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Michela Sesta
Michela Sesta
Medicine
Mutation
Genetics
Gastroenterology
Eculizumab
4
Papers
21
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The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein
2020
Genes
Nicola Laforgia
Lucrezia De Cosmo
Orazio Palumbo
Carlotta Ranieri
Michela Sesta
Donatella Capodiferro
Antonino Pantaleo
Pierluigi Iapicca
Patrizia Lastella
Manuela Capozza
Federico Schettini
Nenad Bukvić
Rosanna Bagnulo
Nicoletta Resta
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A pediatric neurologic assessment score may drive the eculizumab-based treatment of Escherichia coli-related hemolytic uremic syndrome with neurological involvement
2019
Pediatric Nephrology
Paolo Giordano
Giuseppe Stefano Netti
Luisa Santangelo
Giuseppe Castellano
Vincenza Carbone
Diletta Domenica Torres
Marida Martino
Michela Sesta
Franca Di Cuonzo
M. Resta
Alberto Gaeta
Leonardo Milella
Maria Chironna
Cinzia Germinario
Gaia Scavia
Loreto Gesualdo
Mario Giordano
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Citations (14)
PCDH19 mutations in female patients from Southern Italy
2015
Seizure-european Journal of Epilepsy
Monica Gagliardi
Grazia Annesi
Michela Sesta
Patrizia Tarantino
Pasquale Conti
Angelo Labate
Gabriella Di Rosa
Aldo Quattrone
Antonio Gambardella
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Citations (6)
Description of Six Cases of Child Cauda Equina Leptomeningitis: An Emerging Disease
2008
Immunopharmacology and Immunotoxicology
Franca Dicuonzo
Michele Palma
Michele Tangari
Roberta De Nicolo
Marilena Maghenzani
Stefano Andresciani
Michela Sesta
Carella Aristide
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Citations (1)
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