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Publications by József Stankovics
A Novel IL2RG Mutation Associated With Maternal T Lymphocyte Engraftment in a Patient With Severe Combined Immunodeficiency
Journal of Human Genetics
Genetics
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A Novel Mutation in ORAI1 Presenting With Combined Immunodeficiency and Residual T-Cell Function
Journal of Allergy and Clinical Immunology
Allergy
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The Clinical Spectrum of Hypomorphic IL2RG Severe Combined Immunodeficiency (SCID)
Journal of Allergy and Clinical Immunology
Allergy
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Epstein-Barr Virus-Associated Γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Cytotoxic T-Lymphocyte-Associated Protein 4-Ig Effectively Controls Immune Activation and Inflammatory Disease in a Novel Murine Model of Leaky Severe Combined Immunodeficiency
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A Novel KAL1 Mutation Is Associated With Combined Pituitary Hormone Deficiency
Human Genome Variation
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Clinical Resistance Associated With a Novel MAP2K1 Mutation in a Patient With Langerhans Cell Histiocytosis
Pediatric Blood and Cancer
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Child Health
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Perinatology
Medicine
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Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain of Function Mutation
Gastroenterology
Hepatology
Gastroenterology
A Novel APOC2 Gene Mutation Identified in a Chinese Patient With Severe Hypertriglyceridemia and Recurrent Pancreatitis
Lipids in Health and Disease
Biochemistry
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Clinical Biochemistry
Metabolism
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A Novel NaV1.5 Voltage Sensor Mutation Associated With Severe Atrial and Ventricular Arrhythmias
Journal of Molecular and Cellular Cardiology
Cardiovascular Medicine
Molecular Biology
Cardiology