Cinzia Magnani

Parma, Italy

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants.

Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants.

Journal: Disease markers

Published: February 02, 2022

Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns.

Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns.

Journal: Nucleic acids research

Published: May 20, 2020

Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literature.

Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literature.

Journal: Early human development

Published: December 27, 2019

Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome.

Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome.

Journal: American journal of medical genetics. Part A

Published: November 04, 2019

Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6.

Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6.

Journal: Genes

Published: August 30, 2019

Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotype.

Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotype.

Journal: Human genetics

Published: July 23, 2018

Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.

Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.

Journal: Gene

Published: July 13, 2017

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.

Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.

Journal: European journal of medical genetics

Published: February 04, 2015

Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen.

Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagen.

Journal: Pediatric dermatology

Published: February 03, 2015

Universal newborn hearing screening: the experience of the University Hospital of Parma.

Universal newborn hearing screening: the experience of the University Hospital of Parma.

Journal: Acta bio-medica : Atenei Parmensis

Published: January 27, 2015

Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire.

Characterization of 14 novel deletions underlying Rubinstein-Taybi syndrome: an update of the CREBBP deletion repertoire.

Journal: Human genetics

Published: January 20, 2015

Neonatal forearm compartment syndrome: look for cerebral stroke.

Neonatal forearm compartment syndrome: look for cerebral stroke.

Journal: The Journal of pediatrics

Published: September 11, 2013

Showing 1-12 of 17

Last Updated: 09/26/2026