Tokushima University / Educator and Researcher Directory --- Gohji, Aya

Field of Study

Subject of Study

Book / Paper

Book:

1.	Yoshihiro Touda, Aya Gohji, Tatsuo Mori, Shoji Kagami, 青天目信 and 下野九理子 : A case of glucose transporter 1 (GLUT1) deficiency treated with ketone diet for a long time., 特殊ミルク共同安全開発委員会, Tokyo, Nov. 2019. (Keyword) グルコーストランスポーター1欠損症 / GLUT1

Academic Paper (Judged Full Paper):

1.	Tatsuo Mori, Mutsuki Nakano, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, Shinichi Kameyama, Takeshi Mizuguchi, Maki Urushihara and Naomichi Matsumoto : A female case of L1 syndrome that may have developed due to skewedXinactivation., Brain & Development, 46, 6, 230-233, 2024. (Summary) Heterozygous L1CAM variants cause L1 syndrome with hydrocephalus and aplasia/hypoplasia of the corpus callosum. L1 syndrome usually has an X-linked recessive inheritance pattern; however, we report a rare case occurring in a female child. The patient's family history was unremarkable. Fetal ultrasonography revealed enlarged bilateral ventricles of the brain and hypoplasia of the corpus callosum. The patient was born at 38 weeks and 4 days of gestation. Brain MRI performed on the 8th day of life revealed enlargement of the brain ventricles, marked in the lateral and third ventricles with irregular margins, and hypoplasia of the corpus callosum. Exome sequencing at the age of 2 years and 3 months revealed a de novo heterozygous L1CAM variant (NM_000425.5: c.2934_2935delp. (His978Glnfs * 25). X-chromosome inactivation using the human androgen receptor assay revealed that the pattern of X-chromosome inactivation in the patients was highly skewed (96.6 %). The patient is now 4 years and 11 months old and has a mild developmental delay (developmental quotient, 56) without significant progression of hydrocephalus. In this case, we hypothesized that the dominant expression of the variant allele arising from skewed X inactivation likely caused L1 syndrome. Symptomatic female carriers may challenge the current policies of prenatal and preimplantation diagnoses. (Keyword) Humans / Female / X Chromosome Inactivation / Neural Cell Adhesion Molecule L1 / Hydrocephalus / Child, Preschool / Agenesis of Corpus Callosum (Tokushima University Institutional Repository) ● Metadata: 2012240 (Link to Publication Site) ● Publication site (DOI): 10.1016/j.braindev.2024.03.001 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 38480026 ● Summary page in Scopus @ Elsevier: 2-s2.0-85187576992 (Tokushima University Institutional Repository: 2012240, DOI: 10.1016/j.braindev.2024.03.001, PubMed: 38480026, Elsevier: Scopus)
2.	Natsue Nozaki, Kenji Mori, Tetsuya Tanioka, Keiko Mori, Kumi Takahashi, Hiroko Hashimoto, Takahiro Tayama, Aya Gohji and Tatsuo Mori : Bilateral Prefrontasl Cortex Blood Flow Dynamics during Silent and Oral Reading Using Near-Infrared Spectroscopy, The Journal of Medical Investigation : JMI, 71, 1,2, 92-101, 2024. (Summary) This study aimed to investigate blood flow dynamics in the bilateral prefrontal cortex during silent and oral reading using near-infrared spectroscopy (NIRS). The subjects were 40 right-handed university students (20.5±1.8 years old, 20 men and 20 women). After completing the NIRS measurements, the subjects were asked to rate their level of proficiency in silent and oral reading, using a 5-point Likert scale. During oral reading, the left lateral prefrontal cortex (Broca's area) was significantly more active than the right side. During silent reading, prefrontal cortex activity was lower than that during oral reading, and there was no significant difference between both sides of the brain. A significant negative correlation was found between the change in oxy-hemoglobin (oxy-Hb) concentration in the left and right lateral prefrontal cortex during silent reading and silent reading speed. In addition, students with lower self-reported reading proficiency had significantly greater changes in oxy-Hb concentrations in the left and right lateral prefrontal cortex during silent/oral reading than did students with higher self-reported reading proficiency. Reading task assessment using NIRS may be useful for identifying language lateralization and Broca's area. The results demonstrate that NIRS is useful for assessing effortful reading and may be used to diagnose developmental dyslexia in children. J. Med. Invest. 71 : 92-101, February, 2024. (Keyword) near infrared spectroscopy / Silent and Oral Reading (Tokushima University Institutional Repository) ● Metadata: 2011958 (Link to Publication Site) ● Publication site (DOI): 10.2152/jmi.71.92 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 38735731 ● Search Scopus @ Elsevier (PMID): 38735731 ● Search Scopus @ Elsevier (DOI): 10.2152/jmi.71.92 (Tokushima University Institutional Repository: 2011958, DOI: 10.2152/jmi.71.92, PubMed: 38735731)
3.	森慶子, Kenji Mori, 野崎夏江, 岡本里恵, Fumiko Murao, Kumi Takahashi, Hiroko Hashimoto, Takahiro Tayama, Aya Gohji and Tatsuo Mori : 個別学習支援を行った限局性学習症を有する子どもの脳機能評価, 小児保健とくしま, 30, 28-33, 2023. (Keyword) 限局性学習症 / 脳機能評価 / NIRS (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1010021218921958144 (CiNii: 1010021218921958144)
