Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Lawrence W. O'Neal"'
Autor:
Andrew J.M. Boulton, John H. Bowker, James W. Brodsky, Peter R. Cavanagh, Paul Cianci, Curtis R. Clark, William Coleman, John A. Colwell, Kevin P. Conway, Kenrick J. Dennis, Peter D. Donofrio, Dorothy B. Doughty, Michelle Draznin, Robert Eison, Robert G. Frykberg, Robert S. Gailey, Ignacio A. Gaunaurd, Jeffrey S. Gonzalez, Linda Haas, Allen D. Hamdan, K.G. Harding, Lawrence B. Harkless, Irl B. Hirsch, Hanno Hoppe, Thomas K. Hunt, Arthur Huntley, Joseph J. Hurley, Dennis J. Janisse, Jeffrey E. Johnson, Rudolf J. Jokl, John A. Kaufman, Janet L. Kelly, Richard L. Klein, Shelley H. Leinicke, Steven Y. Leinicke, Joseph W. LeMaster, Benjamin A. Lipsky, Mary D. Litchford, Maria E. Lopes-Virella, Timothy J. Lyons, Emanual Maverakis, Donald E. McMillan, Michael J. Mueller, Lawrence W. O'Neal, Walter J. Pedowitz, Michael A. Pfeifer, Jeffrey M. Pitcher, Frank B. Pomposelli, Gayle E. Reiber, Lee J. Sanders, V. Kathleen Satterfield, David R. Sinacore, Jay S. Skyler, Robert J. Tanenberg, Andrew Brian Thomson, Jan S. Ulbrecht, Loretta Vileikyte, William A. Wooden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5690c03749ad51cc126b76bf2bc1983
https://doi.org/10.1016/b978-0-323-04145-4.50004-1
https://doi.org/10.1016/b978-0-323-04145-4.50004-1
Publikováno v:
Journal of Pediatric Surgery. 25:939-943
Medullary thyroid carcinoma (MTC) develops in all patients with multiple endocrine neoplasia type IIb (MEN IIb), a rare syndrome that either occurs sporadically or is inherited in an autosomal dominant pattern. The MTC in patients with MEN IIb has be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d629fb9b0063dae6894167206f9dead6
https://doi.org/10.1016/0022-3468(90)90234-z
https://doi.org/10.1016/0022-3468(90)90234-z
Autor:
Lawrence W. O'Neal
Publikováno v:
JAMA: The Journal of the American Medical Association. 284:1382-1383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecb74c1f04962eb9cf978076e4b8ebdf
https://doi.org/10.1001/jama.284.11.1382
https://doi.org/10.1001/jama.284.11.1382
Autor:
James C. Sisson, Robert A. Norum, Lawrence W. O'Neal, John P. Delaney, Charles E. Jackson, Bruce A.J. Ponder, Ronald G. Lafreniere, Gilbert M. Lenoir, Hagay Sobol, Thomas F. Nikolai, Huntington F. Willard
Publikováno v:
Genomics. 8(2)
The syndrome of multiple endocrine neoplasia type 2B (MEN 2B) resembles that of MEN 2A in that both include medullary carcinoma of the thyroid, pheochromocytoma, and autosomal dominant inheritance, but is distinct in that MEN 2B patients have neuroma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e96fee36444ab9830b0a8afb6e67a3
https://pubmed.ncbi.nlm.nih.gov/1979053
https://pubmed.ncbi.nlm.nih.gov/1979053