29 TURNER SYNDROME AND XP DELETIONS : CLINICAL AND MOLECULAR STUDIES IN 47 PATIENTS
スポンサーリンク
概要
著者
-
Ogata T
Tokyo Ohka Kogyo Co. Ltd. Kanagawa Jpn
-
Horikawa R
National Center for Child Health and Development
-
HASEGAWA T
Keio University
-
ADACHI M
Kanagawa Children's Medical Center
-
TACHIBANA K
Kanagawa Children's Medical Center
-
Sato S
Saitama Metropolitan Hospital
-
Naiki Y
Division Of Endocrinology And Metabolism Adolescent Medicine National Center For Child Health And De
-
Matsuo N
National Center for Child Health and Development
-
Hanew K
Hanew Endocrine Clinic
-
Muroya K
Tokyo Dental College Ichikawa General Hospital
-
Nakagomi Y
Yamanashi University School Of Medicine
-
Shinohara O
Tokai University
-
Ogawa E
Tohoku University
-
Yorifuji T
Kyoto University
-
Minagawa M
Chiba University
-
Igarashi N
Toyama Prefecture Central Hospital
-
Nose O
Nose Clinic
-
Ogawa M
Ogawa Clinic
-
Aikawa T
Aikawa Station Clinic
-
Hasegawa Y
Kiyose Children's Hospital
-
Aizu K
Saitama Children's Medical Center
-
Nishi Y
Hiroshima Red-cross Hospital
-
Horikawa R
Division Of Endocrinology And Metabolism Adolescent Medicine National Center For Child Health And De
-
Ogata T
Department Of Endocrinology And Metabolism National Research Institute For Child Health And Developm
-
Aizu K
Saitama Children's Medical Center
-
Hasegawa T
Department Of Paediatrics Keio University School Of Medicine
-
Tachibana K
Kanagawa Children's Medical Center
-
Ogata T
Tokyo Electric Power Company Hospital
-
Horikawa R
Division Of Adolescent Medicine And Division Of Endocrinology & Metabolism
-
Adachi M
Kanagawa Children's Medical Center
-
Hasegawa Y
Tokyo Metropolitan Kiyose Children's Hospital
-
Matsuo N
Department Of Paediatrics Keio University School Of Medicine
関連論文
- 55 GROWTH RRESPONSE TO GROWTH HORMONE
- 67 THE ROLE OF KAL1 GENE AND KAL2 GENE (FGFR1) IN KALLMANN SYNDROME : MUTATION ANALYSIS AND CLINICAL ASSESSMENT IN 35 PATIENTS WITH KALLMANN SYNDROME
- 64 ADRENO-GENITO-RENAL DISORDER WITH SEVERE GROWTH FAILURE : A NEW DISEASE
- 77 PTPN11 GENE AND NOONAN/LEOPARD SYNDROME, MUTATIONS ANALYSIS AND COMPARISIONS OF THE CLINlCAL FEATURES OF 45 JAPANESE PATIENTS
- 82 MATERNAL UNIPARENTAL ISODISOMY FOR CHROMOSOME 7 IN A CASE WITH SILVER-RUSSELL SYNDROME
- 132 A CASE OF VIRILIZING ADRENOCORTICAL TUMOR
- 152 Dose an anabolic steroid rescue final heights of gonadal suppression therapy?
- 19 GROWTH HORMONE-RELEASING HORMONE (GHRH) RECEPTOR MUTATION THAT ACTS AS A DOMINANT NEGATIVE.
- 11 CAN GH TREATMENT IMPROVE THE FINAL HEIGHT OF CHILDREN WITH NON-GHD SHORT STATURE?
