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Immunotherapy Advances
|
March 29, 2024
Janus kinase inhibitors ameliorate clinical symptoms in patients with STAT3 gain-of-function
Shuya Kaneko, Fumiaki Sakura, Kay Tanita, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
May 28, 2026
Anti-Integrin αvβ6 Autoantibodies as Diagnostic and Monitoring Biomarkers for Pediatric-Onset Primary Sclerosing Cholangitis
Yukako Maeda, Shuichiro Umetsu, Eitaro Hiejima, et al.
Journal of the Pediatric Infectious Diseases Society
|
July 4, 2025
Decline of Pediatric Acute Hepatitis of Unknown Etiology During the Coronavirus Disease 2019 Pandemic in Japan
Hiroki Kondou, Keiko Tanaka-Taya, Kiyoko Amo, et al.
Molecular Genetics and Metabolism
|
January 3, 2017
Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment
Hironori Nagasaka, Haruki Komatsu, Ayano Inui, et al.
JIMD Reports
|
April 15, 2018
Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period
Teruo Miyazaki, Hironori Nagasaka, Haruki Komatsu, et al.
Ebiomedicine
|
November 7, 2017
Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages
Hisamitsu Hayashi, Sotaro Naoi, Takao Togawa, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
May 20, 2022
Diagnostic criteria for acute-on-chronic liver failure and related disease conditions in Japan
Satoshi Mochida, Nobuaki Nakayama, Shuji Terai, et al.
Journal of Inherited Metabolic Disease
|
September 14, 2012
Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children
Hironori Nagasaka, Tohru Yorifuji, Robert H J Bandsma, et al.
Nature Communications
|
November 22, 2023
Intestinal Atp8b1 dysfunction causes hepatic choline deficiency and steatohepatitis
Ryutaro Tamura, Yusuke Sabu, Tadahaya Mizuno, et al.
Scientific Reports
|
November 21, 2019
Effect of food on the pharmacokinetics and therapeutic efficacy of 4-phenylbutyrate in progressive familial intrahepatic cholestasis
Satoshi Nakano, Shuhei Osaka, Yusuke Sabu, et al.
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of 15
Search research articles
Search
Showing results (121-130 of 144) with videos related to
Sort By:
Page
of 15
Immunotherapy Advances
|
March 29, 2024
Janus kinase inhibitors ameliorate clinical symptoms in patients with STAT3 gain-of-function
Shuya Kaneko, Fumiaki Sakura, Kay Tanita, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
May 28, 2026
Anti-Integrin αvβ6 Autoantibodies as Diagnostic and Monitoring Biomarkers for Pediatric-Onset Primary Sclerosing Cholangitis
Yukako Maeda, Shuichiro Umetsu, Eitaro Hiejima, et al.
Journal of the Pediatric Infectious Diseases Society
|
July 4, 2025
Decline of Pediatric Acute Hepatitis of Unknown Etiology During the Coronavirus Disease 2019 Pandemic in Japan
Hiroki Kondou, Keiko Tanaka-Taya, Kiyoko Amo, et al.
Molecular Genetics and Metabolism
|
January 3, 2017
Circulating tricarboxylic acid cycle metabolite levels in citrin-deficient children with metabolic adaptation, with and without sodium pyruvate treatment
Hironori Nagasaka, Haruki Komatsu, Ayano Inui, et al.
JIMD Reports
|
April 15, 2018
Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period
Teruo Miyazaki, Hironori Nagasaka, Haruki Komatsu, et al.
Ebiomedicine
|
November 7, 2017
Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages
Hisamitsu Hayashi, Sotaro Naoi, Takao Togawa, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology
|
May 20, 2022
Diagnostic criteria for acute-on-chronic liver failure and related disease conditions in Japan
Satoshi Mochida, Nobuaki Nakayama, Shuji Terai, et al.
Journal of Inherited Metabolic Disease
|
September 14, 2012
Sustained high plasma mannose less sensitive to fluctuating blood glucose in glycogen storage disease type Ia children
Hironori Nagasaka, Tohru Yorifuji, Robert H J Bandsma, et al.
Nature Communications
|
November 22, 2023
Intestinal Atp8b1 dysfunction causes hepatic choline deficiency and steatohepatitis
Ryutaro Tamura, Yusuke Sabu, Tadahaya Mizuno, et al.
Scientific Reports
|
November 21, 2019
Effect of food on the pharmacokinetics and therapeutic efficacy of 4-phenylbutyrate in progressive familial intrahepatic cholestasis
Satoshi Nakano, Shuhei Osaka, Yusuke Sabu, et al.
Page
of 15