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Author

Takao Togawa

ORCID: 0009-0001-3940-1245
Observed ORCID: 0009-0001-3940-1245
OpenAlex ID: A5006831955
Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing
2016 · Takao Togawa, Tokio Sugiura, et al. · The Journal of Pediatrics · 108
Clinical, Pathologic, and Genetic Features of Neonatal Dubin-Johnson Syndrome: A Multicenter Study in Japan
2018 · Takao Togawa, Tatsuki Mizuochi, et al. · The Journal of Pediatrics · 49
A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly
2017 · Yutaka Negishi, Fuyuki Miya, et al. · BMC Medical Genetics · 30
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Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
2017 · Yuji Nakamura, Yasuko Togawa, et al. · Brain and Development · 27
Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism
2017 · Kohei Aoyama, Haruo Mizuno, et al. · Journal of Pediatric Endocrinology and Metabolism · 22
Intraoperative indocyanine green fluorescence cholangiography can rule out biliary atresia: A preliminary report
2022 · Chiyoe Shirota, Akinari Hinoki, et al. · Frontiers in Pediatrics · 20
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Bile Acid Synthesis Disorders in Japan: Long-Term Outcome and Chenodeoxycholic Acid Treatment
2021 · Akihiko Kimura, Tatsuki Mizuochi, et al. · Digestive Diseases and Sciences · 20
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Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages
2017 · Hisamitsu Hayashi, Sotaro Naoi, et al. · EBioMedicine · 19
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Long‐term Outcomes of Living‐donor Liver Transplantation for Progressive Familial Intrahepatic Cholestasis Type 1
2020 · Tatsuya Okamoto, Mari Sonoda, et al. · Journal of Pediatric Gastroenterology and Nutrition · 18
Neurodevelopmental Outcomes at 18 Months’ Corrected Age of Infants Born at 22 Weeks of Gestation
2011 · Tokio Sugiura, Masanori Kouwaki, et al. · Neonatology · 18
Nemaline myopathy with KLHL40 mutation presenting as congenital totally locked-in state
2015 · Koya Kawase, Ichizo Nishino, et al. · Brain and Development · 17
Case Report: A Rare Case of Benign Recurrent Intrahepatic Cholestasis-Type 1 With a Novel Heterozygous Pathogenic Variant of ATP8B1
2022 · Hiroyuki Suzuki, Teruko Arinaga-Hino, et al. · Frontiers in Medicine · 13
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Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome
2017 · Kei Ohashi, Takao Togawa, et al. · Acta Paediatrica · 12
Assessment of Adenosine Triphosphatase Phospholipid Transporting 8B1 (ATP8B1) Function in Patients With Cholestasis With ATP8B1 Deficiency by Using Peripheral Blood Monocyte-Derived Macrophages
2020 · Ayumu Mizutani, Yusuke Sabu, et al. · Hepatology Communications · 11
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Neurodevelopmental outcomes at 3 years old for infants with birth weights under 500 g
2017 · Syunsuke Nagara, Masanori Kouwaki, et al. · Pediatrics & Neonatology · 10
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Real‐life Progression of the Use of a Genetic Panel in to Diagnose Neonatal Cholestasis
2022 · Shogo Ito, Takao Togawa, et al. · JPGN Reports · 9
Clinicopathologic Features, Genetics, Treatment, and Long-Term Outcomes in Japanese Children and Young Adults with Benign Recurrent Intrahepatic Cholestasis: A Multicenter Study
2023 · Ken Kato, Shuichiro Umetsu, et al. · Journal of Clinical Medicine · 8
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Successful treatment of adult-onset type II citrullinemia with a low-carbohydrate diet and l-arginine after DNA analysis produced a definitive diagnosis
2020 · Satoshi Unita, Noboru Hirashima, et al. · Clinical Journal of Gastroenterology · 6
Effects of 4‐phenylbutyrate therapy in a preterm infant with cholestasis and liver fibrosis
2016 · Shogo Ito, Hisamitsu Hayashi, et al. · Pediatrics International · 6
Living donor liver transplantation for myocerebrohepatopathy spectrum due to POLG mutations
2023 · Masashi Kadohisa, Tatsuya Okamoto, et al. · Pediatric Transplantation · 5
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Urine bile acid profile of a Japanese patient with a bile acid amidation defect
2022 · Nakayuki Naritaka, Rieko Sakamoto, et al. · Pediatrics International · 5
Single nucleotide polymorphisms in AGTR1, TFAP2B, and TRAF1 are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants
2015 · Koya Kawase, Tokio Sugiura, et al. · Pediatrics International · 4
Risk Factors for Early Death in Transient Myeloproliferative Disorder Without Phenotypic Features of Down Syndrome: A Case Report and Literature Review
2012 · Koya Kawase, Eiichi Azuma, et al. · Journal of Pediatric Hematology/Oncology · 4
Antenatal Growth, Gestational Age, Birth, Enteral Feeding, and Blood Citrulline Levels in Very Low Birth Weight Infants
2024 · Midori Obayashi, Sachiko Iwata, et al. · Nutrients · 2
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Adult-onset Type II Citrullinemia Developed under Dietary Restrictions during Imprisonment
2023 · Takanori Suzuki, Kentaro Matsuura, et al. · Internal Medicine · 2
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Works count: 32
Citation count: 446
H-index: 12
I10-index: 15
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