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1. 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 RCRNS Study Grp and Rituximab for Childhood-onset Refractory Nephrotic Syndrome (RCRNS) Study Group
Lancet, The, ISSN 0140-6736, 2014, Volume 384, Issue 9950, pp. 1273 - 1281
Summary Background Rituximab could be an effective treatment for childhood-onset, complicated, frequently relapsing nephrotic syndrome (FRNS) and... 
Internal Medicine | B-CELLS | MEDICINE, GENERAL & INTERNAL | THERAPY | FOLLOW-UP | SAFE | CYCLOSPORINE | CHILDREN | 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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2. Investigator-initiated clinical trials of rituximab for complicated frequently-relapsing or steroid-dependent nephrotic syndrome in children
by Iijima, Kazumoto
Japanese Journal of Nephrology, ISSN 0385-2385, 2016, Volume 58, Issue 8, pp. 1267 - 1270
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3. Full Text Recent Advances in Genetic Aspects and Treatments for Steroid-Sensitive Nephrotic Syndrome in Children
by Iijima, Kazumoto and Nozu, Kandai
Current Pediatrics Reports, ISSN 2167-4841, 12/2018, Volume 6, Issue 4, pp. 291 - 296
This article reviews recent advances in genetic aspects and treatments for steroid-sensitive nephrotic syndrome (SSNS) in children over the previous... 
Rituximab | Pediatrics | Children | Medicine & Public Health | HLA | Idiopathic nephrotic syndrome
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4. Rituximab for the treatment of nephrotic syndrome
by Iijima, Kazumoto
Japanese Journal of Nephrology, ISSN 0385-2385, 2014, Volume 56, Issue 4, pp. 471 - 477
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5. Full Text Rituximab for childhood refractory nephrotic syndrome
: Rituximab for nephrotic syndrome
by Iijima, Kazumoto
Pediatrics International, ISSN 1328-8067, 10/2011, Volume 53, Issue 5, pp. 617 - 621
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6. Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: An investigator initiated, multicenter, double-blind, randomized, placebo-controlled trial
by Iijima, Kazumoto
Japanese Pharmacology and Therapeutics, ISSN 0386-3603, 2014, Volume 42, pp. s82 - s84
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7. Full Text Hepatitis B vaccine: Immunogenicity in an extremely low‐birthweight infant
by Yamana, Keiji and Iwatani, Sota and Fujioka, Kazumichi and Iijima, Kazumoto and Morioka, Ichiro
Pediatrics International, ISSN 1328-8067, 05/2018, Volume 60, Issue 5, pp. 489 - 490
mother‐to‐child infection | extremely low‐birthweight infant | hepatitis B vaccine | hepatitis B virus | immunogenicity | mother-to-child infection | extremely low-birthweight infant | IMMUNIZATION | PEDIATRICS | Immunogenicity, Vaccine | Infant, Extremely Low Birth Weight - immunology | Humans | Immunization Schedule | Infant | Male | Hepatitis B Vaccines - immunology | Hepatitis B - prevention & control | Infectious Disease Transmission, Vertical - prevention & control | Infant, Newborn | Hepatitis B - transmission | Hepatitis B vaccine | Health aspects | Hepatitis B | Hepatitis | Birth weight | Hepatitis B virus | Immunogenicity | Index Medicus
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8. Full Text Loss of Surfacten® during bolus administration with a feeding catheter
by Fujioka, Kazumichi and Kuroda, Jumpei and Yamana, Keiji and Iijima, Kazumoto and Morioka, Ichiro
Pediatrics International, ISSN 1328-8067, 11/2017, Volume 59, Issue 11, pp. 1174 - 1177
BackgroundSurfactant replacement therapy is widely used for treating neonatal respiratory distress syndrome, but insufficient evidence is available on the use... 
intratracheal | intubation | instrumentation | equipment design | surfactant | CONTROLLED-TRIAL | INFANTS | PEDIATRICS | SURFACTANT REPLACEMENT THERAPY | RESPIRATORY-DISTRESS-SYNDROME | Acute respiratory distress syndrome | Neonates | Flushing | Syringes | Respiratory distress syndrome | Medical instruments | Weight loss | Tubes | Surfactants | Variance analysis | Catheters | Feeding | Index Medicus
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9. Full Text Acute kidney injury in type 3 Bartter syndrome: Angiotensin‐converting enzyme inhibitors as a cause
by Nagao, Ryuhei and Suzuki, Shinzi and Kawashima, Hisashi and Nozu, Kandai and Iijima, Kazumoto
Pediatrics International, ISSN 1328-8067, 12/2016, Volume 58, Issue 12, pp. 1373 - 1374
Bartter syndrome | acute kidney injury | angiotensin‐converting enzyme inhibitor | genetic test | infant | angiotensin-converting enzyme inhibitor | PEDIATRICS | ACE inhibitors | Angiotensin | Enzyme inhibitors
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10. Full Text Rituximab for patients with nephrotic syndrome – Authors' reply
by Iijima, Kazumoto and Sako, Mayumi and Nozu, Kandai and Nakamura, Hidefumi and Ito, Shuichi
Lancet, The, ISSN 0140-6736, 2015, Volume 385, Issue 9964, pp. 226 - 227
  Mandy Keijzer-Veen and colleagues reported no difference in relapse rates between the two treatment groups of rituximab and conventional immunosuppressive... 
