Paul Szabolcs, MD
Rare Disease Specialist
UPMC Children's Hospital of Pittsburgh
Pittsburgh, Pennsylvania
PI on 7 trials
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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- MAGIC syndrome
- Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- Dyskeratosis congenita
- Leukocyte adhesion deficiency type I
- Non-severe combined immunodeficiency
- Genetic chronic primary adrenal insufficiency
- Beta-thalassemia-X-linked thrombocytopenia syndrome
- Severe combined immunodeficiency
- Primary hemophagocytic lymphohistiocytosis
- Osteopetrosis and related disorders
- Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
- Immunodeficiency by defective expression of MHC class II
- X-linked alpha-thalassemia-intellectual disability syndrome
- Primary autoimmune enteropathy
- X-linked skeletal dysplasia-intellectual disability syndrome
- X-linked mendelian susceptibility to mycobacterial diseases
- Immune dysregulation disease with immunodeficiency
- Autoimmune hypoparathyroidism
- Aplasia cutis congenita
- Albers-Schönberg osteopetrosis
- Alpha-thalassemia
- Autoimmune polyendocrinopathy
- Genetic polyendocrinopathy
- Common variable immunodeficiency phenotype due to CD19/CD81 deficiency
- Adult Krabbe disease
- Beta-mannosidosis
- Omenn syndrome
- Sickle cell anemia
- Chronic primary adrenal insufficiency
- Primary immunodeficiency
Clinical trials (7)
Verify independently
Other specialists for MAGIC syndrome
Peers ranked by clinical-trial PI role, publications, and verification quality.