Publications by authors named "Alessandra Ferrarini"

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Skin Eruptions in Acute Hemorrhagic Edema of Young Children: Systematic Review of the Literature.
Gabriel Bronz, Pietro O Rinoldi, Camilla Lavagno, Mario G Bianchetti, Sebastiano A G Lava, Alessandra Ferrarini

Dermatology· May 2022

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Acute hemorrhagic edema: Uncommon features.
Pietro Olmo Rinoldi, Gabriel Bronz, Alessandra Ferrarini, Cristina Mangas, Mario G Bianchetti

J Am Acad Dermatol· December 2021

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De novo missense variants in are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features.
Alka Malhotra, Alban Ziegler, Li Shu, Renee Perrier, Louise Amlie-Wolf, Alessandra Ferrarini

J Med Genet· October 2021

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IQSEC2 disorder: A new disease entity or a Rett spectrum continuum?
Diego Lopergolo, Flavia Privitera, Giuseppe Castello, Caterina Lo Rizzo, Maria Antonietta Mencarelli, Alessandra Ferrarini

Clin Genet· March 2021

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Atypical Bacterial Pathogens and Small-Vessel Leukocytoclastic Vasculitis of the Skin in Children: Systematic Literature Review.
Céline Betti, Pietro Camozzi, Viola Gennaro, Mario G Bianchetti, Martin Scoglio, Alessandra Ferrarini

Pathogens· January 2021

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Acute Hemorrhagic Edema of Infancy With Associated Hemorrhagic Lacrimation.
Gregorio P Milani, Mario G Bianchetti, Alessandra Ferrarini, Pietro O Rinoldi, Sebastiano A G Lava

Pediatr Emerg Care· October 2020

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Pathologic fracture revealed a rare syndromic form of genetic lipodystrophy.
Gabriel Bronz, Corinna Leoni-Foglia, Sebastiano G Lava, Giacomo D Simonetti, Alessandra Ferrarini

Clin Dysmorphol· January 2020

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Immune deposits in skin vessels of patients with acute hemorrhagic edema of young children: A systematic literature review.
Giorgia Pellanda, Sebastiano A G Lava, Gregorio P Milani, Mario G Bianchetti, Alessandra Ferrarini

Pediatr Dermatol· January 2020

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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
Anne H O'Donnell-Luria, Lynn S Pais, Víctor Faundes, Jordan C Wood, Abigail Sveden, Alessandra Ferrarini

Am J Hum Genet· June 2019

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Effects of multiwalled carbon nanotubes and carbofuran on metabolism in Astyanax ribeirae, a native species.
Edison Barbieri, Alessandra Maria Tegon Ferrarini, Karina Fernandes Oliveira Rezende, Diego Stéfani Teodoro Martinez, Oswaldo Luiz Alves

Fish Physiol Biochem· February 2019

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Sporadic acute benign calf myositis: Systematic literature review.
Gioele Capoferri, Gregorio P Milani, Gian Paolo Ramelli, Alessandra Ferrarini, Mario G Bianchetti

Neuromuscul Disord· May 2018

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Acute hemorrhagic edema of young children: a prospective case series.
Alessandra Ferrarini, Cecilia Benetti, Pietro Camozzi, Alessandro Ostini, Giacomo D Simonetti

Eur J Pediatr· April 2016

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Familial Henoch-Schönlein Syndrome.
Alessandro Ostini, Giacomo D Simonetti, Giorgia Pellanda, Mario G Bianchetti, Alessandra Ferrarini

J Clin Rheumatol· March 2016

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Recurrent Finkelstein-Seidlmayer Disease in Four First-degree Relatives.
Alessandro Ostini, Gian Paolo Ramelli, Carlo Mainetti, Mario G Bianchetti, Alessandra Ferrarini

Acta Derm Venereol· May 2015

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High prevalence of pathologic copy number variants detected by chromosomal microarray in Swiss-Italian children with autism spectrum disorders.
Giorgia Pellanda, Sebastiano A G Lava, Alessandra Ferrarini, Gian Paolo Ramelli

Eur J Paediatr Neurol· May 2015

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Taste acceptability of pulverized brand-name and generic drugs containing amlodipine or candesartan.
Peter Uestuener, Alessandra Ferrarini, Maristella Santi, Chiara Mardegan, Mario G Bianchetti

Int J Pharm· July 2014

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Influenzavirus B-associated acute benign myalgia cruris: an outbreak report and review of the literature.
Alessandra Ferrarini, Sebastiano A G Lava, Giacomo D Simonetti, Gian Paolo Ramelli, Mario G Bianchetti

Neuromuscul Disord· April 2014

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Chromosomal microarray among children with intellectual disability: a useful diagnostic tool for the clinical geneticist.
Stephanie Capobianco, Sebastiano Ag Lava, Mario G Bianchetti, Danielle Martinet, Marco Belfiore, Alessandra Ferrarini

Dev Med Child Neurol· March 2014

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Ureteral or vesical involvement in Henoch-Schönlein syndrome: a systematic review of the literature.
Giordano M Siegenthaler, Mattia Rizzi, Alberto Bettinelli, Giacomo D Simonetti, Alessandra Ferrarini

Pediatr Nephrol· February 2014

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Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.
Alessandra Ferrarini, Muriel Gaillard, Frederic Guerry, Gianpaolo Ramelli, Fodstad Heidi

Am J Med Genet A· February 2014

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What can we do to make antihypertensive medications taste better for children?
Alessandra Ferrarini, Alesandra A Bianchetti, Emilio F Fossali, Pietro B Faré, Giacomo D Simonetti

Int J Pharm· November 2013

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Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum.
Cristina Gervasini, Silvia Russo, Anna Cereda, Ilaria Parenti, Maura Masciadri, Alessandra Ferrarini

Am J Med Genet A· November 2013

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Prevention of vitamin D insufficiency in Switzerland: a never-ending story.
Sebastiano A G Lava, Giacomo D Simonetti, Alessandra A Bianchetti, Alessandra Ferrarini, Mario G Bianchetti

Int J Pharm· November 2013

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Primary hypertension in childhood.
Barbara S Bucher, Alessandra Ferrarini, Nico Weber, Marina Bullo, Mario G Bianchetti

Curr Hypertens Rep· October 2013

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Regional differences in symptomatic fever management among paediatricians in Switzerland: the results of a cross-sectional Web-based survey.
Sebastiano A G Lava, Giacomo D Simonetti, Alessandra Ferrarini, Gian Paolo Ramelli, Mario G Bianchetti

Br J Clin Pharmacol· January 2013

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