Hasegawa T | Department Of Paediatrics Keio University School Of Medicine

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概要

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著作論文

67 THE ROLE OF KAL1 GENE AND KAL2 GENE (FGFR1) IN KALLMANN SYNDROME : MUTATION ANALYSIS AND CLINICAL ASSESSMENT IN 35 PATIENTS WITH KALLMANN SYNDROME
77 PTPN11 GENE AND NOONAN/LEOPARD SYNDROME, MUTATIONS ANALYSIS AND COMPARISIONS OF THE CLINlCAL FEATURES OF 45 JAPANESE PATIENTS
49 THE CROSS-SECTIONAL BMI GROWTH CURVES FOR JAPANESE FROM BIRTH TO 17 YEARS OF AGE : THE 2000-2001 NATIONAL SURVEY DATA : the comparison with the 1990-1994 data and the 1978-1981 data
37 WIDE PHENOTYPIC SPECTRUM OF GATA3 HAPLOINSUFFICIENCY : ANALYSIS OF 11 JAPANESE FAMILIES
29 TURNER SYNDROME AND XP DELETIONS : CLINICAL AND MOLECULAR STUDIES IN 47 PATIENTS
68 Four cases of Kallmann syndrome with FGFR1 mutations
33 LONG-TERM PROGNOSIS IN ADULT MALES WITH CLASSICAL 21-HYDROXYLASE DEFICIENCY
97 A FEMALE INFANT WITH 21-HYDROXYLASE DEFICIENCY WHO HAD THE VAGINAL ENLARGEMENT
94 MEASUREMENTS OF SERUM 17-HYDROXYPROGESTERONE IN NEWBORN INFANTS BY STABLE ISOTOPE DILUTION / GAS CHROMATOGRAPHY-MASS SPECTROMETRY
111 EFFECTS OF LONG-TERM TESTOSTERONE THERAPY ON BONE MINERAL DENSITY IN MALE WITH HYPOGONADOTROPIC HYPOGONADISM
36 CONGENITAL ADRENAL HYPOPLASIA AND MENTAL RETARDATION : IMPORTNACE OF THE IL1RAPL GENE ANALYSIS
30 SHOX NULLIZYGOSITY AND HAPLOINSUFFICIENCY IN A JAPANESE FAMILY : IMPLICATION FOR THE DEVELOPMENT OF TURNER SKELETAL FEATURES.
66 URINE 5β/5α-REDUCED STEROID RATIO : INFLUENCE OF MUTAIONS AND POLYMORPHISM OF THE STEROID 5α REDUCTASE-2 GENE
155 SHOX HAPLOINSUFFICIENCY AND NORMAL OVARIAN FUNCTION VS. SHOX OVERDOSAGE AND GONADAL ESTROGEN DEFICIENCY : LONGITUDINALAUXOLOGICAL STUDY

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