Internal Medicine | Glucocorticoids - therapeutic use | Humans | Immunosuppressive Agents - therapeutic use | Female | Male | Nephrotic Syndrome - drug therapy | Antibodies, Monoclonal, Murine-Derived - therapeutic use | Care and treatment | Kidney diseases | Drug therapy | Rodents | Pharmaceuticals | Index Medicus | Abridged Index Medicus
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11. Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome
by Matsunoshita, Natsuki and Nozu, Kandai and Yoshikane, Masahide and Kawaguchi, Azusa and Fujita, Naoya and Morisada, Naoya and Ishimori, Shingo and Yamamura, Tomohiko and Minamikawa, Shogo and Horinouchi, Tomoko and Nakanishi, Keita and Fujimura, Junya and Ninchoji, Takeshi and Morioka, Ichiro and Nagase, Hiroaki and Taniguchi-Ikeda, Mariko and Kaito, Hiroshi and Iijima, Kazumoto
Journal of Human Genetics, ISSN 1434-5161, 07/2018, Volume 63, Issue 8, pp. 887 - 892
Pseudo-Bartter/Gitelman syndrome (p-BS/GS) encompasses a clinically heterogeneous group of inherited or acquired disorders similar to Bartter syndrome (BS) or... 
DIFFERENTIAL-DIAGNOSIS | PANEL | CHANNEL | GENE | GENETICS & HEREDITY | COTRANSPORTER | SALT-LOSING TUBULOPATHIES | HYPOKALEMIC ALKALOSIS | MUTATIONS | Diagnosis, Differential | Diarrhea - congenital | Humans | Bartter Syndrome - diagnosis | Infant | Male | Metabolism, Inborn Errors - genetics | Sequence Analysis, DNA | Diarrhea - diagnosis | Metabolism, Inborn Errors - diagnosis | Bartter Syndrome - genetics | Diarrhea - genetics | Base Sequence | Gitelman Syndrome - diagnosis | Female | Gitelman Syndrome - genetics | Child
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12. Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: A comparison with Caucasian cases
by Bo, Ryosuke and Yamada, Kenji and Kobayashi, Hironori and Jamiyan, Purevsuren and Hasegawa, Yuki and Taketani, Takeshi and Fukuda, Seiji and Hata, Ikue and Niida, Yo and Shigematsu, Yosuke and Iijima, Kazumoto and Yamaguchi, Seiji
Journal of Human Genetics, ISSN 1434-5161, 09/2017, Volume 62, Issue 9, pp. 809 - 814
Mitochondrial trifunctional protein (TFP) deficiency is an inherited metabolic disorder of mitochondrial fatty-acid oxidation. Isolated long-chain... 
ALPHA-SUBUNIT | MITOCHONDRIAL TRIFUNCTIONAL PROTEIN | GENETICS & HEREDITY | FOLLOW-UP | BETA-SUBUNIT MUTATIONS | ACID OXIDATION DISORDERS | ENZYME COMPLEX | HADHB GENE | BEZAFIBRATE | 3-HYDROXYACYL-COA DEHYDROGENASE-DEFICIENCY | LONG-CHAIN 3-HYDROXYACYL-COENZYME | Mitochondrial Trifunctional Protein, beta Subunit - genetics | Genetic Testing | Lipid Metabolism, Inborn Errors - genetics | Mitochondrial Trifunctional Protein, alpha Subunit - genetics | Humans | Asian Continental Ancestry Group - genetics | Mitochondrial Trifunctional Protein, beta Subunit - metabolism | Child, Preschool | Infant | Male | Nervous System Diseases - genetics | Nervous System Diseases - diagnosis | Cardiomyopathies - genetics | Rhabdomyolysis - diagnosis | Cardiomyopathies - diagnosis | Female | Mitochondrial Myopathies - diagnosis | Child | Infant, Newborn | Mitochondrial Trifunctional Protein - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genetic Association Studies | Lipid Metabolism, Inborn Errors - diagnosis | Genotype | Mitochondrial Myopathies - genetics | Mitochondrial Trifunctional Protein, alpha Subunit - metabolism | Rhabdomyolysis - genetics | Adolescent | Family | Enzyme Activation | Mutation | Mitochondrial Trifunctional Protein - deficiency
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13. Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes
by Yamamura, Tomohiko and Nozu, Kandai and Ueda, Hiroaki and Fujimaru, Rika and Hisatomi, Ryutaro and Yoshida, Yoko and Kato, Hideki and Nangaku, Masaomi and Miyata, Toshiyuki and Sawai, Toshihiro and Minamikawa, Shogo and Kaito, Hiroshi and Matsuo, Masafumi and Iijima, Kazumoto
Journal of Human Genetics, ISSN 1434-5161, 06/2018, Volume 63, Issue 6, pp. 755 - 759
Pathogenic variants in specific complement-related genes lead to atypical hemolytic uremic syndrome (aHUS). Some reports have indicated that patients with... 
