Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Lisa A. Teot"'
Autor:
Douglas J. Harrison, Yueh‐Yun Chi, Jing Tian, Pooja Hingorani, Leo Mascarenhas, Geoffrey B. McCowage, Brenda J. Weigel, Rajkumar Venkatramani, Suzanne L. Wolden, Torunn I. Yock, David A. Rodeberg, Andrea A. Hayes‐Jordan, Lisa A. Teot, Sheri L. Spunt, William H. Meyer, Douglas S. Hawkins, Barry L. Shulkin, Marguerite T. Parisi
Publikováno v:
Cancer Medicine, Vol 10, Iss 3, Pp 857-866 (2021)
ABSTRACT Background Strategies to optimize management in rhabdomyosarcoma (RMS) include risk stratification to assign therapy aiming to minimize treatment morbidity yet improve outcomes. This analysis evaluated the relationship between complete metab
Externí odkaz:
https://doaj.org/article/312b8738271c49eb906d6d54f8fea79b
Autor:
Pooja Hingorani, Mark Krailo, Allen Buxton, Paul Hutson, Paul M. Sondel, Mitchell Diccianni, Alice Yu, Carol D. Morris, Richard B. Womer, Brian Crompton, R Lor Randall, Lisa A. Teot, Steven G. DuBois, Katherine A. Janeway, Richard G. Gorlick, Michael S. Isakoff
Publikováno v:
European Journal of Cancer. 172:264-275
Novel effective therapies are urgently needed in recurrent osteosarcoma. GD2 is expressed in human osteosarcoma tumours and cell lines. This study evaluated the disease control rate (DCR) in patients with recurrent osteosarcoma treated with the anti-
Autor:
Steven G. DuBois, Dinesh Rakheja, Allen Buxton, Lisa A. Teot, Julia Glade-Bender, Katherine A. Janeway, Mark Krailo, Richard Gorlick, Stephen L. Lessnick, Brian D. Crompton
Publikováno v:
Arch Pathol Lab Med
Context.— Molecular diagnostics play an increasing role in the diagnosis of Ewing sarcoma. The type of molecular testing used in clinical practice has been poorly described. Objective.— To describe patterns of translocation testing for newly diag
Autor:
Marguerite T. Parisi, Lisa A. Teot, Pooja Hingorani, Yueh-Yun Chi, William H. Meyer, Douglas J. Harrison, Geoffrey McCowage, Douglas S. Hawkins, Andrea Hayes-Jordan, Barry L. Shulkin, Torunn I. Yock, Suzanne L. Wolden, Rajkumar Venkatramani, Brenda J. Weigel, Jing Tian, David A. Rodeberg, Leo Mascarenhas, Sheri L. Spunt
Publikováno v:
Cancer Medicine. 10:857-866
Background Strategies to optimize management in rhabdomyosarcoma (RMS) include risk stratification to assign therapy aiming to minimize treatment morbidity yet improve outcomes. This analysis evaluated the relationship between complete metabolic resp
Autor:
Josephine H. Haduong, Christine M. Heske, Wendy Allen‐Rhoades, Wei Xue, Lisa A. Teot, David A. Rodeberg, Sarah S. Donaldson, Aaron Weiss, Douglas S. Hawkins, Rajkumar Venkatramani
Publikováno v:
Pediatr Blood Cancer
Children and adolescents with rhabdomyosarcoma (RMS) comprise a heterogeneous population with variable overall survival rates ranging between approximately 6% and 100% depending on defined risk factors. Although the risk stratification of patients ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2242353372fb5a29feb962487871b05c
https://europepmc.org/articles/PMC8976559/
https://europepmc.org/articles/PMC8976559/
Autor:
Weizhen Tan, Francesco Emma, Tina Storm, Carina Frykholm, Shrikant Mane, Tarak Srivastava, Sejin Nam, Lisa A. Teot, Friedhelm Hildebrandt, Kevin M. Bennett, Jennifer R. Charlton, François Jouret, Aleksandra Cwiek, Seymour Rosen, Lisbeth Tranebjærg, Rikke Nielsen, Erik Ilsø Christensen, Ghaleb Daouk, João Paulo Oliveira
Publikováno v:
Charlton, J R, Tan, W, Daouk, G, Teot, L, Rosen, S, Bennett, K M, Cwiek, A, Nam, S, Emma, F, Jouret, F, Oliveira, J P, Tranebjærg, L, Frykholm, C, Mane, S, Hildebrandt, F, Srivastava, T, Storm, T, Christensen, E I & Nielsen, R 2020, ' Beyond the tubule : pathological variants of LRP2, encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease ', American journal of physiology. Renal physiology, vol. 319, no. 6, pp. F988-F999 . https://doi.org/10.1152/ajprenal.00295.2020
Pathogenic variants in the LRP2 gene, encoding the multiligand receptor megalin, cause a rare autosomal recessive syndrome: Donnai-Barrow/Facio-Oculo-Acoustico-Renal (DB/FOAR) syndrome. Because of the rarity of the syndrome, the long-term consequence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4876af5172ff2e902f3b8dfff44775e0
https://pure.au.dk/portal/da/publications/beyond-the-tubule(09281d1c-d21e-430f-99d7-b2e71eed7af7).html
https://pure.au.dk/portal/da/publications/beyond-the-tubule(09281d1c-d21e-430f-99d7-b2e71eed7af7).html
Autor:
Douglas J, Harrison, Yueh-Yun, Chi, Jing, Tian, Pooja, Hingorani, Leo, Mascarenhas, Geoffrey B, McCowage, Brenda J, Weigel, Rajkumar, Venkatramani, Suzanne L, Wolden, Torunn I, Yock, David A, Rodeberg, Andrea A, Hayes-Jordan, Lisa A, Teot, Sheri L, Spunt, William H, Meyer, Douglas S, Hawkins, Barry L, Shulkin, Marguerite T, Parisi
Publikováno v:
Cancer Medicine
Background Strategies to optimize management in rhabdomyosarcoma (RMS) include risk stratification to assign therapy aiming to minimize treatment morbidity yet improve outcomes. This analysis evaluated the relationship between complete metabolic resp
Autor:
Javed Khan, Susan M. Hiniker, Minjie Li, Archana Shenoy, David M. Parham, Jack F. Shern, Erin R. Rudzinski, Lisa A. Teot, Yueh Yun Chi, Douglas S. Hawkins, Candace F. Granberg, Elysia Alvarez
Publikováno v:
Eur J Cancer
Background Established prognostic indicators in rhabdomyosarcoma (RMS), the most common childhood soft tissue sarcoma, include several clinicopathologic features. Among pathologic features, anaplasia has been suggested as a potential prognostic indic
Autor:
Brenda J. Weigel, Yueh-Yun Chi, James R. Anderson, Douglas S. Hawkins, Barry L. Shulkin, David M. Parham, William H. Meyer, Jing Tian, David A. Rodeberg, Suman Malempati, Torunn I. Yock, Sheri L. Spunt, Lisa A. Teot
Publikováno v:
Cancer. 125:290-297
Background The outcome for patients with metastatic rhabdomyosarcoma (RMS) remains poor. A previous Children's Oncology Group (COG) study (ARST0431) for patients with metastatic RMS produced no improvement in outcome using multiple cytotoxic agents i
Publikováno v:
Pediatric Radiology. 47:484-487
Gaucher disease is a hereditary lipid storage disorder that affects the enzyme beta glucocerebrosidase, causing accumulation of glucocerebroside in macrophages of the reticuloendothelial system. Accumulation can occur in the liver and spleen, manifes