Base de dados : HANSEN
Pesquisa : MINOCICLINA [Descritor de assunto]
Referências encontradas : 19 [refinar]
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  1 / 19 HANSEN  
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Id:27305
Autor:Mane, Ibrahima; Cartel, Jean-Louis; Grosset, Jacques-Henri.
Título:Field trial on efficacy of supervised monthly dose of 600mg rifampin, 400mg ofloxacin and 100mg minocycline for the treatment of leprosy; first results.
Fonte:Int. J. Lepr;65(2):224-229, Jun. 1997. tab.
Resumo:In 1995, a field trial was implemented in Senegal in order to evaluate the efficacy of a regimen based on the monthly supervised intake of rifampin 600 mg, ofloxacin 400 mg and minocycline 100 mg to treat leprosy. During the first year of the trial, 220 patients with active leprosy (newly detected or relapsing after dapsone monotherapy) were recruited: 102 paucibacillary (PB) (60 males and 42 females) and 118 multibacillary (MB) (71 males and 47 females). All of them accepted the new treatment (none requested to be preferably put under standard WHO/MDT), no clinical sign which could be considered as a toxic effect of the drug was noted, and none of the patients refused to continue treatment because of any clinical trouble. The compliance was excellent: the 113 patients (PB and MB) detected during the first 6 months of the trial have taken six monthly doses in 6 months, as planned. The rate of clearance and the progressive decrease of cutaneous lesions was satisfactory. Although it is too soon to give comprehensive results, it should be noted that no treatment failure was observed in the 56 PB patients who have completed treatment and have been followed up for 6 months. The long-term efficacy of the new regimen is to be evaluated on the rate of relapse during the years following the cessation of treatment. If that relapse rate is acceptable (similar to that observed in patients after treatment with current standard WHO/ MDT), the new regimen could be a solution to treat, for instance, patients very irregular and/or living in remote or inaccessible areas since no selection of rifampin-resistant Mycobacterium leprae should be possible (a monthly dose of ofloxacin and minocycline being as effective as a dose of dapsone and clofazimine taken daily for 1 month). Nevertheless, until longer term results of this and other trials become available, there is no justification for any change in the treatment strategy, and all leprosy patients should be put under standard WHO/MDT. (AU)^ien.
Descritores:Hanseníase/quimioter
Rifampina/admin
Rifampina/ef adv
Rifampina/uso terap
Ofloxacino/admin
Ofloxacino/ef adv
Ofloxacino/uso terap
Minociclina/admin
Minociclina/ef adv
Minociclina/uso terap
Limites:Humanos
Masculino
Feminino
Localização:BR191.1


  2 / 19 HANSEN  
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Texto Completo-en
Id:27041
Autor:Fajardo, Tranquilino T Jr; Villahermos, Laarni G; Cruz, Eduardo C. Dela; Abalos, Rodolfo M; Franzblau, Scoott G; Walsh, Gerald P.
Título:Minocycline in Lepromatous Leprosy.
Fonte:Int. J. Lepr;63(1):8-17, 1995. ^btab.
Resumo:Twelve patients were treated with three dose levels of minocycline for 30 days, primarily to detect the dose-related effects on Mycobacterium leprae viability, followed by another 5 months of daily minocycline for overall efficacy and persistence of clinical and antibacterial effects. Subsequently, the patients were given standard WHO/MDT chemotherapy for multibacillary leprosy. Clinical improvement was recognizable during the first month, occurring much earlier among those on minocycline 200 mg daily than those who received minocycline 100 mg daily. A similar change also was observed in one patient 11 days after three daily doses of 100 mg of minocycline. At the end of 6 months, all patients were clinically improved with a slight reduction in the average bacterial index (BI) and logarithmic index of bacilli in biopsy (LIB). The effects of minocycline on viability by mouse foot pad inoculation and palmitic acid oxidation assays were noted beginning at 10 to 14 days of daily dosing and becoming more definite after 30 days of treatment. Both tests correlated fairly well. Doses of 200 mg daily did not appear to be more efficient than minocycline 100 daily. Phenolic glycolipid-I (PGL-I) antigen determinations done on some patients during the first month remained positive and did not correlate with changes in viability results. At the end of 6 months, after 5 months of 100 mg of minocycline monotherapy, no viable organisms could be demonstrated by mouse foot pad inoculation and palmitic acid oxidation assays; assays for PGL-I antigen were all negative.
Descritores:Hanseníase Virchowiana/imunol
Hanseníase Virchowiana/fisiopatol
Minociclina/imunol
Limites:Humanos
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/1995/pdf/v63n1/v63n1a02.pdf - en.
Localização:BR191.1


