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155 results on '"Eyal Grunebaum"'

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1. Characterizing CD38 expression in terminally differentiated B cells using variable lymphocyte receptor B tetramers

2. Case report: A case of spinal muscular atrophy in a preterm infant: risks and benefits of treatment

3. Purine nucleoside phosphorylase deficiency induces p53-mediated intrinsic apoptosis in human induced pluripotent stem cell-derived neurons

4. Monitoring patients with uncomplicated common variable immunodeficiency: a systematic review

5. Homozygous duplication identified by whole genome sequencing causes LRBA deficiency

6. Skin prick test in milk allergic patients undergoing oral immunotherapy: Does the milk form used for skin tests matter?

7. Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome

8. The Use of Induced Pluripotent Stem Cells to Study the Effects of Adenosine Deaminase Deficiency on Human Neutrophil Development

9. An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell Composition

10. Partial Purine Nucleoside Phosphorylase Deficiency Helps Determine Minimal Activity Required for Immune and Neurological Development

11. Canadian Society of Allergy and Clinical Immunology annual scientific meeting 2016

12. Early Enzyme Replacement Therapy Improves Hearing and Immune Defects in Adenosine Deaminase Deficient-Mice

13. Detection of Human CD38 Using Variable Lymphocyte Receptor (VLR) Tetramers

14. Cerebellar abnormalities in purine nucleoside phosphorylase deficient mice

15. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

16. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

19. Homozygous duplication identified by whole genome sequencing causes LRBA deficiency

20. Hematopoietic Cell Transplantation in 240 Patients with Chronic Granulomatous Disease: A Pidtc Report

21. Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data

22. Allogenic Hematopoietic Cell Transplantations Are Effective in Patients with p47phox Chronic Granulomatous Disease: A Primary Immune Deficiency Treatment Consortium Study

23. Platelet Activating Factor (PAF): A Mediator of Inflammation

24. Progressive decline of T and B cell numbers and function in a patient with CDC42 deficiency

25. FCRL4 Is an Fc Receptor for Systemic IgA, but Not Mucosal Secretory IgA

26. Novel mutations in the CYBB gene causing X-linked chronic granulomatous disease: a case report of 2 patients

27. Epigenetic and immunological indicators of IPEX disease in subjects with FOXP3 gene mutation

30. Platelet-activating factor acetylhydrolase is a biomarker of severe anaphylaxis in children

31. A Sherlock Approach to a Kindred With a Variable Immunohematologic Phenotype

36. Monitoring patients with uncomplicated common variable immunodeficiency: a systematic review

37. Comparison of elapegademase and pegademase in ADA-deficient patients and mice

38. Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency

39. SARS-CoV-2-Reactive Mucosal B Cells in the Upper Respiratory Tract of Uninfected Individuals

40. Short dosing intervals during oral challenge increase the risk of severe adverse reactions in children with milk allergy

41. Conversion from tacrolimus to sirolimus as a treatment modality in de novo allergies and immune‐mediated disorders in pediatric liver transplant recipients

42. Liver-associated immune abnormalities

43. Use of induced pluripotent stem cells to investigate the effects of purine nucleoside phosphorylase deficiency on neuronal development

44. Elevated Cow’s Milk–Specific IgE Levels Prior to Oral Immunotherapy Decrease the Likelihood of Reaching the Maintenance Dose

45. Adenosine deaminase deficiency: current treatments and emerging therapeutics

46. Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency

47. A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency

48. NK cell defects in X-linked pigmentary reticulate disorder

49. Alveolar-like Stem Cell–derived Myb− Macrophages Promote Recovery and Survival in Airway Disease

50. DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis

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