- 39 TWENTY CHILDREN WITH CUSHING SYNDROME (CS) TREATED IN EIGHT MEDICAL CENTRES
- 52 STUDIES OF HEPATOCYTE NUCLER FACTER-4α HNF4-α AND HNF-1β GENES IN JUVENILE ONSET DIABETES MELLITUS WITHOUT OBESITY
- 69 SKEWED X-INACTIVATION PATTERNS IN THREE FEMALE CARRIERS WITH VASOPRESSIN TYPE 2 RECEPTOR GENE MUTATIONS
- 120 Assessment of psychosocial effect on short-stature children and their families with and without growth hormone therapy
- 125 EFFECT OF ANABOLIC STEROID HORMONE ON GROWTH PROMOTION AND GONADAL FUNCTION IN PUBERTAL BOYS
- Investigation of Resist Characteristics of Fluoropolymer for 157nm Lithography
- 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
- 48 TARGET HEIGHT AND TARGET RANGE FOR THE JAPANESE : REVISITED
- 133 THE ORIGIN OF ANDROGEN EXCESS IN JAPANESE GIRLS WITH PREMATURE PUBARCHE IN COMPARISON WITH CENTRAL PRECOCIOUS PUBERTY
- 86 THE AIRE MUTATIONS IN A JAPANESE APECED PATIENT
- 90 MUTATION ANALYSIS IN A JAPANESE KIDRED WITH SPONDYLOEPIPHYSEAL DYSPLASIA TARDA
- 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
- 129 A novel mutation of PROP 1 gene in 2 siblings with multiple pituitary hormone deficiency from Japan
- 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
- 54 Excessive Mid-Growth Spurt (MGS) induced by GH therapy started at early childhood in 3 male siblings with non-endcrine short stature (NESS)
- 63 ARX IS THE CAUSATIVE GENE FOR X-LINKED LISSCENCEPHALY WITH AMBIGUOUS GENITALIA
- 36 CONGENITAL ADRENAL HYPOPLASIA AND MENTAL RETARDATION : IMPORTNACE OF THE IL1RAPL GENE ANALYSIS
- 16 PREVALENCE OF SHOX HAPLOINSUFFICIENCY IN 900 PATIENTS WITH IDIOPATHIC SHORT STATURE
- 30 SHOX NULLIZYGOSITY AND HAPLOINSUFFICIENCY IN A JAPANESE FAMILY : IMPLICATION FOR THE DEVELOPMENT OF TURNER SKELETAL FEATURES.
- 149 QUESTIONNAIRE SURVEY ON AUTOINJECTER Konyjecter(R) Pen, AN AUXIALLY DEVICE FOR GH INJECTION : CAN KONYJECTER(R)PEN BE A PAIN RELIEVING TOOL?
- 148 PREVALENCE OF DIABETIC NEPHROPATHY IN CHILDHOOD ONSET TYPE1 DIABETES OVER THE AGE OF TWENTY
- 4 CUSHING SYNDROME IN CHILDHOOD : ETIOLOGY, DIAGNOSIS AND TREATMENT
- 66 URINE 5β/5α-REDUCED STEROID RATIO : INFLUENCE OF MUTAIONS AND POLYMORPHISM OF THE STEROID 5α REDUCTASE-2 GENE
- 158 TRANSDERMAL DIHYDROTESTOSTERONE TREATMENT FOR THREE PATIENTS WITH STEROID 5α REDUCTASE-2 DEFICIENCY
- 155 SHOX HAPLOINSUFFICIENCY AND NORMAL OVARIAN FUNCTION VS. SHOX OVERDOSAGE AND GONADAL ESTROGEN DEFICIENCY : LONGITUDINALAUXOLOGICAL STUDY
- 106 CLlNICAL DEFINITION OF POLYCYSTIC OVARY SYNDROME(PCOS) IN ADOLESCENCE
- 51 A STUDY ON INSULIN DOSE IN ITT AS A GROWTH HORMONE PROVOCATIVE TEST
- 137 TWO CASES OF TURNER SYNDROME WITH TALL STATURE
- 17 HETEROGENEITYOF GH-1 GENE ABNORMALITIES AMONG JAPANESE IGHD TYPE II PATIENTS
- 運動ストレスによる免疫能(natural killer cell活性)低下と微量元素による回復 (特集 微量元素研究 up-to-date) -- (免疫機能における微量元素の栄養と毒)