Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Judith Stamberg"'
Publikováno v:
Clinical Genetics. 23:380-385
Two siblings were found with different structural abnormalities involving their maternally inherited chromosome 13. The proband exhibited a ring 13 and a small fragment: 46, XX, r(13) (pllq34), +f, while her clinically normal brother carried a dicent
Publikováno v:
Clinical Genetics. 19:122-125
We report a stillborn infant with partial trisomy 6q who had several major congenital malformations not previously associated with the chromosomal aberration. These included occipital encephalocele, ambiguous genitalia with imperforate anus, omphaloc
Publikováno v:
Clinical Genetics. 23:447-453
A patient with clinical features of Turner syndrome and a 45,X karyotype in repeated blood cultures was re-evaluated when she spontaneously entered puberty. A ring X cell line was found in a small proportion of fibroblasts. A review of 35 previously
Autor:
Andrew J. Carroll, Colin G. Edwards, Frederick R. Davey, Prasad Koduru, Robert J. Mayer, John C. Byrd, Mark J. Pettenati, Krzysztof Mrózek, Clara D. Bloomfield, Amy S. Ruppert, Richard A. Larson, Diane C. Arthur, Judith Stamberg, Joseph O. Moore
Publikováno v:
Journal of Clinical Oncology. 22:1087-1094
Purpose To study the impact of repetitive (three to four courses) versus a single course of high-dose cytarabine (HDAC) consolidation therapy on outcome of patients with acute myeloid leukemia (AML) and inv(16)(p13q22) or t(16;16)(p13;q22). Patients
Autor:
Judith Stamberg, Chen Chih Sun, Jeffrey A. Toretsky, Allen E. Eskenazi, Andrew B. Campbell, Stephen P. Hunger, Christopher N. Frantz, James Jenson, J. Laurance Hill, Aimee Caires
Publikováno v:
American Journal of Clinical Oncology. 26:300-306
Thymic carcinoma is a rare epithelial neoplasm of the thymus. The presence of a specific chromosomal abnormality may augment diagnosis and therapeutic stratification. We report a 15-year-old boy diagnosed with thymic carcinoma who presented with a la
Autor:
Allen R. Chen, Chris Frantz, Thomas Ried, Eileen M. Everly, Allen E. Eskenazi, Judith Stamberg, Lynne V. Abruzzo, Jeffrey A. Toretsky, Hesed Padilla-Nash
Publikováno v:
Journal of Pediatric Hematology/Oncology. 25:396-402
The authors report a unique translocation in a patient with M7 acute myeloid leukemia and review the literature. A 22-month-old girl without Down syndrome was diagnosed with acute myeloid leukemia, subtype M7 (AML-M7), and died with relapsed disease
Publikováno v:
American Journal of Medical Genetics. 93:215-218
We report on a boy with mosaicism for trisomy 15 and Prader-Willi syndrome (PWS) due to maternal isodisomy for chromosome 15. His phenotype is consistent with PWS and trisomy 15 mosaicism. Although our patient is unusual in having maternal isodisomy
Autor:
E. L.C. Alonsozana, C. Frantz, S. Kerman, Elaine S. Jaffe, Celia A. Schiffer, D. Kumar, Sanford A. Stass, L. J. Medeiros, B. A. O'Connell, Judith Stamberg, Lynne V. Abruzzo
Publikováno v:
Leukemia. 11:1367-1372
Malignant lymphomas often have complex, nonrandom chromosomal abnormalities. Hepatosplenic gammadelta T cell lymphoma (gammadelta TCL) is an unusual post-thymic T cell lymphoma that primarily involves liver and spleen, often in young adult males. Few
Autor:
Kimberly F. Doheny, Marcia F. Schwartz, Sonja A. Rasmussen, George H. Thomas, Julie Rutberg, Gail Stetten, Judith Stamberg, Denise A.S. Batista, Gregg L. Semenza
Publikováno v:
American Journal of Medical Genetics. 69:188-193
An interchromosomal insertion in 3 generations of a family was ascertained through two developmentally delayed first cousins. Cytogenetic analysis using G-banding and chromosome painting showed an apparently balanced direct insertion of chromosome 10
Autor:
Amy S. Ruppert, Sherif S. Farag, Prasad Koduru, Richard A. Larson, Joseph O. Moore, Judith Stamberg, Robert J. Mayer, James W. Vardiman, Richard Stone, Jonathan E. Kolitz, Bayard L. Powell, Andrew J. Carroll, Mark J. Pettenati, AnneMarie W. Block, Charles A. Schiffer, Krzysztof Mrózek, Clara D. Bloomfield, Maria R. Baer
Publikováno v:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology. 23(3)
Purpose Evaluate the outcome of induction and postremission therapy in adults younger than 60 years with normal cytogenetics acute myeloid leukemia (AML). Patients and Methods In 490 patients, induction included cytarabine and daunorubicin (AD) or cy