4.	Takahiro Tayama, Shunsuke Takeuchi, Mikiko Takei, Keisuke Fujioka, Akemi Ono, Miki Shono, 七條光市, Shuji Kondo, Shoko Fukura, Aya Gohji, Tatsuo Mori and Toshiyuki Takahashi : A case of MOG antibody-associated disease with encephalomyelitis after the onset of subacute meningitis, No to Hattatsu, 55, 5, 363-367, 2023. (Keyword) MOG antibody-associated disease / aseptic meningitis / encephalitis / myelitis / plasma exchange therapy (Link to Publication Site) ● Publication site (DOI): 10.11251/ojjscn.55.363 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1390016262462269056 ● Search Scopus @ Elsevier (DOI): 10.11251/ojjscn.55.363 (DOI: 10.11251/ojjscn.55.363, CiNii: 1390016262462269056)
5.	Kouhei Kamoi, 大山正弘, Keiichiro Watanabe, Ryuji Nakagawa, Tatsuo Mori, Satoshi Koyama, Aya Gohji, Junya Fukuda and 富永賢 : ピエール・ロバン症候群乳児における維持と調整機構を付与したPre-epiglottic baton plateの製作, Journal of Japanese Academy of Oral and Maxillofacial Rehabilitation Technology, 22, 1, 9-15, 2022. (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1520578448257550336 (CiNii: 1520578448257550336)
6.	Shunsuke Takeuchi, Tatsuo Mori, Aya Gohji, Toshiyuki Takahashi and Yoshihiro Touda : Effective plasmapheresis treatment of intractable visual symptoms of MOG antibody-related disorders, No to Hattatsu, 54, 6, 421-425, 2022. (Keyword) MOG抗体 / 視神経炎 / 血漿交換 / 急性散在性脳脊髄炎 / 維持療法 / myelin oligodendrocyte glycoprotein / optic neuritis / plasmapheresis / acute disseminated encephalomyelitis / maintenance steroids (Link to Publication Site) ● Publication site (DOI): 10.11251/ojjscn.54.421 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1390294341169669632 ● Search Scopus @ Elsevier (DOI): 10.11251/ojjscn.54.421 (DOI: 10.11251/ojjscn.54.421, CiNii: 1390294341169669632)
7.	Shun Aoi, Hidehiro Umehara, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, 高橋幸利 and Tetsuro Ohmori : 免疫療法が著効し，髄液中の抗グルタミン酸受容体抗体が陽性であった小児自己免疫性溶連菌感染関連性精神神経障害が疑われた1例, Psychiatria et Neurologia Japonica, 124, 7, 447-456, 2022. (Keyword) 小児自己免疫性溶連菌感染関連性精神神経障害 / チック症候群 / 強迫性障害 / 免疫療法 / pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections (PANDAS) / tic disorder / obsessive-compulsive disorder (OCD) / immunotherapy / ショウニジコメンエキセイヨウレンキンカンセンカンレンセイセイシンシンケイショウガイ / チックショウコウグン / キョウハクセイショウガイ / メンエキリョウホウ (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1520011638683069824 (CiNii: 1520011638683069824)
8.	Kenji Mori, 森慶子, 野崎夏江, 河井ちひろ, Kumi Takahashi, Hiroko Hashimoto, Aya Gohji and Tatsuo Mori : 読字障害と脳活動に関する最新の研究, Psychiatry, 41, 1, 126-132, 2022. (Keyword) dyslexia / near-infrared spectroscopy(NIRS) / brain activity / reading aloud / silent reading (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1520574181168742656 (CiNii: 1520574181168742656)
9.	Tatsuo Mori, Aya Gohji, Yoshihiro Touda, Asami Okada, Yumiko Kotani and Shoji Kagami : Usefulness of individual support and medication for autism spectrum disorder traits in a boy with cyclic vomiting syndrome, No to Hattatsu, 53, 1, 54-57, 2021. (Summary) Herein we report the case of a 7-year-old boy with cyclic vomiting syndrome (CVS) successfully treated with judicious management and medication of autism spectrum disorder (ASD) traits. Radical surgery for esophageal atresia (Gross C) was performed during the neonatal period. The patient's mother and grandmother both had migraines. The cyclic vomiting began when he was 1 year and 4 months of age, and the episodes occurred 1-3 times monthly. Various drug treatments were tested, but were not effective in controlling the vomiting events. The patient was referred to our hospital at the age of 7 years and 4 months for consultation and treatment. We arrived at a diagnosis of ASD due to observable traits including avoidance of eye contact, obsessiveness, and difficulty in communication. Subsequently, we began individual support and medication for ASD traits to alleviate the CVS. The school has begun to support for his behaviors associated with ASD. Consequently, the psychological anxiety regarding school attendance was addressed, allowing the patient to return to school. When prophylactic drug treatment was changed to the combination of risperidone, amitriptin, and sodium valproate, the vomiting attacks discontinued. The patient is now aged 9 years and 3 months, and has experienced no recurrent vomiting episodes in the past 14 months. In conclusion, it is important to consider the possible coexistence of developmental disorders in patients with intractable CVS, and to provide the reasonable accommodation and treatment for optimal outcomes. (Keyword) 周期性嘔吐症 / 自閉スペクトラム症 / risperidone / amitriptin / 個別支援 (Link to Publication Site) ● Publication site (DOI): 10.11251/ojjscn.53.54 (Link to Search Site for Scientific Articles) ● CiNii @ National Institute of Informatics (CRID): 1390005667266618880 ● Summary page in Scopus @ Elsevier: 2-s2.0-85105807980 (DOI: 10.11251/ojjscn.53.54, CiNii: 1390005667266618880, Elsevier: Scopus)
