Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Mariana M. Cajaiba"'
Autor:
James I. Geller, Nicholas G. Cost, Elizabeth Mullen, Brett Tornwall, Elizabeth J. Perlman, Geetika Khanna, Conrad V. Fernandez, Mariana M. Cajaiba, Yueh-Yun Chi, Jeffrey S. Dome, Najat C. Daw, Yeonil Kim, Richard D. Glick, Peter F. Ehrlich
Publikováno v:
Cancer
To the authors' knowledge, AREN0321 is the first prospective clinical study of pediatric and adolescent renal cell carcinoma (RCC). Goals of the study included establishing epidemiological, treatment, and outcome data and confirming that patients wit
Autor:
Donald A. Barkauskas, Mariana M. Cajaiba, Jeffrey S. Dome, Stacey L. Berg, Joseph G. Pressey, James I. Geller, Steve Y. Cho, Brenda J. Weigel, David Hall, Elizabeth Fox, Rachel A. Kudgus, Stephen D. Voss, Malcolm A. Smith, Joel M. Reid
Publikováno v:
Cancer
Background Lorvotuzumab mertansine (IMGN901) is an antibody-drug conjugate linking an antimitotic agent (DM1) to an anti-CD56 antibody (lorvotuzumab). Preclinical efficacy has been noted in Wilms tumor, rhabdomyosarcoma, and neuroblastoma. Synovial s
Autor:
Mariana M. Cajaiba, Samantha Gadd, Elizabeth J. Perlman, Min Yu, Lily Marsden, Lawrence J. Jennings
Publikováno v:
Human Pathology. 60:32-36
Metanephric stromal tumors (MSTs) are rare renal stromal tumors that predominantly affect children. They belong to the metanephric family of tumors, along with metanephric adenofibroma and metanephric adenoma. The previous documentation of BRAF exon
Publikováno v:
Genes, Chromosomes and Cancer. 55:814-817
Autor:
Elizabeth J. Perlman, Lawrence J. Jennings, Jonathan A. Fletcher, Katrin M. Leuer, Julia A. Bridge, James I. Geller, Mariana M. Cajaiba, Adrián Mariño-Enríquez, Antonio R. Perez-Atayde, Stephen Rohan
Publikováno v:
Genes, Chromosomes and Cancer. 55:442-451
Knowledge of the clinicopathological and molecular spectrum of pediatric renal cell carcinomas (RCC) remains limited, and approximately 16%-24% of these neoplasms cannot be classified into specific subtypes. In this review of 168 pediatric RCC prospe
Autor:
Jeffrey S. Dome, Ethan A. Smith, Mariana M. Cajaiba, Lan L. Gellert, Elizabeth J. Perlman, Geetika Khanna, Dana A. Hill, Elizabeth Mullen, James I. Geller, Yueh-Yun Chi
Publikováno v:
Human Pathology. 48:81-87
Cystic nephromas (CNs) are uncommon benign renal neoplasms that present with a bimodal age distribution, affecting either infants/young children or adult females. Although differences between these age groups have been suggested, large studies of ped
Publikováno v:
Rare Kidney Tumors ISBN: 9783319969886
TFE/translocation renal cell carcinoma (tRCC) was formally recognized by the WHO in 2004 as a distinct, typically translocation-associated, RCC with characteristic morphology and immunohistochemical expression of TFE3 or TFEb. Cytogenetic translocati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac86e225fd3a40e98d64c40efe96527
https://doi.org/10.1007/978-3-319-96989-3_8
https://doi.org/10.1007/978-3-319-96989-3_8
Autor:
Jeffrey S. Dome, Elizabeth Mullen, Stephen Rohan, James I. Geller, Nicholas G. Cost, Dawn A. Kirschmann, Elizabeth J. Perlman, Lawrence J. Jennings, Geetika Khanna, Lisa M. Dyer, Conrad V. Fernandez, David George, Mariana M. Cajaiba
Background Renal cell carcinomas (RCCs) are rare in young patients. Knowledge of their pathologic and molecular spectrum remains limited, and no prospective studies have been performed to date in this population. This study analyzes patients diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2577eac87419dd4a84eed3c05b9c5e10
https://europepmc.org/articles/PMC6108909/
https://europepmc.org/articles/PMC6108909/
Autor:
Elizabeth Mullen, Ethan A. Smith, Mariana M. Cajaiba, Elizabeth J. Perlman, Conrad V. Fernandez, Geetika Khanna, Sabah Servaes, Jeffrey S. Dome, Nicholas G. Cost, Jesse K. Sandberg, James I. Geller, Peter F. Ehrlich
Renal medullary carcinoma is a rare renal malignancy of childhood. There are no large series describing the imaging appearance of renal medullary carcinoma in children. To characterize the clinical and imaging features of pediatric renal medullary ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd4b79f4ec7479f2abd4f42ddeb4f2c
https://europepmc.org/articles/PMC5768308/
https://europepmc.org/articles/PMC5768308/
Publikováno v:
Applied immunohistochemistrymolecular morphology : AIMM. 26(10)
Pediatric renal tumors (PRT) with small round blue or spindle cell morphology can be diagnostically challenging and only a limited number of immunohistochemical markers have been documented to help in the diagnosis: paired box (Pax) 2 and nerve growt