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David W. Kimmel
Researcher at Mayo Clinic
Publications - 39
Citations - 4066
David W. Kimmel is an academic researcher from Mayo Clinic. The author has contributed to research in topics: Cancer & Glioma. The author has an hindex of 27, co-authored 39 publications receiving 3925 citations. Previous affiliations of David W. Kimmel include Johns Hopkins University.
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Journal ArticleDOI
Alterations of chromosome arms 1p and 19q as predictors of survival in oligodendrogliomas, astrocytomas, and mixed oligoastrocytomas
Justin S. Smith,Arie Perry,Thomas J. Borell,Hyun K. Lee,Judith R. O'Fallon,Sandra M. Hosek,David W. Kimmel,Allan J. Yates,Peter C. Burger,Bernd W. Scheithauer,Robert B. Jenkins +10 more
TL;DR: Combined loss of 1p and 19q is a statistically significant predictor of prolonged survival in patients with pure oligodendroglioma, independent of tumor grade, and could potentially improve existing strategies for patient stratification and management.
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Paraneoplastic and oncologic profiles of patients seropositive for type 1 antineuronal nuclear autoantibodies
TL;DR: Seropositivity for ANNA-1 can expedite the diagnosis and treatment of otherwise occult cancer in patients, especially tobacco abusers, with varied neurologic and gastroenterologic presentations.
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Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype
Justin S. Smith,Benjamin Alderete,Yuriko A. Minn,Thomas J. Borell,Arie Perry,Gayatry Mohapatra,Sandra M. Hosek,David W. Kimmel,Judith R. O'Fallon,Allan J. Yates,Burt G. Feuerstein,Peter C. Burger,Bernd W. Scheithauer,Robert B. Jenkins +13 more
TL;DR: Using 115 human diffuse gliomas, regions of common allelic loss on chromosomes 1 and 19 were localized and the association of these deletion intervals with glioma histological subtypes was assessed, suggesting not only locations of putative tumor suppressor genes, but also a simple assay for assessment of 1p and 19q alterations as diagnostic and prognostic markers.
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A cytogenetic study of 53 human gliomas.
Robert B. Jenkins,David W. Kimmel,Cheryl A. Moertel,Cloann G. Schultz,Bernd W. Scheithauer,Patrick J. Kelly,Gordon W. Dewald +6 more
TL;DR: It is suggested that grade 3 and 4 tumors are more likely to contain an abnormal clone than tumors of grade 1 or 2 (p less than 0.01), and cytogenetic studies can be successful on nearly all human gliomas, including those derived from small stereotactic biopsies.
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Immunomodulatory treatment trial for paraneoplastic neurological disorders
TL;DR: Aggressive immunosuppression early in the clinical course should be considered in patients who have paraneoplastic neurological disorders, even when there is no evidence of active malignancy.