  3 / 19 HANSEN  
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Texto Completo-en
Id:26908
Autor:Rea, Thomas H.
Título:Trials of Daily, long-term minocycline and rifampin of clarithromycin and rifampin in the treatment of borderlinne lepromatous and lepromatous leprosy.
Fonte:Int. J. Lepr;68(2):129-135, Jun., 2000. graf.
Resumo:Daily, long-term treatment with minocycline 100 mg and rifampin 600 mg was initiated in 24 previously untreated borderline lepromatous (BL) and lepromatous (LL) patients for a total of 646 patient-months, averaging 26.9 months per patient. The same regimen was started in 12 BL and LL patients having a bacteriologic relapse for a total of 379 patient-months, averaging 32.5 months per patient, and in 12 patients judged to be at high risk for relapse for a total of 354 patient-months, averaging 29.5 months per patient. Daily, long-term treatment with clarithromycin 500 mg and rifampin 600 mg was initiated in 8 previously untreated BL and LL patients for a total of 174 patient-months, averaging 21.8 months per patient. The results in these 56 patients were compared to those obtained in 34 previously untreated BL and LL patients who were treated concurrently receiving daily, long-term dapsone 100 mg and rifampin 600 mg. No evidence of dangerous drug reactions or bone marrow, kidney or liver toxicity was seen in any of these five patient groups. Drug intolerance in 10 of the 90 patients studied necessitated discontinuing the chosen regimen, 4 from rifampin, 3 from dapsone, 2 from minocycline and 1 of undetermined attribution. The use of either minocycline or clarithromycin in conjunction with rifampin appears to pose no great risk when used long term. (AU)^ien.
Descritores:Hanseníase Virchowiana/quimioter
Hanseníase Virchowiana/imunol
Minociclina/uso terap
Rifampina/uso terap
Claritromicina/uso terap
Meio Eletrônico:http://hansen.bvs.ilsl.br/textoc/revistas/intjlepr/2000/pdf/v68n2/v68n2a02.pdf - en.
Localização:BR191.1


