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C Romano

Showing results (851-860 of 889) with videos related to

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The Journal of Pediatrics|March 11, 2026
Genetic Syndromes Do Not Affect Survival but Increase Morbidity in Neonates with Symptomatic Tetralogy of FallotJoanna E Nelson, Christopher J Petit, Bryan H Goldstein, et al.
Ocular Immunology and Inflammation|May 12, 2021
COVID-19 Retinal Findings in Patients Admitted to Intensive Care Units and WardsPaula M Marinho, Alléxya A A Marcos, Ana M C Branco, et al.
Gut|December 19, 2015
T cell neoepitope discovery in colorectal cancer by high throughput profiling of somatic mutations in expressed genesDaniele Mennonna, Cristina Maccalli, Michele C Romano, et al.
The Journal of Pediatrics|May 30, 2024
Outcomes of Neonates Born with Symptomatic Tetralogy of Fallot and Absent Ductus ArteriosusShiraz A Maskatia, Andrew C Glatz, Bryan H Goldstein, et al.
Annals of Human Genetics|February 12, 1998
Genetic history of cystic fibrosis mutations in Italy. I. Regional distributionS Rendine, F Calafell, N Cappello, et al.
Pediatric Cardiology|April 6, 2022
Palliation Strategy to Achieve Complete Repair in Symptomatic Neonates with Tetralogy of FallotMark A Law, Andrew C Glatz, Jennifer C Romano, et al.
Molecular Psychiatry|February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDB W M van Bon, B P Coe, R Bernier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 18, 2020
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlationsR Villa, V G C Fergnani, R Silipigni, et al.
European Review for Medical and Pharmacological Sciences|May 18, 2021
Clinical application of lung ultrasound score on COVID-19 setting: a regional experience in Southern ItalyM Lugara, G Oliva, P C Pafundi, et al.
Molecular Psychiatry|July 30, 2014
In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cellsH Ito, H Shiwaku, C Yoshida, et al.
Pageof 89

Showing results (851-860 of 889) with videos related to

Sort By:
Pageof 89
The Journal of Pediatrics|March 11, 2026
Genetic Syndromes Do Not Affect Survival but Increase Morbidity in Neonates with Symptomatic Tetralogy of FallotJoanna E Nelson, Christopher J Petit, Bryan H Goldstein, et al.
Ocular Immunology and Inflammation|May 12, 2021
COVID-19 Retinal Findings in Patients Admitted to Intensive Care Units and WardsPaula M Marinho, Alléxya A A Marcos, Ana M C Branco, et al.
Gut|December 19, 2015
T cell neoepitope discovery in colorectal cancer by high throughput profiling of somatic mutations in expressed genesDaniele Mennonna, Cristina Maccalli, Michele C Romano, et al.
The Journal of Pediatrics|May 30, 2024
Outcomes of Neonates Born with Symptomatic Tetralogy of Fallot and Absent Ductus ArteriosusShiraz A Maskatia, Andrew C Glatz, Bryan H Goldstein, et al.
Annals of Human Genetics|February 12, 1998
Genetic history of cystic fibrosis mutations in Italy. I. Regional distributionS Rendine, F Calafell, N Cappello, et al.
Pediatric Cardiology|April 6, 2022
Palliation Strategy to Achieve Complete Repair in Symptomatic Neonates with Tetralogy of FallotMark A Law, Andrew C Glatz, Jennifer C Romano, et al.
Molecular Psychiatry|February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDB W M van Bon, B P Coe, R Bernier, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 18, 2020
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlationsR Villa, V G C Fergnani, R Silipigni, et al.
European Review for Medical and Pharmacological Sciences|May 18, 2021
Clinical application of lung ultrasound score on COVID-19 setting: a regional experience in Southern ItalyM Lugara, G Oliva, P C Pafundi, et al.
Molecular Psychiatry|July 30, 2014
In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cellsH Ito, H Shiwaku, C Yoshida, et al.
Pageof 89