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Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences | 論文
- Autosomal dominant onychodystrophy and congenital sensorineural deafness
- A severe case of Moebius syndrome with calcification on the fourth ventricular floor
- New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome
- A NAGER ACROFACIAL DYSOSTOSIS SYNDROME PATIENT WITH SEVERE RESPIRATORY DISTRESS SYNDROME (RDS)
- Neuropsychological and MRI Assessment of Young Adults with Hemiplegic Cerebral Palsy
- Epidemiological and clinical studies of West syndrome in Nagasaki
- Developmental Assessment-Based Surgical Intervention for Intractable Epilepsies in Infants and Young Children
- A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia
- Acute pancreatitis associated with systemic lupus erythematosus: Successful treatment with plasmapheresis followed by aggressive immunosuppressive therapy.
- Maternal Uniparental Disomy for Chromosome 14 with Diabetes Mellitus
- The calming effect of a maternal breast milk odor on the human newborn infant
- Severe subaortic stenosis that progressed over a 12-year period after cardiac surgery
- Case with Small Testes Associated with Skeletal Dysplasia
- PROP1 Abnormality
- Detection of cytomegalovirus in preserved umbilical cord from a boy with autistic disorder
- 長崎県妊婦におけるサイトメガロウイルス感染の血清疫学的調査
- 168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
- Miller syndrome with novel dihydroorotate dehydrogenase gene mutations
- 40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1
- 53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY