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Annals of Human Genetics
|
June 2, 2021
External hydrocephalus as a prenatal feature of noonan syndrome
Gioia Mastromoro, Alessandro De Luca, Enrica Marchionni, et al.
Journal of Neurogenetics
|
November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy
Francesco Nicita, Giacomo Garone, Laura Papetti, et al.
Annali Italiani Di Chirurgia
|
September 19, 2023
Neither inguinoscrotal hernia nor hydrocele misunderstood giant testicular neoplasm. Case report and literature review
Alessandro De Luca, Lucia Franzoso, Viviana Danese, et al.
Sensors (Basel, Switzerland)
|
August 26, 2022
Lamb Wave Detection for Structural Health Monitoring Using a ϕ-OTDR System
Rizwan Zahoor, Enis Cerri, Raffaele Vallifuoco, et al.
Indian Journal of Pediatrics
|
June 20, 2020
Neonatal Marfan Syndrome by Inherited Mutation
Gioia Mastromoro, Valentina Guida, Raffaella Cellitti, et al.
JPRAS Open
|
December 18, 2023
Evaluating the Quality of Online Patient Information for Prepectoral Breast Reconstruction Using Polyurethane-Coated Breast Implants
Edoardo Bruno, Gianluca Borea, Roberto Valeriani, et al.
Archives of Pathology & Laboratory Medicine
|
April 7, 2011
Immunohistochemical expression of neurotrophic tyrosine kinase receptors 1 and 2 in lung carcinoma: potential discriminators between squamous and nonsquamous subtypes
Jefferson Terry, Alessandro De Luca, Samuel Leung, et al.
Human Mutation
|
February 22, 2002
Reliability of DHPLC in mutational screening of beta-globin (HBB) alleles
Alessia Colosimo, Valentina Guida, Alessandro De Luca, et al.
Cancer Cell International
|
January 27, 2018
A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgery
Alessio Metere, Francesca Frezzotti, Claire Elizabeth Graves, et al.
American Journal of Medical Genetics. Part A
|
May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletion
Irene Bottillo, Isabella Torrente, Valentina Lanari, et al.
Page
of 20
Search research articles
Search
Showing results (21-30 of 192) with videos related to
Sort By:
Page
of 20
Annals of Human Genetics
|
June 2, 2021
External hydrocephalus as a prenatal feature of noonan syndrome
Gioia Mastromoro, Alessandro De Luca, Enrica Marchionni, et al.
Journal of Neurogenetics
|
November 13, 2015
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy
Francesco Nicita, Giacomo Garone, Laura Papetti, et al.
Annali Italiani Di Chirurgia
|
September 19, 2023
Neither inguinoscrotal hernia nor hydrocele misunderstood giant testicular neoplasm. Case report and literature review
Alessandro De Luca, Lucia Franzoso, Viviana Danese, et al.
Sensors (Basel, Switzerland)
|
August 26, 2022
Lamb Wave Detection for Structural Health Monitoring Using a ϕ-OTDR System
Rizwan Zahoor, Enis Cerri, Raffaele Vallifuoco, et al.
Indian Journal of Pediatrics
|
June 20, 2020
Neonatal Marfan Syndrome by Inherited Mutation
Gioia Mastromoro, Valentina Guida, Raffaella Cellitti, et al.
JPRAS Open
|
December 18, 2023
Evaluating the Quality of Online Patient Information for Prepectoral Breast Reconstruction Using Polyurethane-Coated Breast Implants
Edoardo Bruno, Gianluca Borea, Roberto Valeriani, et al.
Archives of Pathology & Laboratory Medicine
|
April 7, 2011
Immunohistochemical expression of neurotrophic tyrosine kinase receptors 1 and 2 in lung carcinoma: potential discriminators between squamous and nonsquamous subtypes
Jefferson Terry, Alessandro De Luca, Samuel Leung, et al.
Human Mutation
|
February 22, 2002
Reliability of DHPLC in mutational screening of beta-globin (HBB) alleles
Alessia Colosimo, Valentina Guida, Alessandro De Luca, et al.
Cancer Cell International
|
January 27, 2018
A possible role for selenoprotein glutathione peroxidase (GPx1) and thioredoxin reductases (TrxR1) in thyroid cancer: our experience in thyroid surgery
Alessio Metere, Francesca Frezzotti, Claire Elizabeth Graves, et al.
American Journal of Medical Genetics. Part A
|
May 27, 2010
Germline mosaicism in neurofibromatosis type 1 due to a paternally derived multi-exon deletion
Irene Bottillo, Isabella Torrente, Valentina Lanari, et al.
Page
of 20