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Francesca Rivieri
Observed names:
F RIVIERI,
F Rivieri,
F. Rivieri,
Francesca RIVIERI,
Rivieri, Francesca
Institution:
Ospedale Santa Chiara
Observed institutions:
University of Modena and Reggio Emilia,
University of Ferrara,
Ospedale Santa Chiara,
Santa Maria Nuova Hospital,
Azienda Ospedaliero-Universitaria di Modena,
Arcispedale Sant'Anna
show all 6
ORCID:
0000-0001-7791-1046
Observed ORCID:
0000-0001-7791-1046
OpenAlex ID:
A5019946781
Associated anomalies in multi‐malformed infants with cleft lip and palate: An epidemiologic study of nearly 6 million births in 23 EUROCAT registries
2007
·
Elisa Calzolari
, Anna Pierini
, et al.
·
American Journal of Medical Genetics Part A
·
249
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis
2017
·
Viviana Palazzo
, Aldesia Provenzano
, et al.
·
Kidney International
·
135
PDF
Mowat–Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature
2009
·
L. Garavelli
, M. Zollino
, et al.
·
American Journal of Medical Genetics Part A
·
111
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care
2018
·
Ivan Ivanovski
, Olivera Djuric
, et al.
·
Genetics in Medicine
·
103
PDF
Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy)
2003
·
E. Calzolari
, G. Garani
, et al.
·
European Journal of Epidemiology
·
94
Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients
2016
·
Livia Garavelli
, Ivan Ivanovski
, et al.
·
Genetics in Medicine
·
59
PDF
Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype
2013
·
Duccio Maria Cordelli
, Livia Garavelli
, et al.
·
American Journal of Medical Genetics Part A
·
51
Mandibuloacral dysplasia type A in childhood
2009
·
L. Garavelli
, M.R. D'Apice
, et al.
·
American Journal of Medical Genetics Part A
·
51
Adverse pregnancy outcomes in a population exposed to the emissions of a municipal waste incinerator
2008
·
M VINCETI
, C MALAGOLI
, et al.
·
The Science of The Total Environment
·
49
Risk of congenital anomalies around a municipal solid waste incinerator: a GIS-based case-control study
2009
·
Marco Vinceti
, Carlotta Malagoli
, et al.
·
International Journal of Health Geographics
·
45
PDF
Familial Poland anomaly revisited
2011
·
Anwar Baban
, Michele Torre
, et al.
·
American Journal of Medical Genetics Part A
·
37
Syndromic intellectual disability: A new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant
2015
·
Claudio Graziano
, Anita Wischmeijer
, et al.
·
Gene
·
30
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype
2018
·
Lorenzo Nanetti
, Elisa Sarto
, et al.
·
Journal of Neurology
·
29
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype
2005
·
Anna Baroncini
, Francesca Rivieri
, et al.
·
European Journal of Medical Genetics
·
25
Holt–Oram syndrome associated with anomalies of the feet
2008
·
L. Garavelli
, D. De Brasi
, et al.
·
American Journal of Medical Genetics Part A
·
20
Concomitant IDH wild‐type glioblastoma and IDH1‐mutant anaplastic astrocytoma in a patient with constitutional mismatch repair deficiency syndrome
2017
·
F. Galuppini
, E. Opocher
, et al.
·
Neuropathology and Applied Neurobiology
·
18
A novel SLC5A6 homozygous variant in a family with multivitamin-dependent neurometabolic disorder: Phenotype expansion and long-term follow-up
2023
·
Martino Montomoli
, Annalisa Vetro
, et al.
·
European Journal of Medical Genetics
·
13
PDF
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individuals
2021
·
Emilia Ricci
, Anna Fetta
, et al.
·
Epilepsy & Behavior
·
13
Generalized Arterial Calcification of Infancy Type 1 (GACI1): Identification of a Novel Pathogenic Variant (c.1715T>C (p.Leu572Ser))
2021
·
Gaetano Pietro Bulfamante
, Laura Carpenito
, et al.
·
Diagnostics
·
7
PDF
De Novo Unbalanced Translocations in Prader-Willi and Angelman Syndrome Might Be the Reciprocal Product of inv dup(15)s
2012
·
Elena Rossi
, Roberto Giorda
, et al.
·
PLoS ONE
·
6
PDF
Mutational Screening of NOTCH3 Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis
2014
·
Lorena Mosca
, Francesca Rivieri
, et al.
·
Journal of Molecular Neuroscience
·
3
Prevalence at Birth of Congenital Anomalies in a Population Living Around a Modern Municipal Solid Waste Inciderator
2006
·
M Vinceti
, C Malagoli
, et al.
·
Epidemiology
·
2
An Unusual Liver and Kidney Involvement in Congenital Hyperinsulinism with HNF1A Mutation: A Case Report
2025
·
Evelina Maines
, Arianna Maiorana
, et al.
·
Hormone Research in Paediatrics
·
1
Biochemical Pattern of Methylmalonyl-CoA Epimerase Deficiency Identified in Newborn Screening: A Case Report
2024
·
Evelina Maines
, Roberto Franceschi
, et al.
·
International Journal of Neonatal Screening
·
1
PDF
Residence Near High-voltage Power Lines and Risk of Birth Defects
2010
·
Carlotta Malagoli
, Rossella Rodolfi
, et al.
·
Epidemiology
·
1
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Works count:
34
Citation count:
1,153
H-index:
16
I10-index:
18
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