X-linked agammaglobulinemia

Known as: AGMX1, Bruton's Agammaglobulinemia, BRUTON-TYPE AGAMMAGLOBULINEMIA 
X-linked agammaglobulinemia. An immunodeficiency state characterized (usually) by profoundly low concentrations of serum immunoglobulins of all… (More)
National Institutes of Health

Papers overview

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2008
2008
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by germline mutation of the Bruton tyrosine… (More)
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2006
2006
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency characterized by a failure to generate immunoglobulins of all… (More)
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2002
2002
X-linked agammaglobulinemia (XLA) is characterized by a severe B-cell deficiency, resulting from a differentiation arrest in the… (More)
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Highly Cited
2001
Highly Cited
2001
Recombinant vectors based on adeno-associated virus (AAV) or human immunodeficiency 1 (lentivirus) are promising tools for long… (More)
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2001
2001
X-linked agammaglobulinemia (XLA), caused by mutations in Bruton's tyrosine kinase (BTK), typically presents in early childhood… (More)
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Review
1996
Review
1996
X-linked agammaglobulinemia (XLA), characterized by a profound deficiency of B lymphocytes due to an arrest in B lymphocyte… (More)
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1996
1996
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia… (More)
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Highly Cited
1994
Highly Cited
1994
X-linked agammaglobulinemia (XLA) is an inherited human immunodeficiency disease, characterized by an arrest in B-cell… (More)
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Review
1991
Review
1991
X-linked agammaglobulinemia (XLA) patients manifest a very low production of immunoglobulins (Ig) of all classes and plasma cells… (More)
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1987
1987
We used a recently developed strategy to analyze patterns of X-chromosome inactivation in human cell populations in order to… (More)
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