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1. Full Text Idiopathic nephrotic syndrome in children
by Noone, Damien G and Iijima, Kazumoto and Parekh, Rulan
The Lancet (British edition), ISSN 0140-6736, 07/2018, Volume 392, Issue 10141, pp. 61 - 74
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Medical policy | Medical colleges | Corticosteroids | Chronic kidney failure | Children's hospitals | Nephrotic syndrome | Prednisone | Thromboembolism | Urine | End-stage renal disease | Edema | Kidneys | Complications | Pathogenesis | Abnormalities | Health risks | Risk | Minority & ethnic groups | Immunosuppressive agents | Endothelium | Proteins | Disease resistance | Microscopy | Biopsy | Mutation | Kidney diseases | Children | Steroids | Index Medicus | Abridged Index Medicus
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2. Full Text Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial
by Iijima, Kazumoto, Prof and Sako, Mayumi, MD and Nozu, Kandai, MD and Mori, Rintaro, MD and Tuchida, Nao, MD and Kamei, Koichi, MD and Miura, Kenichiro, MD and Aya, Kunihiko, MD and Nakanishi, Koichi, MD and Ohtomo, Yoshiyuki, MD and Takahashi, Shori, Prof and Tanaka, Ryojiro, MD and Kaito, Hiroshi, MD and Nakamura, Hidefumi, MD and Ishikura, Kenji, MD and Ito, Shuichi, MD and Ohashi, Yasuo, Prof and on behalf of the Rituximab for Childhood-onset Refractory Nephrotic Syndrome (RCRNS) Study Group and RCRNS Study Grp and Rituximab for Childhood-onset Refractory Nephrotic Syndrome (RCRNS) Study Group
The Lancet (British edition), ISSN 0140-6736, 2014, Volume 384, Issue 9950, pp. 1273 - 1281
Internal Medicine | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Glomerulonephritis | Nephrology. Urinary tract diseases | Biological and medical sciences | General aspects | Medical sciences | Nephropathies. Renovascular diseases. Renal failure | Recurrence | Glucocorticoids - therapeutic use | Double-Blind Method | Humans | Immunosuppressive Agents - therapeutic use | Kaplan-Meier Estimate | Child, Preschool | Rituximab | Male | Nephrotic Syndrome - drug therapy | Nephrotic Syndrome - immunology | Young Adult | B-Lymphocytes - drug effects | Adolescent | Lymphocyte Count | Female | Immunosuppressive Agents - adverse effects | Prednisolone - therapeutic use | Drug Therapy, Combination | Antibodies, Monoclonal, Murine-Derived - adverse effects | Child | Antibodies, Monoclonal, Murine-Derived - therapeutic use | Nephrotic syndrome | Children | Drug therapy | Diseases | Monoclonal antibodies | Clinical trials | Kidneys | Kidney diseases | Drug dosages | Index Medicus | Abridged Index Medicus
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3. Full Text Rituximab for nephrotic syndrome in children
by Iijima, Kazumoto and Sako, Mayumi and Nozu, Kandai
Clinical and experimental nephrology, ISSN 1342-1751, 04/2017, Volume 21, Issue 2, pp. 193 - 202
Rituximab | Children | Complicated frequently relapsing/steroid-dependent nephrotic syndrome | Idiopathic nephrotic syndrome | Proteinuria | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Kidney Failure, Chronic - immunology | Age Factors | Humans | Immunosuppressive Agents - therapeutic use | Risk Factors | Treatment Outcome | Nephrotic Syndrome - drug therapy | Nephrotic Syndrome - congenital | Disease Progression | Nephrotic Syndrome - immunology | Rituximab - therapeutic use | Kidney Failure, Chronic - prevention & control | Adolescent | Immunosuppressive Agents - adverse effects | Child | Nephrotic Syndrome - diagnosis | Rituximab - adverse effects | Medical research | Medical colleges | Immunotherapy | Medicine, Experimental | Nephrotic syndrome | Health aspects | Immunosuppressive agents | Diseases | Index Medicus | Complicated frequently relapsing | Review | steroid-dependent nephrotic syndrome
