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Photocatalytic hydrogen production from aqueous glycerol solution using NiO/TiO2 catalysts: Effects of preparation and reaction conditions

Applied catalysis. B, Environmental, 2016-02, Vol.181, p.818-824

2016

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The diagnosis and treatment of hereditary angioedema patients in Japan: A patient reported outcome survey

Allergology International, 2021-04, Vol.70 (2), p.235-243

2021

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Fibrin and fibrinogen degradation products/D-dimer ratio can be a useful marker for differentiating an acute attack of hereditary angioedema from thrombotic conditions

Allergology international, 2024-01, Vol.73 (1), p.174-176

2024

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Uric acid-lowering and renoprotective effects of topiroxostat, a selective xanthine oxidoreductase inhibitor, in patients with diabetic nephropathy and hyperuricemia: a randomized, double-blind, placebo-controlled, parallel-group study (UPWARD study)

Clinical and experimental nephrology, 2018-08, Vol.22 (4), p.860-870

2018

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Oral berotralstat for the prophylaxis of hereditary angioedema attacks in patients in Japan: A phase 3 randomized trial

Allergy (Copenhagen), 2021-06, Vol.76 (6), p.1789-1799

2021

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Hereditary angioedema with an acute attack resolved after bone marrow transplantation for acute myeloid leukemia: a case report

Allergy, asthma, and clinical immunology, 2023-05, Vol.19 (1), p.42-42, Article 42

2023

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Diminished capacity of opsonization and immune complex solubilization, and detection of anti-C1q antibodies in sera from patients with hereditary angioedema

Allergology international, 2017-10, Vol.66 (4), p.603-609

2017

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Thraustochytrid Aurantiochytrium sp. 18W-13a Accummulates High Amounts of Squalene

Bioscience, biotechnology, and biochemistry, 2011, Vol.75 (11), p.2246-2248

2011

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Clinical manifestations, diagnosis, and treatment of hereditary angioedema: survey data from 94 physicians in Japan

Annals of allergy, asthma, & immunology, 2015-06, Vol.114 (6), p.492-498

2015

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Correction: Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

BMC nephrology, 2023-11, Vol.24 (1), p.1-327, Article 327

2023

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Suffocation due to Acute Airway Edema in a Patient with Hereditary Angioedema Highlighted the Need for Urgent Improvements in Treatment Availability in Japan

Internal Medicine, 2018/11/01, Vol.57(21), pp.3193-3197

2018

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Clinical Features of Hereditary and Mast Cell-mediated Angioedema Focusing on the Differential Diagnosis in Japanese Patients

Internal Medicine, 2018/02/01, Vol.57(3), pp.319-324

2018

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Clinical and Laboratory Characteristics That Differentiate Hereditary Angioedema in 72 Patients with Angioedema

Allergology international, 2014, Vol.63 (4), p.595-602

2014

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A case of hereditary angioedema due to C1-inhibitor deficiency with recurrent abdominal pain diagnosed 40 years after the occurrence of the initial symptom

Clinical journal of gastroenterology, 2021-08, Vol.14 (4), p.1175-1179

2021

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Study on the formulation of maintenance and inspection guidelines for life support devices

Transactions of Japanese Society for Medical and Biological Engineering, 2020, Vol.Annual58(Abstract), pp.243-243

2020

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Berotralstat for long-term prophylaxis of hereditary angioedema in Japan: Parts 2 and 3 of the randomized APeX-J Phase III trial

The World Allergy Organization journal, 2024-03, Vol.17 (3), p.100882-100882, Article 100882

2024

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Quantitative evaluation of the role of cysteine and methionine residues in the antioxidant activity of human serum albumin using recombinant mutants

IUBMB life, 2012-05, Vol.64 (5), p.450-454

2012

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Optimization of culture conditions for growth and docosahexaenoic acid production by a marine thraustochytrid, Aurantiochytrium limacinum mh0186

Journal of oleo science, 2009, Vol.58 (12), p.623

2009

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Survey of actual conditions of erythema marginatum as a prodromal symptom in Japanese patients with hereditary angioedema

The World Allergy Organization journal, 2021-02, Vol.14 (2), p.100511-100511, Article 100511

2021

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Leukocytosis and high hematocrit levels during abdominal attacks of hereditary angioedema

