91 results on '"Ida, Shinobu"'
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2. Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study-
3. 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
4. Very young children with Prader-Willi syndrome are refractory to growth hormone-associated decreases in free thyroxine levels
5. Evaluations for Wilms Tumor and Late‐onset Nephrotic Syndrome in 46, XY DSD
6. Subcutaneous adipose tissue is a positive predictor for bone mineral density in prepubertal children with Prader–Willi syndrome independent of lean mass
7. Dosage of hydrocortisone during late infancy is positively associated with changes in body mass index during early childhood in patients with 21-hydroxylase deficiency
8. 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
9. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)
10. Circulating insulin‐like growth factor 1 levels are reduced in very young children with Prader–Willi syndrome independent of anthropometric parameters and nutritional status
11. Psychological Changes and Adaptation: Primary Amenorrhea Associated with Disorders of Sex Development
12. Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan
13. Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype
14. Development of an efficient one-step real-time reverse transcription polymerase chain reaction method for severe acute respiratory syndrome-coronavirus-2 detection
15. Renal function in short‐statured children born small for gestational age and treated with growth hormone
16. Male assignment in 5α‐reductase type 2 deficiency with female external genitalia
17. Growth hormone treatment for extremely low birthweight children born small for gestational age
18. Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists
19. Central hypothyroidism improves with age in very young children with Prader‐Willi syndrome
20. Fat distribution in short‐stature children born small for gestational age
21. Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited
22. A Multicenter Prospective Survey on Early-Onset Inflammatory Bowel Disease in Japan
23. MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene
24. Policy statement of enteral nutrition for preterm and very low birthweight infants
25. Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis
26. Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan
27. Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial
28. Present status of prophylactic thyroidectomy in pediatric multiple endocrine neoplasia 2: a nationwide survey in Japan 1997–2017
29. Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome
30. Gonadal function and testicular histology in males with Prader-Willi syndrome
31. Shwachman-Diamond syndrome: Nationwide survey and systematic review in Japan
32. Vitamin B1 Deficiency Related to Excessive Soft Drink Consumption in Japan
33. Three patients with Schaaf-Yang syndrome exhibiting arthrogryposis and endocrinological abnormalities
34. Visceral adipose tissue increases shortly after the cessation of GH therapy in adults with Prader-Willi syndrome
35. Thyroid hormone status in patients with severe selenium deficiency
36. Endoscopic findings of esophagogastric junction in children
37. Pediatric‐onset Chronic Nonspecific Multiple Ulcers of Small Intestine
38. Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature
39. Endocrine status of patients with septo-optic dysplasia: fourteen Japanese cases
40. Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia
41. Pathological examination of the placenta in small for gestational age (SGA) children with or without postnatal catch-up growth
42. Mo1197 Mitochondrial Respiratory Chain Complex Disorders Associated With NAFLD in Childhood Cancer Survivors
43. Negative feedback loop of cholesterol regulation is impaired in the livers of patients with Alagille syndrome
44. Pediatric chronic intestinal pseudo-obstruction is a rare, serious, and intractable disease: A report of a nationwide survey in Japan
45. Selenium deficiency in children and adolescents nourished by parenteral nutrition and/or selenium-deficient enteral formula
46. Esophago-gastric motility and nutritional management in a child with ATR-X syndrome
47. Tu1140 Primary Antibiotics Susceptibility and Efficacy of Susceptibility-Guided Triple Therapy for Helicobacter pylori Among Japanese Children in the Last Decade -A Multi-Center Observational Study
48. Tu1132 High Incidence of Selenium Deficiency in Children With Gastrointestinal or Neurological Dysfunction Treated With Parenteral Nutrition and/or Enteral Medical Nutritional Products
49. Endocrinological Characteristics of 25 Japanese Patients with CHARGE Syndrome
50. Tumors of Bilateral Streak Gonads in Patients with Disorders of Sex Development Containing Y Chromosome Material
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