Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lindsay W. Cole"'
Publikováno v:
Journal of Bioethical Inquiry. 9:77-83
We use the format of a hypothetical case study to review issues related to pharmaceutical product approval and physician prescribing practices. In this case, a new FDA-approved drug is recommended for a patient who subsequently experiences an adverse
Autor:
Qun-Yong Zhou, Chengkang Zhang, Guy VanVliet, Richard Quinton, Lindsay W. Cole, Andrew A. Dwyer, Duarte Pignatelli, Lacey Plummer, Simon Pearce, Céline Huot, Virginia A. Hughes, Phyllis W. Speiser, Nathalie Alos, Akira Takeshita, William F. Crowley, Frances J. Hayes, Nelly Pitteloud, Stephanie B. Seminara, Yisrael Sidis, Taneli Raivio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 93:3551-3559
Mice deficient in prokineticin 2(PROK2) and prokineticin receptor2 (PROKR2) exhibit variable olfactory bulb dysgenesis and GnRH neuronal migration defects reminiscent of human GnRH deficiency.We aimed to screen a large cohort of patients with Kallman
Autor:
Lacey Plummer, Lindsay W. Cole, John L. Falardeau, Richard Quinton, Andrew A. Dwyer, Céline Huot, Andrew Beenken, Anna V. Eliseenkova, Jinghong Ma, Simon H. S. Pearce, Nelly Pitteloud, Elka Jacobson-Dickman, Wilson C. J. Chung, Yisrael Sidis, Natalie Alois, Sandra Na, Janet E. Hall, Pei Tsai, Moosa Mohammadi, Taneli Raivio, Virginia A. Hughes
Publikováno v:
Journal of Clinical Investigation. 118:2822-2831
Idiopathic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS) or with a normal sense of smell (normosmic IHH; nIHH) are heterogeneous genetic disorders associated with deficiency of gonadotropin-releasing hormone (GnRH). While l
Autor:
Frances J. Hayes, Richard Quinton, John L. Falardeau, Simon H. S. Pearce, Taneli Raivio, William F. Crowley, Nelly Pitteloud, Virginia A. Hughes, Paul A. Boepple, Andrew A. Dwyer, Lindsay W. Cole, Hang Lee
Publikováno v:
New England Journal of Medicine. 357:863-873
Idiopathic hypogonadotropic hypogonadism, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense of smell, is a treatable form of male infertility caused by a congenital defect in the secretion or action of gonadotropin-r
Autor:
William F. Crowley, Taneli Raivio, Qun-Yong Zhou, Lacey Plummer, Jia-Da Li, Elka Jacobson-Dickman, Pamela L. Mellon, Chengkang Zhang, Nelly Pitteloud, Duarte Pignatelli, Lindsay W. Cole
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 104(44)
Gonadotropin-releasing hormone (GnRH) deficiency in the human presents either as normosmic idiopathic hypogonadotropic hypogonadism (nIHH) or with anosmia [Kallmann syndrome (KS)]. To date, several loci have been identified to cause these disorders,