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Bruno Angelo Drera
Observed names:
B Drera,
B. Drera,
Bruno Drera
Institutions:
Istituti Ospitalieri di Cremona,
Azienda Socio Sanitaria Territoriale di Cremona
Observed institutions:
Istituti Ospitalieri di Cremona,
Azienda Socio Sanitaria Territoriale di Cremona,
University of Brescia
ORCID:
0000-0002-3589-0221
Observed ORCID:
0000-0002-3589-0221
OpenAlex ID:
A5004224386
Remdesivir and three other drugs for hospitalised patients with COVID-19: final results of the WHO Solidarity randomised trial and updated meta-analyses
2022
·
Hongchao Pan
, Richard Peto
, et al.
·
The Lancet
·
434
PDF
Dystrophic epidermolysis bullosa pruriginosa in Italy: clinical and molecular characterization
2006
·
B Drera
, D Castiglia
, et al.
·
Clinical Genetics
·
41
Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome
2006
·
Bruno Drera
, Andrea Guala
, et al.
·
American Journal of Medical Genetics Part A
·
34
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): study protocol for a multicentric longitudinal project
2020
·
Livio Provenzi
, Serena Grumi
, et al.
·
BMJ Open
·
32
PDF
Loeys-Dietz syndrome type I and type II: clinical findings and novel mutations in two Italian patients
2009
·
Bruno Drera
, Marco Ritelli
, et al.
·
Orphanet Journal of Rare Diseases
·
32
PDF
Mutations in TGFBR2 gene cause spontaneous cervical artery dissection
2011
·
A. Pezzini
, B. Drera
, et al.
·
Journal of Neurology Neurosurgery & Psychiatry
·
27
PDF
Arterial tortuosity syndrome in two Italian paediatric patients
2009
·
Marco Ritelli
, Bruno Drera
, et al.
·
Orphanet Journal of Rare Diseases
·
26
PDF
Identification of a novel TGFBR1 mutation in a Loeys–Dietz syndrome type II patient with vascular Ehlers–Danlos syndrome phenotype
2007
·
B Drera
, G Tadini
, et al.
·
Clinical Genetics
·
24
Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations
2011
·
Bruno Drera
, Nicoletta Zoppi
, et al.
·
Journal of Dermatological Science
·
19
De novo occurrence of the 730insG recurrent mutation in an Italian family with the ichthyotic variant of Vohwinkel syndrome, loricrin keratoderma
2007
·
B Drera
, G Tadini
, et al.
·
Clinical Genetics
·
15
Clinical, neuroradiological and molecular features of a patient affected by pseudoxhantoma elasticum associated to carotid rete mirabile: Case report
2012
·
Elisabetta Del Zotto
, Marco Ritelli
, et al.
·
Clinical Neurology and Neurosurgery
·
11
A case of neonatal Jeune syndrome expanding the phenotype
2014
·
Bruno Drera
, Daniela Ferrari
, et al.
·
Clinical Case Reports
·
9
PDF
Ultrasound follow-up of an unusual giant urinoma in a newborn
2016
·
Bruno Drera
, Carlo Poggiani
·
Journal of Ultrasound
·
7
Recurrence of the p.R156X TNNI2 mutation in distal arthrogryposis type 2B
2006
·
B Drera
, N Zoppi
, et al.
·
Clinical Genetics
·
7
Ischemic Stroke in an Adolescent With Arterial Tortuosity Syndrome
2007
·
Bruno Drera
, Sergio Barlati
, et al.
·
Neurology
·
6
The novel p.G150R missense mutation in the cartilage matrix protein subdomain of type VII collagen in compound heterozigosity with the c.682+1G>A COL7A1 splicing mutation leads to mild dystrophic epidermolysis bullosa
2008
·
B. Drera
, M. Ritelli
, et al.
·
Journal of Dermatological Science
·
4
Congenital Unilesional Cutaneous Langerhans Cell Histiocytosis: A Case Report
2020
·
Marco Ungari
, Gioachino Caresana
, et al.
·
American Journal of Dermatopathology
·
3
Brain ultrasound in Canavan disease
2014
·
B. Drera
, C. Poggiani
·
Journal of Ultrasound
·
3
PDF
Branch point and donor splice-siteCOL7A1mutations in mild recessive dystrophic epidermolysis bullosa
2009
·
B. Drera
, G. Floriddia
, et al.
·
British Journal of Dermatology
·
3
The risk of hospitalisation from RSV is not increased by co-infection in children under 24-months-of-age
2024
·
Alessandra Chiara Francesca Ferrari
, Elisa Giani
, et al.
·
European Journal of Pediatrics
·
2
Erratum to “Letter to the Editor – Diagnosis of vascular Ehlers-Danlos syndrome in Italy: Clinical findings and novel COL3A1 mutations” [J. Dermatol. Sci. 64 (2011) 237–248]
2011
·
Bruno Drera
, Nicoletta Zoppi
, et al.
·
Journal of Dermatological Science
·
2
Waardenburg–Shah syndrome: A case of neonatal palliative care
2024
·
Michael Colpani
, Maria del Carmen Rodriguez Perez
, et al.
·
Pediatric Discovery
·
1
PDF
Hypercalcemia and nephrocalcinosis complicating subcutaneous fat necrosis in a newborn after therapeutic hypothermia.
2016
·
Elisa Milanesi
, Cristina Loda
, et al.
·
PubMed
·
1
The MOM-COPE research project: Measuring the outcomes of maternal COVID19-related prenatal exposure
2020
·
Livio Provenzi
, Roberto Giorda
, et al.
·
Psychoneuroendocrinology
Compound heterozygosity for a novel and a recurrent ABCC6 gene mutation in an Italian family with Pseudoxanthoma elasticum
2007
·
Bruno Drera
, Andrea Brezzi
, et al.
·
Journal of Dermatological Science
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Works count:
25
Citation count:
743
H-index:
11
I10-index:
11
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