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Contemporary Clinical Trials
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June 1, 2022
Clinic navigation and home visits to improve asthma care in low income adults with poorly controlled asthma: Before and during the pandemic
Andrea J Apter, Tyra Bryant-Stephens, Xiaoyan Han, et al.
Genes
|
October 23, 2021
Pendred Syndrome, or Not Pendred Syndrome? That Is the Question
Paola Tesolin, Sofia Fiorino, Stefania Lenarduzzi, et al.
Materials (Basel, Switzerland)
|
June 1, 2018
A Single-Step Surface Modification of Electrospun Silica Nanofibers Using a Silica Binding Protein Fused with an RGD Motif for Enhanced PC12 Cell Growth and Differentiation
Wen Shuo Chen, Ling Yu Guo, Amien Mohamed Masroujeh, et al.
European Journal of Human Genetics : EJHG
|
October 21, 2018
TBL1Y: a new gene involved in syndromic hearing loss
Mariateresa Di Stazio, Chiara Collesi, Diego Vozzi, et al.
Hearing Research
|
August 7, 2019
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss
Stefania Lenarduzzi, Anna Morgan, Flavio Faletra, et al.
Scientific Reports
|
December 23, 2015
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss
Giorgia Girotto, Déborah I Scheffer, Anna Morgan, et al.
Biomolecules
|
January 8, 2025
In-Depth Phenotyping of <i>PIGW</i>-Related Disease and Its Role in 17q12 Genomic Disorder
Agnese Feresin, Mathilde Lefebvre, Emilie Sjøstrøm, et al.
Genes
|
October 27, 2020
Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
Anna Morgan, Stefania Lenarduzzi, Beatrice Spedicati, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection
Dragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, et al.
Mutation Research
|
May 15, 2017
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families
Moza K Alkowari, Diego Vozzi, Shruti Bhagat, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 86) with videos related to
Sort By:
Page
of 9
Contemporary Clinical Trials
|
June 1, 2022
Clinic navigation and home visits to improve asthma care in low income adults with poorly controlled asthma: Before and during the pandemic
Andrea J Apter, Tyra Bryant-Stephens, Xiaoyan Han, et al.
Genes
|
October 23, 2021
Pendred Syndrome, or Not Pendred Syndrome? That Is the Question
Paola Tesolin, Sofia Fiorino, Stefania Lenarduzzi, et al.
Materials (Basel, Switzerland)
|
June 1, 2018
A Single-Step Surface Modification of Electrospun Silica Nanofibers Using a Silica Binding Protein Fused with an RGD Motif for Enhanced PC12 Cell Growth and Differentiation
Wen Shuo Chen, Ling Yu Guo, Amien Mohamed Masroujeh, et al.
European Journal of Human Genetics : EJHG
|
October 21, 2018
TBL1Y: a new gene involved in syndromic hearing loss
Mariateresa Di Stazio, Chiara Collesi, Diego Vozzi, et al.
Hearing Research
|
August 7, 2019
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss
Stefania Lenarduzzi, Anna Morgan, Flavio Faletra, et al.
Scientific Reports
|
December 23, 2015
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss
Giorgia Girotto, Déborah I Scheffer, Anna Morgan, et al.
Biomolecules
|
January 8, 2025
In-Depth Phenotyping of <i>PIGW</i>-Related Disease and Its Role in 17q12 Genomic Disorder
Agnese Feresin, Mathilde Lefebvre, Emilie Sjøstrøm, et al.
Genes
|
October 27, 2020
Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
Anna Morgan, Stefania Lenarduzzi, Beatrice Spedicati, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection
Dragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, et al.
Mutation Research
|
May 15, 2017
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families
Moza K Alkowari, Diego Vozzi, Shruti Bhagat, et al.
Page
of 9