  4 / 19 HANSEN  
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Id:25458
Autor:Ebenezer, G. J; Norman, G; Joseph, G. A; Daniel, S; Job, C. K
Título:Drug resistant-Mycobacterium leprae- results of mouse footpad studies from a laboratory in South India
..-
Fonte:s.l; s.n; 2002. 12 p. tab.
Resumo:Out of 265 biopsies of leprosy patients received at the Experimental Laboratory of Schieffelin Leprosy Research and Training Centre from 1987 to 1997 for evaluating resistant strains of M. leprae using the mouse footpad technique, 49 showed resistant strains of M. leprae to varying concentration of dapsone, rifampicin and clofazimine. 23 (47%) of these were from a control area. With 369 skin-smear positive multibacillary (MB) patients as the risk group (denominator), 23 (6.23%) were resistant to one or more drugs. 18 (4.88%) had dapsone resistance, 5 (1.36%) were resistant to rifampicin and 9 (2.44%) had resistance to low concentrations of clofazimine (0.0001%). Out of the 23 biopsies with drug resistance from the control area, primary dapsone resistance was seen in 7 (30%) biopsies and secondary dapsone resistance in 11 (48%). Primary rifampicin resitance was seen in 4 (17.4%) patients, secondary rifampicin resistance in 1 (4.35%) and primary clofazimine resistance in 7 (30%). 3 (13%) of the strains showed secondary clofazimine resistance. One biopsy had resistent strains to all the three drugs. In a control area where properly supervised effective multidrug therapy (MDT) was regularly administered over the years, the emergence of drug resistance is negligible. It may not be the case if the content, duration and regularity of the drug regimen were not satisfactory. Aware of the possible shortcomings in mass administration of MDT, it is emplasized that mouse footpad studies on drug resistance should be made available at least in endemic areas where the incidence of the disease has not changed despite good MDT coverage in order to monitor the emergence of drug resistance. Research into molecular biological identification of drug resistant-M.leprae should be intensified. These steps would help to institute timely measures to check the spread of any drug-resistant organisms in the community (AU).
Descritores:MYCOBACTERIUM LEPRAE/cresc
MYCOBACTERIUM LEPRAE/isol
MYCOBACTERIUM LEPRAE/metab
MYCOBACTERIUM LEPRAE/patogen
MYCOBACTERIUM LEPRAE/ultraest
RESISTÊNCIA A DROGAS
DAPSONA/uso terap
CLOFAZIMINA/uso terap
RIFAMPINA/uso terap
TESTES DE SENSIBILIDADE MICROBIANA/métodos
TESTES DE SENSIBILIDADE MICROBIANA/vet
HANSENIASE/clas
 HANSENIASE/compl
 HANSENIASE/quimioter
 HANSENIASE/imunol
 HANSENIASE/microbiol
 HANSENIASE/patol
 OFLOXACINO/uso terap
 MINOCICLINA/uso terap
Limites:HUMANO
Localização:BR191.1; 09299/s


  5 / 19 HANSEN  
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Id:25453
Autor:Consigny, Sophie; Bentoucha, Abdelhalim; Bonnafous, Pascale; Grosset, Jacques; Ji, Baohong
Título:Bactericidal activities of HMR 3647, moxifloxacin, and rifapentine against Mycobacterium leprae in mice
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Fonte:s.l; s.n; 2000. 3 p. tab.
Resumo:Bactericidal activities of HMR 3647 (HMR), moxifloxacin (MXFX), and rifapentine (RPT) against Mycobacterium leprae, measured by the proportional bactericidal technique in the mouse footpad system, were compared with those of the established antileprosy drugs clarithromycin (CLARI), ofloxacin (OFLO), and rifampin (RMP. Administered in five daily doses of 100 mg/kg of body weight, HMR appeared slightly more bactericidal than CLARI. In a single dose, MXFX at 150 mg/kg was more active than the same dose of OFLO and displayed exactly the same level of activity as RMP at 10 mg/kg; the combination MXFX-minocycline (MINO) (MM) was more bactericidal than the combination OFLO-MINO (OM); RPT at 10mg/kg was more bactericidal than the same dose of RMP and even more active than the combination RMP-OFLO-MINO (ROM); the combination RPT-MXFX-MINO (PMM) killed 99.9% of viable M. leprae and was slighthy more bactericidal than RPT alone, indicating that the combination PMM showed an additive effect against M. leprae (AU).
Descritores:HANSENIASE/quimioter
HANSENOSTATICOS/admin
HANSENOSTATICOS/farmacol
HANSENOSTATICOS/farmacocin
HANSENOSTATICOS/uso terap
MYCOBACTERIUM LEPRAE
TESTES DE SENSIBILIDADE MICROBIANA/métodos
DROGAS EM INVESTIGACAO/admin
DROGAS EM INVESTIGACAO/anal
DROGAS EM INVESTIGACAO/uso terap
BACTERICIDAS
 QUIMIOTERAPIA COMBINADA
 MYCOBACTERIUM LEPRAE/metab
 MYCOBACTERIUM LEPRAE/fisiol
 DAPSONA/uso terap
 RIFAMPINA/uso terap
 CLOFAZIMINA/uso terap
 OFLOXACINO/uso terap
 MINOCICLINA/uso terap
 CLARITROMICINA/uso terap
Limites:ESTUDO COMPARATIVO
Localização:BR191.1; 09311/s


