Shimomura Hideki Department
Hyogo Medical University(Specialty Division)
Pediatrics, Clinical Medicine Seminars
Hyogo Medical University(Corporation/Other Facilities)
Medical Education Center, Medical Education Center
Position
■ Journal
1.
Introduction
Possible roles of pontine respiratory neuron groups in the autonomic nervous system 2014/03
2.
Case report
Chronic ileocolic intussusception due to transmural infiltration of diffuse large B cell lymphoma in a 14-year-old boy: a case report 2015/07
3.
Original article
Glycine plays a crucial role as a co-agonist of NMDA receptors in the neuronal circuit generating body movements in rat fetuses. 2015/08
4.
Original article
Reconsideration of the diagnosis and treatment of childhood migraine: A practical review of clinical experiences. 2017/05
5.
Case report
Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutation 2018/08
6.
Case report
Two closely spaced mutations incis result in Ullrich congenital muscular dystrophy 2019/04
7.
Original article
Clinical and upper gastrointestinal endoscopy feature of seven adolescents with Helicobacter pylori infection 2020/04
8.
Original article
Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan. 2021/07
9.
Original article
Underlying diseases in sporadic presentation of high creatine kinase levels in girls. 2021/08
10.
Original article
Views of the General Population on Newborn Screening for Spinal Muscular Atrophy in Japan. 2021/08
11.
Original article
Emotional and behavioral problems in pediatric patients with migraine and tension-type headache. 2021/09
12.
Original article
Early Developmental Signs in Children with Autism Spectrum Disorder: Results from the Japan Environment and Children's Study. 2022/01
13.
Other
Reply to letter to editor "Children with migraine and tension-type headache: Do they have behavioral and emotional issues?". 2022/01
14.
Original article
Effects of Screen Viewing Time on Sleep Duration and Bedtime in Children Aged 1 and 3 Years: Japan Environment and Children's Study 2022/03
15.
Original article
Analysis of the preventive treatment for migraines and Tension-type headaches. 2022/04
16.
Introduction
Emotional Problems in Pediatric Headache Patients. 2022/06
17.
Original article
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan. 2022/11
18.
Case report
A Pediatric Case of COLQ-Related Congenital Myasthenic Syndrome with Marked Fatigue. 2023/04
19.
Original article
Association between maternal use of spray formulations and offspring urological anomalies: The Japan Environment and Children's Study. 2023/10
20.
Original article
Newborn Screening for Spinal Muscular Atrophy: A 2.5-Year Experience in Hyogo Prefecture, Japan. 2023/12
21.
Case report
A novel DLG4 variant causes DLG4-related synaptopathy with intellectual regression. 2024/01
Orexinergic modulation on fetal movement in brainstem-spinal cord preparation (Poster presentation,General Lecture) 2013/06/20
2.
Analysis of modulation on respiratoru neurons in the hypoxia during perinatal period (Poster presentation,General Lecture) 2013/06/21
3.
Modulation of orexin on respiratory neuron in parabrachial nucleus. (Poster presentation,General Lecture) 2013/06/21
4.
Hypoxic modulation on respiratory neuron network during perinatal period (Poster presentation,General Lecture) 2013/11/11
5.
Hypoxic modulation on respiratory neuron and TRPA1 channel during perinatal period (Poster presentation,General Lecture) 2014/03/18
6.
A new antisense oligonucleotide composed of RNA/ENA chimera (AO85) against dystrophin exon 45 significantly increased six-minute walk distance in Duchenne muscular dystrophy (Poster presentation,General Lecture) 2016/03/14
7.
RNA/ENA chimera antisense oligonucleotide (AO85) was safely administered and shown to induce dystrophin exon 45 skipping in Duchenne muscular dystrophy patient: the first clinical study (Oral presentation,General Lecture) 2016/04/07
8.
A case with late-onset Ornithine transcarbamylase deficiency caused by a somatic mosaic framshift mutation (Oral presentation,General Lecture) 2017/10/16
9.
Clinical background of hyper-creatine-kinase-emia girls without a family history of genetic muscular diseases (Oral presentation,General Lecture) 2019/06/15
10.
A manifesting carrier of Duchenne Muscular Dystrophy with a balanced X-autosome translocation with a breakpoint in the dystrophin gene. (Poster presentation,General Lecture) 2019/10/01
11.
A Pediatric Case of COLQ-related Congenital Myasthenic Syndrome with Marked Fatigue (Poster presentation,General Lecture) 2023/08/05
12.
Cases of Becker muscular dystrophy with nonsense mutations in the dystrophin gene (Poster presentation,General Lecture) 2023/10/12