Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Wessel, H B"'
Autor:
Wang, J., Zhou, J., Todorovic, S. M., Feero, W. G., Barany, F., Conwit, R., Hausmanowa-Petrusewicz, I., Fidzianska, A., Arahata, K., Wessel, H. B., Sillen, A., Marks, H. G., Hartlage, P., Galloway, G., Ricker, K., Lehmann-Horn, F., Hayakawa, H., Hoffman, E. P.
We present a correlation of molecular genetic data (mutations) and genetic data (dinucleotide-repeat polymorphisms) for a cohort of seven hyperkalemic periodic paralysis (HyperPP) and two paramyotonia congenita (PC) families from diverse ethnic backg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83b4d29628e6dfea84e1bd9810ed049b
https://europepmc.org/articles/PMC1682261/
https://europepmc.org/articles/PMC1682261/
Akademický článek
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Autor:
ORENSTEIN, S. R., DENT, J., DENEAULT, L. G., LUTZ, J. W., WESSEL, H. B., KELSEY, S. F., SHALABY, T. M.
Publikováno v:
Neurogastroenterology & Motility; Dec1994, Vol. 6 Issue 4, p271-277, 7p
Autor:
Bergman, Ira, May, Mark, Wessel, Henry B., Stool, Sylvan E., Bergman, I, May, M, Wessel, H B, Stool, S E
Publikováno v:
Laryngoscope; 1986, Vol. 96 Issue 4, p381-384, 4p
Autor:
Feero, W. G., Wang, J., Barany, F., Zhou, J., Todorovic, S. M., Conwit, R., Galloway, G., Hausmanowa-Petrusewicz, I., Fidzianska, A., Arahata, K., Wessel, H. B., Wadelius, C., Marks, H. G., Hartlage, P., Hayakawa, H., Hoffman, E. P.
Publikováno v:
Neurology; Apr1993, Vol. 43 Issue 4, p668-673, 6p
Autor:
Pegoraro, E., Schimke, R. N., Garcia, C., Stern, H., Cadaldini, M., Angelini, C., Barbosa, E., Carroll, J., Marks, W. A., Neville, H. E., Marks, H., Appleton, S., Toriello, H., Wessel, H. B., Donnelly, J., Bernes, S. M., Taber, J. W., Weiss, L., Hoffman, E. P.
Publikováno v:
Neurology (Ovid); April 1995, Vol. 45 Issue: 4 p677-690, 14p
Autor:
Hoffman, E. P., Arahata, K., Minetti, C., Bonilla, E., Rowland, L. P., Angelini, C., Arikawa, E., Baba, C., Barkhaus, P. E., Bauserman, S. C., Butler, I. J., Cook, J. D., Chutkow, J. G., Cordone, G., Evans, O. B., Fideianska, A., Garcia, C., Gilchrist, J. M., Glasberg, M., Hamada, K., Ishihara, T., Ishikawa, N., Johnsen, S. D., Kamakura, K., Kikumoto, O., Kinoshita, M., Kumagai, K., Marks, H., Marks, W., Maytal, J., Moggio, M., Moser, E., Nigro, M. A., Noll, W., Nonaka, I., Prelle, A., Iieyes, M. G., Ricci, E., Roses, AD., Sakuta, R., Satoyoshi, E., Servidei, S., Smith, A., Steele, M., Subramony, S. H., Sunohara, N., Wang, J. Z., Wessel, H. B., Yanagawa, T., Munsat, T., Hausmanowa-Petrusewicz, I., Sugita, H.
Publikováno v:
Neurology (Ovid); May 1992, Vol. 42 Issue: 5 p967-975, 9p
Autor:
Fang, Xiaolan1 (AUTHOR), Butler, Kameryn M.1 (AUTHOR), Abidi, Fatima1 (AUTHOR), Gass, Jennifer2 (AUTHOR), Beisang, Arthur3 (AUTHOR), Feyma, Timothy3 (AUTHOR), Ryther, Robin C.4 (AUTHOR), Standridge, Shannon5,6 (AUTHOR), Heydemann, Peter7 (AUTHOR), Jones, Mary8 (AUTHOR), Haas, Richard9 (AUTHOR), Lieberman, David N10 (AUTHOR), Marsh, Eric D.11 (AUTHOR), Benke, Tim A.12 (AUTHOR), Skinner, Steve1 (AUTHOR), Neul, Jeffrey L.13 (AUTHOR), Percy, Alan K.14 (AUTHOR), Friez, Michael J.1 (AUTHOR), Caylor, Raymond C.1 (AUTHOR) rcaylor@ggc.org
Publikováno v:
Molecular Genetics & Genomic Medicine. May2022, Vol. 10 Issue 5, p1-14. 14p.
Autor:
Wang, Xiaoyuan1 (AUTHOR), Xiao, Huijie1 (AUTHOR), Su, Baige1 (AUTHOR), Ren, Yali2 (AUTHOR), Ding, Jie1 (AUTHOR) djnc_5855@126.com, Wang, Fang1 (AUTHOR) wangfangped@163.com
Publikováno v:
Molecular Genetics & Genomic Medicine. Jul2021, Vol. 9 Issue 7, p1-8. 8p.
Autor:
Monaghan, Rosemary1,2 (AUTHOR) monaghar@tcd.ie, O'Dwyer, Máire1 (AUTHOR), Luus, Retha3 (AUTHOR), Mulryan, Niamh2,4 (AUTHOR), McCallion, Philip5 (AUTHOR), McCarron, Mary3 (AUTHOR), Henman, Martin C.1 (AUTHOR)
Publikováno v:
Journal of Applied Research in Intellectual Disabilities. May2021, Vol. 34 Issue 3, p818-829. 12p.