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Study of Genetic and Molecular Defects in Primary Immunodeficiency Disorders

This study is ongoing, but not recruiting participants.
Study NCT00004341.   Last updated on June 23, 2005.   Information provided by Office of Rare Diseases (ORD)

Find Related Studies by Searching for the Conditions, Interventions, and Sponsors found in this study:
1 Conditions listed in this trial
X-Linked Agammaglobulinemia
X-Linked Hyper IgM Syndrome
Wiskott-Aldrich Syndrome
2 Additional conditions recognized in this trial
Adhesions
Agammaglobulinemia
Hyper-IgM Immunodeficiency Syndrome
Hyper-IgM Immunodeficiency Syndrome, Type 1
Leukocyte-Adhesion Deficiency Syndrome
Syndrome
3 More general conditions related to this trial
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Blood Platelet Disorders
Blood Protein Disorders
Disease
Dysgammaglobulinemia
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Hematologic Diseases
Hemorrhagic Disorders
Immune System Diseases
Immunologic Deficiency Syndromes
Lymphatic Diseases
Lymphoproliferative Disorders
Pathologic Processes
Purpura, Thrombocytopenic
Thrombocytopenia
4 Sponsors listed in this trial
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
University of Washington




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