990 results on '"Dattani, Mehul"'
Search Results
152. Urinary Conjugated Metabolites of α-Tocopherol (Vitamin E) in Children and Young People with Type 1 Diabetes Mellitus
153. Factors Associated with Obesity in Children with Septo-Optic Dysplasia
154. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
155. Pituitary Masses in Children and Young People — To Operate or Not?
156. Understanding the Cellular Origin of Pituitary Tumors: Isolation and Characterization of Putative Tumorigenic Progenitors/Stem Cells from a Mouse Model of Human Adamantinomatous Craniopharyngioma
157. Clinical Manifestations of a NovelSOX2Mutation May Result from Failure to Repress β-Catenin-Mediated Target Activation: Suggestion for a New Mechanism for the Interaction between SOX2 and β-Catenin
158. LIN28 in Human Ovary Development and Function
159. Pituitary
160. Endocrinology of Fetal Development
161. Enhancement of the Canonical Wnt Pathway in Rathke's Pouch Results in Pituitary Tumours Reminiscent of Human Adamantinomatous Craniopharyngioma.
162. Congenital Disorders of the Hypothalamo-Pituitary-Somatotrope Axis
163. Growth Hormone Deficiency in Children
164. Contributors
165. Pituitary
166. Growth and Growth Factors
167. Role of Transcription Factors in Midline Central Nervous System and Pituitary Defects
168. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
169. An Infant with Pseudohyperkalemia, Hemolysis, and Seizures: Cation-Leaky GLUT1-Deficiency Syndrome due to a SLC2A1 Mutation
170. How to use insulin-like growth factor 1 (IGF1)
171. Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and −202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiency
172. Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia
173. Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency
174. A Mutation in the Thyroid Hormone Receptor Alpha Gene
175. Effect of growth hormone deficiency on brain structure, motor function and cognition
176. Contributors
177. SOX3 and Infundibular Hypoplasia
178. EMX2 and HESX1 and Type I Schizencephaly and Septo-Optic Dysplasia
179. Growth and Growth Factors
180. SOX2 haploinsufficiency is associated with slow progressing hypothalamo-pituitary tumours
181. Novel FGF8 Mutations Associated with Recessive Holoprosencephaly, Craniofacial Defects, and Hypothalamo-Pituitary Dysfunction
182. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency
183. Increased Transactivation Associated with SOX3 Polyalanine Tract Deletion in a Patient with Hypopituitarism
184. Sterol O-Acyltransferase 1 (SOAT1, ACAT) Is a Novel Target of Steroidogenic Factor-1 (SF-1, NR5A1, Ad4BP) in the Human Adrenal
185. Pubertal Presentation in Seven Patients with Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency
186. Letrozole: a new treatment for delayed puberty in boys?
187. Congenital growth hormone deficiency associated with hip dysplasia and Legg‐Calve‐Perthes disease
188. Mutations in LAMB2 are associated with albuminuria and optic nerve hypoplasia with hypopituitarism
189. Clinical benefits of sex steroids given as a priming prior to GH provocative test or as a growth‐promoting therapy in peripubertal growth delays: Results of a retrospective study among ENDO‐ERN centres
190. MON-LB014 Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178g>A Mutation in the GH1 Gene Is Caused by Alternative Splicing to Produce a Small GH Isoform
191. Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178G>A Mutation in the GH1 Gene is Caused by Alternative Splicing to Produce a Small GH Isoform
192. OR16-04 OTX2 Mutations in Congenital Hypopituitarism Patients
193. SUN-070 European Registries for Rare Endocrine Conditions (EuRRECa): Results from the Platform for E-reporting of Rare Endocrine Conditions (e-REC)
194. Development of the Pituitary Gland
195. Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism
196. Growth and Growth Factors
197. Genetic causes and treatment of isolated growth hormone deficiency—an update
198. A novel method for the direct measurement of urinary conjugated metabolites of α-tocopherol and its use in diabetes
199. Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action
200. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
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