  6 / 19 HANSEN  
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Id:24508
Autor:Aguas, José Terencio de las.
Título:Multiterapia de la hanseniasis en Europa / Multherapeutic leprosy in Europe
Fonte:Hansen. int;(n.esp):137-140, Jun. 1998. tab.
Conferência:Apresentado em: Congresso da Associação Brasileira de Hansenologia, IX, Foz do Iguaçu, 04-08 junho 1997.
Descritores:HANSENIASE/quimioter
HANSENIASE/prev
HANSENIASE/reabil
HANSENIASE/terap
CLARITROMICINA/bios
CLARITROMICINA/farmacol
CLARITROMICINA/uso terap
MINOCICLINA/farmacol
MINOCICLINA/uso terap
EUROPA (CONTINENTE)/epidemiol
Limites:RELATO DE CASO
ESTUDO COMPARATIVO
HUMANO
Localização:BR191.1


  7 / 19 HANSEN  
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Id:22742
Autor:Stefani, Mariane M. A; Martelli, Celina M. T; Gillis, Thomas P; Krahenbuhl, James L
Título:In situ type 1 cytokine gene expression and mechanism associated with early leprosy progression
..-
Fonte:s.l; s.n; 2003. 8 p. ilus.
Resumo:We explored the prognostic value of in situ cytokine patterns in 39 patients with single-skin-lesion paucibacillary leprosy before single-dose therapy, with 3 years of follow-up. Interferon (IFN)-gamma, interleukin (IL)-12, IL-10, IL-4, tumor necrosis factor (TNF)-alpha, and macrophage inflammatory protein (MIP)-1alpha mRNA was quantified in skin biopsy samples at diagnosis, and Mycobacterium leprae DNA was detected in 51.4% of cases. Type 1 immunity predominance with measurable IFN-gamma and undetectable IL-4, which is indicative of effective cell-mediated immunity, is compatible with both the reversal reactions (33.3%) and the resolution of lesions (64.1%) observed. A positive correlation between IL-12 and IFN-gamma indicated type 1 polarization via IL-12. The TNF-alpha/MIP-1alpha correlation implied the TNF-alpha induction of chemokines, which is important for granuloma formation. Positive correlations between key regulatory cytokines-IL-10 and IFN-gamma, IL-10 and IL-12, and IL-10 and TNF-alpha-suggests that there may be some level of an intralesional pro- or anti-inflammatory mechanism essential in avoiding immunopathology. (AU).
Descritores:Anticorpos Antibacterianos/BL
Biópsia
Estudos de Coortes
Citocinas/BI/*GE/IM
Regulação Bacteriana da Expressão Gênica/*IM
Hanseníase/DT/*GE/IM
Minociclina/TU
Mycobacterium leprae/*GE/IM
Ofloxacino/TU
Prognóstico
RNA Mensageiro/BI/GE
RNA Viral/BI/GE
Reação em Cadeia da Polimerase Via Transcriptase Reversa
Rifampina/TU
Limites:Adolescente
Adulto
Criança
Feminino
Humano
Masculino
Células Th1/IM
Localização:BR191.1; 01884/s


  8 / 19 HANSEN  
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Id:15783
Autor:Sehgal, Virendra N; Kumar, Sunil; Jain, Sanjiv; Bhattacharya, Samit N
Título:Relapse (reactivation) in borderline tuberculoid (BT) leprosy
..-
Fonte:s.l; s.n; 1998. 2 p. ilus.
Descritores:HANSENIASE DIMORFA
HANSENIASE DIMORFA
HANSENIASE TUBERCULOIDE
HANSENIASE TUBERCULOIDE
LEPROSTATICOS
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
ANTIBIOTICOS TETRACICLINICOS
DAPSONA
GRANULOMA
HISTIOCITOS
LINFOCITOS
MINOCICLINA
RECIDIVA
RIFAMPINA
Limites:ADULTO
HUMANO
MASCULINO
Localização:BR191.1; 07324/s


