Download e-book for iPad: Annual Review of Medicine Volume 55 2004 by C. Thomas Caskey

By C. Thomas Caskey

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About the Authors
Dr. Da Cheng Hao is an affiliate Professor and precept investigator on the institution of surroundings and Chemical Engineering, established on the Biotechnology Institute, Dalian Jiaotong college, Dalian, P. R China. he's a visitor Prof. of Institute of Medicinal Plant improvement (IMPLAD), chinese language Academy of clinical Sciences (CAMS), Beijing, P. R China.

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Professor Pei Gen Xiao is an Academician of chinese language Academy of Engineering and the pinnacle of Key Laboratory of Bioactive ingredients and assets usage of chinese language natural drugs, Ministry of schooling, established at IMPLAD, CAMS, Beijing, P. R China.

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Extra resources for Annual Review of Medicine Volume 55 2004

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24. 25. 26. 27. 28. 29. sgm LaTeX2e(2002/01/18) P1: GBC WEINSTEIN renal tubular dysfunction similar to that seen in tumor-induced osteomalacia. J. Bone Miner. Res. 16:806–13 Kim I, Kim ER, Nam HJ, et al. 1999. Activating mutation of Gsα in McCuneAlbright syndrome causes skin pigmentation by tyrosinase gene activation on affected melanocytes. Horm. Res. 52:235–40 Weinstein LS, Yu S, Warner DR, et al. 2001. Endocrine manifestations of stimulatory G protein α-subunit mutations and the role of genomic imprinting.

Rev. Med. 55:41-60. org by Universitaet Heidelberg on 10/04/05. For personal use only. PARKINSON’S DISEASE P1: GBC 47 Figure 3 (a) Comparison of frequency of developing dyskinesia in 3 different doubleblind prospective trials in which patients have been randomized to initiate treatment with a dopamine agonist or levodopa (derived from References 33 and 34). In each study, the frequency of dyskinesias was significantly lower in patients started on the dopamine agonist than in those started on levodopa.

Horm. Res. 52:235–40 Weinstein LS, Yu S, Warner DR, et al. 2001. Endocrine manifestations of stimulatory G protein α-subunit mutations and the role of genomic imprinting. Endocr. Rev. 22:675– 705 Spiegel AM, Weinstein LS. 2001. Pseudohypoparathyroidism. In The Metabolic and Molecular Bases of Inherited Disease, ed. CR Scriver, AL Beaudet, WS Sly, D Valle, pp. 4205–21. New York: McGraw-Hill Shore EM, Ahn J, Jan de Beur S, et al. 2002. Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia.

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Annual Review of Medicine Volume 55 2004 by C. Thomas Caskey


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