10.	Ken-ichi Suga, Issei Imoto, Hiromichi Ito, Takuya Naruto, Aya Gohji, Keita Osumi, Narumi Tokaji, Yukako Homma, Akemi Ono, Yuko Ichihara, Miki Shono, Tatsuo Mori, Maki Urushihara, Ryuji Nakagawa, Yasunobu Hayabuchi and Shoji Kagami : Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilities, The Journal of Medical Investigation : JMI, 67, 3, 4, 246-249, 2020. (Summary) Background : In clinical practice, a large proportion of patients with multiple congenital anomalies and/or intellectual disabilities (MCA / ID) lacks a specific diagnosis. Recently, next-generation sequencing (NGS) has become an efficient strategy for genetic diagnosis of patients with MCA/ID. To review the utility of NGS for the diagnosis of patients with MCA / ID. Patients with MCA/ID were recruited between 2013 and 2017. Molecular diagnosis was performed using NGS-based targeted panel sequencing for 4,813 genes. Promising causative variants underwent confirmation by Sanger sequencing or chromosomal microarray. Eighteen patients with MCA/ID were enrolled in this study. Of them, 8 cases (44%) were diagnosed by targeted panel sequencing. Most of diagnosed patients were able to receive better counseling and more appropriate medical management. NGS-based targeted panel sequencing seems to be an effective testing strategy for diagnosis of patients with MCA/ID. J. Med. Invest. 67 : 246-249, August, 2020. (Keyword) intellectual disability / multiple congenital anomalies / next-generation sequencing / targeted panel sequencing (Tokushima University Institutional Repository) ● Metadata: 2008342 (Link to Publication Site) ● Publication site (DOI): 10.2152/jmi.67.246 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 33148896 ● Summary page in Scopus @ Elsevier: 2-s2.0-85095598029 (Tokushima University Institutional Repository: 2008342, DOI: 10.2152/jmi.67.246, PubMed: 33148896, Elsevier: Scopus)
11.	Keita Osumi, Ken-ichi Suga, Akemi Ono, Aya Gohji, Tatsuo Mori, Yukiko Kinoshita, Mikio Sugano, Yoshihiro Touda, Maki Urushihara, Ryuji Nakagawa, Yasunobu Hayabuchi, Issei Imoto and Shoji Kagami : Molecular diagnosis of an infant with TSC2/ PKD1 contiguous gene syndrome, Human Genome Variation, 7, 21, 2020. (Summary) A 1-month-old Japanese infant with cardiac rhabdomyoma was diagnosed with / contiguous gene syndrome by targeted panel sequencing with subsequent quantitative polymerase chain reaction that revealed gross monoallelic deletion, including parts of two genes: exons 19-42 of and exons 2-46 of . Early molecular diagnosis can help to detect bilateral renal cyst formation and multidisciplinary follow-up of this multisystem disease. (Tokushima University Institutional Repository) ● Metadata: 2009119 (Link to Publication Site) ● Publication site (DOI): 10.1038/s41439-020-0108-0 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 32695431 ● Summary page in Scopus @ Elsevier: 2-s2.0-85088011488 (Tokushima University Institutional Repository: 2009119, DOI: 10.1038/s41439-020-0108-0, PubMed: 32695431, Elsevier: Scopus)
12.	Kenji Mori, 田山貴広, Aya Gohji, Tatsuo Mori and Yoshihiro Touda : けいれんと間違えやすい生理的運動・異常行動., 小児内科, 50, 541-544, 2018.
13.	Hiromichi Ito, Kenji Mori, Masafumi Harada, Sonoka Hisaoka, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, Yoko Abe, Masahito Miyazaki and Shoji Kagami : A Proton Magnetic Resonance Spectroscopic Study in Autism Spectrum Disorder Using a 3-Tesla Clinical Magnetic Resonance Imaging (MRI) System: The Anterior Cingulate Cortex and the Left Cerebellum., Journal of Child Neurology, 32, 8, 731-739, 2017. (Summary) The pathophysiology of autism spectrum disorder (ASD) is not fully understood. We used proton magnetic resonance spectroscopy to investigate metabolite concentration ratios in the anterior cingulate cortex and left cerebellum in ASD. In the ACC and left cerebellum studies, the ASD group and intelligence quotient- and age-matched control group consisted of 112 and 114 subjects and 65 and 45 subjects, respectively. In the ASD group, γ-aminobutyric acid (GABA)+/ creatine/phosphocreatine (Cr) was significantly decreased in the anterior cingulate cortex, and glutamate (Glu)/Cr was significantly increased and GABA+/Cr was significantly decreased in the left cerebellum compared to those in the control group. In addition, both groups showed negative correlations between Glu/Cr and GABA+/Cr in the left cerebellum, and positive correlations between GABA+/Cr in the anterior cingulate cortex and left cerebellum. ASD subjects have hypoGABAergic alterations in the anterior cingulate cortex and hyperglutamatergic/hypoGABAergic alterations in the left cerebellum. (Keyword) Adolescent / Aspartic Acid / Autism Spectrum Disorder / cerebellum / Child / Child, Preschool / Choline / Creatine / Female / Gyrus Cinguli / Humans / Imaging, Three-Dimensional / magnetic resonance imaging / Male / Proton Magnetic Resonance Spectroscopy / gamma-Aminobutyric Acid (Link to Publication Site) ● Publication site (DOI): 10.1177/0883073817702981 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 28420309 ● Summary page in Scopus @ Elsevier: 2-s2.0-85021191879 (DOI: 10.1177/0883073817702981, PubMed: 28420309, Elsevier: Scopus)

