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Hisamitsu Hayashi

Showing results (41-50 of 68) with videos related to

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Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 18, 2025
Lipolysis-Stimulated Lipoprotein Receptor Gene Variants as a Cause of Progressive Familial Intrahepatic Cholestasis: A Case ReportYugo Takaki, Shuichiro Umetsu, Yoshihiko Sugino, et al.
Molecular Genetics and Metabolism Reports|December 9, 2024
Efficacy and safety of switching therapy from chenodeoxycholic acid to cholic acid in Japanese patients with bile acid synthesis disordersMitsuyoshi Suzuki, Hajime Takei, Hiromi Suzuki, et al.
JPGN Reports|November 30, 2023
Healthy Patients With <i>AKR1D1</i> Mutation Not Requiring Primary Bile Acid Therapy: A Case SeriesAkihiko Kimura, Jun Mori, Anh-Hoa Nguyen Pham, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 31, 2015
Successful treatment with 4-phenylbutyrate in a patient with benign recurrent intrahepatic cholestasis type 2 refractory to biliary drainage and bilirubin absorptionHisamitsu Hayashi, Sotaro Naoi, Yu Hirose, et al.
American Journal of Otolaryngology|June 25, 2021
Differences in responsiveness of intratympanic steroid injection for intractable vertigo in Meniere's diseaseHiroshi Okuda, Mitsuhiro Aoki, Bakushi Ogawa, et al.
Frontiers in Pediatrics|April 22, 2024
Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosisHiroshi Nittono, Mitsuyoshi Suzuki, Hiromi Suzuki, et al.
Journal of Human Genetics|March 7, 2018
Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasisKazuo Imagawa, Hisamitsu Hayashi, Yusuke Sabu, et al.
Molecular Genetics and Metabolism Reports|September 15, 2021
Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disordersYoko Nakajima, Shuhei Osaka, Tadahaya Mizuno, et al.
Molecular Genetics and Metabolism|March 12, 2010
Favorable effect of 4-phenylacetate on liver functions attributable to enhanced bile salt export pump expression in ornithine transcarbamylase-deficient childrenHironori Nagasaka, Tohru Yorifuji, Kunihiko Kobayashi, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 8, 2022
Serum Fibrinogen Level and Cytokine Production as Prognostic Biomarkers for Idiopathic Sudden Sensorineural Hearing LossHiroshi Okuda, Mitsuhiro Aoki, Toshimitsu Ohashi, et al.
Pageof 7

Showing results (41-50 of 68) with videos related to

Sort By:
Pageof 7
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 18, 2025
Lipolysis-Stimulated Lipoprotein Receptor Gene Variants as a Cause of Progressive Familial Intrahepatic Cholestasis: A Case ReportYugo Takaki, Shuichiro Umetsu, Yoshihiko Sugino, et al.
Molecular Genetics and Metabolism Reports|December 9, 2024
Efficacy and safety of switching therapy from chenodeoxycholic acid to cholic acid in Japanese patients with bile acid synthesis disordersMitsuyoshi Suzuki, Hajime Takei, Hiromi Suzuki, et al.
JPGN Reports|November 30, 2023
Healthy Patients With <i>AKR1D1</i> Mutation Not Requiring Primary Bile Acid Therapy: A Case SeriesAkihiko Kimura, Jun Mori, Anh-Hoa Nguyen Pham, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|July 31, 2015
Successful treatment with 4-phenylbutyrate in a patient with benign recurrent intrahepatic cholestasis type 2 refractory to biliary drainage and bilirubin absorptionHisamitsu Hayashi, Sotaro Naoi, Yu Hirose, et al.
American Journal of Otolaryngology|June 25, 2021
Differences in responsiveness of intratympanic steroid injection for intractable vertigo in Meniere's diseaseHiroshi Okuda, Mitsuhiro Aoki, Bakushi Ogawa, et al.
Frontiers in Pediatrics|April 22, 2024
Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosisHiroshi Nittono, Mitsuyoshi Suzuki, Hiromi Suzuki, et al.
Journal of Human Genetics|March 7, 2018
Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasisKazuo Imagawa, Hisamitsu Hayashi, Yusuke Sabu, et al.
Molecular Genetics and Metabolism Reports|September 15, 2021
Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disordersYoko Nakajima, Shuhei Osaka, Tadahaya Mizuno, et al.
Molecular Genetics and Metabolism|March 12, 2010
Favorable effect of 4-phenylacetate on liver functions attributable to enhanced bile salt export pump expression in ornithine transcarbamylase-deficient childrenHironori Nagasaka, Tohru Yorifuji, Kunihiko Kobayashi, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 8, 2022
Serum Fibrinogen Level and Cytokine Production as Prognostic Biomarkers for Idiopathic Sudden Sensorineural Hearing LossHiroshi Okuda, Mitsuhiro Aoki, Toshimitsu Ohashi, et al.
Pageof 7