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Spectrum and the In Vitro Antifungal Susceptibility Pattern of Yeast Isolates in Ethiopian HIV Patients with Oropharyngeal Candidiasis.

International journal of microbiology

Moges B, Bitew A, Shewaamare A.
PMID: 26880925
Int J Microbiol. 2016;2016:3037817. doi: 10.1155/2016/3037817. Epub 2016 Jan 05.

Background. In Ethiopia, little is known regarding the distribution and the in vitro antifungal susceptibility profile of yeasts. Objective. This study was undertaken to determine the spectrum and the in vitro antifungal susceptibility pattern of yeasts isolated from HIV...

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Moges B, Bitew A, Shewaamare A. Spectrum and the In Vitro Antifungal Susceptibility Pattern of Yeast Isolates in Ethiopian HIV Patients with Oropharyngeal Candidiasis. Int J Microbiol. 2016;2016:3037817doi: 10.1155/2016/3037817.
Moges, B., Bitew, A., & Shewaamare, A. (2016). Spectrum and the In Vitro Antifungal Susceptibility Pattern of Yeast Isolates in Ethiopian HIV Patients with Oropharyngeal Candidiasis. International journal of microbiology, 20163037817. https://doi.org/10.1155/2016/3037817
Moges, Birhan, et al. "Spectrum and the In Vitro Antifungal Susceptibility Pattern of Yeast Isolates in Ethiopian HIV Patients with Oropharyngeal Candidiasis." International journal of microbiology vol. 2016 (2016): 3037817. doi: https://doi.org/10.1155/2016/3037817
Moges B, Bitew A, Shewaamare A. Spectrum and the In Vitro Antifungal Susceptibility Pattern of Yeast Isolates in Ethiopian HIV Patients with Oropharyngeal Candidiasis. Int J Microbiol. 2016;2016:3037817. doi: 10.1155/2016/3037817. Epub 2016 Jan 05. PMID: 26880925; PMCID: PMC4736391.
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Combining cytochrome P-450 3A4 modulators and cyclosporine or everolimus in transplantation is successful.

World journal of transplantation

González F, Valjalo R.
PMID: 26722662
World J Transplant. 2015 Dec 24;5(4):338-47. doi: 10.5500/wjt.v5.i4.338.

AIM: To describe the long term follow-up of kidney allograft recipients receiving ketoconazole with calcineurin inhibitors (CNI) alone or combined with everolimus.METHODS: This is an open-label, prospective observational clinical trial in low immunologic risk patients who, after signing an...

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González F, Valjalo R. Combining cytochrome P-450 3A4 modulators and cyclosporine or everolimus in transplantation is successful. World J Transplant. 2015;5(4):338-47doi: 10.5500/wjt.v5.i4.338.
González, F., & Valjalo, R. (2015). Combining cytochrome P-450 3A4 modulators and cyclosporine or everolimus in transplantation is successful. World journal of transplantation, 5(4), 338-47. https://doi.org/10.5500/wjt.v5.i4.338
González, Fernando, and Valjalo, Ricardo. "Combining cytochrome P-450 3A4 modulators and cyclosporine or everolimus in transplantation is successful." World journal of transplantation vol. 5,4 (2015): 338-47. doi: https://doi.org/10.5500/wjt.v5.i4.338
González F, Valjalo R. Combining cytochrome P-450 3A4 modulators and cyclosporine or everolimus in transplantation is successful. World J Transplant. 2015 Dec 24;5(4):338-47. doi: 10.5500/wjt.v5.i4.338. PMID: 26722662; PMCID: PMC4689945.
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Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1.

Avicenna journal of phytomedicine

Adzu B, Mustapha KB, Masimirembwa C, Obodozie O, Kirim RA, Gamaniel KS.
PMID: 25050275
Avicenna J Phytomed. 2013;3(3):201-4.

OBJECTIVE: To evaluate the effect of NIPRD-AM1 on CYP3A4 in order to generate clinically significant data for its safe and efficacious use.MATERIALS AND METHODS: NIPRD-AM1 is a phytomedicine developed from aqueous root extracts of Nauclea latifolia Smith (Rubiaceae) for...

