Tokyo Metropolitan Kiyose Children's Hospital

Recent papers from Tokyo Metropolitan Kiyose Children's Hospital

1. Relationship between plasma insulin concentration and plasma remnant lipoprotein response to an oral fat load in patients with type 2 diabetesJournal of the American College of Cardiology · 2001
2. SCN2A-related neonatal-onset epilepsy responding significantly to lidocaine and lacosamide: A case reportBrain and Development Case Reports · 2026
3. Factors Affecting Quality of Life Among Independent Community-Dwelling Senior Citizens in Sri Lanka: A Narrative StudyAsian Journal of Social Science Studies · 2019
4. Hypomorphic mutations of TRIP11 cause odontochondrodysplasiaJCI Insight · 2019
5. Neural tube defects: Risk factors and preventive measuresCongenital Anomalies · 2017
6. A tumor lysate is an effective vaccine antigen for the stimulation of CD4⁺T-cell function and subsequent induction of antitumor immunity mediated by CD8⁺T cellsCancer Biology & Therapy · 2015
7. Combination of pulse methylprednisolone infusions with cyclosporine‐based immunosuppression is safe and effective to treat recurrent focal segmental glomerulosclerosis after pediatric kidney transplantationClinical Transplantation · 2013
8. Whole‐exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D‐2‐hydroxyglutaric aciduria (MC‐HGA)American Journal of Medical Genetics Part A · 2011
9. Predicting response to immunosuppressive therapy in childhood aplastic anemiaHaematologica · 2011
10. A Backflip Flap: A New Surgical Correction for Severe Cicatricial EntropionPlastic & Reconstructive Surgery · 2010
11. Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia familyJournal of Medical Genetics · 2010
12. A dominant mesomelic dysplasia associated with a 1.0-Mb microduplication of HOXD gene cluster at 2q31.1Journal of Medical Genetics · 2010
13. Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndromeHuman Mutation · 2010
14. A new Ehlers–Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility‐related manifestationsAmerican Journal of Medical Genetics Part A · 2010
15. Spondylo‐epiphyseal dysplasia, Maroteaux type (pseudo‐Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutationsAmerican Journal of Medical Genetics Part A · 2010
16. A variant of Desbuquois dysplasia characterized by advanced carpal bone age, short metacarpals, and elongated phalanges: Report of seven casesAmerican Journal of Medical Genetics Part A · 2010
17. Urinary Neutrophil-Gelatinase Associated Lipocalin is a Potential Noninvasive Marker for Renal Scarring in Patients With Vesicoureteral RefluxThe Journal of Urology · 2010
18. Effect of anakinra on arthropathy in CINCA/NOMID syndromePediatric Rheumatology · 2010
19. Bifid epiglottis: Syndromic constituent rather than isolated anomalyPediatrics International · 2010
20. Persistent Eosinophilic Infiltration of the Myocardium in a Child in Complete Remission of Acute Lymphoblastic Leukemia and Eosinophilia. Potential Role in Late Cardiac Disease?The Keio Journal of Medicine · 2010