Search research articles
Contact Us
Filters
Showing results (21-30 of 86) with videos related to
Page
of 9
Sort By:
Gene
|
November 12, 2013
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss
Flavio Faletra, Giorgia Girotto, Adamo Pio D'Adamo, et al.
Stress and Health : Journal of the International Society for the Investigation of Stress
|
November 21, 2022
Feasibility of combining biosensor and ecological momentary assessment to measure stress experiences among economically disadvantaged adolescents
Desiree W Murray, Ty A Ridenour, Margaret M Swingler, et al.
Gene
|
May 20, 2014
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta
Elisa Rubinato, Anna Morgan, Angela D'Eustacchio, et al.
The Veterinary Record
|
May 6, 2020
Inducing weight loss in native ponies: is straw a viable alternative to hay?
Miranda Carlotta Maria Dosi, Roxane Kirton, Sarah Hallsworth, et al.
Nursing Older People
|
May 17, 2005
Ask the experts? Integrated falls service
Clare Abley, Nicky Hayes, Dianne Lewis, et al.
Audiology Research
|
December 22, 2023
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders
Paola Tesolin, Aurora Santin, Anna Morgan, et al.
The Journal of International Advanced Otology
|
February 19, 2021
Non-Syndromic Sensorineural Prelingual and Postlingual Hearing Loss due to COL11A1 Gene Mutation
Andrea Ciorba, Virginia Corazzi, Michela Melegatti, et al.
Cancers
|
April 14, 2025
The Co-Expression and Cellular Location of HER Family Members, EGFRvIII, Putative Cancer Stem Cell Biomarkers CD44 and CD109 in Patients with Glioblastoma, and Their Impacts on Prognosis
Ermira Mulliqi, Said Khelwatty, Izhar Bagwan, et al.
Genes
|
August 6, 2021
Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the <i>NCOA3</i> Gene
Paola Tesolin, Anna Morgan, Michela Notarangelo, et al.
Molecular Medicine (Cambridge, Mass.)
|
March 23, 2025
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct
Emanuele Bernardinelli, Raffaella Liuni, Rapolas Jamontas, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 86) with videos related to
Sort By:
Page
of 9
Gene
|
November 12, 2013
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss
Flavio Faletra, Giorgia Girotto, Adamo Pio D'Adamo, et al.
Stress and Health : Journal of the International Society for the Investigation of Stress
|
November 21, 2022
Feasibility of combining biosensor and ecological momentary assessment to measure stress experiences among economically disadvantaged adolescents
Desiree W Murray, Ty A Ridenour, Margaret M Swingler, et al.
Gene
|
May 20, 2014
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta
Elisa Rubinato, Anna Morgan, Angela D'Eustacchio, et al.
The Veterinary Record
|
May 6, 2020
Inducing weight loss in native ponies: is straw a viable alternative to hay?
Miranda Carlotta Maria Dosi, Roxane Kirton, Sarah Hallsworth, et al.
Nursing Older People
|
May 17, 2005
Ask the experts? Integrated falls service
Clare Abley, Nicky Hayes, Dianne Lewis, et al.
Audiology Research
|
December 22, 2023
Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders
Paola Tesolin, Aurora Santin, Anna Morgan, et al.
The Journal of International Advanced Otology
|
February 19, 2021
Non-Syndromic Sensorineural Prelingual and Postlingual Hearing Loss due to COL11A1 Gene Mutation
Andrea Ciorba, Virginia Corazzi, Michela Melegatti, et al.
Cancers
|
April 14, 2025
The Co-Expression and Cellular Location of HER Family Members, EGFRvIII, Putative Cancer Stem Cell Biomarkers CD44 and CD109 in Patients with Glioblastoma, and Their Impacts on Prognosis
Ermira Mulliqi, Said Khelwatty, Izhar Bagwan, et al.
Genes
|
August 6, 2021
Non-Syndromic Autosomal Dominant Hearing Loss: The First Italian Family Carrying a Mutation in the <i>NCOA3</i> Gene
Paola Tesolin, Anna Morgan, Michela Notarangelo, et al.
Molecular Medicine (Cambridge, Mass.)
|
March 23, 2025
Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct
Emanuele Bernardinelli, Raffaella Liuni, Rapolas Jamontas, et al.
Page
of 9