Publications by authors named "Aya Goji"

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Hemodynamics of the left cerebral hemisphere during silent reading:analysis using near-infrared spectroscopy.
Ruriko Yamashita, Kumi Takahashi, Keiko Mori, Takahiro Tayama, Mitsunori Daibatake, Aya Goji

J Med Invest· October 2024

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A female case of L1 syndrome that may have developed due to skewed X inactivation.
Tatsuo Mori, Mutsuki Nakano, Takahiro Tayama, Aya Goji, Yoshihiro Toda

Brain Dev· June 2024

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Bilateral Prefrontal Cortex Blood Flow Dynamics during Silent and Oral Reading Using Near-Infrared Spectroscopy.
Natsue Nozaki, Kenji Mori, Tetsuya Tanioka, Keiko Mori, Kumi Takahashi, Aya Goji

J Med Invest· May 2024

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A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation.
Tatsuo Mori, Masamune Sakamoto, Takahiro Tayama, Aya Goji, Yoshihiro Toda

Brain Dev· August 2023

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Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilities.
Kenichi Suga, Issei Imoto, Hiromichi Ito, Takuya Naruto, Aya Goji

J Med Invest· October 2021

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Survey of patients with spinal muscular atrophy on the island of Shikoku, Japan.
Kentaro Okamoto, Takahiro Motoki, Isao Saito, Risako Urate, Kaori Aibara, Aya Goji

Brain Dev· September 2020

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Molecular diagnosis of an infant with / contiguous gene syndrome.
Keita Osumi, Kenichi Suga, Akemi Ono, Aya Goji, Tatsuo Mori

Hum Genome Var· July 2020

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Improvement of epilepsy with lacosamide in a patient with ring chromosome 20 syndrome.
Takahiro Tayama, Tatsuo Mori, Aya Goji, Yoshihiro Toda, Shoji Kagami

Brain Dev· June 2020

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Multi-delay arterial spin labeling brain magnetic resonance imaging study for pediatric autism.
Tatsuo Mori, Hiromichi Ito, Masafumi Harada, Sonoka Hisaoka, Yuki Matsumoto, Aya Goji

Brain Dev· April 2020

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A 16q22.2-q23.1 deletion identified in a male infant with West syndrome.
Tatsuo Mori, Aya Goji, Yoshihiro Toda, Hiromichi Ito, Kenji Mori

Brain Dev· November 2019

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A rare male patient with classic Rett syndrome caused by MeCP2_e1 mutation.
Narumi Tokaji, Hiromichi Ito, Tomohiro Kohmoto, Takuya Naruto, Rizu Takahashi, Aya Goji

Am J Med Genet A· March 2018

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Assessment of Anterior Cingulate Cortex (ACC) and Left Cerebellar Metabolism in Asperger's Syndrome with Proton Magnetic Resonance Spectroscopy (MRS).
Aya Goji, Hiromichi Ito, Kenji Mori, Masafumi Harada, Sonoka Hisaoka

PLoS One· August 2017

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The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via mutation detection.
Asami Okada, Tomohiro Kohmoto, Takuya Naruto, Ichiro Yokota, Yumiko Kotani, Aya Goji

Hum Genome Var· August 2017

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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.
Hiromichi Ito, Kenji Mori, Masafumi Harada, Sonoka Hisaoka, Yoshihiro Toda, Aya Goji

J Child Neurol· July 2017

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A case of generalized lymphatic anomaly causing skull-base leakage and bacterial meningitis.
Kenichi Suga, Aya Goji, Miki Inoue, Masami Kawahito, Masako Taki

Brain Dev· May 2017

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Neuroimaging in autism spectrum disorders: 1H-MRS and NIRS study.
Kenji Mori, Yoshihiro Toda, Hiromichi Ito, Tatsuo Mori, Keiko Mori, Aya Goji

J Med Invest· December 2016

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Exome-first approach identified a novel gloss deletion associated with Lowe syndrome.
Miki Watanabe, Ryuji Nakagawa, Tomohiro Kohmoto, Takuya Naruto, Ken-Ichi Suga, Aya Goji

Hum Genome Var· November 2016

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A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndrome.
Miki Watanabe, Ryuji Nakagawa, Takuya Naruto, Tomohiro Kohmoto, Ken-Ichi Suga, Aya Goji

Hum Genome Var· September 2016

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A case of acute acalculous cholecystitis complicated by primary Epstein-Barr virus infection.
Kenichi Suga, Miki Shono, Aya Goji, Sato Matsuura, Miki Inoue

J Med Invest· May 2016

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Mumps encephalitis with akinesia and mutism.
Kenichi Suga, Aya Goji, Miki Shono, Sato Matsuura, Miki Inoue

Pediatr Int· August 2015

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Case of early childhood-onset narcolepsy with cataplexy: comparison with a monozygotic co-twin.
Hiromichi Ito, Kenji Mori, Tatsuo Mori, Aya Goji, Shoji Kagami

Pediatr Int· October 2014

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A case of Barber-Say syndrome in a male Japanese newborn.
Kenichi Suga, Miki Shono, Aya Goji, Sato Matsuura, Miki Inoue

Clin Case Rep· October 2014

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[Hemodynamic activities in children with autism while imitating emotional facial expressions: a near-infrared spectroscopy study].
Kenji Mori, Tatsuo Mori, Aya Goji, Hiromichi Ito, Yoshihiro Toda

No To Hattatsu· July 2014

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Age-related changes in a patient with Pelizaeus-Merzbacher disease determined by repeated 1H-magnetic resonance spectroscopy.
Tatsuo Mori, Kenji Mori, Hiromichi Ito, Aya Goji, Masahito Miyazaki

J Child Neurol· February 2014

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A proton magnetic resonance spectroscopic study in autism spectrum disorders: amygdala and orbito-frontal cortex.
Kenji Mori, Yoshihiro Toda, Hiromichi Ito, Tatsuo Mori, Aya Goji

Brain Dev· February 2013

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