27EC McGeady, Stephen J. - Thomas Jefferson University - Thomas Jefferson University
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Stephen J. McGeady, MD

Contact Dr. McGeady

833 Chestnut Street
Suite 300
Philadelphia, PA 19107

(215) 955-5800

Most Recent Peer-reviewed Publications

  1. Transient Hypogammaglobulinemia of Infancy
  2. Phenotypic parameters predict time to normalization in infants with hypogammaglobulinemia
  3. Early intervention with high-dose inhaled corticosteroids for control of acute asthma exacerbations at home and improved outcomes: A randomized controlled trial
  4. The prevalence of antibiotic skin test reactivity in a pediatric population
  5. Uncommon reaction to nonsteroidal anti-inflammatory drugs in a teenager.
  6. Infants with low immunoglobulin levels: Isolated low IgA level vs other immunoglobulin abnormalities
  7. Efficacy of Chest Physiotherapy in Pediatric Patients with Acute Asthma Exacerbations
  8. Radiologic outcomes in children with chronic rhinosinusitis and ostiomeatal complex obstruction after medical management
  9. A 15-year-old girl with recurrent pneumonia
  10. Selective IgM deficiency and 22q11.2 deletion syndrome
  11. Diagnosis of common variable immunodeficiency in a patient with primary ciliary dyskinesia
  12. Patient, home residence, and neighborhood characteristics in pediatric emergency department visits for asthma
  13. Antenatal risk factors, cytokines and the development of atopic disease in early childhood
  14. Lack of cross-reactivity between 5-aminosalicylic acid-based drugs: A case report and review of the literature
  15. A 5-month-old boy with recurrent respiratory infections, failure to thrive, and borderline elevated sweat chloride levels
  16. Two cases of accidental epinephrine injection into a finger [1]
  17. Infants presenting with recurrent infections and low immunoglobulins: Characteristics and analysis of normalization
  18. Cutaneous vasculitis associated with zafirlukast use in asthma
  19. Developing resources to teach and assess the core competencies: A collaborative approach
  20. 22q11.2 deletion syndrome and selective IgM deficiency: An association of a common chromosomal abnormality with a rare immunodeficiency [1]