  9 / 19 HANSEN  
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Id:15490
Autor:Costa Neto, Julio
Título:Possibilidades secundárias no tratamento da hanseníase
Secondary possibilities in lweprosy's therapy-
Fonte:s.l; s.n; set. 2000. 5 p. .
Descritores:HANSENIASE
HANSENIASE
FORMAS DE DOSAGEM
ANTIBIOTICOS
TERAPIAS ALTERNATIVAS
PROTEINAS NA DIETA
VITAMINA E
VACINA BCG
OLEOS VEGETAIS
ETIONAMIDA
ESTREPTOMICINA
KANAMICINA
CICLOSSERINA
MINOCICLINA
CLARITROMICINA
QUINOLONAS
CEFALOSPORINAS
Localização:BR191.1; 08341/s


  10 / 19 HANSEN  
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Id:15474
Autor:Bernier, C; Dréno, B
Título:Minocycline
..-
Fonte:s.l; s.n; 2001. 11 p. .
Descritores:ACNE VULGAR
ANTIBIOTICOS TETRACICLINICOS
ANTIBIOTICOS TETRACICLINICOS
ANTIBIOTICOS TETRACICLINICOS
DOENÇAS AUTO-IMUNES
ESQUEMA DE MEDICAÇAO
CITOCINAS
HANSENIASE
DOENÇA DE LYME
MINOCICLINA
MINOCICLINA
MINOCICLINA
MICOBACTERIOSE
NOCARDIOSE
PRURIGO
PIODERMA GANGRENOSO
PROJETOS DE PESQUISA
DOENÇAS SEXUALMENTE TRANSMISSIVEIS
DERMATOPATIAS VESICULOBOLHOSAS
RESULTADO DE TRATAMENTO
Localização:BR191.1; 08329/s


  11 / 19 HANSEN  
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Id:14995
Autor:Ji, Baohong; Sow, Samba; Perani, Evelyne; Lienhardt, Christian; Diderot, Vimala; Grosset, Jacques
Título:Bactericidal activity of a single-dos combination of ofloxacin plus minocycline, with or without rifampin, against mycobacterium leprae in mice and in lepromatous patients
..-
Fonte:s.l; s.n; may, 1998. 6 p. tab.
Descritores:HANSENIASE
MYCOBACTERIUM LEPRAE
OFLOXACINA
OFLOXACINA
MINOCICLINA
MINOCICLINA
RIFAMPINA
RIFAMPINA
LEPROSTATICOS
LEPROSTATICOS
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS COMBINADOS
Localização:BR191.1; 07327/s


  12 / 19 HANSEN  
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Id:14078
Autor:Mandal, Ashim Kumar
Título:Single dose "ROM" therapy-Is it really effective? (Correspondence)
..-
Fonte:s.l; s.n; 1998. 1 p. .
Descritores:HANSENIASE
QUIMIOTERAPIA COMBINADA
LEPROSTATICOS
MINOCICLINA
RIFAMPINA
RESULTADO DE TRATAMENTO
Localização:BR191.1; 07138/s


  13 / 19 HANSEN  
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Id:14032
Autor:Gelber, Robert H; Baohong, Ji; Grosset, Jacques H
Título:Another view of the therapy of leprosy
..-
Fonte:s.l; s.n; 1998. 3 p. .
Descritores:HANSENIASE
LEPROSTATICOS
LEPROSTATICOS
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS TETRACICLINICOS
DAPSONA
MINOCICLINA
RIFAMPINA
Localização:BR191.1; 06998/s


  14 / 19 HANSEN  
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Id:13869
Autor:Baohong, J. I; Jamet, Pierre; Perani, Evelyne G; Sow, Samba; Lienhardt, Christian; Petinon, Corinne; Grosset, Jacques H
Título:Bactericidal activity of single dose of clarithromycin plus minocycline, with or without ofloxacin, against Mycobacterium leprae in patients
..-
Fonte:s.l; s.n; 1996. 5 p. tab.
Descritores:ADOLESCENCIA
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS MACROLIDIOS
ANTIBIOTICOS MACROLIDIOS
ANTIBIOTICOS TETRACICLINICOS
ANTIBIOTICOS TETRACICLINICOS
CLARITROMICINA
CLARITROMICINA
QUIMIOTERAPIA COMBINADA
HANSENIASE LEPROMATOSA
HANSENIASE LEPROMATOSA
CAMUNDONGOS
MINOCICLINA
MINOCICLINA
MYCOBACTERIUM LEPRAE
OFLOXACINA
OFLOXACINA
PELE
Limites:ANIMAL
Localização:BR191.1; 06806/s


