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Fanni Szumutku

Observed name: Szumutku, Fanni
Observed institution: Semmelweis University
OpenAlex ID: A5066822844
A 22q11.2-microdeletiós szindróma klinikai jellemzői
2022 · Fanni Szumutku, Krisztina Kádár, et al. · Orvosi Hetilap · 2
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Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome
2026 · Fanni Szumutku, Anna Lengyel, et al. · Molecular and Cellular Pediatrics · 1
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Complete recovery after complement factor I deficiency associated fulminant acute hemorrhagic leukoencephalitis: a case report
2025 · Fanni Szumutku, Léna Szabó, et al. · Frontiers in Immunology · 1
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Clinical aspects of 22q11.2 microdeletion syndrome
2022 · Fanni Szumutku, Krisztina Kádár, et al. · PubMed · 1
Expanding the clinical spectrum of pediatric CASPR2 antibody-associated autoimmune encephalitis: a multicenter case series
2026 · Fanni Szumutku, Léna Szabó, et al. · Frontiers in Immunology
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Additional file 1 of Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome
2026 · Szumutku, Fanni, Lengyel, Anna, et al. · Figshare
Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome
2026 · Szumutku, Fanni, Lengyel, Anna, et al. · Figshare
Functional Characterization of a Novel Intronic Complement Factor I Variant in Factor I Deficiency and Atypical Hemolytic Uremic Syndrome
2026 · Simon Péter Nagy, Sarolta Dobner, et al. · Kidney International Reports
Works count: 8
Citation count: 5
H-index: 1
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