Lau, Sharon Tsui Hang Fung, Kam Hung Ma, Christine Wai Ling Lau, Man Mut Yau, Chun Hung Ko, Kwing Wan Tsui, Che Kwan Ma Tags: Original article Source Type: research

Cranial shapes of Japanese preterm infants at one month of age using a three-dimensional scanner
Recently, cranial shape measurements of preterm infants have been performed using handheld three-dimensional (3D) scanners and can now be objectively quantified. (Source: Brain and Development)
Source: Brain and Development - July 26, 2022 Category: Neurology Authors: Hiroshi Miyabayashi, Nobuhiko Nagano, Risa Kato, Shin Hashimoto, Katsuya Saito, Takanori Noto, Shoko Ohashi, Ken Masunaga, Ichiro Morioka Tags: Original article Source Type: research