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4. Full Text A review of clinical characteristics and genetic backgrounds in Alport syndrome
by Nozu, Kandai and Nozu, Kandai and Nakanishi, Koichi and Nakanishi, Koichi and Abe, Yoshifusa and Abe, Yoshifusa and Udagawa, Tomohiro and Udagawa, Tomohiro and Okada, Shinichi and Okada, Shinichi and Okamoto, Takayuki and Okamoto, Takayuki and Kaito, Hiroshi and Kaito, Hiroshi and Kanemoto, Katsuyoshi and Kanemoto, Katsuyoshi and Kobayashi, Anna and Kobayashi, Anna and Tanaka, Eriko and Tanaka, Eriko and Tanaka, Kazuki and Tanaka, Kazuki and Hama, Taketsugu and Hama, Taketsugu and Fujimaru, Rika and Fujimaru, Rika and Miwa, Saori and Miwa, Saori and Yamamura, Tomohiko and Yamamura, Tomohiko and Yamamura, Natsusmi and Yamamura, Natsusmi and Horinouchi, Tomoko and Horinouchi, Tomoko and Minamikawa, Shogo and Minamikawa, Shogo and Nagata, Michio and Nagata, Michio and Iijima, Kazumoto and Iijima, Kazumoto
Clinical and experimental nephrology, ISSN 1342-1751, 2/2019, Volume 23, Issue 2, pp. 158 - 168
Nephrology | Thin basement membrane | Medicine & Public Health | Genotype–phenotype correlation | Urology | ACE inhibitor | Bardoxolone | Genetic Predisposition to Disease | Prognosis | Genetic Association Studies | Kidney - pathology | Humans | Risk Factors | Nephritis, Hereditary - genetics | Male | Heredity | Autoantigens - genetics | Nephritis, Hereditary - diagnosis | Nephritis, Hereditary - therapy | Young Adult | Phenotype | Animals | Collagen Type IV - genetics | Adult | Female | Kidney - chemistry | Mutation | Genetic research | Medical colleges | Eye diseases | Enzyme inhibitors | Chronic kidney failure | Angiotensin-converting enzyme inhibitors | End-stage renal disease | Phenotypes | Clinical trials | Drug development | Genetic screening | Hearing loss | Peptidyl-dipeptidase A | Genetic analysis | Alport syndrome | Angiotensin | Kidney diseases | Diagnosis | Genotypes | Index Medicus | Invited Review
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5. Full Text Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials
by Iijima, Kazumoto and Iijima, Kazumoto and Sako, Mayumi and Sako, Mayumi and Kamei, Koichi and Kamei, Koichi and Nozu, Kandai and Nozu, Kandai
Pediatric Nephrology, ISSN 0931-041X, 9/2018, Volume 33, Issue 9, pp. 1449 - 1455
Pediatrics | Nephrology | Steroid-dependent nephrotic syndrome | Randomized | Clinical management | Medicine & Public Health | Rituximab | Clinical trial | Urology | Frequently relapsing nephrotic syndrome | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | Care and treatment | Analysis | Clinical trials | Nephrotic syndrome | Research | Non-Hodgkin's lymphomas | Drug therapy | Risk factors | Lymphocytes B | CD20 antigen | Monoclonal antibodies | Remission | Children | Health risk assessment | Lymphoma | Patients | Immunosuppressive agents | Review
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6. Full Text Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
by Nagano, China and Yamamura, Tomohiko and Horinouchi, Tomoko and Aoto, Yuya and Ishiko, Shinya and Sakakibara, Nana and Shima, Yuko and Nakanishi, Koichi and Nagase, Hiroaki and Iijima, Kazumoto and Nozu, Kandai
Scientific reports, ISSN 2045-2322, 01/2020, Volume 10, Issue 1, pp. 270 - 270