Academic Paper (Unrefereed Paper):

1.	Asuna Sugimoto, 河原林啓太, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, Shoji Kagami and Tsutomu Iwamoto : 口腔筋機能療法の可能性と展望, 小児保健とくしま, 27, 1, 23-26, 2019.
2.	Narumi Tokaji, Hiromichi Ito, Tomohiro Kohmoto, Takuya Naruto, Rizu Takahashi, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, Masako Saito, Shoichiro Tange, Kiyoshi Masuda, Shoji Kagami and Issei Imoto : A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation, American Journal of Medical Genetics. Part A., 176A, 3, 699-702, 2018. (Summary) Rett syndrome (RTT) is a severe neurodevelopmental disorder typically affecting females. It is mainly caused by loss-of-function mutations that affect the coding sequence of exon 3 or 4 of methyl-CpG-binding protein 2 (MECP2). Severe neonatal encephalopathy resulting in death before the age of 2 years is the most common phenotype observed in males affected by a pathogenic MECP2 variant. Mutations in MECP2 exon 1 affecting the MeCP2_e1 isoform are relatively rare causes of RTT in females, and only one case of a male patient with MECP2-related severe neonatal encephalopathy caused by a mutation in MECP2 exon 1 has been reported. This is the first reported case of a male with classic RTT caused by a 5-bp duplication in the open-reading frame of MECP2 exon 1 (NM_001110792.1:c.23_27dup) that introduced a premature stop codon [p.(Ser10Argfs*36)] in the MeCP2_e1 isoform, which has been reported in one female patient with classic RTT. Therefore, both males and females displaying at least some type of MeCP2_e1 mutation may exhibit the classic RTT phenotype. (Keyword) Alternative Splicing / Base Sequence / brain / Child, Preschool / DNA Mutational Analysis / Exons / Genetic Association Studies / Genetic Predisposition to Disease / Humans / magnetic resonance imaging / male / Methyl-CpG-Binding Protein 2 / Mutation / Phenotype / Rett Syndrome (Link to Publication Site) ● Publication site (DOI): 10.1002/ajmg.a.38595 (Link to Search Site for Scientific Articles) ● PubMed @ National Institutes of Health, US National Library of Medicine (PMID): 29341476 ● Summary page in Scopus @ Elsevier: 2-s2.0-85042076423 (DOI: 10.1002/ajmg.a.38595, PubMed: 29341476, Elsevier: Scopus)
3.	Kenji Mori, 森慶子, Kaoru Furukawa, Kumi Takahashi, Hiroko Hashimoto, Hiromichi Ito, Aya Gohji, Tatsuo Mori, Yoshihiro Touda and Shoji Kagami : 脳科学から読み解く発達障害, 小児保健とくしま, 26, 10-18, 2018.

Proceeding of International Conference:

1.	Aya Gohji, Hiromichi Ito, N Tokaji, T Kohmoto, T Naruto, R Takahashi, Tatsuo Mori, Yoshihiro Touda, M Saito, S Tange, K Masuda, Shoji Kagami and I Imoto : A Rare Male Patient with Classic Rett Syndrome Caused by MeCP2_e1 Mutation., ASHG 2017 annual meeting, Oct. 2017.
2.	Aya Gohji, Hiromichi Ito, Kenji Mori, S Hisaoka, Yoshihiro Touda, Tatsuo Mori, Y Abe, M Miyazaki and Shoji Kagami : Metabolic dysfunction in anterior cingulate cortex using a magnetic resonance spectroscopy in Asperger's syndrome., Pediatric Academic Societies Meeting, May 2016.