Introns | Humans | RNA, Messenger - genetics | Infant | Male | Hemolytic-Uremic Syndrome - genetics | Phenotype | RNA Splicing | Age of Onset | Polymerase Chain Reaction | Membrane Cofactor Protein - genetics | Mutation | Complement C3 - genetics
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14. Full Text A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment
by Yoshikawa, Norishige and Nakanishi, Koichi and Sako, Mayumi and Oba, Mari S and Mori, Rintaro and Ota, Erika and Ishikura, Kenji and Hataya, Hiroshi and Honda, Masataka and Ito, Shuichi and Shima, Yuko and Kaito, Hiroshi and Nozu, Kandai and Nakamura, Hidefumi and Igarashi, Takashi and Ohashi, Yasuo and Iijima, Kazumoto and Japanese Study Grp Kidney Dis Chil and Japanese Study Group of Kidney Disease in Children
Kidney International, ISSN 0085-2538, 01/2015, Volume 87, Issue 1, pp. 225 - 232
In this multicenter, open-label, randomized controlled trial, we determined whether 2-month prednisolone therapy for steroid-sensitive nephrotic syndrome was... 
initial treatment | nephrotic syndrome | pediatric nephrology | randomized controlled trial | steroid | Initial treatment | THERAPY | MANAGEMENT | EPISODE | DISEASE | UROLOGY & NEPHROLOGY | CHILDREN | LONG | Recurrence | Glucocorticoids - administration & dosage | Prednisolone - administration & dosage | Humans | Adolescent | Child, Preschool | Female | Infant | Male | Nephrotic Syndrome - drug therapy | Child | Index Medicus | Clinical Trial
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15. Full Text Neonatal vitamin K deficiency in the son of a mother with short bowel syndrome
by Ashina, Mariko and Fujioka, Kazumichi and Nishida, Kosuke and Iijima, Kazumoto
Pediatrics International, ISSN 1328-8067, 10/2018, Volume 60, Issue 10, pp. 991 - 992
protein induced by vitamin K absence or antagonist | maternal malnutrition | neonate | short bowel syndrome | vitamin K deficiency bleeding | protein induced by vitamin K absence or antagonist-II | PROPHYLAXIS | PEDIATRICS | INTRACRANIAL HEMORRHAGE | Vitamin K 2 - therapeutic use | Vitamin K Deficiency Bleeding - drug therapy | Humans | Vitamin K Deficiency Bleeding - etiology | Male | Mothers | Short Bowel Syndrome - complications | Young Adult | Vitamin K 2 - analogs & derivatives | Blood Coagulation Tests - methods | Female | Hemostatics - therapeutic use | Hirschsprung Disease - surgery | Colectomy - adverse effects | Infant, Newborn | Vitamin K Deficiency Bleeding - diagnosis | Infants (Newborn) | Vitamin K deficiency | Malabsorption syndromes | Vitamins | Neonates | Nutrient deficiency | Short bowel syndrome | Intestine | Vitamin K | Index Medicus
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16. Full Text Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome
by Okamoto, Takayuki and Nozu, Kandai and Iijima, Kazumoto and Ariga, Tadashi
Journal of Nephrology, ISSN 1121-8428, 2/2019, Volume 32, Issue 1, pp. 155 - 159
Approximately 80% of patients with Alport syndrome have X-linked Alport syndrome (XLAS), which is caused by mutations in the type IV collagen alpha 5 gene... 
