Tibor Kalmár
16PUBLICATIONS
22CO-AUTHORS
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Publications (16)
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|Jan 25, 2025
Fibronectin Glomerulopathy Without Typical Renal Biopsy Features in a 4-Year-Old Girl with Incidentally Discovered Proteinuria and a G417V <i>FN1</i> Gene Mutation.Tibor Kalmár, Dániel Jakab, Zoltán Maróti
|Nov 06, 2024
A Patient Diagnosed with Mosaic Trisomy 18 Presenting New Symptoms: Diaphragmatic Relaxation and Cyclic Vomiting Syndrome. Updated Review of Mosaic Trisomy 18 Cases.Magdolna Kósa, Emese Horváth, Tibor Kalmár
|Jun 19, 2024
Phenotypic and Genotypic Features of the <i>FAN1</i> Mutation-Related Disease in a Large Hungarian Family.Ildikó Császár, Tibor Kalmár, Zoltán Maróti
|Jan 23, 2024
The Apical Endocytic-Lysosomal Apparatus in CLCN5 Mutations with Phenotypic-Genotypic Correlations in Three Cases.Tibor Kalmár, Dániel Jakab, Zoltán Maróti
|Dec 23, 2023
Phenotype-Genotype Correlations in Three Different Cases of Adult-Onset Genetic Focal Segmental Glomerulosclerosis.Tibor Kalmár, Sándor Turkevi-Nagy, László Bitó
|Feb 11, 2023
Spinocerebellar Ataxia in a Hungarian Female Patient with a Novel Variant of Unknown Significance in the <i>CCDC88C</i> Gene.Fanni Annamária Boros, László Szpisjak, Renáta Bozó
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Frequent Collaborators
6 joint publications
Zoltán Maróti
3 joint publications
Endre Neparáczki
2 joint publications
Tibor Török
2 joint publications
István Nagy
2 joint publications
Béla Iványi
1 joint publications
Ildikó Pap
1 joint publications
Dóra Tombácz
1 joint publications
Michael Snyder
1 joint publications
Sándor Turkevi-Nagy
1 joint publications
Katalin Havasi