Proceeding of Domestic Conference:

1.	Kenji Mori, 森慶子, Kumi Takahashi, Hiroko Hashimoto, Mutsuki Nakano, TAYAMA Takahiro, Aya Gohji, Tatsuo Mori, Hiromichi Ito, Yoshihiro Touda and 宮崎雅仁 : 音読・黙読時の左大脳半球の血流動態 NIRSによる解析, No to Hattatsu, 57, Suppl, 244, Jun. 2025.
2.	Mutsuki Nakano, Tatsuo Mori, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, 輿水江里子, 宮武聡子, 松本直通 and Maki Urushihara : PNKP遺伝子の複合ヘテロ接合性変異によるmicrocephaly,seizures,and developmental delay(MCSZ)の女児例, No to Hattatsu, 56, 6, 463, Jul. 2024.
3.	Mutsuki Nakano, Tatsuo Mori, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, 輿水江里子, 宮武聡子, 松本直通 and Maki Urushihara : PNKP遺伝子の複合ヘテロ接合性変異によるmicrocephaly,seizures,and developmental delay(MCSZ)の女児例, The Journal of the Japan Pediatric Society, Jun. 2024.
4.	Tatsuo Mori, Mutsuki Nakano, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, 亀山真一, 水口剛, 松本直通 and Maki Urushihara : X染色体不活化パターンの偏りにより発症した可能性のあるL1症候群の女児例, No to Hattatsu, 56, Suppl, 251, May 2024.
5.	森慶子, Kenji Mori, 野崎夏江, 岡本里恵, Fumiko Murao, Kumi Takahashi, Hiroko Hashimoto, Takahiro Tayama, Aya Gohji and Tatsuo Mori : 個別学習支援を行った限局性学習症を有する子どもの脳機能評価, 小児保健とくしま, 30, Sep. 2023. (Keyword) 限局性学習症 / 脳機能評価 / NIRS
6.	Takahiro Tayama, Tatsuo Mori, Mutsuki Nakano, Aya Gohji and Maki Urushihara : COVID-19罹患後に発症した多発性脳梗塞の乳児例, No to Hattatsu, 56, 1, 70, Jul. 2023.
7.	Kenji Mori, 森慶子, Kumi Takahashi, Hiroko Hashimoto, 野崎夏江, Tatsuo Mori, Aya Gohji, Takahiro Tayama, Hiromichi Ito, Yoshihiro Touda and 宮崎雅仁 : 読字障害を有する小学1年生におけるNIRSを用いた脳機能評価, 第65回日本小児神経学会学術集会, 55, 353, May 2023. (Keyword) 読字障害 / 脳機能評価 / NIRS
8.	Tatsuo Mori, Yoshiteru Tada, Masahito Nakataki, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, Toshitaka Fujihara, Hiroki Yamazaki and Kenji Mori : 徳島大学病院てんかんセンターにおけるトランジションの現状と今後の課題, 第10回全国てんかんセンター協議会総会栃木大会 2023, Mar. 2023.
9.	Yoshiteru Tada, Masahito Nakataki, Tatsuo Mori, Toshitaka Fujihara, Aya Gohji, Hiroki Yamazaki, 泉千恵, 高尾里沙, 多田雅美, 阿部修司, Kenji Mori and Yasushi Takagi : 地方におけるてんかん支援拠点病院の役割, 第10回全国てんかんセンター協議会, Feb. 2023.
10.	Aya Gohji, Hiroyuki Morino, Asami Okada, Tatsuo Mori, Ken-ichi Suga, Yumiko Kotani, Rie Seyama, Yuri Uchiyama and Naomichi Matsumoto : Coffin-siris syndrome with persistent open anterior fontanelle in a boy arising from a novel de novo ARID2 variant, 日本人類遺伝学会第67回大会, Dec. 2022.
11.	Yuki Sakaki, Tatsuo Mori, Takahiro Tayama, Aya Gohji, Yoshihiro Touda and Maki Urushihara : 乳児期の異常眼球運動発作の存在が診断の契機になったGLUT1欠損症の男児例, 中国四国小児科学会プログラム・抄録集, 74, 50, Oct. 2022.
12.	Tatsuo Mori, Takahiro Tayama, Aya Gohji, Yoshihiro Touda, 坂本正宗, 松本直通 and Maki Urushihara : A girl case with myoclonic atonic epilepsy caused by SLC6A1 gene rupture due to a balanced chromosomal translocation, てんかん研究, 40, 2, 407, Sep. 2022.
13.	Mai Azumi, Kohhei Nakajima, 大野卓也, Aya Gohji, Tatsuo Mori, Kenji Mori and Yasushi Takagi : けいれん重積型急性脳症に類似した症状を呈し，West症候群に移行した乳児頭部外傷の1例, 第50回日本小児神経外科学会, Jun. 2022.
14.	Kenji Mori, 森慶子, Kumi Takahashi, Hiroko Hashimoto, 野﨑夏江, 河井ちひろ, Tatsuo Mori, Aya Gohji, 伊藤弘道, Yoshihiro Touda and 宮崎雅仁 : Evaluation of brain function in dyslexic children : a near-infrared spectroscopy study, 第64回日本小児神経学会学術集会, Jun. 2022. (Keyword) 読字障害 / NIRS / 脳機能評価