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Adzu B, Mustapha KB, Masimirembwa C, et al. Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1. Avicenna J Phytomed. 2013;3(3):201-4
Adzu, B., Mustapha, K. B., Masimirembwa, C., Obodozie, O., Kirim, R. A., & Gamaniel, K. S. (2013). Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1. Avicenna journal of phytomedicine, 3(3), 201-4.
Adzu, Bulus, et al. "Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1." Avicenna journal of phytomedicine vol. 3,3 (2013): 201-4.
Adzu B, Mustapha KB, Masimirembwa C, Obodozie O, Kirim RA, Gamaniel KS. Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1. Avicenna J Phytomed. 2013;3(3):201-4. PMID: 25050275; PMCID: PMC4075716.
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Similarity of metabolism for CAI (NSC 609974) in human liver tissue in vitro and in humans in vivo.

Clinical cancer research : an official journal of the American Association for Cancer Research

Ludden LK, Strong JM, Kohn EC, Collins JM.
PMID: 9815997
Clin Cancer Res. 1995 Apr;1(4):399-405.

Metabolism of a new antitumor agent, CAI (NSC 609974), was investigated in human liver tissue in vitro and in plasma and urine of patients receiving CAI. Metabolites identified by HPLC following C-labeled CAI incubation with human liver microsomes and...

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Ludden LK, Strong JM, Kohn EC, et al. Similarity of metabolism for CAI (NSC 609974) in human liver tissue in vitro and in humans in vivo. Clin Cancer Res. 1995;1(4):399-405
Ludden, L. K., Strong, J. M., Kohn, E. C., & Collins, J. M. (1995). Similarity of metabolism for CAI (NSC 609974) in human liver tissue in vitro and in humans in vivo. Clinical cancer research : an official journal of the American Association for Cancer Research, 1(4), 399-405.
Ludden, et al. "Similarity of metabolism for CAI (NSC 609974) in human liver tissue in vitro and in humans in vivo." Clinical cancer research : an official journal of the American Association for Cancer Research vol. 1,4 (1995): 399-405.
Ludden LK, Strong JM, Kohn EC, Collins JM. Similarity of metabolism for CAI (NSC 609974) in human liver tissue in vitro and in humans in vivo. Clin Cancer Res. 1995 Apr;1(4):399-405. PMID: 9815997.
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Polycyclic aromatic hydrocarbons inhibit in vitro ovarian steroidogenesis in the flounder (Platichthys flesus L.).

Aquatic toxicology (Amsterdam, Netherlands)

Rocha Monteiro PR, Reis-Henriques MA, Coimbra J.
PMID: 10794836
Aquat Toxicol. 2000 Apr 01;48(4):549-559. doi: 10.1016/s0166-445x(99)00055-7.

The in vitro effect of polycyclic aromatic hydrocarbons (PAHs) on ovarian steroidogenesis of the flounder (Platichthys flesus L.) was determined. Fully vitellogenic ovary tissue was in vitro incubated in the presence of phenanthrene, benzo[a]pyrene or chrysene, using 17alpha-hydroxyprogesterone or...

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Rocha Monteiro PR, Reis-Henriques MA, Coimbra J. Polycyclic aromatic hydrocarbons inhibit in vitro ovarian steroidogenesis in the flounder (Platichthys flesus L.). Aquat Toxicol. 2000;48(4):549-559doi: 10.1016/s0166-445x(99)00055-7.
Rocha Monteiro PR, Reis-Henriques, M. A., & Coimbra, J. (2000). Polycyclic aromatic hydrocarbons inhibit in vitro ovarian steroidogenesis in the flounder (Platichthys flesus L.). Aquatic toxicology (Amsterdam, Netherlands), 48(4), 549-559. https://doi.org/10.1016/s0166-445x(99)00055-7
Rocha Monteiro PR, et al. "Polycyclic aromatic hydrocarbons inhibit in vitro ovarian steroidogenesis in the flounder (Platichthys flesus L.)." Aquatic toxicology (Amsterdam, Netherlands) vol. 48,4 (2000): 549-559. doi: https://doi.org/10.1016/s0166-445x(99)00055-7
Rocha Monteiro PR, Reis-Henriques MA, Coimbra J. Polycyclic aromatic hydrocarbons inhibit in vitro ovarian steroidogenesis in the flounder (Platichthys flesus L.). Aquat Toxicol. 2000 Apr 01;48(4):549-559. doi: 10.1016/s0166-445x(99)00055-7. PMID: 10794836.
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Unusual presentation of cutaneous leishmaniasis.

