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Daiki Abukawa

Clinical pictures of 75 patients with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD)
2007 · T. Ohura, K. Kobayashi, et al. · Journal of Inherited Metabolic Disease · 152
Neonatal presentation of adult-onset type II citrullinemia
2001 · Toshihiro Ohura, Keiko Kobayashi, et al. · Human Genetics · 135
Infantile cholestatic jaundice associated with adult-onset type II citrullinemia
2001 · Yusaku Tazawa, Keiko Kobayashi, et al. · The Journal of Pediatrics · 113
Pathology of chronic hepatitis C in children
1997 · M Kage, T Fujisawa, et al. · Hepatology · 107
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Diagnostic Accuracy of The 13C-Urea Breath Test for Childhood Helicobacter Pylori Infection: A Multicenter Japanese Study
2002 · Seiichi Kato, Kyoko Ozawa, et al. · The American Journal of Gastroenterology · 88
Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn’s disease
2018 · The CEAS study group, Junji Umeno, et al. · Journal of Gastroenterology · 81
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Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients
2004 · Yusaku Tazawa, Keiko Kobayashi, et al. · Molecular Genetics and Metabolism · 65
Helicobacter pylori Reinfection Rates in Children After Eradication Therapy
1998 · Seiichi Kato, Daiki Abukawa, et al. · Journal of Pediatric Gastroenterology and Nutrition · 61
Effects of Citrin Deficiency in the Perinatal Period: Feasibility of Newborn Mass Screening for Citrin Deficiency
2004 · Akiko Tamamori, Akie Fujimoto, et al. · Pediatric Research · 51
A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: neonatal intrahepatic cholestasis caused by citrin deficiency
2003 · Toshihiro Ohura, Keiko Kobayashi, et al. · European Journal of Pediatrics · 48
Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity
2023 · Kunihiko Moriya, Tomohiro Nakano, et al. · The Journal of Experimental Medicine · 47
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Pilot study of screening for Wilson disease using dried blood spots obtained from children seen at outpatient clinics
1999 · T. Ohura, D. Abukawa, et al. · Journal of Inherited Metabolic Disease · 42
Two Novel Mutations in the Lactase Gene in a Japanese Infant with Congenital Lactase Deficiency
2012 · Nao Uchida, Osamu Sakamoto, et al. · The Tohoku Journal of Experimental Medicine · 39
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Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
2010 · Akihiko Kimura, Masayoshi Kage, et al. · Hepatology Research · 39
Targeted Sequencing and Immunological Analysis Reveal the Involvement of Primary Immunodeficiency Genes in Pediatric IBD: a Japanese Multicenter Study
2016 · Tasuku Suzuki, Yoji Sasahara, et al. · Journal of Clinical Immunology · 37
Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC
1999 · Laura N. Bull, Jenneke A. Juijn, et al. · Human Genetics · 35
Current role of colonoscopy in infants and young children: a multicenter study
2019 · Ryusuke Nambu, Shin-ichiro Hagiwara, et al. · BMC Gastroenterology · 32
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Pediatric Patient and Parental Anxiety and Impressions Related to Initial Gastrointestinal Endoscopy: A Japanese Multicenter Questionnaire Study
2015 · Shin-ichiro Hagiwara, Yoshiko Nakayama, et al. · Scientifica · 32
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Direct enzymatic assay of urinary sulfated bile acids to replace serum bilirubin testing for selective screening of neonatal cholestasis
1996 · Akira Matsui, Yasuo Kasano, et al. · The Journal of Pediatrics · 32
Immunochemical study in three patients with cytochromec oxidase deficiency presenting leigh's encephalomyelopathy
1987 · S. Miyabayashi, T. Ito, et al. · Journal of Inherited Metabolic Disease · 30
Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early‐onset Refractory Diarrhea
2020 · Takashi Uchida, Tasuku Suzuki, et al. · Journal of Pediatric Gastroenterology and Nutrition · 29
Genetic Analysis of Shwachman-Diamond Syndrome: Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
2005 · Takako Kawakami, Tetsuo Mitsui, et al. · The Tohoku Journal of Experimental Medicine · 28
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Pediatric‐onset Chronic Nonspecific Multiple Ulcers of Small Intestine: A Nationwide Survey and Genetic Study in Japan
2016 · Keiichi Uchida, Atsushi Nakajima, et al. · Journal of Pediatric Gastroenterology and Nutrition · 26
Selective expansion of donor‐derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome
2013 · Satoshi Horino, Yoji Sasahara, et al. · Pediatric Transplantation · 25
Neonatal lactic acidosis with methylmalonic aciduria due to novel mutations in the SUCLG1 gene
2011 · Osamu Sakamoto, Toshihiro Ohura, et al. · Pediatrics International · 25
Works count: 96
Citation count: 1,935
H-index: 25
I10-index: 55
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