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Clinical Genetics
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February 10, 2016
Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant
D Salvatore, D Dell'Edera, C Colangelo, et al.
European Review for Medical and Pharmacological Sciences
|
February 20, 2024
A novel BRCA2 pathogenic variant c.7094_7100del (p.His2365LeufsTer9) in an Italian family with hereditary breast cancer
D Dell'Edera, A Allegretti, F La Rocca, et al.
European Review for Medical and Pharmacological Sciences
|
October 22, 2011
Salvage utilization of selective and super selective embolization in emergency by use of a-magnetic coil and nano-particles in gynecology
A Tinelli, R Prudenzano, M Torsello, et al.
Journal of Medical Case Reports
|
April 4, 2018
16p11.2 microdeletion syndrome: a case report
D Dell'Edera, C Dilucca, A Allegretti, et al.
European Review for Medical and Pharmacological Sciences
|
March 9, 2011
Importance of molecular biology in the characterization of beta-thalassemia carriers
D Dell'Edera, E Pacella, A A Epifania, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 26, 2011
Biochemical and molecular characterization of von Willebrand disease type 2N in a pregnant patient who gave birth under analgesia with remifentanil
D Dell'Edera, P Guanciali Franchi, M B Lioi, et al.
European Review for Medical and Pharmacological Sciences
|
August 4, 2017
Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results
D Dell'Edera, F Sarlo, A Allegretti, et al.
European Review for Medical and Pharmacological Sciences
|
February 3, 2011
Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies
D Dell'Edera, A Malvasi, E Vitullo, et al.
European Review for Medical and Pharmacological Sciences
|
March 8, 2011
Stickler syndrome in Pierre-Robin sequence prenatal ultrasonographic diagnosis and postnatal therapy: two cases report
E Pacella, A Malvasi, A Tinelli, et al.
European Review for Medical and Pharmacological Sciences
|
April 20, 2021
7q35q36.3 deletion and concomitant 20q13.2q13.33 duplication in a newborn: familiar case
D Dell'Edera, A Allegretti, F Forte, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Clinical Genetics
|
February 10, 2016
Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant
D Salvatore, D Dell'Edera, C Colangelo, et al.
European Review for Medical and Pharmacological Sciences
|
February 20, 2024
A novel BRCA2 pathogenic variant c.7094_7100del (p.His2365LeufsTer9) in an Italian family with hereditary breast cancer
D Dell'Edera, A Allegretti, F La Rocca, et al.
European Review for Medical and Pharmacological Sciences
|
October 22, 2011
Salvage utilization of selective and super selective embolization in emergency by use of a-magnetic coil and nano-particles in gynecology
A Tinelli, R Prudenzano, M Torsello, et al.
Journal of Medical Case Reports
|
April 4, 2018
16p11.2 microdeletion syndrome: a case report
D Dell'Edera, C Dilucca, A Allegretti, et al.
European Review for Medical and Pharmacological Sciences
|
March 9, 2011
Importance of molecular biology in the characterization of beta-thalassemia carriers
D Dell'Edera, E Pacella, A A Epifania, et al.
Journal of Biological Regulators and Homeostatic Agents
|
October 26, 2011
Biochemical and molecular characterization of von Willebrand disease type 2N in a pregnant patient who gave birth under analgesia with remifentanil
D Dell'Edera, P Guanciali Franchi, M B Lioi, et al.
European Review for Medical and Pharmacological Sciences
|
August 4, 2017
Prevention of neural tube defects and maternal gestational diabetes through the inositol supplementation: preliminary results
D Dell'Edera, F Sarlo, A Allegretti, et al.
European Review for Medical and Pharmacological Sciences
|
February 3, 2011
Androgen insensitivity syndrome (or Morris syndrome) and other associated pathologies
D Dell'Edera, A Malvasi, E Vitullo, et al.
European Review for Medical and Pharmacological Sciences
|
March 8, 2011
Stickler syndrome in Pierre-Robin sequence prenatal ultrasonographic diagnosis and postnatal therapy: two cases report
E Pacella, A Malvasi, A Tinelli, et al.
European Review for Medical and Pharmacological Sciences
|
April 20, 2021
7q35q36.3 deletion and concomitant 20q13.2q13.33 duplication in a newborn: familiar case
D Dell'Edera, A Allegretti, F Forte, et al.
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of 1