15.	Takahiro Tayama, 竹内竣亮, 武井美貴子, Keisuke Fujioka, Akemi Ono, Miki Shono, 七條光市, Shuji Kondo, 福良翔子, Aya Gohji, Tatsuo Mori and 高橋利幸 : 髄膜炎で発症後に，脳脊髄炎を呈した抗MOG抗体関連疾患の1例, No to Hattatsu, 54, Suppl, S352, May 2022.
16.	Yukako Honma, Aya Gohji, Tatsuo Mori, Yasunobu Hayabuchi, Mikio Sugano, Takashi Kitaichi and Hiroki Hata : 憤怒痙攣が診断の契機となった完全大血管転位症術後における冠状動脈狭窄・心筋虚血の1乳児例, 第36回日本小児循環器学会近畿・中四国地方会, Mar. 2022.
17.	Yoshiteru Tada, Masahito Nakataki, Tatsuo Mori, Toshitaka Fujihara, Aya Gohji, Hiroki Yamazaki, 高尾里沙, 泉千恵, 多田雅美, 安部修司 and Kenji Mori : 今後の徳島県におけるてんかん地域診療連携整備事業の展望について, 第9回全国てんかんセンター協議会総会, Mar. 2022.
18.	Tomoshi Koyama, Aya Gohji, Tatsuo Mori, Ryuji Nakagawa, Keiichiro Watanabe, Kouhei Kamoi and Junya Fukuda : Pre-epiglottic baton plateを用いて上気道狭窄に対応したPierre-Robin Sequenceの1例, 第73回中国四国小児科学会, Nov. 2021.
19.	佐藤宏紀, Tatsuo Mori, Aya Gohji, Yoshihiro Touda and Masashi Ohta : 興奮, 暴行を伴う発作後精神病の管理に難渋したLennox-Gastaut症候群の男児例., 第1回四国小児てんかんEducation Seminar., Oct. 2021.
20.	田中真波, 福良翔子, Aya Gohji, Tatsuo Mori and Yoshihiro Touda : BCG接種から約1か月でACTH療法を導入したWest症候群の1例., 第32回日本小児神経学会中国・四国地方会., Jul. 2021.
21.	Hiroki Sato, Yukako Honma, Mikio Sugano, Takashi Kitaichi, Aya Gohji, Tatsuo Mori and Yasunobu Hayabuchi : 憤怒痙攣が診断の契機となった完全大血管転位術後における冠状動脈狭窄・心筋虚血の1乳児例, 第135回日本小児科学会徳島地方会, Jun. 2021.
22.	Kenji Mori, 森慶子, Kumi Takahashi, Hiroko Hashimoto, 野﨑夏江, 河井ちひろ, Tatsuo Mori, Aya Gohji, Hiromichi Ito, Yoshihiro Touda and 宮崎雅仁 : 読字活動時における脳反応について―NIRSによる解析―．, 第63回日本小児神経学会学術集会, May 2021.
23.	竹内竣亮, Tatsuo Mori, Aya Gohji, 高橋利幸 and Yoshihiro Touda : 視覚症状のみが遷延したが，血漿交換後に症状改善を得た抗myelin oligodendrocyte glycoprotein(MOG)抗体関連疾患の男児例, No to Hattatsu, 53, Suppl, S350, May 2021.
24.	Kenji Mori, 森慶子, 高橋久美, Saori Kamishirakawa, 河合ちひろ, Hiroko Hashimoto, Tatsuo Mori, Aya Gohji, Hiromichi Ito, Yoshihiro Touda and 宮崎雅仁 : 絵本の読み聞かせ聴取時における脳反応について-NIRS および心拍変動を用いた解析-, 第62回日本小児神経学会学術集会, Aug. 2020.
25.	Tatsuo Mori, Aya Gohji, Yoshihiro Touda, Hiromichi Ito, Toshitaka Kawarai, 藤田京志, 松本直通 and Kenji Mori : 薬剤抵抗性てんかんを合併したARID1B 遺伝子欠失を伴うCoffin-Siris症候群の女児例., 第31回日本小児神経学会中国・四国地方会, Jul. 2020.
26.	Masahito Nakataki, Hiroaki Edo, Yoshiteru Tada, Yoshihiro Touda, Toshitaka Fujihara, Tatsuo Mori, Aya Gohji, Kenji Mori and Tetsuro Ohmori : てんかん発作や精神症状と関連しない生活の質, 第53回日本てんかん学会学術集会, Nov. 2019.
27.	Yoshiteru Tada, Yoshihiro Touda, Masahito Nakataki, Toshitaka Fujihara, Tatsuo Mori, Aya Gohji, 飯田幸治, Kenji Mori and Yasushi Takagi : 徳島県におけるてんかん地域診療連携整備事業の紹介, 第53回日本てんかん学会学術集会, Oct. 2019.
28.	宮本容子, Toshitaka Kawarai, Tatsuo Mori, Aya Gohji and Masami Morimoto : Genetic counseling for children with congenital disease diagnosed with PTEN Hamartoma Tumor Syndrome by IRUD, 第43回日本遺伝カウンセリング学会, Aug. 2019.
29.	青井駿, Hidehiro Umehara, Aya Gohji, 東田義広, Shinya Watanabe, Masahito Nakataki, Shusuke Numata and Tetsuro Ohmori : 感冒症状後にチック症状と強迫症状の出現増悪を認め，PANDASが疑われた1例, 第115回日本精神神経学会学術総会, Jun. 2019.
30.	Tatsuo Mori, Hiromichi Ito, Aya Gohji, Yoshihiro Touda, Kenji Mori, Masafumi Harada and Shoji Kagami : 自閉症スペクトラム症におけるArterial Spin Labeling法を用いた脳血流評価, 第61回日本小児神経学会学術集会, May 2019.