BMC gastroenterology, 2013-08, Vol.13 (1), p.123-123, Article 123

2013

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Impact of Body Mass Index on Progression of IgA Nephropathy Among Japanese Patients

Journal of clinical laboratory analysis, 2015-09, Vol.29 (5), p.353-360

2015

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p-Cresyl sulfate causes renal tubular cell damage by inducing oxidative stress by activation of NADPH oxidase

Kidney international, 2013-04, Vol.83 (4), p.582-592

2013

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Properdin has an ascendancy over factor H regulation in complement-mediated renal tubular damage

BMC nephrology, 2014-05, Vol.15 (1), p.82-82, Article 82

2014

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Efficacy and Safety of Upacicalcet in Hemodialysis Patients with Secondary Hyperparathyroidism: A Phase 3 Study: TH-OR20

Journal of the American Society of Nephrology, 2020-10, Vol.31 (10S), p.6-7

2020

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Upacicalcet, a Novel Non-Peptide Calcimimetic for the Treatment of Secondary Hyperparathyroidism, Has a Low Risk of Hypocalcemia: PO0318

Journal of the American Society of Nephrology, 2020-10, Vol.31 (10S), p.148-148

2020

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Photocatalytic hydrogen production from aqueous glycerol solution using NiO/TiO2 catalysts: Effects of preparation and reaction conditions

The diagnosis and treatment of hereditary angioedema patients in Japan: A patient reported outcome survey

Fibrin and fibrinogen degradation products/D-dimer ratio can be a useful marker for differentiating an acute attack of hereditary angioedema from thrombotic conditions

Uric acid-lowering and renoprotective effects of topiroxostat, a selective xanthine oxidoreductase inhibitor, in patients with diabetic nephropathy and hyperuricemia: a randomized, double-blind, placebo-controlled, parallel-group study (UPWARD study)

Oral berotralstat for the prophylaxis of hereditary angioedema attacks in patients in Japan: A phase 3 randomized trial

Hereditary angioedema with an acute attack resolved after bone marrow transplantation for acute myeloid leukemia: a case report

Diminished capacity of opsonization and immune complex solubilization, and detection of anti-C1q antibodies in sera from patients with hereditary angioedema

Thraustochytrid Aurantiochytrium sp. 18W-13a Accummulates High Amounts of Squalene

Clinical manifestations, diagnosis, and treatment of hereditary angioedema: survey data from 94 physicians in Japan

Correction: Atypical histological abnormalities in an adult patient with nephronophthisis harboring NPHP1 deletion: a case report

Suffocation due to Acute Airway Edema in a Patient with Hereditary Angioedema Highlighted the Need for Urgent Improvements in Treatment Availability in Japan

Clinical Features of Hereditary and Mast Cell-mediated Angioedema Focusing on the Differential Diagnosis in Japanese Patients

Clinical and Laboratory Characteristics That Differentiate Hereditary Angioedema in 72 Patients with Angioedema

A case of hereditary angioedema due to C1-inhibitor deficiency with recurrent abdominal pain diagnosed 40 years after the occurrence of the initial symptom

Study on the formulation of maintenance and inspection guidelines for life support devices

Berotralstat for long-term prophylaxis of hereditary angioedema in Japan: Parts 2 and 3 of the randomized APeX-J Phase III trial

Quantitative evaluation of the role of cysteine and methionine residues in the antioxidant activity of human serum albumin using recombinant mutants

Optimization of culture conditions for growth and docosahexaenoic acid production by a marine thraustochytrid, Aurantiochytrium limacinum mh0186

Survey of actual conditions of erythema marginatum as a prodromal symptom in Japanese patients with hereditary angioedema

Leukocytosis and high hematocrit levels during abdominal attacks of hereditary angioedema

Impact of Body Mass Index on Progression of IgA Nephropathy Among Japanese Patients

p-Cresyl sulfate causes renal tubular cell damage by inducing oxidative stress by activation of NADPH oxidase

Properdin has an ascendancy over factor H regulation in complement-mediated renal tubular damage

Efficacy and Safety of Upacicalcet in Hemodialysis Patients with Secondary Hyperparathyroidism: A Phase 3 Study: TH-OR20

Upacicalcet, a Novel Non-Peptide Calcimimetic for the Treatment of Secondary Hyperparathyroidism, Has a Low Risk of Hypocalcemia: PO0318

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