Indian journal of dermatology, venereology and leprology

Lahiry AK.
PMID: 17656914
Indian J Dermatol Venereol Leprol. 2002 May-Jun;68(3):145-6.

Cutaneous leishmaniasis is endemic in some regions of Saudi Arabia. A case with uncommon hyperkeratotic type of lesion was seen. Being an endemic zone, a slit-skin smear was done and stained with Giemsa's stain. Smears showed Leishman Donovan bodies...

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Lahiry AK. Unusual presentation of cutaneous leishmaniasis. Indian J Dermatol Venereol Leprol. 2002;68(3):145-6
Lahiry, A. K. (2002). Unusual presentation of cutaneous leishmaniasis. Indian journal of dermatology, venereology and leprology, 68(3), 145-6.
Lahiry, Anup Kumar. "Unusual presentation of cutaneous leishmaniasis." Indian journal of dermatology, venereology and leprology vol. 68,3 (2002): 145-6.
Lahiry AK. Unusual presentation of cutaneous leishmaniasis. Indian J Dermatol Venereol Leprol. 2002 May-Jun;68(3):145-6. PMID: 17656914.
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Synthesis and antifungal activity of metal complexes containing dichloro-tetramorpholino-cyclophosphazatriene.

Metal-based drugs

Guran C, Barboiu M, Diaconescu P, Iluc V, Bojin M, Scozzafava A, Supuran CT.
PMID: 18475860
Met Based Drugs. 1998;5(5):287-94. doi: 10.1155/MBD.1998.287.

Metal complexes of dichloro-tetramorpholino-cyclophosphazatriene containing divalent cations such as Ni(II), Co(II), and Mn(II) have been prepared and characterised by standard physico-chemical procedures (elemental chemical analysis, IR and UV-VIS spectra, conductimetric measurement). The newly synthesised compounds possessed antifungal activity against...

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Guran C, Barboiu M, Diaconescu P, et al. Synthesis and antifungal activity of metal complexes containing dichloro-tetramorpholino-cyclophosphazatriene. Met Based Drugs. 1998;5(5):287-94doi: 10.1155/MBD.1998.287.
Guran, C., Barboiu, M., Diaconescu, P., Iluc, V., Bojin, M., Scozzafava, A., & Supuran, C. T. (1998). Synthesis and antifungal activity of metal complexes containing dichloro-tetramorpholino-cyclophosphazatriene. Metal-based drugs, 5(5), 287-94. https://doi.org/10.1155/MBD.1998.287
Guran, C, et al. "Synthesis and antifungal activity of metal complexes containing dichloro-tetramorpholino-cyclophosphazatriene." Metal-based drugs vol. 5,5 (1998): 287-94. doi: https://doi.org/10.1155/MBD.1998.287
Guran C, Barboiu M, Diaconescu P, Iluc V, Bojin M, Scozzafava A, Supuran CT. Synthesis and antifungal activity of metal complexes containing dichloro-tetramorpholino-cyclophosphazatriene. Met Based Drugs. 1998;5(5):287-94. doi: 10.1155/MBD.1998.287. PMID: 18475860; PMCID: PMC2365132.
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Functionalized Derivatives of Benzo-Crown Ethers. Part 4. Antifungal Macrocyclic Supramolecular Complexes of Transition Metal Ions Acting as Lanosterol-14-alpha-Demethylase Ihibitors.

Metal-based drugs

Barboiu M, Supuran CT, Scozzafava A, Guran C, Diaconescu P, Bojin M, Iluc V, Cot L.
PMID: 18475888
Met Based Drugs. 1999;6(2):101-10. doi: 10.1155/MBD.1999.101.

Poly- and mononuclear metal complexes of 2,3,11,12-bis[4-(10-aminodecylcarbonyl)]benzo-18- crown-6 (L) and Cu(II); Ni(II); Co(II) and Cr(III) have been synthesized and characterized by standard physico-chemical procedures. In the newly prepared complexes the crown moiety oxygen atoms of the macrocyclic host did...

