Search Results - Maria Michela D'Alessandro

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  1. 1
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    Tubulointerstitial nephritis and uveitis syndrome post‐COVID‐19 by Maria Cristina Maggio, Filippo Collura, Maria Michela D'Alessandro, Barbara Gramaglia, Giovanni Corsello

    Published 2023
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  2. 2
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    Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town by Gregorio Serra, Vincenzo Antona, Maria Michela D'Alessandro, Maria Cristina Maggio, Vincenzo Verde, Giovanni Corsello

    Published 2021
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  3. 3
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    Renal angiomyolipomatosis and bleeding aneurysms in a tuberous sclerosis context: selective artery embolization in a girl with end-stage renal failure by Gloria Pelizzo, Mario Giuseppe Vallone, Mario Milazzo, Gregorio Rosone, Salvatore Amoroso, Giovanni Pavone, Maria Michela D'Alessandro, Elettra Unti, Valeria Calcaterra

    Published 2020
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  4. 4
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    A novel NF1 mutation in a pediatric patient with renal artery aneurysm by Ilenia Chillura, Giulia Angela Restivo, Simonetta Callari, Sabrina Cibella, Maria Michela D'Alessandro, Ciro Corrado, Mario Vallone, Vincenzo Antona, Giovanni Corsello

    Published 2022
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  5. 5
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    Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report by Ingrid Anne Mandy Schierz, Mario Giuffrè, Marcello Cimador, Maria Michela D'Alessandro, Gregorio Serra, Federico Favata, Vincenzo Antona, Ettore Piro, Giovanni Corsello

    Published 2022
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  6. 6
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    Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome by Gregorio Serra, Giovanni Corsello, Vincenzo Antona, Maria Michela D'Alessandro, Nicola Cassata, Marcello Cimador, Mario Giuffrè, Ingrid Anne Mandy Schierz, Ettore Piro

    Published 2020
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