31.	Kenji Mori, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, Hiromichi Ito, 宮崎雅仁 and Shoji Kagami : NIRSを用いた読字課題時の前頭葉機能評価, 第61回日本小児神経学会学術集会, May 2019.
32.	Tatsuo Mori, 田山貴広, Aya Gohji, Yoshihiro Touda and Shoji Kagami : 均衡型相互転座(46XX t(3;11)(p25;q13.1))を伴ったミオクロニー脱力発作を伴うてんかんの一女児例, 第52回日本てんかん学会学術集会, Oct. 2018.
33.	Yoshihiro Touda, Aya Gohji, Tatsuo Mori and Shoji Kagami : 小児難治性てんかんに対する新規抗てんかん薬の使用経験, 第52回日本てんかん学会学術集会, Oct. 2018.
34.	Kenji Mori, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, Hiromichi Ito, 宮崎雅仁 and Shoji Kagami : 多チャンネルNIRSを用いた表情処理過程の解析, 第60回日本小児神経学会学術集会, May 2018.
35.	Hiromichi Ito, Kenji Mori, Masafumi Harada, 久岡園花, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, 高見容子, 宮崎雅仁 and Shoji Kagami : 自閉スペクトラム症の頭部1H-MRSによる検討―前部帯状回と左小脳について―, 第60回日本小児神経学会学術集会, May 2018.
36.	Yoshiteru Tada, Toshitaka Fujihara, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, Kenji Mori, 飯田幸治, Junichiro Satomi and Yasushi Takagi : 術前精査中にバルブロ酸の追加が著効したrolandic crtical dysplasiaに1例, 第41回日本てんかん外科学会, Jan. 2018.
37.	Yoshihiro Touda, Aya Gohji, Tatsuo Mori, Yukiko Kinoshita, Yasunobu Hayabuchi, Shoji Kagami and Issei Imoto : バルプロ酸の投与によりてんかん発症を抑制できた結節性硬化症の一例, 第51回日本てんかん学会学術集会, Nov. 2017.
38.	Kaoru Furukawa, Kenji Mori, Hiroko Hashimoto, Kumi Takahashi, Saori Kamishirakawa, Aya Gohji, Tatsuo Mori, Yoshihiro Touda, 宮崎雅仁 and Shoji Kagami : 自閉症スペクトラムにおけるNIRSを用いた表情処理過程の評価, 第118回日本小児精神神経学会, 10, Nov. 2017. (Keyword) 自閉症スペクトラム / NIRS / 表情処理 / 脳機能評価
39.	Hiromichi Ito, Kenji Mori, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, 阿部容子, 宮崎雅仁 and Shoji Kagami : 注意欠如・多動症におけるてんかん・脳波異常の検討, 第59回日本小児神経学会学術集会, Jun. 2017.
40.	Kenji Mori, Aya Gohji, Tatsuo Mori, Hiromichi Ito, Yoshihiro Touda and 宮崎雅仁 : NIRSによる読字能力評価 - 無意味単語速読・単語逆唱課題による検討 -, 第59回日本小児神経学会学術集会, Jun. 2017.
41.	Ryuji Nakagawa, Ken-ichi Suga, Aya Gohji, Shoji Kagami, Takashi Kaji, Atsuko Hichijyo and Naoto Yonetani : 先天性サイトメガロウイルス感染症の2例, 第147回日本小児科学会徳島地方会, Dec. 2016.
42.	Aya Gohji, Yoshihiro Touda, 武井美貴子, Tatsuo Mori, Hiromichi Ito and Shoji Kagami : 発作時99mTc-ECD SPECTが診断に有用であった限局性皮質異形成の乳児例, 第147回日本小児科学会徳島地方会, Dec. 2016.
43.	鈴木智子, Aya Gohji, Tatsuo Mori, Hiromichi Ito, Yoshihiro Touda, Kenji Mori and Shoji Kagami : フェノバルビタール大量投与が奏功した皮質形成異常を認める難治性てんかんの一例, 第34回四国小児神経症例検討会, Sep. 2016.
44.	大隅敬太, Hiromichi Ito, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, Shoji Kagami, 佐々木亜由美 and Kazuhiro Mori : 急性弛緩性麻痺様症状を呈した選択性IgA欠損症の幼児例, 第146回日本小児科学会徳島地方会, Jun. 2016.
45.	阿部容子, Aya Gohji, Tatsuo Mori, Hiromichi Ito, Yoshihiro Touda and Shoji Kagami : 補足運動野発作が疑われるも，発作間欠期に側頭部棘波を示す1例, 第146回日本小児科学会徳島地方会, Jun. 2016.
46.	Aya Gohji, Hiromichi Ito, Kenji Mori, Masafumi Harada, 久岡園花, Yoshihiro Touda, Tatsuo Mori, 阿部容子, 宮崎雅仁 and Shoji Kagami : Metabolic alteration in the brain of Asperger`s syndrome by using a magnetic resonance spectroscopy, 第58回日本小児神経学会学術集会, Jun. 2016.
47.	Hiromichi Ito, Kenji Mori, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, 阿部容子, 宮崎雅仁 and Shoji Kagami : 自閉症スペクトラム障害におけるてんかん・脳波異常の検討, 第58回日本小児神経学会学術集会, Jun. 2016.
48.	Hiromichi Ito, Kenji Mori, Masafumi Harada, 久岡園花, Yoshihiro Touda, Tatsuo Mori, Aya Gohji, 阿部容子, 宮崎雅仁 and Shoji Kagami : 自閉症スペクトラム障害における頭部MRI所見の目視的検討, 第58回日本小児神経学会学術集会, Jun. 2016.

