Zobrazeno 1 - 10
of 30
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:
Wenger SL; Department of Pediatrics, University of Pittsburgh, Children's Hospital of Pittsburgh, Pennsylvania 15213-2583, USA., Giangreco CA, Tarleton J, Wessel HB
Publikováno v:
American journal of medical genetics [Am J Med Genet] 1996 Dec 02; Vol. 66 (1), pp. 60-3.
Autor:
Pegoraro E; Department of Molecular Genetics, University of Pittsburgh, School of Medicine, PA 15261., Schimke RN, Arahata K, Hayashi Y, Stern H, Marks H, Glasberg MR, Carroll JE, Taber JW, Wessel HB, et. al.
Publikováno v:
American journal of human genetics [Am J Hum Genet] 1994 Jun; Vol. 54 (6), pp. 989-1003.