Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Helen S. Maurer"'
Publikováno v:
The Journal of Pediatrics. 107:748-751
bly account for the previous lack of recognition of hypoglycorrhachia as a prominent feature of HSV-ME. However, on subsequent taps, all nine patients developed hypoglycorrhachia, with the majority (seven of nine) demonstrating markedly decreased lev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958323544873f9e22573b259ea740884
https://doi.org/10.1016/s0022-3476(85)80407-8
https://doi.org/10.1016/s0022-3476(85)80407-8
Autor:
Arthur J. Provisor, Janet K. Hamilton, David T. Purtilo, Helen S. Maurer, Kathryn Clausen, Margaret L. Grunnet, Frank G. Cruzi, Louise A. Paquin, Jo Ann Cornet, C. Philip Steuber, Gerald Z. Finkelstein, Edith P. Hawkins, Benjamin H. Landing, David H. Yawn, John L. Sullivan
Publikováno v:
The Journal of Pediatrics. 96:669-673
Immune deficiency, especially to the Epstein-Barr virus, and increased susceptibility to fatal infectious mononucleosis, acquired agammoglobulinemia, and lymphoma are the cardinal features of the X-linked lymphoproliferative syndrome. Since the estab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0468eddf752f331c5ac823418e101c7a
https://doi.org/10.1016/s0022-3476(80)80735-9
https://doi.org/10.1016/s0022-3476(80)80735-9
Publikováno v:
Cancer. 43:205-208
Wilms' tumor was diagnosed in two children each of whom has an identical twin. In one of the pairs of twins the aniridia syndrome with psychomotor retardation was present in both children, but Wilms' tumor was found in only one. In the other twins he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d718f011491587b29c55675a6a520b8a
https://doi.org/10.1002/1097-0142(197901)43:1<205::aid-cncr2820430130>3.0.co
https://doi.org/10.1002/1097-0142(197901)43:1<205::aid-cncr2820430130>3.0.co
Autor:
Helen S. Maurer, Helen R. Salwen, C. V. Herst, Elaine R. Morgan, Steven T. Rosen, Susan L. Cohn, Michael L. Nieder
Publikováno v:
Cancer. 62:723-726
Patients with neuroblastoma who present with the syndrome of opsoclonus and myoclonus enjoy a remarkably good prognosis independent of their stage of disease or their age at diagnosis. The presence of N-myc amplification also has been found to be an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c42ac3994ed7b5b75f8ea4f21f4a3fe2
https://doi.org/10.1002/1097-0142(19880815)62:4<723::aid-cncr2820620413>3.0.co
https://doi.org/10.1002/1097-0142(19880815)62:4<723::aid-cncr2820620413>3.0.co
Publikováno v:
Journal of Clinical Oncology. 5:1441-1444
N-myc amplification is most frequently found in neuroblastoma from patients with stage III and IV disease. Recently a significant association between genomic amplification and poor prognosis has been demonstrated. The primary tumors studied from pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4111c07711544967a8c55ad44a56b53
https://doi.org/10.1200/jco.1987.5.9.1441
https://doi.org/10.1200/jco.1987.5.9.1441
Publikováno v:
Cancer. 37:2224-2231
Four cases of malignant lymphoma all in male members of a family are described. In three of the affected individuals the primary tumor arose in the small intestine and in the other the site of origin was the retroperitoneum. Immunologic studies were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a745fae82c29dac1bb5befa6b552542d
https://doi.org/10.1002/1097-0142(197605)37:5<2224::aid-cncr2820370511>3.0.co
https://doi.org/10.1002/1097-0142(197605)37:5<2224::aid-cncr2820370511>3.0.co
Autor:
Robert T. Collins, Gordon F. Vawter, Shinji Harada, George Klein, Vanessa M. Barnabei, Werner Henle, Kiyoshi Sakamoto, Robert Maier, Martin R. Klemperer, J. Greally, George Bucchanan, Lauren M. Pachman, Paul K. Pattengale, Benjamin H. Landing, Sevre Lie, Helen S. Maurer, David T. Purtilo, Izet Berkel, Gertrude Henle, Hans D. Ochs, Elvin Kaplan, Geraldine Rogers, Margaret Grunet, Joanne Yetz, Gerald Z. Finkelstein, Frank G. Cruzi, Carter D. Brooks, Anders Glomstein, Arthur J. Provisor, Thomas Bechtold, Gary R. Pearson, Janet Seeley, Michael Medici
Publikováno v:
The American Journal of Medicine. 73:49-56
Analyses of 100 subjects with the X-linked lymphoproliferative syndrome (XLP) in 25 kindreds revealed four major interrelated phenotypes: infectious mononucleosis, malignant B-cell lymphoma, aplastic anemia, and hypogammaglobulinemia. Eighty-one of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c1170814d822a1f7f16f35ffef9f50f
https://doi.org/10.1016/0002-9343(82)90923-8
https://doi.org/10.1016/0002-9343(82)90923-8
Publikováno v:
Human Pathology. 9:635-648
The present report is a neuropathologic study of three patients who died from a severe form of necrotizing encephalopathy following intrathecal methotrexate therapy and craniospinal irradiation for acute lymphoblastic leukemia. During the early phase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc66eae3c82dc9e9d32d799ece2441ad
https://doi.org/10.1016/s0046-8177(78)80047-1
https://doi.org/10.1016/s0046-8177(78)80047-1
Publikováno v:
Blood. 60:389-399
We studied the karyotype in 26 children with ANLL, which was diagnosed on the basis of the FAB classification. Clonal chromosome abnormalities were found in 21 of 26 patients. Four patients, including 3 with Down's syndrome, had AML(M1). Nine patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6012fc6649027284ecf9e3c621eaad31
https://doi.org/10.1182/blood.v60.2.389.bloodjournal602389
https://doi.org/10.1182/blood.v60.2.389.bloodjournal602389
Publikováno v:
The American Journal of Surgical Pathology. 6:599-612
This is a clinicopathologic study summarizing the experience with hepatoblastomas at Children's Memorial Hospital of Chicago between 1954 and 1981. Of 21 patients studied, 13 (61.9%) died. Three major histologic epithelial patterns were identified: f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04106a32757622597831bc0e0644a193
https://doi.org/10.1097/00000478-198210000-00002
https://doi.org/10.1097/00000478-198210000-00002