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Barboiu M, Supuran CT, Scozzafava A, et al. Functionalized Derivatives of Benzo-Crown Ethers. Part 4. Antifungal Macrocyclic Supramolecular Complexes of Transition Metal Ions Acting as Lanosterol-14-alpha-Demethylase Ihibitors. Met Based Drugs. 1999;6(2):101-10doi: 10.1155/MBD.1999.101.
Barboiu, M., Supuran, C. T., Scozzafava, A., Guran, C., Diaconescu, P., Bojin, M., Iluc, V., & Cot, L. (1999). Functionalized Derivatives of Benzo-Crown Ethers. Part 4. Antifungal Macrocyclic Supramolecular Complexes of Transition Metal Ions Acting as Lanosterol-14-alpha-Demethylase Ihibitors. Metal-based drugs, 6(2), 101-10. https://doi.org/10.1155/MBD.1999.101
Barboiu, M, et al. "Functionalized Derivatives of Benzo-Crown Ethers. Part 4. Antifungal Macrocyclic Supramolecular Complexes of Transition Metal Ions Acting as Lanosterol-14-alpha-Demethylase Ihibitors." Metal-based drugs vol. 6,2 (1999): 101-10. doi: https://doi.org/10.1155/MBD.1999.101
Barboiu M, Supuran CT, Scozzafava A, Guran C, Diaconescu P, Bojin M, Iluc V, Cot L. Functionalized Derivatives of Benzo-Crown Ethers. Part 4. Antifungal Macrocyclic Supramolecular Complexes of Transition Metal Ions Acting as Lanosterol-14-alpha-Demethylase Ihibitors. Met Based Drugs. 1999;6(2):101-10. doi: 10.1155/MBD.1999.101. PMID: 18475888; PMCID: PMC2365158.
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[Minimal inhibitory concentrations of Candida species to five antifungals by using the reference dilution micromethod and the E-test.].

Revista iberoamericana de micologia

Torres-Rodríguez JM, Madrenys N, Jiménez T, Saballs P.
PMID: 17655386
Rev Iberoam Micol. 1997 Sep;14(3):115-8.

It is accepted that the frequency of candidosis has increased during the last decade, specially in hospitalized patients. The more frequent use of azole antifungals and the recognition of isolates of Candida sp resistant to these and other drugs...

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Torres-Rodríguez JM, Madrenys N, Jiménez T, et al. Concentraciones mínimas inhibitorias de levaduras a cinco antifúngicos utilizando un micrométodo de dilución estandarizado y el E-test. [Minimal inhibitory concentrations of Candida species to five antifungals by using the reference dilution micromethod and the E-test.]. Rev Iberoam Micol. 1997;14(3):115-8
Torres-Rodríguez, J. M., Madrenys, N., Jiménez, T., & Saballs, P. (1997). Concentraciones mínimas inhibitorias de levaduras a cinco antifúngicos utilizando un micrométodo de dilución estandarizado y el E-test. [Minimal inhibitory concentrations of Candida species to five antifungals by using the reference dilution micromethod and the E-test.]. Revista iberoamericana de micologia, 14(3), 115-8.
Torres-Rodríguez, J M, et al. "Concentraciones mínimas inhibitorias de levaduras a cinco antifúngicos utilizando un micrométodo de dilución estandarizado y el E-test." [Minimal inhibitory concentrations of Candida species to five antifungals by using the reference dilution micromethod and the E-test.]. Revista iberoamericana de micologia vol. 14,3 (1997): 115-8.
Torres-Rodríguez JM, Madrenys N, Jiménez T, Saballs P. Concentraciones mínimas inhibitorias de levaduras a cinco antifúngicos utilizando un micrométodo de dilución estandarizado y el E-test. [Minimal inhibitory concentrations of Candida species to five antifungals by using the reference dilution micromethod and the E-test.]. Rev Iberoam Micol. 1997 Sep;14(3):115-8. Spanish. PMID: 17655386.
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Prevalence and in vitro antifungal susceptibility of Candida spp isolated from clinical specimens in São Paulo, Brazil.