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Next-generation sequencing | Genes | Point mutation | Remission | Nephrotic syndrome | Diagnosis | Mutation | Sclerosis | Immunosuppressive agents | Genetic screening | Proteinuria | Index Medicus
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7. Full Text Rituximab for childhood refractory nephrotic syndrome
by Iijima, Kazumoto
Pediatrics international, ISSN 1328-8067, 10/2011, Volume 53, Issue 5, pp. 617 - 621
clinical trial | refractory nephrotic syndrome | rituximab | Life Sciences & Biomedicine | Pediatrics | Science & Technology | Humans | Rituximab | Clinical Trials as Topic | Nephrotic Syndrome - drug therapy | Antibodies, Monoclonal, Murine-Derived - pharmacology | Child | Immunologic Factors - pharmacology | Antibodies, Monoclonal, Murine-Derived - therapeutic use | Immunologic Factors - therapeutic use | Lupus | Medical colleges | Rheumatoid factor | Rheumatoid arthritis | Nephrotic syndrome | Non-Hodgkin's lymphomas | Immunosuppressive agents | Clinical trials | Monoclonal antibodies | Kidney diseases | Children & youth | Index Medicus
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8. Full Text Soft tissue tumor with novel NR1D1-MAML1 fusion in a pediatric case
by Komatsu, Masato and Yamamoto, Nobuyuki and Kawamoto, Teruya and Kawakami, Yohei and Hara, Hitomi and Uemura, Suguru and Nishimura, Noriyuki and Akisue, Toshihiro and Kuroda, Ryosuke and Lijima, Kazumoto and Limbo, Naoe and Kanzawa, Maki and Kajimoto, Kazuyoshi and Itoh, Tomoo and Hirose, Takanori
Virchows Archiv : an international journal of pathology, ISSN 0945-6317, 12/2020, Volume 477, Issue 6, pp. 891 - 895
Life Sciences & Biomedicine | Pathology | Science & Technology | Nuclear Receptor Subfamily 1, Group D, Member 1 - genetics | Humans | Male | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Myoepithelioma - pathology | Myoepithelioma - genetics | Leg | Oncogene Fusion | Soft Tissue Neoplasms - pathology | Carcinoma - genetics | Carcinoma - pathology | Child | Soft Tissue Neoplasms - genetics | RNA sequencing | Medical colleges | Pediatrics | Keratin | Sarcoma | Children | Nucleotide sequencing | Health aspects | Cancer | DNA sequencing | Translocation | Cytokeratin | Tumor cells | Ribonucleic acid--RNA | Neoplasms | Mimicry | Gene sequencing | Soft tissues | Proteins | Polymerase chain reaction | Gene rearrangement | Growth patterns | Alveoli | Clear cell-type renal cell carcinoma | Tumors | Index Medicus
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9. Full Text Recombinant human thrombomodulin attenuated sepsis severity in a non-surgical preterm mouse model
by Ashina, Mariko and Fujioka, Kazumichi and Nishida, Kosuke and Okubo, Saki and Ikuta, Toshihiko and Shinohara, Masakazu and Iijima, Kazumoto
Scientific reports, ISSN 2045-2322, 01/2020, Volume 10, Issue 1, pp. 333 - 333
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neonates | Sepsis | Inflammation | Immune response | Thrombomodulin | Slurries | Index Medicus
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10. Full Text MPPH syndrome with aortic coarctation and macrosomia due to CCND2 mutations
by Sameshima, Tomohiro and Morisada, Naoya and Egawa, Tsuyoshi and Kugo, Masaaki and Iijima, Kazumoto
Pediatrics international, ISSN 1328-8067, 01/2020, Volume 62, Issue 1, pp. 115 - 117
MPPH syndrome | CCND2 | hydrocephalus | aortic coarctation | postaxial polydactyly | Life Sciences & Biomedicine | Pediatrics | Science & Technology | Aorta | Mutation | Index Medicus
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