733 results on '"Hasegawa, Yukihiro"'
Search Results
202. A Randomized Phase II Trial of Gemcitabine plus Carboplatin: Biweekly versus Standard Schedules in Patients with Advanced Non-Small Cell Lung Cancer
203. Functional Characterization of c.870+3_6delGAGT Splice Site Mutation in NR5A1.
204. Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism
205. Phase II study of amrubicin (AMR) combined with carboplatin (CBDCA) for refractory relapsed small cell lung cancer (SCLC): North Japan Lung Cancer Group 0802.
206. Computer Simulations of Silicon Nanowires and its Visualization with ^|^pi;-CAVE System
207. First-principles calculations of electron states of a silicon nanowire with 100,000 atoms on the K computer
208. Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome
209. High iFGF23 level despite hypophosphatemia is one of the clinical indicators to make diagnosis of XLH
210. THREE CHILDREN WITH PLASTIC BRONCHITIS ASSOCIATED WITH 2009 H1N1 INFLUENZA VIRUS INFECTION
211. Serum FSH level below 10 mIU/mL at twelve years old is an index of spontaneous and cyclical menstruation in Turner syndrome
212. Adult Heights of 258 Girls with Turner Syndrome on Low Dose of Growth Hormone Therapy in Japan
213. Patients with Hypophosphatemic Osteomalacia Need Continuous Treatment during Adulthood
214. Stress Doses of Glucocorticoids Cannot Prevent Progression of All Adrenal Crises
215. Feasibility and safety of platinum-doublet therapy in patients with small-cell lung cancer in the third-line setting: A multi-institutional retrospective study.
216. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q11.21 and 9p12 (or 7p11.2 and 9q12) in three generations
217. The Range of 2.2-3.3 mg/gCr of Pregnanetriol in the First Morning Urine Sample as an Index of Optimal Control in CYP21 Deficiency
218. Ovarian Histological Findings in an Adult Patient with the Steroidogenic Acute Regulatory Protein (StAR) Deficiency Reveal the Impairment of Steroidogenesis by Lipoid Deposition
219. Pregnanetriol in the Range of 1.2-2.1mg/m2/day as an Index of Optimal Control in CYP21A2 Deficiency
220. P-07 A NEW HETEROZYGOUS MUTATION IN THE REGION OF AN INTRONIC XGGG REPEAT OF THE GH-1 GENE LEADING TO GH DEFICIENCY BY PERTURBING ALTERNATIVE SPLICING
221. Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency: Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan
222. Limitations of G-banding Karyotype Analysis with Peripheral Lymphocytes in Diagnosing Mixed Gonadal Dysgenesis
223. Mutational Analysis of Androgen Receptor (AR) Gene in 46, XY Patients with Ambiguous Genitalia and Normal Testosterone Secretion: Endocrinological Characteristics of Three Patients with AR Gene Mutations
224. No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment
225. Dose Adjustments of Hydrocortisone and L-thyroxine in Hypopituitarism Associated with Cholestasis
226. Gonadal Function in 15 Patients Associated with WT1 Gene Mutations
227. Genetic and enzymatic analysis for two Japanese patients with idiopathic infantile arterial calcification
228. Studies of Very Severe Short Stature with Severe GH Deficiency: From the Data Registered with the Foundation for Growth Science
229. Utility of Computed Tomography in Identifying an Ectopic Thyroid in Infants and Pre-school Children
230. Vascular Endothelial Growth Factor Level as a Prognostic Determinant of Small Cell Lung Cancer in Japanese Patients
231. Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome
232. Side Effects of Therapy
233. Neonatal Diabetes Mellitus and Neonatal Polycystic, Dysplastic Kidneys: Phenotypically Discordant Recurrence of a Mutation in the Hepatocyte Nuclear Factor-1β Gene Due to Germline Mosaicism
234. Clinical Assessment and Mutation Analysis of Kallmann Syndrome 1 (KAL1) and Fibroblast Growth Factor Receptor 1 (FGFR1, orKAL2) in Five Families and 18 Sporadic Patients
235. Deficits in long-term retention of learned motor skills in patients with cortical or subcortical degeneration
236. Statural Growth in 31 Japanese Patients with SHOX Haploinsufficiency: Support for a Disadvantageous Effect of Gonadal Estrogens
237. Adrenocorticotropic Hormone and 17-Hydroxyprogesterone Levels during High-dose Glucocorticoid Supplement for the Management of Clitoroplasty of CYP21A2 Deficiency
238. First-principles calculations of electron states of a silicon nanowire with 100,000 atoms on the K computer.
239. Intratracheal Fire Ignited by a Gallium-Arsenide-Aluminum Diode Laser During Treatment of Airway Obstruction With Lung Cancer
240. First-principles calculations of electron states of a silicon nanowire with 100,000 atoms on the K computer.
241. Intravenous glycerol therapy should not be used in patients with unrecognized fructose-1,6-bisphosphatase deficiency
242. Evaluation of IGF-I Levels in Subjects whose GH Secretion Status was Judged Mainly by Auxological Data
243. A Sudden Death Due to Central Hypoventilation in A 3-Year-Old Boy with Idiopathic Hypothalamic Dysfunction
244. Lymphstasis in Boy with Noonan Syndrome: Implication for the Development of Skeletal Features
245. Eotaxin Level in Induced Sputum Is Increased in Patients with Bronchial Asthma and in Smokers
246. POU1F1/Pou1f1c.143-83A > G Variant Disrupts the Branch Site in Pre-mRNA and Leads to Dwarfism
247. TIME – A DISTRIBUTED RESOURCE HANDLING TOOL
248. Increased Circulatory Level of Biologically Active Full-Length FGF-23 in Patients with Hypophosphatemic Rickets/Osteomalacia
249. Infrequent voiding in nephrogenic diabetes insipidus as a cause of renal failure
250. Airflow through the auxiliary line of the laser fiber prevents ignition of intra-airway fire during endoscopic laser surgery
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