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206. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Menieres disease

220. Hepatic Failure and Enhanced Oxidative Stress in Mitochondrial Diabetes

223. Growth Hormone Reverses Nonalcoholic Steatohepatitis in a Patient With Adult Growth Hormone Deficiency

224. Neither intravenous nor intracerebroventricular administration of obestatin affects the secretion of GH, PRL, TSH and ACTH in rats

225. McCune-Albright Syndrome with Acromegaly and Fibrous Dysplasia Associated with the GNAS Gene Mutation Identified by Sensitive PNA-clamping Method

230. OR01-4 A METABOLIC SYNDROME MODEL FOR ADULT GROWTH HORMONE (GH) DEFICIENCY IN GH-DEFICIENT SPONTANEOUS DWARF RAT

232. OR09-4 GHRP-2, A GHRELIN RECEPTOR AGONIST, DIRECTLY ACTS ON MYOCYTES TO SUPPRESS THE EXPRESSIONS OF E3 UBIQUITIN-LIGATING ENZYMES, ATROGIN-1 AND MuRF1

249. The Indication of ICSI

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