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Incorrect Holding Angle of Dry Powder Inhaler during the Drug-Loading Step Significantly Decreases Output Efficiency

Biological and Pharmaceutical Bulletin, 2021/06/01, Vol.44(6), pp.822-829

2021

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Pre-existing autoimmune disease as a risk factor for immune-related adverse events in cancer patients receiving immune checkpoint inhibitors

PloS one, 2024-07, Vol.19 (7), p.e0306995

2024

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Assessment of inhalation flow patterns of soft mist inhaler co-prescribed with dry powder inhaler using inspiratory flow meter for multi inhalation devices

PloS one, 2018-02, Vol.13 (2), p.e0193082-e0193082

2018

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Previous Dosage of Allopurinol Is a Strong Determinant of Febuxostat Efficacy

Biological and Pharmaceutical Bulletin, 2017/05/01, Vol.40(5), pp.681-686

2017

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Substrate-dependent effects of molecular-targeted anticancer agents on activity of organic anion transporting polypeptide 1B1

Xenobiotica, 2018-10, Vol.48 (10), p.1059-1071

2018

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Severe Skin Disorders Due to Sorafenib Use After Nivolumab Treatment in Renal Cell Carcinoma Patients

In vivo (Athens), 2021, Vol.35 (5), p.2969-2974

2021

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Cooperative inhibitory effects of uremic toxins and other serum components on OATP1B1-mediated transport of SN-38

Cancer chemotherapy and pharmacology, 2017-04, Vol.79 (4), p.783-789

2017

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Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype

Journal of human genetics, 2009-02, Vol.54 (2), p.94-97

2009

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Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A MT-TS2 pathogenic variant in a Japanese family

Molecular genetics and metabolism reports, 2023-06, Vol.35, p.100966, Article 100966

2023

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Concomitant administration of candesartan cilexetil in patients on paclitaxel and carboplatin combination therapy increases risk of severe neutropenia

International journal of clinical pharmacology and therapeutics, 2018-07, Vol.56 (7), p.328-336

2018

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Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

Journal of human genetics, 2012-05, Vol.57 (5), p.338-341

2012

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A 14-year-old girl with lissencephaly and craniofacial dysmorphism

Neuropathology, 2012-12, Vol.32 (6), p.675-678

2012

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In Vitro Evidence of Potential Interactions between CYP2C8 and Candesartan Acyl- β -D-glucuronide in the Liver

Drug metabolism and disposition, 2021-04, Vol.49 (4), p.289-297

2021

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Erratum: Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

Journal of human genetics, 2012-06, Vol.57 (6), p.399-399

2012

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Analysis of Risk Factors for High-dose Cisplatin-induced Renal Impairment in Head and Neck Cancer Patients

In vivo (Athens), 2022-09, Vol.36 (5), p.2465-2472

2022

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Acceleration of carboxylesterase-mediated activation of irinotecan to SN-38 by serum from patients with end-stage kidney disease

Cancer chemotherapy and pharmacology, 2018-06, Vol.81 (6), p.1121-1128

2018

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Pre-existing autoimmune disease as a risk factor for immune-related adverse events in cancer patients receiving immune checkpoint inhibitors

PloS one, 2024-01, Vol.19 (7), p.e0306995

2024

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Severe Skin Disorders Due to Sorafenib Use After Nivolumab Treatment in Renal Cell Carcinoma Patients

In vivo (Athens), 2021-09, Vol.35 (5), p.2969-2974

2021

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Novel Mutations and Genotype-Phenotype Relationships in 107 Families With Fukuyama-Type Congenital Muscular Dystrophy (FCMD)

Human molecular genetics, 1999-11, Vol.8 (12), p.2303-2309

1999

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Three cases of hyponatremia during administration of pimozide

No to hattatsu, 1991-09, Vol.23 (5), p.502

Koide, H

1991

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Neuropathology of brainstem in severe cerebral palsy mainly due to perinatal asphyxia

No to hattatsu, 1985, Vol.17 (4), p.293

Koide, H

1985

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Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A MT-TS2 pathogenic variant in a Japanese family

Molecular genetics and metabolism reports, 2023, Vol.35, p.100966-100966

2023

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Idiopathic torsion dystonia and writing tremor within a family

Brain & development (Tokyo. 1979), 1997-12, Vol.19 (8), p.556-558

1997

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Two Patients with Angelman Syndrome Followed Beyond 20 Years of Age

Epilepsia (Copenhagen), 1998-05, Vol.39 (S5), p.67-67

1998

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A case of Klippel-Trenaunay-Weber syndrome accompanied by congenital hydrocephalus and micropolygyria

No to hattatsu, 1992-07, Vol.24 (4), p.353

1992

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Incorrect Holding Angle of Dry Powder Inhaler during the Drug-Loading Step Significantly Decreases Output Efficiency

Pre-existing autoimmune disease as a risk factor for immune-related adverse events in cancer patients receiving immune checkpoint inhibitors

Assessment of inhalation flow patterns of soft mist inhaler co-prescribed with dry powder inhaler using inspiratory flow meter for multi inhalation devices

Previous Dosage of Allopurinol Is a Strong Determinant of Febuxostat Efficacy

Substrate-dependent effects of molecular-targeted anticancer agents on activity of organic anion transporting polypeptide 1B1

Severe Skin Disorders Due to Sorafenib Use After Nivolumab Treatment in Renal Cell Carcinoma Patients

Cooperative inhibitory effects of uremic toxins and other serum components on OATP1B1-mediated transport of SN-38

Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype

Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A MT-TS2 pathogenic variant in a Japanese family

Concomitant administration of candesartan cilexetil in patients on paclitaxel and carboplatin combination therapy increases risk of severe neutropenia

Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

A 14-year-old girl with lissencephaly and craniofacial dysmorphism

In Vitro Evidence of Potential Interactions between CYP2C8 and Candesartan Acyl- β -D-glucuronide in the Liver

Erratum: Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions

Analysis of Risk Factors for High-dose Cisplatin-induced Renal Impairment in Head and Neck Cancer Patients

Acceleration of carboxylesterase-mediated activation of irinotecan to SN-38 by serum from patients with end-stage kidney disease

Pre-existing autoimmune disease as a risk factor for immune-related adverse events in cancer patients receiving immune checkpoint inhibitors

Severe Skin Disorders Due to Sorafenib Use After Nivolumab Treatment in Renal Cell Carcinoma Patients

Novel Mutations and Genotype-Phenotype Relationships in 107 Families With Fukuyama-Type Congenital Muscular Dystrophy (FCMD)

Three cases of hyponatremia during administration of pimozide

Neuropathology of brainstem in severe cerebral palsy mainly due to perinatal asphyxia

Association between maternally inherited deafness, epilepsy, and intellectual disability and the m.12207G > A MT-TS2 pathogenic variant in a Japanese family

Idiopathic torsion dystonia and writing tremor within a family

Two Patients with Angelman Syndrome Followed Beyond 20 Years of Age

A case of Klippel-Trenaunay-Weber syndrome accompanied by congenital hydrocephalus and micropolygyria

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