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Journal of Pediatric Hematology/Oncology
|
April 28, 2004
Resolution of orbitocerebral aspergillosis during combination treatment with voriconazole and amphotericin plus adjunctive cytokine therapy
Delia Bethell, Georgina Hall, T Robin Goodman, et al.
The British Journal of Ophthalmology
|
June 8, 2013
Valuing the benefits of genetic testing for retinitis pigmentosa: a pilot application of the contingent valuation method
Martin Eden, Katherine Payne, Ryan M Combs, et al.
Journal of Community Genetics
|
January 9, 2015
Variation in healthcare services for specialist genetic testing and implications for planning genetic services: the example of inherited retinal dystrophy in the English NHS
Mark Harrison, Stephen Birch, Martin Eden, et al.
Journal of Genetic Counseling
|
January 22, 2013
Building the genetic counsellor profession in the United Kingdom: two decades of growth and development
Heather Skirton, Lauren Kerzin-Storrar, Chris Barnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2017
Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example
Niall Davison, Katherine Payne, Martin Eden, et al.
Journal of Medical Genetics
|
May 15, 2012
A paradigm shift in the delivery of services for diagnosis of inherited retinal disease
James O'Sullivan, Brendan G Mullaney, Sanjeev S Bhaskar, et al.
Rheumatology (Oxford, England)
|
August 5, 2019
Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra
Noémi B A Roy, Ahmad I Zaal, Georgina Hall, et al.
The British Journal of Ophthalmology
|
June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophies
Ryan Combs, Georgina Hall, Katherine Payne, et al.
European Journal of Human Genetics : EJHG
|
February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophy
Ryan Combs, Marion McAllister, Katherine Payne, et al.
Eye (London, England)
|
February 3, 2025
Real-world outcomes of Voretigene Neparvovec: a single-centre consecutive case series
Assad Jalil, Mariantonia Ferrara, Myrta Lippera, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Journal of Pediatric Hematology/Oncology
|
April 28, 2004
Resolution of orbitocerebral aspergillosis during combination treatment with voriconazole and amphotericin plus adjunctive cytokine therapy
Delia Bethell, Georgina Hall, T Robin Goodman, et al.
The British Journal of Ophthalmology
|
June 8, 2013
Valuing the benefits of genetic testing for retinitis pigmentosa: a pilot application of the contingent valuation method
Martin Eden, Katherine Payne, Ryan M Combs, et al.
Journal of Community Genetics
|
January 9, 2015
Variation in healthcare services for specialist genetic testing and implications for planning genetic services: the example of inherited retinal dystrophy in the English NHS
Mark Harrison, Stephen Birch, Martin Eden, et al.
Journal of Genetic Counseling
|
January 22, 2013
Building the genetic counsellor profession in the United Kingdom: two decades of growth and development
Heather Skirton, Lauren Kerzin-Storrar, Chris Barnes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 17, 2017
Exploring the feasibility of delivering standardized genomic care using ophthalmology as an example
Niall Davison, Katherine Payne, Martin Eden, et al.
Journal of Medical Genetics
|
May 15, 2012
A paradigm shift in the delivery of services for diagnosis of inherited retinal disease
James O'Sullivan, Brendan G Mullaney, Sanjeev S Bhaskar, et al.
Rheumatology (Oxford, England)
|
August 5, 2019
Majeed syndrome: description of a novel mutation and therapeutic response to bisphosphonates and IL-1 blockade with anakinra
Noémi B A Roy, Ahmad I Zaal, Georgina Hall, et al.
The British Journal of Ophthalmology
|
June 7, 2013
Understanding the expectations of patients with inherited retinal dystrophies
Ryan Combs, Georgina Hall, Katherine Payne, et al.
European Journal of Human Genetics : EJHG
|
February 14, 2013
Understanding the impact of genetic testing for inherited retinal dystrophy
Ryan Combs, Marion McAllister, Katherine Payne, et al.
Eye (London, England)
|
February 3, 2025
Real-world outcomes of Voretigene Neparvovec: a single-centre consecutive case series
Assad Jalil, Mariantonia Ferrara, Myrta Lippera, et al.
Page
of 5