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19 Oct 2015 |
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Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
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Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2
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The global, regional, and national burden of cancer, 1990–2023, with forecasts to 2050: a systematic analysis for the Global Burden of Disease Study 2023
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DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
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Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia
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Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria
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Epstein-Barr Virus in Pediatric Multiple Sclerosis
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Mutations in PYCR1 cause cutis laxa with progeroid features
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Mutations in the Gene Encoding Capillary Morphogenesis Protein 2 Cause Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis
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DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation
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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
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Effect of Awake Prone Positioning on Endotracheal Intubation in Patients With COVID-19 and Acute Respiratory Failure
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Characteristics, risk factors and outcomes among the first consecutive 1096 patients diagnosed with COVID-19 in Kuwait
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IL-21 is the primary common γ chain-binding cytokine required for human B-cell differentiation in vivo
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A Prospective Survey of Pediatric Dermatology Clinic Patients in Kuwait: An Analysis of 10,000 Cases
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CHD2variants are a risk factor for photosensitivity in epilepsy
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X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world
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Spectrum of autoimmune bullous diseases in Kuwait
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Radiation Exposure to Patients During Interventional Procedures in 20 Countries: Initial IAEA Project Results
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A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton
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Distinguishing the four genetic causes of jouberts syndrome–related disorders
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A Phenotypic Approach for IUIS PID Classification and Diagnosis: Guidelines for Clinicians at the Bedside
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Molecular Characterization of α-Thalassemia Determinants, β-Thalassemia Alleles, and β s Haplotypes among Kuwaiti Arabs
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Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency
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