Germline mosaicism | Nephrology | Genetic counseling | Medicine & Public Health | Isolated | Urology | XLAS
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17. Full Text Incidence and Neonatal Risk factors of Short Stature and Growth Hormone treatment in Japanese Preterm Infants Born Small for Gestational Age
by Matsumoto, M and Nagano, N and Awanol, H and Ohyamal, S and Fujioka, K and Iwatani, S and Urakami, T and Iijima, K and Morioka, I
SCIENTIFIC REPORTS, ISSN 2045-2322, 08/2019, Volume 9, Issue 1, pp. 1 - 7
Incidence and neonatal risk factors for short stature in preterm children born small for gestational age (SGA) have not been fully investigated in Japan. In... 
STATEMENT | RETARDATION | MANAGEMENT | FINAL HEIGHT | MULTIDISCIPLINARY SCIENCES | BINDING PROTEIN-3 | BIRTH | CHILDREN | Neonates | Newborn babies | Lung diseases | Growth hormones | Birth weight | Infants | Children | Growth hormone | Physical growth | Risk factors | Age | Gestational age | Index Medicus
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18. Clinically diverse phenotypes and genotypes of patients with branchio-oto-renal syndrome
by Unzaki, Ai and Morisada, Naoya and Nozu, Kandai and Ye, Ming Juan and Ito, Shuichi and Matsunaga, Tatsuo and Ishikura, Kenji and Ina, Shihomi and Nagatani, Koji and Okamoto, Takayuki and Inaba, Yuji and Ito, Naoko and Igarashi, Toru and Kanda, Shoichiro and Ito, Ken and Omune, Kohei and Iwaki, Takuma and Ueno, Kazuyuki and Yahata, Mayumi and Ohtsuka, Yasufumi and Nishi, Eriko and Takahashi, Nobuya and Ishikawa, Tomoaki and Goto, Shunsuke and Okamoto, Nobuhiko and Iijima, Kazumoto
Journal of Human Genetics, ISSN 1434-5161, 05/2018, Volume 63, Issue 5, pp. 647 - 656
Branchio-oto-renal (BOR) syndrome is a rare autosomal dominant disorder characterized by branchiogenic anomalies, hearing loss, and renal anomalies. The aim of... 
BOR SYNDROME | SALL1 | EYA1 | SIX2 | GENES | GENETICS & HEREDITY | KIDNEY DEVELOPMENT | MUTATIONS
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19. Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis
by Nozu, Kandai and Minamikawa, Shogo and Yamada, Shiro and Oka, Masafumi and Yanagita, Motoko and Morisada, Naoya and Fujinaga, Shuichiro and Nagano, China and Gotoh, Yoshimitsu and Takahashi, Eihiko and Morishita, Takahiro and Yamamura, Tomohiko and Ninchoji, Takeshi and Kaito, Hiroshi and Morioka, Ichiro and Nakanishi, Koichi and Vorechovsky, Igor and Iijima, Kazumoto
Journal of Human Genetics, ISSN 1434-5161, 07/2017, Volume 62, Issue 7, pp. 733 - 735
Alport syndrome-diffuse leiomyomatosis (AS-DL, OMIM: 308940) is a rare variant of the X-linked Alport syndrome that shows overgrowth of visceral smooth muscles... 
GENETICS & HEREDITY | Leiomyomatosis - complications | Nephritis, Hereditary - complications | Base Sequence | Gene Deletion | Humans | Collagen Type IV - genetics | Nephritis, Hereditary - genetics | Leiomyomatosis - genetics
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20. Cryptic exon activation in SLC12A3 in Gitelman syndrome
by Nozu, Kandai and Nozu, Yoshimi and Nakanishi, Keita and Konomoto, Takao and Horinouchi, Tomoko and Shono, Akemi and Morisada, Naoya and Minamikawa, Shogo and Yamamura, Tomohiko and Fujimura, Junya and Nakanishi, Koichi and Ninchoji, Takeshi and Kaito, Hiroshi and Morioka, Ichiro and Taniguchi-Ikeda, Mariko and Vorechovsky, Igor and Iijima, Kazumoto
Journal of Human Genetics, ISSN 1434-5161, 02/2017, Volume 62, Issue 2, pp. 335 - 337
Gitelman syndrome (GS) is an autosomal recessive renal tubulopathy characterized by hypokalemic metabolic alkalosis with hypocalciuria and hypomagnesemia. GS... 
NA-CL COTRANSPORTER | DIAGNOSIS | MUTATIONS | GENE | GENETICS & HEREDITY | Gitelman Syndrome - pathology | Kidney Tubules, Distal - pathology | Introns - genetics | Humans | Child, Preschool | Exons - genetics | Mutation - genetics | Sequence Analysis, DNA | Base Sequence | Solute Carrier Family 12, Member 3 - genetics | Gitelman Syndrome - diagnosis | Female | Gitelman Syndrome - genetics | High-Throughput Nucleotide Sequencing | Solute Carrier Family 12, Member 3 - metabolism
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