Revista iberoamericana de micologia

Sugizaki MF, Rhoden CR, Bombonatti DM, Montelli AC, Martinson ME, de Magalhães Lopes CA.
PMID: 17655397
Rev Iberoam Micol. 1998 Mar;15(1):16-8.

We examined the prevalence and the in vitro susceptibility to antifungal drugs of Candida spp isolated from clinical specimens at our university hospital in São Paulo, Brazil. Among 6,417 samples studied, positive cultures, were obtained from 222 (3.5%) most...

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Sugizaki MF, Rhoden CR, Bombonatti DM, et al. Prevalence and in vitro antifungal susceptibility of Candida spp isolated from clinical specimens in São Paulo, Brazil. Rev Iberoam Micol. 1998;15(1):16-8
Sugizaki, M. F., Rhoden, C. R., Bombonatti, D. M., Montelli, A. C., Martinson, M. E., & de Magalhães Lopes, C. A. (1998). Prevalence and in vitro antifungal susceptibility of Candida spp isolated from clinical specimens in São Paulo, Brazil. Revista iberoamericana de micologia, 15(1), 16-8.
Sugizaki, M F, et al. "Prevalence and in vitro antifungal susceptibility of Candida spp isolated from clinical specimens in São Paulo, Brazil." Revista iberoamericana de micologia vol. 15,1 (1998): 16-8.
Sugizaki MF, Rhoden CR, Bombonatti DM, Montelli AC, Martinson ME, de Magalhães Lopes CA. Prevalence and in vitro antifungal susceptibility of Candida spp isolated from clinical specimens in São Paulo, Brazil. Rev Iberoam Micol. 1998 Mar;15(1):16-8. PMID: 17655397.
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Mizolastine: a review of its use in allergic rhinitis and chronic idiopathic urticaria.

BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy

Prakash A, Lamb HM.
PMID: 18020585
BioDrugs. 1998 Jul;10(1):41-63. doi: 10.2165/00063030-199810010-00004.

UNLABELLED: Mizolastine is a second generation antihistamine agent with high affinity and specificity for histamine H(1) receptors. Mizolastine has demonstrated antiallergic effects in animals and healthy volunteers and anti-inflammatory activity in animal models. Double-blind trials have shown mizolastine to...

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Prakash A, Lamb HM. Mizolastine: a review of its use in allergic rhinitis and chronic idiopathic urticaria. BioDrugs. 1998;10(1):41-63doi: 10.2165/00063030-199810010-00004.
Prakash, A., & Lamb, H. M. (1998). Mizolastine: a review of its use in allergic rhinitis and chronic idiopathic urticaria. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 10(1), 41-63. https://doi.org/10.2165/00063030-199810010-00004
Prakash, A, and Lamb, H M. "Mizolastine: a review of its use in allergic rhinitis and chronic idiopathic urticaria." BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy vol. 10,1 (1998): 41-63. doi: https://doi.org/10.2165/00063030-199810010-00004
Prakash A, Lamb HM. Mizolastine: a review of its use in allergic rhinitis and chronic idiopathic urticaria. BioDrugs. 1998 Jul;10(1):41-63. doi: 10.2165/00063030-199810010-00004. PMID: 18020585.
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Flare Associated with LHRH-Agonist Therapy.

Reviews in urology

Thompson IM.
PMID: 16986003
Rev Urol. 2001;3:S10-4.

The most common form of hormonal treatment for prostate cancer is luteinizing hormone-releasing hormone (LHRH)-agonist therapy. During the first 1 to 3 weeks of LHRH-agonist therapy, an initial increase in testosterone is associated with a condition known as "flare."...

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Thompson IM. Flare Associated with LHRH-Agonist Therapy. Rev Urol. 2001;3:S10-4
Thompson, I. M. (2001). Flare Associated with LHRH-Agonist Therapy. Reviews in urology, 3S10-4.
Thompson, I M. "Flare Associated with LHRH-Agonist Therapy." Reviews in urology vol. 3 (2001): S10-4.
Thompson IM. Flare Associated with LHRH-Agonist Therapy. Rev Urol. 2001;3:S10-4. PMID: 16986003; PMCID: PMC1476081.
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Showing 13 to 24 of 483 entries