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15 in total

Review 1. Cellular and clinical pharmacology of fludarabine.

Authors: Varsha Gandhi; William Plunkett
Journal: Clin Pharmacokinet Date: 2002 Impact factor: 6.447

Review 2. Membrane transport and the antineoplastic action of nucleoside analogues.

Authors: F M Sirotnak; J R Barrueco
Journal: Cancer Metastasis Rev Date: 1987 Impact factor: 9.264

3. Deoxycytidine kinase-mediated toxicity of deoxyadenosine analogs toward malignant human lymphoblasts in vitro and toward murine L1210 leukemia in vivo.

Authors: D A Carson; D B Wasson; J Kaye; B Ullman; D W Martin; R K Robins; J A Montgomery
Journal: Proc Natl Acad Sci U S A Date: 1980-11 Impact factor: 11.205

4. 6-N-substituted derivatives of adenine arabinoside as selective inhibitors of varicella-zoster virus.

Authors: G W Koszalka; D R Averett; J A Fyfe; G B Roberts; T Spector; K Biron; T A Krenitsky
Journal: Antimicrob Agents Chemother Date: 1991-07 Impact factor: 5.191

5. Ocular toxicity of fludarabine: a purine analog.

Authors: Xiaoyan Ding; Alexandra A Herzlich; Rachel Bishop; Jingsheng Tuo; Chi-Chao Chan
Journal: Expert Rev Ophthalmol Date: 2008-02

Review 6. Fludarabine phosphate. A new anticancer drug with significant activity in patients with chronic lymphocytic leukemia and in patients with lymphoma.

Authors: G Rodriguez
Journal: Invest New Drugs Date: 1994 Impact factor: 3.850

7. 9-beta-D-arabinofuranosyl-2-fluoroadenine 5'-monophosphate pharmacokinetics in plasma and tumor cells of patients with relapsed leukemia and lymphoma.

Authors: L Danhauser; W Plunkett; M Keating; F Cabanillas
Journal: Cancer Chemother Pharmacol Date: 1986 Impact factor: 3.333

Review 8. Evolution of the arabinosides and the pharmacology of fludarabine.

Authors: W Plunkett; V Gandhi
Journal: Drugs Date: 1994 Impact factor: 9.546

Review 9. Clinical experience with fludarabine in leukaemia.

Authors: M J Keating; E Estey; S O'Brien; H Kantarjian; L E Robertson; W Plunkett
Journal: Drugs Date: 1994 Impact factor: 9.546

10. Development of modified nucleosides that have supremely high anti-HIV activity and low toxicity and prevent the emergence of resistant HIV mutants.

Authors: Hiroshi Ohrui
Journal: Proc Jpn Acad Ser B Phys Biol Sci Date: 2011 Impact factor: 3.493