スポンサーリンク
Department of Pediatrics, Nagasaki University School of Medicine | 論文
- A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy
- A case of megalocornea-mental retardation syndrome complicated with bilateral sensorineural hearing impairment
- 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)
- A Four-year-old Girl with Pit-1 Gene Mutation, Extremely Short Stature and Hypoglycemia
- Sinus Pericranii Associated with a Cerebellar Venous Angioma : Case Report
- Magnetic resonance imaging in congenital facial palsy
- Development of Growth Hormone and Adrenocorticotropic Hormone Deficiencies in Patients with Prenatal or Perinatal-Onset Hypothalamic Hypopituitarism Having Invisible or Thin Pituitary Stalk on Magnetic Resonance Imaging
- 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
- Quantitative EEG Analyses and Surgical Outcome After Corpus Callosotomy
- Acute pancreatitis associated with systemic lupus erythematosus: Successful treatment with plasmapheresis followed by aggressive immunosuppressive therapy.
- Clinical usefulness of In-111 chloride and Tc-99m Sn colloid scintigraphy in the diagnosis of intrathoracic extramedullary hematopoiesis
- Glutathione Related Enzyme Activities in Spontaneous Hypertensive Rat Heart
- Ignited Combustion Criterion of a Reaction
- The calming effect of a maternal breast milk odor on the human newborn infant
- Mental Retardation in a Boy with Congenital Adrenal Hypoplasia : A Clue to Contiguous Gene Syndrome Involving DAX1 and IL1RAPL