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Milton D. Gross

Researcher at Veterans Health Administration

Publications -  41
Citations -  830

Milton D. Gross is an academic researcher from Veterans Health Administration. The author has contributed to research in topics: Thyroid cancer & Thyroid. The author has an hindex of 18, co-authored 41 publications receiving 781 citations.

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Journal Article

18F-FDG PET/CT in myeloma with presumed solitary plasmocytoma of bone.

TL;DR: The preliminary data in a small number of cases suggests that there are a group of patients with SPB (local disease) in whom FDG PET/CT may detect other unsuspected sites of bone involvement, upstaging the extent of the disease.
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Papillary Thyroid Carcinoma: 35-Year Outcome and Prognostic Factors in 1858 Patients

TL;DR: Assessing the prognostic factors and survival rate in a large cohort of patients treated and followed up in the same center found that the extent of primary surgery and the presence of I-131 positive or negative metastases have similar prognostic significance.
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The role of 18F-FDG PET/CT in detecting metastatic deposits of recurrent medullary thyroid carcinoma: A prospective study

TL;DR: In this study, 18F-FDG PET/CT was the most sensitive imaging modality in detecting metastases in recurrent MTC patients with increased serum calcitonin levels and was useful in some patients to plan a more accurate re-operation.
Journal Article

Functional and scintigraphic evaluation of the silent adrenal mass

TL;DR: There was congruence between the anatomic (CT) and functional (NP-59 scintigraphy and AVC) investigations that depicted asymmetry of the adrenal glands which were not associated with abnormalities of overall adrenal function or hypothalamic-pituitary-adrenal axis integrity.
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A novel multipurpose monoclonal antibody for evaluating human c-Met expression in preclinical and clinical settings.

TL;DR: The developed monoclonal antibody, designated MET4, accurately and reproducibly measures c-MET expression by IHC in FFPE tissues and can be used for molecular imaging in vivo, encourage further development of MET4 as a multipurpose molecular diagnostics reagent to help to guide appropriate selection of patients being considered for treatment with c- MET–antagonistic drugs.