33 results on '"Schaballie, Heidi"'
Search Results
2. The burden and surveillance of RSV disease in young children in Belgium—expert opinion
3. Anterior and posterior tracheopexy for severe tracheomalacia
4. Spiroplasma infection as a cause of severe congenital keratouveitis, cataract and glaucoma
5. Urinary sodium/creatinine ratio is a predictor for fractional sodium excretion and related to age in patients with cystic fibrosis
6. Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent Infections
7. Combined deficient response to polysaccharide-based and protein-based vaccines predicts a severe clinical phenotype.
8. The burden and surveillance of RSV disease in young children in Belgium—expert opinion
9. AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3: a Diagnostic Pursuit Won by Clinical Acuity
10. Physical activity and its correlates in patients with Cystic Fibrosis: a systematic review
11. Physical activity and its correlates in people with cystic fibrosis: a systematic review
12. Clinical characteristics of patients with low functional IL-6 production upon TLR/IL-1R stimulation
13. Liver transplantation for very severe hepatopulmonary syndrome due to vitamin A-induced chronic liver disease in a patient with Shwachman-Diamond syndrome
14. PID in Disguise: Molecular Diagnosis of IRAK-4 Deficiency in an Adult Previously Misdiagnosed With Autosomal Dominant Hyper IgE Syndrome
15. Delayed presentations of severe combined immunodeficiency during the SARS‑CoV‑2 pandemic
16. Urinary sodium/creatinine ratio is a predictor for fractional sodium excretion and related to age in patients with cystic fibrosis
17. Homozygous N-terminal missense mutation in TRNT1 leads to progressive B-cell immunodeficiency in adulthood
18. Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
19. A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency
20. Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency
21. Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding
22. Defining Polysaccharide Antibody Deficiency: Measurement of Anti-Pneumococcal Antibodies and Anti-Salmonella typhi Antibodies in a Cohort of Patients with Recurrent Infections
23. Pulmonary function in children after lobectomy
24. Clinical characteristics of patients with low functional IL-6 production upon TLR/IL-1R stimulation.
25. Fifth Percentile Cutoff Values for Antipneumococcal Polysaccharide and Anti-Salmonella typhi Vi IgG Describe a Normal Polysaccharide Response
26. AD Hyper-IgE Syndrome Due to a Novel Loss-of-Function Mutation in STAT3: a Diagnostic Pursuit Won by Clinical Acuity
27. SALMONELLA TYPHI Vi VACCINE RESPONSE AND ALLOHEMAGGLUTININS VERSUS UNCONJUGATED PNEUMOCOCCAL VACCINE RESPONSE IN THE DIAGNOSIS OF SPECIFIC POLYSACCHARIDE ANTIBODY DEFICIENCY
28. Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
29. Olmsted syndrome: exploration of the immunological phenotype
30. Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency.
31. Anterior and posterior tracheopexy for severe tracheomalacia
32. Combined deficient response to polysaccharide-based and protein-based vaccines predicts a severe clinical phenotype.
33. Anterior and posterior tracheopexy for severe tracheomalacia.
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