Publications by authors named "Bruno Drera"

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Waardenburg-Shah syndrome: A case of neonatal palliative care.
Michael Colpani, Maria Del Carmen Rodriguez Perez, Bruno Angelo Drera, Francesco Maria Risso

Pediatr Discov· December 2024

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The risk of hospitalisation from RSV is not increased by co-infection in children under 24-months-of-age.
Alessandra Chiara Francesca Ferrari, Elisa Giani, Andrea Enzo Scaramuzza, Vera Cutuli, Martina Giambarda, Bruno Angelo Drera

Eur J Pediatr· April 2024

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Congenital Unilesional Cutaneous Langerhans Cell Histiocytosis: A Case Report.
Marco Ungari, Gioachino Caresana, Giulia Tanzi, Bruno Drera, Marta Claudia Frittoli

Am J Dermatopathol· March 2021

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Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): study protocol for a multicentric longitudinal project.
Livio Provenzi, Serena Grumi, Roberto Giorda, Giacomo Biasucci, Renza Bonini, Bruno Drera

BMJ Open· December 2020

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Ultrasound follow-up of an unusual giant urinoma in a newborn.
Bruno Drera, Carlo Poggiani

J Ultrasound· March 2018

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Hypercalcemia and nephrocalcinosis complicating subcutaneous fat necrosis in a newborn after therapeutic hypothermia.
Elisa Milanesi, Cristina Loda, Bruno Drera, Carlo Poggiani

Minerva Pediatr· August 2016

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A case of neonatal Jeune syndrome expanding the phenotype.
Bruno Drera, Daniela Ferrari, Pietro Cavalli, Carlo Poggiani

Clin Case Rep· August 2014

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Clinical, neuroradiological and molecular features of a patient affected by pseudoxhantoma elasticum associated to carotid rete mirabile: case report.
Elisabetta Del Zotto, Marco Ritelli, Alessandro Pezzini, Bruno Drera, Massimo Gamba

Clin Neurol Neurosurg· July 2012

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Mutations in TGFBR2 gene cause spontaneous cervical artery dissection.
Alessandro Pezzini, Bruno Drera, Elisabetta Del Zotto, Marco Ritelli, Monica Carletti

J Neurol Neurosurg Psychiatry· December 2011

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Diagnosis of vascular Ehlers-Danlos syndrome in Italy: clinical findings and novel COL3A1 mutations.
Bruno Drera, Nicoletta Zoppi, Marco Ritelli, Gianluca Tadini, Marina Venturini

J Dermatol Sci· December 2011

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Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients.
Bruno Drera, Marco Ritelli, Nicoletta Zoppi, Anita Wischmeijer, Maria Gnoli

Orphanet J Rare Dis· November 2009

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Arterial tortuosity syndrome in two Italian paediatric patients.
Marco Ritelli, Bruno Drera, Mariano Vicchio, Giovanni Puppini, Paolo Biban

Orphanet J Rare Dis· September 2009

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Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with Pseudoxanthoma elasticum.
Bruno Drera, Andrea Brezzi, Nicoletta Zoppi, Marina Venturini, Sergio Barlati

J Dermatol Sci· March 2008

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Ischemic stroke in an adolescent with arterial tortuosity syndrome.
Bruno Drera, Sergio Barlati, Marina Colombi

Neurology· May 2007

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Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome.
Bruno Drera, Andrea Guala, Nicoletta Zoppi, Rita Gardella, Piergiorgio Franceschini

Am J Med Genet A· January 2007

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