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Lancet, The, ISSN 0140-6736, 2014, Volume 384, Issue 9950, pp. 1273 - 1281
Journal Article
Japanese Journal of Nephrology, ISSN 0385-2385, 2016, Volume 58, Issue 8, pp. 1267 - 1270
Journal Article
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
Journal Article
Japanese Journal of Nephrology, ISSN 0385-2385, 2014, Volume 56, Issue 4, pp. 471 - 477
Journal Article
Pediatrics International, ISSN 1328-8067, 10/2011, Volume 53, Issue 5, pp. 617 - 621
Journal Article
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
Journal Article
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
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 09/2017, Volume 62, Issue 9, pp. 809 - 814
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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