  15 / 19 HANSEN  
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Id:13813
Autor:Baohong, J. I; Perani, Evelyne G; Petinom, Corinne; Grosset, Jacques H
Título:Bactericidal activities of combinations of new drugs against Mycobacterium leprae in nude mice
..-
Fonte:s.l; s.n; 1996. 7 p. tab.
Descritores:HANSENIASE
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
LEPROSTATICOS
LEPROSTATICOS
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
AGENTES ANTIINFECCIOSOS DE FLUOROQUINOLONA
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS MACROLIDIOS
ANTIBIOTICOS MACROLIDIOS
ANTIBIOTICOS TETRACICLINICOS
ANTIBIOTICOS TETRACICLINICOS
CLARITROMICINA
CONTAGEM DE COLONIA MICROBIANA
ESQUEMA DE MEDICAÇAO
COMBINAÇAO DE MEDICAMENTOS
CAMUNDONGOS
MINOCICLINA
RIFAMPINA
RIFAMPINA
Localização:BR191.1; 06733/s


  16 / 19 HANSEN  
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Id:13726
Autor:Gelber, Robert H; Siu, Patricia; Tsang, Mabel; Alley, Patricia; Murray, Lydia P
Título:Effect of low-level and intermittent minocycline therapy on the growth of mycobacterium leprae in mice
..-
Fonte:s.l; s.n; 1991. 3 p. tab.
Descritores:DIETA
ESQUEMA DE MEDICAÇAO
HANSENIASE
HANSENIASE
CAMUNDONGOS
CAMUNDONGOS ENDOGAMICOS BALB C
MINOCICLINA
MINOCICLINA
MINOCICLINA
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
Localização:BR191.1; 06526/s


  17 / 19 HANSEN  
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Id:13305
Autor:Gelber, Robert H; Fukuda, Keiji; Byrd, Sally; Murray, L. P; Siu, P; Tsang, M; Rea, Thomas H
Título:A clinical trial minocycline in lepromatous leprosy
..-
Fonte:s.l; s.n; 1992. 2 p. tab.
Descritores:HANSENIASE LEPROMATOSA
HANSENIASE LEPROMATOSA
CAMUNDONGOS
CAMUNDONGOS ENDOGAMICOS BALB C
MINOCICLINA
MYCOBACTERIUM LEPRAE
PELE
FATORES DE TEMPO
Limites:ANIMAL
Localização:BR191.1; 06484/s


  18 / 19 HANSEN  
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Id:13303
Autor:Lalwani, Anil K; Tami, Thomas A; Gelber, Robert H
Título:Lepromatous leprosy: nasal manifestations and treatment with minocycline
..-
Fonte:s.l; s.n; 1992. 4 p. ilus.
Descritores:DAPSONA
QUIMIOTERAPIA COMBINADA
HANSENIASE LEPROMATOSA
HANSENIASE LEPROMATOSA
HANSENIASE LEPROMATOSA
MINOCICLINA
DOENÇAS NASAIS
RIFAMPINA
Localização:BR191.1; 06438/s


  19 / 19 HANSEN  
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Id:13229
Autor:Baohong, J. I; Perani, Evelyne G; Grosset, Jacques H
Título:Effectiveness of clarithromycin and mynocycline alone and in combination against experimental Mycobacterium leprae infection in mice
..-
Fonte:s.l; s.n; 1991. 3 p. tab.
Descritores:ANTIBIOTICOS COMBINADOS
CLARITROMICINA
ERITROMICINA
ERITROMICINA
ERITROMICINA
HANSENIASE
MINOCICLINA
MINOCICLINA
MYCOBACTERIUM LEPRAE
RIFAMPINA
Localização:BR191.1; 06249/s; BR191.1; 02207/s



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