G. Garani

发表

ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.

I. Scheffer, H. Mefford, G. Cioni, 2021, Brain : a journal of neurology.

Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype

B. V. van Bon, A. Hoischen, H. Brunner, 2017, Journal of Medical Genetics.

Increase of Parkin and ATG5 plasmatic levels following perinatal hypoxic-ischemic encephalopathy

P. Pinton, C. Giorgi, M. Wieckowski, 2022, Scientific reports.

Melatonin as a master regulator of cell death and inflammation: molecular mechanisms and clinical implications for newborn care

P. Pinton, M. Wieckowski, G. Ancora, 2019, Cell Death & Disease.

Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, Italy.

A. Ferlini, M. Marsella, C. Borgna-Pignatti, 2013, Blood transfusion = Trasfusione del sangue.

Secondary prevention of early-onset sepsis: a less invasive Italian approach for managing neonates at risk

G. Piccinini, V. Sambri, L. Corvaglia, 2018, Italian Journal of Pediatrics.

Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay

A. Ferlini, S. Fini, S. Bigoni, 2017, Molecular Syndromology.

Factors affecting yawning frequencies in preterm neonates

H. Oster, C. Borgna-Pignatti, Damiano Menin, 2022, PloS one.

Anencephaly: MRI findings and pathogenetic theories

F. Calzolari, G. Garani, L. Tamisari, 2004, Pediatric Radiology.

Terminal deletion of chromosome 1(q43) in a female infant.

V. Vigi, G. Garani, L. Tamisari, 1988, Journal of medical genetics.

Melatonin as a master regulator of cell death and inflammation: molecular mechanisms and clinical implications for newborn care

P. Pinton, M. Wieckowski, G. Ancora, 2019, Cell Death & Disease.

Displasia fronto-nasale

F. Calzolari, L. Merlo, G. Garani, 1992 .

Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy)

A. Neville, E. Calzolari, L. Garavelli, 2002, European Journal of Epidemiology.

Efficacy of a new technique – INtubate-RECruit-SURfactant-Extubate – “IN-REC-SUR-E” – in preterm neonates with respiratory distress syndrome: study protocol for a randomized controlled trial

F. Cools, J. Pillow, L. Boni, 2016, Trials.

Lung recruitment before surfactant administration in extremely preterm neonates with respiratory distress syndrome (IN-REC-SUR-E): a randomised, unblinded, controlled trial.

F. Cools, J. Pillow, L. Boni, 2020, The Lancet. Respiratory medicine.

Limb reduction defects in Emilia Romagna, Italy: epidemiological and genetic study in 173,109 consecutive births.

E. Calzolari, G. Cocchi, G. Garani, 1990, Journal of medical genetics.

Temporal variability in birth prevalence of congenital heart defects as recorded by a general birth defects registry.

E. Calzolari, G. Bosi, M. Scorrano, 2003, The Journal of pediatrics.

Epidemiological and genetic study of 200 cases of oral cleft in the Emilia Romagna region of northern Italy.

E. Calzolari, G. Cocchi, C. Magnani, 1988, Teratology.

Universal cranial ultrasound screening in preterm infants with gestational age 33-36 weeks. A retrospective analysis of 724 newborns.

C. Borgna-Pignatti, A. Baldan, Anna Tarocco, 2014, Pediatric neurology.

Use of ketamine in a newborn with refractory status epilepticus: a case report.

Anna Tarocco, E. Ballardini, G. Garani, 2014, Pediatric Neurology.

Universal Head Ultrasound Screening in Full-term Neonates: A Retrospective Analysis of 6771 Infants.

C. Borgna-Pignatti, A. Baldan, Anna Tarocco, 2017, Pediatric neurology.

Use of ketamine in a newborn with refractory status epilepticus: a case report.

Anna Tarocco, E. Ballardini, G. Garani, 2014, Pediatric neurology.