Add to ORKGSEVERE COMBINED IMMUNE DEFI-ciency (SCID) is a heterog-eneous group of inherited dis-eases wi th an es t imated frequency of 1 in 50 000 to 100 000 live births.1 It is characterized by signifi-cant impaired immunity leading to death in infancy unless treated by he-matopoietic stem cell transplantation. The optimal treatment for most pa-tients with SCID is bone marrow trans-plantation (BMT) from a related, HLA-identical donor (RID).2 Unfortunately, such donors are found for only a mi-nority of patients with SCID.3,4 As an alternative, stem cell trans-plantations from HLA-mismatched re-lated donors (MMRDs) have been com
BackgroundThe approach to the diagnosis of severe combined immunodeficiency disease (SCID) and relat...
Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment available f...
Inherited defects in adenosine deaminase (ADA) cause a subtype of severe combined immunodeficiency (...
Hematopoietic stem cell transplantation (HSCT) is an effective approach for the treatment of severe ...
AbstractHematopoietic stem cell transplantation (HSCT) is the only curative option for most children...
Severe combined immunodeficiencies (SCIDs) represent a group of distinct congenital disorders affect...
Severe combined immunodeficiency (SCID) is a fatal congenital disorder of the immune system for whic...
Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hemat...
Severe combined immunodeficiencies (SCIDs) are a group of inherited disorders responsible for severe...
Severe combined immunodeficiency (SCID) is one of the most severe forms of primary immunodeficiency ...
Severe combined immunodeficiency (SCID) represents a group of rare, sometimes fatal, congenital diso...
IntroductionNewborn screening has led to a better understanding of the prevalence of Severe Combined...
Severe combined immunodeficiency (SCID), also known as "bubble boy disease," is a rare hereditary pa...
X-linked severe combined immunodeficiency (SCID-X1) is a profound deficiency of T, B, and natural ki...
Abstract Background Severe combined immunodeficiency (SCID) is a group of relatively rare primary im...
BackgroundThe approach to the diagnosis of severe combined immunodeficiency disease (SCID) and relat...
Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment available f...
Inherited defects in adenosine deaminase (ADA) cause a subtype of severe combined immunodeficiency (...
Hematopoietic stem cell transplantation (HSCT) is an effective approach for the treatment of severe ...
AbstractHematopoietic stem cell transplantation (HSCT) is the only curative option for most children...
Severe combined immunodeficiencies (SCIDs) represent a group of distinct congenital disorders affect...
Severe combined immunodeficiency (SCID) is a fatal congenital disorder of the immune system for whic...
Absent T-cell immunity resulting in life-threatening infections provides a clear rationale for hemat...
Severe combined immunodeficiencies (SCIDs) are a group of inherited disorders responsible for severe...
Severe combined immunodeficiency (SCID) is one of the most severe forms of primary immunodeficiency ...
Severe combined immunodeficiency (SCID) represents a group of rare, sometimes fatal, congenital diso...
IntroductionNewborn screening has led to a better understanding of the prevalence of Severe Combined...
Severe combined immunodeficiency (SCID), also known as "bubble boy disease," is a rare hereditary pa...
X-linked severe combined immunodeficiency (SCID-X1) is a profound deficiency of T, B, and natural ki...
Abstract Background Severe combined immunodeficiency (SCID) is a group of relatively rare primary im...
BackgroundThe approach to the diagnosis of severe combined immunodeficiency disease (SCID) and relat...
Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment available f...
Inherited defects in adenosine deaminase (ADA) cause a subtype of severe combined immunodeficiency (...