707 results on '"Ihara, Kenji"'
Search Results
2. Cardiac manifestations of human ACTA2 variants recapitulated in a zebrafish model
3. Characteristic phenotypes of ADH5/ALDH2 deficiency during childhood
4. Long-term trends of pediatric type 1 diabetes incidence in Japan before and after the COVID-19 pandemic
5. Diabetic lipemia as a predisposing state to acute pancreatitis: a case report and literature review
6. Behavioral and neurotransmitter changes on antiepileptic drugs treatment in the zebrafish pentylenetetrazol-induced seizure model
7. Early infantile spontaneous movement in very low birthweight infants is associated with sensory characteristics at the corrected age of 3 years
8. Clinical characteristics of preterm and term infants with Ureaplasma in gastric fluid
9. Abnormal bone marrow T1-weighted MRI images in a pediatric patient with acute lymphoblastic leukemia without peripheral blasts
10. Intrauterine twin environment and genetic factors subliminally affecting general movements in preterm infants
11. Rituximab-induced serum sickness in a girl with nephrotic syndrome
12. Dried blood spot-based newborn screening for bile acid synthesis disorders, Zellweger spectrum disorder, and Niemann-Pick type C1 by detection of bile acid metabolites
13. Myocarditis in 13-Year-Old Monochorionic Diamniotic Twins After COVID-19 Vaccination
14. Asymptomatic 3-methylglutaconic aciduria type 1 detected by high C5-OH on newborn screening
15. Early defibrotide therapy and risk factors for post‐transplant veno‐occlusive disease/sinusoidal obstruction syndrome in childhood.
16. Topoisomerase IIβ immunoreactivity (IR) co-localizes with neuronal marker-IR but not glial fibrillary acidic protein-IR in GLI3-positive medulloblastomas: an immunohistochemical analysis of 124 medulloblastomas from the Japan Children’s Cancer Group
17. Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period
18. Safe management of acute respiratory failure by mediastinal lymphoma: Transient endotracheal stent placement with short-term extracorporeal membrane oxygenation
19. A pH imbalance is linked to autophagic dysregulation of inner ear hair cells in Atp6v1ba-deficient zebrafish
20. Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafish
21. A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscess
22. The association between brain morphological development and the quality of general movements
23. Infantile Hypothalamic Hamartoma: A Rare Presentation of Isolated Obesity.
24. Auto-immune disorders in a child with PIK3CD variant and 22q13 deletion
25. A case of CHARGE syndrome associated with hyperinsulinemic hypoglycemia in infancy
26. Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
27. Predicting Long-Term Ventricular Arrhythmia Risk in Children with Acute Lymphoblastic Leukemia Using Normal Values of Ventricular Repolarization Markers Established from Japanese Cohort Study
28. A severe pulmonary complication in a patient with COL4A1-related disorder: A case report
29. Gastric Carcinoma as Second Malignant Neoplasm in a Survivor From High-risk Neuroblastoma
30. A case of septo-optic dysplasia with hereditary hemorrhagic telangiectasia: a previously unrecognized combination of malformations
31. Identification of Mutations in the c-mpl Gene in Congenital Amegakaryocytic Thrombocytopenia
32. Comparison of physician- and self-assessed pubertal onset in Japanese children
33. The clinical characteristics of Asian patients with classical-type Hutchinson–Gilford progeria syndrome
34. Cardiac manifestations of human ACTA2variants recapitulated in a zebrafish model
35. Serum Amino Acid Profiling in Citrin-Deficient Children Exhibiting Normal Liver Function During the Apparently Healthy Period
36. Therapeutic potential of hepatocyte-like-cells converted from stem cells from human exfoliated deciduous teeth in fulminant Wilson’s disease
37. Celiac Disease Genetics, Pathogenesis, and Standard Therapy for Japanese Patients
38. Multifaceted support for quality of life in childhood cancer survivors: Questionnaire survey
39. Kawasaki disease complicated with posterior reversible encephalopathy syndrome
40. A Seven-Year-Old Girl With Dysphagia Due to Fear of Swallowing: A Favorable Outcome With Cognitive Behavioral Therapy Using an Anxiety Hierarchy Chart
41. An Algorithm for the Detection of General Movements of Preterm Infants Based on the Instantaneous Heart Rate
42. Acute myeloid leukemia associated with CHARGE syndrome
43. Pancreatoblastoma with a novel fusion gene of IQSEC1‐RAF1
44. Secular Trends in Obesity and Serum Lipid Values among Children in Oita City, Japan, during a 27-Year Period
45. Long-term trends of pediatric type 1 diabetes incidence in Japan: before and during the COVID- 19 pandemic years (1999–2021)
46. Sensorineural Hearing Loss in Sjögren’s Syndrome
47. Comprehensive screening for monogenic diabetes in 89 Japanese children with insulin‐requiring antibody‐negative type 1 diabetes
48. De novo missense mutations in NALCN cause developmental and intellectual impairment with hypotonia
49. Coagulopathy by vitamin K deficiency: Clinical pitfall in a case with cerebral palsy under long-term enteral nutrition
50. X-linked mental retardation and severe short stature with a novel mutation of the KDM5C gene
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