Chronic granulomatous disease (CGD) is a rare inherited disorder caused by defective nicotinamide adenine dinucleotide phosphate oxidase enzyme and characterized by recurrent bacterial and fungal infections. Although liver abscess is a common manifestation of CGD, its management in CGD patients is not well-defined. In addition, the generalized guidelines for treating liver abscesses do not necessarily apply to CGD patients. Corticosteroids are commonly used to control granulomatous complications, such as inflammatory gastrointestinal and genitourinary lesions, in patients with CGD, Corticosteroids have also been used in combination with antimicrobials to treat refractory infections in patients with CGD. Because corticosteroids are capable o...
Background and aim: There are no epidemiological studies focusing on the association between oral co...
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infecti...
Background and Aims: Concomitant presence of autoimmune hepatitis (AIH) and primary sclerosing chola...
Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to treat and often re...
Liver abscesses occur in up to one-third of patients with chronic granulomatous disease (CGD). Surge...
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder, characterized by ...
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterized clinically by p...
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated b...
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disease, affecting phagocytic...
Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phago...
Acute-on-chronic liver failure (ACLF) occurs in the presence of a chronic liver disease or cirrhosis...
We describe the spectrum of radiologic appearances of hepatic abscesses in patients with chro...
In chronic granulomatous disease, interferon-gamma (IFN-gamma) significantly reduces the incidence a...
Abstract Background Chronic granulomatous disease (CGD), a rare inherited disorder, is characterized...
In chronic granulomatous disease, interferon-\u3b3 (IFN-\u3b3) significantly reduces the incidence a...
Background and aim: There are no epidemiological studies focusing on the association between oral co...
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infecti...
Background and Aims: Concomitant presence of autoimmune hepatitis (AIH) and primary sclerosing chola...
Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to treat and often re...
Liver abscesses occur in up to one-third of patients with chronic granulomatous disease (CGD). Surge...
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder, characterized by ...
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterized clinically by p...
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated b...
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disease, affecting phagocytic...
Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phago...
Acute-on-chronic liver failure (ACLF) occurs in the presence of a chronic liver disease or cirrhosis...
We describe the spectrum of radiologic appearances of hepatic abscesses in patients with chro...
In chronic granulomatous disease, interferon-gamma (IFN-gamma) significantly reduces the incidence a...
Abstract Background Chronic granulomatous disease (CGD), a rare inherited disorder, is characterized...
In chronic granulomatous disease, interferon-\u3b3 (IFN-\u3b3) significantly reduces the incidence a...
Background and aim: There are no epidemiological studies focusing on the association between oral co...
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infecti...
Background and Aims: Concomitant presence of autoimmune hepatitis (AIH) and primary sclerosing chola...