X International Congress of The Society for the Advancement of Contraception Manila, Philippines, 5–9 November 1998 Abstracts (in alphabetical order of author)

Autor: P. Blumenthal, Maria Otelia D. Costales, I. Spitz, Babatunde A. Gbolade, J. T. Queenan, Delfln A. Tan, P. Mena, S. Rubakaniko, William Fuiyer, R. Ramos, E. Nowalle, N. Mcintosh, Joe Leigh Simpson, T. Samoto, S. Takeuchi, Antonio C. Costales, Jevgenijs Kalejs, Kathy Kennedy, Pilar Ramos-Jimenez, F. Vilar, I. Batár, Victoria Jennings, M. Vrijens, R. G. Walker, C. Cordero, W. Delbarge, Rosemary Kirkman, Diana J. A. Mansour, F. Lubis, E. Johansson, R. Fernandez, Leonard F. Blackwell, D. Wildemeersch, R. Pudgo, R. Youlton, Pamela J. Schwingl, R. Gray, P. Darney, J. Mcgrath, L. J. Canson, Irina Yacobsen, Loreto B. Roquero, R. S. Batani, C. Joanis, Biran Affandi, E. Valles, J. Kasule, A. E. Pollack, Mohammed S. A. Mansour, S. Palmore, X. Zhenming, T. Marou, R. Massai, R. Lu, Catalino M. Lim, K. Hardee, N. Williamson, S. Girvin, H. Sanghvi, Z. M. Chirenje, D. R. Bimo, B. Lee Romeo, V. Orais, S. Diaz, Max Elstein, T. Vaidya, T. Chipato, M. Catalino, B. Gu, L. Gaffikin, Sara Johnson, K. Kamali, R. Rivera, B. Morales, Jose Miguel De La Rosa, G. A. Manuel-Limson, Corazon A. Ngelangel, K. O. Rogo, R. D. Sanchez, J. Collins, A. Perez, H. Nagib, R. De La Paz Ingenie, M. Cabaraban, B. Norman Barwin, T. Grey, E. J. Oloto, Salud B. Zaldlvar, Nina Frankel, P. Makunike, M. Cordero, Marcos Arevalo, H. Croxatto, R. Magarick, R. Vogel, I. Kimsang, Richard A. Grossman, P. Bhiwandi

Publikováno v: Advances in Contraception. 14:N1-N56

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::19743972b75c4a6793525e9fadfcfe5b
https://doi.org/10.1007/bf02884152

[Germline mutations of the ret proto-oncogene in Chilean patients with hereditary and sporadic medullary thyroid carcinoma]

Autor: N, Wohllk, P, Becker, R, Youlton, G J, Cote, R F, Gagel

Publikováno v: Revista medica de Chile. 129(7)

Medullary thyroid carcinoma (MTC) may occur either as a sporadic or familial disease. Multiple endocrine neoplasia (MEN) type 2, inherited as an autosomal dominant disease, is characterized by MTC only (FMTC) or coexistence of MTC with other endocrin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::35e9841ab9e6b9b12d51a360cfc66b5a
https://pubmed.ncbi.nlm.nih.gov/11552438

[Gonadal dysgenesis: diagnosis and therapeutic perspectives]

Autor: R, Youlton

Publikováno v: Revista medica de Chile. 124(1)

Ovarian dysgenesis is the endstage of a process of follicular atresia, Turner syndrome (45,X) being the most common cause, with an incidence of 1 in 2500 female births. In addition to ovarian failure, these patients have short stature and a number of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7efd8232285c4e66effef0fef943cbe0
https://pubmed.ncbi.nlm.nih.gov/8762626

[Molecular genetic study of a severe growth hormone deficiency in a Chilean family]

Autor: E, Aguirre, R, Benítez, R, Youlton, P, Carvallo

Publikováno v: Revista medica de Chile. 121(9)

The first and so far the only form of isolated growth hormone deficiency to accede to molecular genetic analysis is IGHD 1A, which has an autosomal recessive mode of inheritance. Several sizes of growth hormone gene deletions, ranging from 6.7 to 8.5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::93355b8d7c9e3e6590469396b7740fd9
https://pubmed.ncbi.nlm.nih.gov/7910700

[Genetic study in twins]

Autor: V, Daher, R, Youlton, J, Nazer, L, Cifuentes

Publikováno v: Revista chilena de pediatria. 62(1)

During the period june 1987-January 1988, 35 consecutive pairs of twins born at two maternity hospitals in the northern area of Santiago were studied to search evidence of genetic or other factors which could eventually favour twinning. Sixteen of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7ee7ab419f3d02334031cb473749a478
https://pubmed.ncbi.nlm.nih.gov/1843999