Jump Power Concepts and Some Theorems on Switching

Autor: Simone Barcellona, Gabrio SupertiFurga

Publikováno v: Journal of Electrical Systems, Vol 14, Iss 2, Pp 1-15 (2018)

Power-like functions based on Tellegen’s theorem are important tools in the study of electrical networks. Networks containing power converters are nonlinear and/or time-variant. This fact continues to represent a challenge regarding both theoretica

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::0403218c18cd308d6a25be34a6f95c62
https://journal.esrgroups.org/jes/papers/14_2_1.pdf

A variant of Desbuquois dysplasia characterized by advanced carpal bone age, short metacarpals, and elongated phalanges: Report of seven casesHow to cite this article: Kim OH, Nishimura G, Song HR, Matsui Y, Sakazume S, Yamada M, Narumi Y, Alanay Y, Unger S, Cho TJ, Park SS, Ikegawa S, Meinecke P, SupertiFurga A. 2010. A Variant of desbuquois dysplasia characterized by advanced carpal bone age, short metacarpals, and elongated phalanges: Report of seven cases. Am J Med Genet Part A 152A:875–885.

Autor: Kim, OkHwa, Nishimura, Gen, Song, HaeRyong, Matsui, Yoshito, Sakazume, Satoru, Yamada, Masanobu, Narumi, Yoko, Alanay, Yasemin, Unger, Sheila, Cho, TaeJoon, Park, Sung Sup, Ikegawa, Shiro, Meinecke, Peter, SupertiFurga, Andrea

Publikováno v: American Journal of Medical Genetics. Part A; April 2010, Vol. 152 Issue: 4 p875-885, 11p

Holt-Oram syndrome associated with anomalies of the feet

Autor: Garavelli, L., De Brasi, D., Verri, R., Guareschi, E., Cariola, F., Melis, D., Calcagno, G., Salvatore, F., Unger, S., Sebastio, G., Albertini, G., Rivieri, F., Soli, F., SupertiFurga, A., Gentile, M.

Publikováno v: American Journal of Medical Genetics. Part A; May 2008, Vol. 146 Issue: 9 p1185-1189, 5p

Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13

Autor: Gong, Yq, Vikkula, M., Boon, L., Liu, J., Beighton, P., Rajkumar Ramesar, Peltonen, L., Somer, H., Hirose, T., Dallapiccola, B., Depaepe, A., Swoboda, W., Zabel, B., Supertifurga, A., Steinmann, B., Brunner, Hg, Jans, A., Boles, Rg, Adkins, W., Vandenboogaard, Mj, Olsen, Br, Warman, Ml

Publikováno v: Web of Science
American Journal of Human Genetics, 59, 1, pp. 146-151
American Journal of Human Genetics, 59, 146-151
American Journal of Human Genetics, 59, pp. 146-151

Osteoporosis-pseudoglioma syndrome (OPS) is an autosomal recessive disorder characterized by severe juvenile-onset osteoporosis and congenital or juvenile-onset blindness. The pathogenic mechanism is not known. Clinical, biochemical, and microscopic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5473f1f638fea8cbb221966b9df7d856
https://publons.com/wos-op/publon/8588191/

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