Fujieda K | Department Of Pediatrics Asahikawa Medical College

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著作論文

A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
34 NOVEL MUTATIONS IN THE CYP11B1 GENE IN JAPANESEPATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 11β-HYDROXYIASE DEFICIENCY
52 STUDIES OF HEPATOCYTE NUCLER FACTER-4α HNF4-α AND HNF-1β GENES IN JUVENILE ONSET DIABETES MELLITUS WITHOUT OBESITY
Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
Postnatal development of brainstem serotonin-containing neurons projecting to lumbar spinal cord in rats
112 METABOLIC SYNDROME IN SURVIVORS OF CHILDHOOD BRAIN TUMORS WITH ENDOCRINE COMPLICATIONS
18 Sporadic haploinsufficiency of the HESX1 gene causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient
117 Molecular analysis of PHEX and FGF23 gene in hypophosphatemic rickets
182 MOLECULAR ANALYSIS OF PAX8 GENE IN JAPANESE PATIENTS WITH CONGENITAL HYPOTHYROIDISM
65 NOVEL MISSENSE MUTATION OF THE GATA3 GENE IN A PATIENT WITH HDR SYNDROME WHO MANIFESTED PRIMARY HYPOGONADISM
141 A CASE OF CARNEY COMPLEX
161 A NOVEL MUTATION IN SOX9 GENE IN A CASE OF CAMPOMELIC DYSPLASIA
53 EFFECTS OF MUTANT ALLELES OF THE FORKHEAD TRANSCRIPTION FACTOR Foxo1 ON REGULATION OF HEPATIC INSULIN ACTION AND PANCREATIC β-CELL FUNCTION
76 Molecular analysis of the PTPN11 gene in Japanese patients with Noonan syndrome

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