Pages that link to "Q39327528"

The following pages link to Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation (Q39327528):

Displaying 23 items.

• A delayed diagnosis of X-linked hyper IgM syndrome complicated with toxoplasmic encephalitis in a child: A case report and literature review (Q47142358) (← links)
• Hematopoietic cell transplantation in primary immunodeficiency - conventional and emerging indications (Q47210347) (← links)
• Population Pharmacokinetics of Intravenous Busulfan in Japanese Pediatric Patients With Primary Immunodeficiency Diseases. (Q47636752) (← links)
• CD40 ligand deficiency causes functional defects of peripheral neutrophils that are improved by exogenous IFN-γ. (Q52666648) (← links)
• A Novel de Novo Mutation in the CD40 Ligand Gene in a Patient With a Mild X-Linked Hyper-IgM Phenotype Initially Diagnosed as CVID: New Aspects of Old Diseases. (Q54204905) (← links)
• A Tumor Profile in Primary Immune Deficiencies Challenges the Cancer Immune Surveillance Concept. (Q55004131) (← links)
• Reduced-intensity conditioning for hematopoietic cell transplant for HLH and primary immune deficiencies (Q57147939) (← links)
• Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis (Q57289938) (← links)
• Class-Switch Recombination (CSR)/Hyper-IgM (HIGM) Syndromes and Phosphoinositide 3-Kinase (PI3K) Defects (Q57491434) (← links)
• An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation (Q58567287) (← links)
• Site-Specific Gene Editing of Human Hematopoietic Stem Cells for X-Linked Hyper-IgM Syndrome (Q59360193) (← links)
• Transplantation of Hematopoietic Stem Cells for Primary Immunodeficiencies in Brazil: Challenges in Treating Rare Diseases in Developing Countries (Q64042510) (← links)
• Haematopoietic stem cell transplant for hyper-IgM syndrome due to CD40 defects: a single-centre experience (Q64045072) (← links)
• Pneumocystis jirovecii pneumonia as an initial manifestation of hyper-IgM syndrome in an infant: A case report (Q64247663) (← links)
• Gastrointestinal Manifestations and Complications of Primary Immunodeficiency Disorders (Q64289147) (← links)
• Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency. (Q64988277) (← links)
• Global report on primary immunodeficiencies: 2018 update from the Jeffrey Modell Centers Network on disease classification, regional trends, treatment modalities, and physician reported outcomes (Q88622362) (← links)
• Gastrointestinal Disorders Associated with Primary Immunodeficiency Diseases (Q88651319) (← links)
• Hematopoietic Stem Cell Transplantation for Combined Immunodeficiencies, on Behalf of IEWP-EBMT (Q89623057) (← links)
• Humoral immunodeficiencies: conferred risk of infections and benefits of immunoglobulin replacement therapy (Q90398899) (← links)
• Clinical and molecular features of X-linked hyper IgM syndrome - An experience from North India (Q90573330) (← links)
• Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives (Q92802115) (← links)
• Treatment and management of primary antibody deficiency: German interdisciplinary evidence-based consensus guideline (Q98729309) (← links)