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American Journal of Medical Genetics. Part A|March 17, 2009
Multiple joint dislocations: an additional skeletal finding in Lowry-Wood syndrome?Cinzia Magnani, Salvatore Antonio Tedesco, Sara Dallaglio, et al.Genomics|April 5, 2008
Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndromeFrancesco Nonnis Marzano, Milena Maldini, Laura Filonzi, et al.Disease Markers|September 12, 2022
Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight InfantsLaura Filonzi, Serafina Perrone, Maria Luisa Tataranno, et al.Neurogenetics|September 24, 2008
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesisLaura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, et al.Acta Bio-Medica : Atenei Parmensis|December 24, 2015
Universal newborn hearing screening: the experience of the University Hospital of ParmaCinzia Magnani, Giovanna Bacchi, Anna Maria Borghini, et al.Journal of Child Neurology|March 2, 2012
Clinical and polygraphic improvement of breathing abnormalities after valproate in a case of Pitt-Hopkins syndromeIlenia Maini, Gaetano Cantalupo, Emanuela Claudia Turco, et al.Pediatric Dermatology|February 3, 2015
Recessive bullous dermolysis of the newborn in preterm siblings with a missense mutation in type VII collagenValeria Boccaletti, Giovanna Zambruno, Daniele Castiglia, et al.Early Human Development|February 25, 2020
Determinants of neonatal hypoglycemia after antenatal administration of corticosteroids (ACS) for lung maturation: Data from two referral centers and review of the literatureElvira di Pasquo, Gabriele Saccone, Laura Angeli, et al.American Journal of Medical Genetics. Part A|June 2, 2020
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndromeFrancesco Cucco, Patrizia Sarogni, Sara Rossato, et al.American Journal of Medical Genetics. Part A|July 12, 2005
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palateMichele Rubini, Roberto Brusati, Giovanna Garattini, et al.Pageof 3