Et cetera, Workshop:

1.	Hiroki Sato, Ken-ichi Suga, Masashi Suzue, Ryuji Nakagawa, Aya Gohji, Yukako Honma, Shunsuke Takeuchi, Takahiro Tayama, Mikiko Takei, Keisuke Fujioka, Akemi Ono, Miki Shono, Koichi Sichijo, Shuji Kondo and Yasunobu Hayabuchi : Ellis-van Creveld 症候群の1例, 第38階四国新生児医療研究会, Jun. 2021. (Keyword) congenital
2.	Tatsuo Mori, Aya Gohji, Yoshihiro Touda, 武井美貴子, Hiromichi Ito, Shoji Kagami and 瓦井俊孝 : GCH1変異を認めた瀬川病の8歳男児例, 第151会日本小児科学会徳島地方会, Dec. 2018.
3.	Yoshihiro Touda, 田山貴広, Aya Gohji, Tatsuo Mori and Shoji Kagami : 抗てんかん剤の中止により発作が抑制されたWest症候群の男児例, 第36回四国小児神経症例検討会, Sep. 2018.
4.	Tatsuo Mori, Aya Gohji, Yoshihiro Touda, 武井美貴子, Hiromichi Ito, Toshitaka Kawarai and Shoji Kagami : GCH1遺伝子に変異を認めた瀬川病の8歳男児例, 第29回日本小児神経学会中国四国地方会, Jul. 2018.
5.	田山貴広, Tatsuo Mori, Aya Gohji, Yoshihiro Touda and Shoji Kagami : ラコサミドが著効した環状20番染色体の7歳男児例, 第150回日本小児科学会徳島地方会, Jun. 2018.
6.	田山貴広, Yoshihiro Touda, Aya Gohji, Tatsuo Mori and Shoji Kagami : ヒプスアリスミアを伴わない乳児スパズムの一例, 第48回中国四国点頭てんかん研究会, Mar. 2018.
7.	田山貴広, Tatsuo Mori, Aya Gohji, Yoshihiro Touda and Shoji Kagami : ラコサミドが著効した環状20番染色体の7歳男児例, 第 12 回日本てんかん学会中国・四国地方会, Feb. 2018.
8.	田山貴広, Yoshihiro Touda, Aya Gohji, Tatsuo Mori and Shoji Kagami : ヒプスアリスミアを伴わない乳児スパズムの1 例, 第149回日本小児科学会徳島地方会, Dec. 2017.
9.	Aya Gohji, Hiromichi Ito, 戸梶成美, Tatsuo Mori, Yoshihiro Touda, Takuya Naruto, Issei Imoto and Shoji Kagami : MeCP2-e1遺伝子変異を持つRett症候群の男児例, 第28回日本小児神経学会中国・四国地方会, Jul. 2017.
10.	四宮由貴, Aya Gohji, Tatsuo Mori, Yoshihiro Touda and Shoji Kagami : 覚醒時にチアノーゼを伴う複雑部分発作を呈した前頭葉てんかんの一例, 第148回日本小児科学会徳島地方会, Jun. 2017.

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Designated Associate Professor : Gohji, Aya

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Grants-in-Aid for Scientific Research (KAKEN Grants Database @ NII.ac.jp)