314 results on '"Etani, Yuri"'
Search Results
2. A case of early-onset idiopathic chronic pancreatitis associated with a loss-of-function TRPV6 p.R483Q variant successfully treated by pancreatic duct stenting
3. Utility of a rapid assay for prostaglandin E-major urinary metabolite as a biomarker in pediatric ulcerative colitis
4. Association between adeno-associated virus 2 and severe acute hepatitis of unknown etiology in Japanese children
5. Final Analysis of COVID-19 Patients With Inflammatory Bowel Disease in Japan (J-COSMOS): A Multicenter Registry Cohort Study
6. Serum Zinc and Selenium in Children with Inflammatory Bowel Disease: A Multicenter Study in Japan
7. Genotype-Phenotype Correlations in Thirty Japanese Patients with Congenital Hypothyroidism Attributable to TG Defects
8. Genotype–Phenotype Correlations in 30 Japanese Patients With Congenital Hypothyroidism Attributable to TGDefects
9. Constitutional mismatch repair deficiency in childhood colorectal cancer harboring a de novo variant in the MSH6 gene: a case report
10. Antibodies to Crohn’s disease peptide 353 as a diagnostic marker for pediatric Crohn’s disease: a prospective multicenter study in Japan
11. Final analysis of COVID-19 patients with inflammatory bowel disease in Japan (J-COSMOS): a multicenter registry cohort study
12. Comprehensive Targeted Sequencing Identifies Monogenic Disorders in Patients With Early-onset Refractory Diarrhea
13. MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene
14. Serum leucine‐rich alpha‐2 glycoprotein and calprotectin in children with inflammatory bowel disease: a multicenter study in Japan
15. Utility of a rapid assay for Prostaglandin E-major urinary metabolite as a biomarker in pediatric ulcerative colitis
16. Reductions in estimated glomerular filtration rate during puberty in growth hormone-treated children born small for gestational age are associated with prematurity and low birthweight, not the dosage of growth hormone treatment
17. Very young children with Prader-Willi syndrome are refractory to growth hormone-associated decreases in free thyroxine levels
18. Clinical characteristics of seizures associated with viral gastroenteritis in children
19. Evaluations for Wilms Tumor and Late‐onset Nephrotic Syndrome in 46, XY DSD
20. Case of hypereosinophilic syndrome with gastrointestinal involvement showing tissue eosinophil cytolysis
21. Anti–Integrin αvβ6 Antibody as a Diagnostic Marker for Pediatric Patients With Ulcerative Colitis
22. Natural history of chronic hepatitis B virus infection in children in Japan: a comparison of mother-to-child transmission with horizontal transmission
23. Selenium deficiency in children and adolescents nourished by parenteral nutrition and/or selenium-deficient enteral formula
24. Zinc monotherapy for young children with presymptomatic Wilson disease: A multicenter study in Japan
25. Nephrogenic diabetes insipidus caused by a novel missense variant (p.S127Y) in the AVPR2 gene
26. Subcutaneous adipose tissue is a positive predictor for bone mineral density in prepubertal children with Prader–Willi syndrome independent of lean mass
27. Clinical practice guidelines for the management of children with mother‐to‐child transmitted hepatitis C virus infection
28. Dosage of hydrocortisone during late infancy is positively associated with changes in body mass index during early childhood in patients with 21-hydroxylase deficiency
29. Beta-human chorionic gonadotropin-producing neuroblastoma: an unrecognized cause of gonadotropin-independent precocious puberty
30. Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature
31. Circulating insulin‐like growth factor 1 levels are reduced in very young children with Prader–Willi syndrome independent of anthropometric parameters and nutritional status
32. Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype
33. Intussusception Caused by Percutaneous Endoscopic Gastrostomy With Jejunal Extension in Patients With Severe Motor and Intellectual Disabilities
34. Serum Zinc and Selenium in Children with Inflammatory Bowel Disease: A Multicenter Study in Japan
35. Renal function in short‐statured children born small for gestational age and treated with growth hormone
36. Increased type 3 iodothyronine deiodinase activity in a regrown hepatic hemangioma with consumptive hypothyroidism
37. Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter
38. Male assignment in 5α‐reductase type 2 deficiency with female external genitalia
39. Growth hormone treatment for extremely low birthweight children born small for gestational age
40. Graves' disease as an emerging complication of MIRAGE syndrome.
41. Central hypothyroidism improves with age in very young children with Prader‐Willi syndrome
42. Fat distribution in short‐stature children born small for gestational age
43. Diagnostic accuracy of serum proteinase 3 antineutrophil cytoplasmic antibodies in children with ulcerative colitis
44. Interim analysis of a multicenter registry study of COVID-19 patients with inflammatory bowel disease in Japan (J-COSMOS).
45. Circulating insulin‐like growth factor 1 levels are reduced in very young children with Prader–Willi syndrome independent of anthropometric parameters and nutritional status.
46. Efficacy of pegylated interferon-α2a monotherapy in Japanese children with chronic hepatitis C
47. A novel de novo SLC26A3 mutation causing congenital chloride diarrhea in a Japanese neonate
48. Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis
49. A FAVORABLE RESPONSE TO STEROID THERAPY IN A CHILD WITH DRUG-ASSOCIATED ACUTE VANISHING BILE DUCT SYNDROME AND SKIN DISORDER
50. Successful stenting for renal artery stenosis in a patient with Alagille syndrome
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