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Lenalidomide is an immunomodulatory agent which has been approved for multiple myeloma. Lenalidomide is also effective in and tolerated well by patients with follicular lymphoma, diffuse large B-cell lymphoma, and transformed large cell lymphoma. This review summarizes the results of current preclinical and clinical studies of lenalidomide, alone or in(More)
We propose an approach for decomposing Boolean satisfiability problems while extending recent results of [12] on solving Boolean systems of equations. Developments in [12] were aimed at the expansion of functions f in orthonormal (ON) sets of base functions as a generalization of the Boole-Shannon expansion and the derivation of the consistency condition(More)
  • Praveen Kumar Kolla, Madhav Desai, Ram Mohan Pathapati, B. Mastan Valli, Suneetha Pentyala, G. Madhusudhan Reddy +1 other
  • 2012
Cutaneous disorders can precede or follow the initiation of hemodialysis treatment. We evaluated the prevalence of various dermatological manifestations in patients undergoing hemodialysis at least twice a week for minimum of three months at our center. Patients were excluded if they were undergoing hemodialysis less than twice a week or on hemodialysis(More)
Given a CNF formula F , we present a new algorithm for deciding the satisfiability (SAT) of F and computing all solutions of assignments. The algorithm is based on the concept of cofactors known in the literature. This paper is a fallout of the previous work by authors on Boolean satisfiability [11, 12, 13], however the algorithm is essentially independent(More)
Introduction. Gitelman's syndrome (GS) is autosomal recessive renal tubular disorder characterized by hypokalemia, hypomagnesemia, hypocalciuria, metabolic alkalosis, and hyperreninemic hyperaldosteronism. It is usually associated with normal serum calcium. We report a patient presented with hypocalcemic tetany, and evaluation showed Gitelman's syndrome(More)
INTRODUCTION Presentation of the ischemic stroke due to vasoactive intestinal peptide producing tumor (VIPoma) or Verner Morrison syndrome is rare. This is first of its kind case which we are reporting here which was later turned out to be multiple endocrine neoplasia type 1 (MEN 1) syndrome with diagnosis of primary hyperparathyroidism in the same patient(More)
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