Laboratory confirmed miltefosine resistant cases of visceral leishmaniasis from India
暂无分享,去创建一个
[1] G. H. Coombs,et al. In vitro selection of miltefosine resistance in promastigotes of Leishmania donovani from Nepal: genomic and metabolomic characterization , 2016, Molecular microbiology.
[2] A. Kulshrestha,et al. Comparative transcript expression analysis of miltefosine-sensitive and miltefosine-resistant Leishmania donovani , 2014, Parasitology Research.
[3] M. Rai,et al. In vitro susceptibility of Leishmania donovani to miltefosine in Indian visceral leishmaniasis. , 2013, The American journal of tropical medicine and hygiene.
[4] Sarman Singh,et al. Miltefosine resistance in Leishmania donovani involves suppression of oxidative stress-induced programmed cell death. , 2013, Experimental parasitology.
[5] J. Beijnen,et al. Increasing failure of miltefosine in the treatment of Kala-azar in Nepal and the potential role of parasite drug resistance, reinfection, or noncompliance. , 2013, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[6] R. Dey,et al. A new model of progressive visceral leishmaniasis in hamsters by natural transmission via bites of vector sand flies. , 2013, The Journal of infectious diseases.
[7] R. Madhubala,et al. Visceral and post-Kala-Azar dermal leishmaniasis isolates show significant difference in their in vitro drug susceptibility pattern , 2013, Parasitology Research.
[8] S. Sundar,et al. Efficacy of miltefosine in the treatment of visceral leishmaniasis in India after a decade of use. , 2012, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[9] S. Sundar,et al. Drug Susceptibility in Leishmania Isolates Following Miltefosine Treatment in Cases of Visceral Leishmaniasis and Post Kala-Azar Dermal Leishmaniasis , 2012, PLoS neglected tropical diseases.
[10] J. Le bras,et al. Leishmania Resistance to Miltefosine Associated with Genetic Marker , 2012, Emerging infectious diseases.
[11] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer , 2011, Nature Biotechnology.
[12] Matthew Berriman,et al. Iterative Correction of Reference Nucleotides (iCORN) using second generation sequencing technology , 2010, Bioinform..
[13] O. Kaneko,et al. Relapse of visceral leishmaniasis after miltefosine treatment in a Nepalese patient. , 2009, The American journal of tropical medicine and hygiene.
[14] P. Leprohon,et al. Parasite susceptibility to amphotericin B in failures of treatment for visceral leishmaniasis in patients coinfected with HIV type 1 and Leishmania infantum. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[15] S. Croft,et al. Inactivation of the miltefosine transporter, LdMT, causes miltefosine resistance that is conferred to the amastigote stage of Leishmania donovani and persists in vivo. , 2007, International journal of antimicrobial agents.
[16] O. Zerpa,et al. Diffuse cutaneous leishmaniasis responds to miltefosine but then relapses , 2007, The British journal of dermatology.
[17] H. Sindermann,et al. Relapse of new world diffuse cutaneous leishmaniasis caused by Leishmania (Leishmania) mexicana after miltefosine treatment. , 2006, The American journal of tropical medicine and hygiene.
[18] S. Croft,et al. Miltefosine: issues to be addressed in the future. , 2006, Transactions of the Royal Society of Tropical Medicine and Hygiene.
[19] S. Castanys,et al. Phospholipid Translocation and Miltefosine Potency Require Both L. donovani Miltefosine Transporter and the New Protein LdRos3 in Leishmania Parasites* , 2006, Journal of Biological Chemistry.
[20] K. Chang,et al. Cloning, expression, and purification of a novel recombinant antigen from Leishmania donovani. , 2006, Protein expression and purification.
[21] J. Berman. Visceral leishmaniasis in the New World & Africa. , 2006, The Indian journal of medical research.
[22] S. Croft,et al. Mechanisms of experimental resistance of Leishmania to miltefosine: Implications for clinical use. , 2006, Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy.
[23] S. Filteau,et al. Plasma 25-hydroxyvitamin D does not vary over the course of a malarial infection. , 2003, Transactions of the Royal Society of Tropical Medicine and Hygiene.
[24] S. Sundar,et al. Treatment options for visceral leishmaniasis: a systematic review of clinical studies done in India, 1980-2004. , 2005, The Lancet. Infectious diseases.
[25] J. Berman,et al. Advances in leishmaniasis , 2005, The Lancet.
[26] P. Loiseau,et al. Alteration of Fatty Acid and Sterol Metabolism in Miltefosine-Resistant Leishmania donovani Promastigotes and Consequences for Drug-Membrane Interactions , 2005, Antimicrobial Agents and Chemotherapy.
[27] M. Chatterjee,et al. Development of a modified MTT assay for screening antimonial resistant field isolates of Indian visceral leishmaniasis. , 2005, Parasitology international.
[28] S. Sundar,et al. Availability of miltefosine for the treatment of kala-azar in India. , 2005, Bulletin of the World Health Organization.
[29] Sarman Singh,et al. Challenges and new discoveries in the treatment of leishmaniasis , 2004, Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy.
[30] M. Ouellette,et al. Functional Cloning of the Miltefosine Transporter , 2003, Journal of Biological Chemistry.
[31] G. Matlashewski,et al. Heterologous expression of a mammalian protein tyrosine phosphatase gene in Leishmania: effect on differentiation , 2003, Molecular microbiology.
[32] S. Croft,et al. Characterisation of Leishmania donovani promastigotes resistant to hexadecylphosphocholine (miltefosine). , 2003, International journal of antimicrobial agents.
[33] J. Nichols,et al. Lem3p Is Essential for the Uptake and Potency of Alkylphosphocholine Drugs, Edelfosine and Miltefosine* , 2003, Journal of Biological Chemistry.
[34] Shyam Sundar,et al. Visceral leishmaniasis: current status of control, diagnosis, and treatment, and a proposed research and development agenda. , 2002, The Lancet. Infectious diseases.
[35] D. Ellis. Amphotericin B: spectrum and resistance. , 2002, The Journal of antimicrobial chemotherapy.
[36] L. Oskam,et al. Leishmania donovani: intraspecific polymorphisms of Sudanese isolates revealed by PCR-based analyses and DNA sequencing. , 2001, Experimental parasitology.
[37] S. Sundar,et al. Failure of pentavalent antimony in visceral leishmaniasis in India: report from the center of the Indian epidemic. , 2000, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[38] J. Berman,et al. U.S Food and Drug Administration approval of AmBisome (liposomal amphotericin B) for treatment of visceral leishmaniasis. , 1999, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[39] A. Pandey,et al. Do the diminishing efficacy and increasing toxicity of sodium stibogluconate in the treatment of visceral leishmaniasis in Bihar, India, justify its continued use as a first-line drug? An observational study of 80 cases , 1998 .
[40] C. P. Thakur,et al. Do the diminishing efficacy and increasing toxicity of sodium stibogluconate in the treatment of visceral leishmaniasis in Bihar, India, justify its continued use as a first-line drug? An observational study of 80 cases. , 1998, Annals of tropical medicine and parasitology.
[41] S. Reed,et al. Diagnostic and prognostic value of K39 recombinant antigen in Indian leishmaniasis. , 1995, The Journal of parasitology.