Add to ORKGSera from Indian patients with parasitologically confirmed visceral leishmaniasis were studied by immu-noblot analysis in order to identify a specific pattern for Leishmania infection. A soluble extract of Leishmania donovani was used as antigen. At diagnosis the sera from patients with visceral leishmaniasis specifically recognized fractions represented by bands of 201 kDa (50 % of serum samples), 193 kDa (60%), 147 kDa (50%)
Leishmania promastigotes polypeptides are analyzed by immunoblotting with sera from patients infecte...
The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was inves...
Sera of kala-azar patients from Bihar, India, were used to identify Leishmania donovani antigens enc...
Sera from Indian patients with parasitologically confirmed visceral leishmaniasis were studied by im...
Using the immunoblot technique, we have compared the reactions of Leishmania donovani infantum polyp...
Abstract. Soluble antigens from Leishmania donovani chagasi were studied in terms of their ability t...
The biggest challenge in the serological diagnosis of visceral leishmaniasis (VL) is to find a bioma...
The biggest challenge in the serological diagnosis of visceral leishmaniasis (VL) is to find a bioma...
The unreliability of most of the existing antibody-based diagnostic kits to discriminate between act...
<div><p>The unreliability of most of the existing antibody-based diagnostic kits to discriminate bet...
The antibody response in patients with American cutaneous leishmaniasis was analyzed by immunoblotti...
A purified 200-kDa antigenic fraction from Leishmania donovani axenic amastigotes was evaluated by E...
A purified 200-kDa antigenic fraction from Leishmania donovani axenic amastigotes was evaluated by E...
The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was inves...
Leishmania promastigotes polypeptides are analyzed by immuno-blotting with sera from patients infect...
Leishmania promastigotes polypeptides are analyzed by immunoblotting with sera from patients infecte...
The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was inves...
Sera of kala-azar patients from Bihar, India, were used to identify Leishmania donovani antigens enc...
Sera from Indian patients with parasitologically confirmed visceral leishmaniasis were studied by im...
Using the immunoblot technique, we have compared the reactions of Leishmania donovani infantum polyp...
Abstract. Soluble antigens from Leishmania donovani chagasi were studied in terms of their ability t...
The biggest challenge in the serological diagnosis of visceral leishmaniasis (VL) is to find a bioma...
The biggest challenge in the serological diagnosis of visceral leishmaniasis (VL) is to find a bioma...
The unreliability of most of the existing antibody-based diagnostic kits to discriminate between act...
<div><p>The unreliability of most of the existing antibody-based diagnostic kits to discriminate bet...
The antibody response in patients with American cutaneous leishmaniasis was analyzed by immunoblotti...
A purified 200-kDa antigenic fraction from Leishmania donovani axenic amastigotes was evaluated by E...
A purified 200-kDa antigenic fraction from Leishmania donovani axenic amastigotes was evaluated by E...
The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was inves...
Leishmania promastigotes polypeptides are analyzed by immuno-blotting with sera from patients infect...
Leishmania promastigotes polypeptides are analyzed by immunoblotting with sera from patients infecte...
The antibody response against an amastigote-specific protein (A2) from Leishmania donovani was inves...
Sera of kala-azar patients from Bihar, India, were used to identify Leishmania donovani antigens enc...