Search research articles
Contact Us
Filters
Showing results (21-30 of 47) with videos related to
Page
of 5
Sort By:
Journal of Immunology (Baltimore, Md. : 1950)
|
January 8, 2008
CpG drives human transitional B cells to terminal differentiation and production of natural antibodies
Federica Capolunghi, Simona Cascioli, Ezio Giorda, et al.
Australasian Journal of Ultrasound in Medicine
|
July 2, 2025
Vertebral Bone Density Abnormalities in Fetal Ultrasound: A Distinctive Clinical Sign of Spondylocarpotarsal Synostosis Syndrome <i>MYH3</i>-Related
Immacolata Blasi, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.
Pathology, Research and Practice
|
January 22, 2021
Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review
Giovanni Innella, Sara Miccoli, Dora Colussi, et al.
The New Microbiologica
|
April 6, 2018
Infectious meningitis/encephalitis: evaluation of a rapid and fully automated multiplex PCR in the microbiological diagnostic workup
Giulia Piccirilli, Angela Chiereghin, Liliana Gabrielli, et al.
European Journal of Human Genetics : EJHG
|
February 7, 2013
Where Birt-Hogg-Dubé meets Cowden syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours
Laura Maria Pradella, Martin Lang, Ivana Kurelac, et al.
Frontiers in Medicine
|
August 13, 2021
<i>PTEN</i> Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis
Giovanni Innella, Elena Bonora, Iria Neri, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2018
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients
Michele Ciavarella, Sara Miccoli, Anna Prossomariti, et al.
Human Molecular Genetics
|
April 8, 2011
Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma
Flora Guerra, Ivana Kurelac, Antonella Cormio, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
January 29, 2025
Myoclonic reflex and non-reflex seizures in a female child with Coffin-Lowry syndrome: Clinical vignette
Agnese Pantani, Susanna Rizzi, Carlotta Spagnoli, et al.
International Journal of Molecular Sciences
|
June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 47) with videos related to
Sort By:
Page
of 5
Journal of Immunology (Baltimore, Md. : 1950)
|
January 8, 2008
CpG drives human transitional B cells to terminal differentiation and production of natural antibodies
Federica Capolunghi, Simona Cascioli, Ezio Giorda, et al.
Australasian Journal of Ultrasound in Medicine
|
July 2, 2025
Vertebral Bone Density Abnormalities in Fetal Ultrasound: A Distinctive Clinical Sign of Spondylocarpotarsal Synostosis Syndrome <i>MYH3</i>-Related
Immacolata Blasi, Marzia Pollazzon, Stefano Giuseppe Caraffi, et al.
Pathology, Research and Practice
|
January 22, 2021
Colorectal polyposis as a clue to the diagnosis of Cowden syndrome: Report of two cases and literature review
Giovanni Innella, Sara Miccoli, Dora Colussi, et al.
The New Microbiologica
|
April 6, 2018
Infectious meningitis/encephalitis: evaluation of a rapid and fully automated multiplex PCR in the microbiological diagnostic workup
Giulia Piccirilli, Angela Chiereghin, Liliana Gabrielli, et al.
European Journal of Human Genetics : EJHG
|
February 7, 2013
Where Birt-Hogg-Dubé meets Cowden syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours
Laura Maria Pradella, Martin Lang, Ivana Kurelac, et al.
Frontiers in Medicine
|
August 13, 2021
<i>PTEN</i> Hamartoma Tumor Syndrome: Skin Manifestations and Insights Into Their Molecular Pathogenesis
Giovanni Innella, Elena Bonora, Iria Neri, et al.
European Journal of Human Genetics : EJHG
|
January 26, 2018
Somatic APC mosaicism and oligogenic inheritance in genetically unsolved colorectal adenomatous polyposis patients
Michele Ciavarella, Sara Miccoli, Anna Prossomariti, et al.
Human Molecular Genetics
|
April 8, 2011
Placing mitochondrial DNA mutations within the progression model of type I endometrial carcinoma
Flora Guerra, Ivana Kurelac, Antonella Cormio, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
January 29, 2025
Myoclonic reflex and non-reflex seizures in a female child with Coffin-Lowry syndrome: Clinical vignette
Agnese Pantani, Susanna Rizzi, Carlotta Spagnoli, et al.
International Journal of Molecular Sciences
|
June 2, 2021
Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?
Roberta Zuntini, Elena Bonora, Laura Maria Pradella, et al.
Page
of 5