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1.
Autosomal Recessive Bestrophinopathy: Clinical Features, Natural History, and Genetic Findings in Preparation for Clinical Trials.
Ophthalmology
; 128(5): 706-718, 2021 05.
Article
in English
| MEDLINE | ID: mdl-33039401
2.
Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom.
Ophthalmology
; 127(10): 1384-1394, 2020 10.
Article
in English
| MEDLINE | ID: mdl-32423767
3.
Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females.
Hum Mutat
; 39(1): 80-91, 2018 01.
Article
in English
| MEDLINE | ID: mdl-28967191
4.
Clinician and parent views on urine collection in precontinent children in the UK: a qualitative interview study.
BMJ Open
; 14(4): e081306, 2024 Apr 29.
Article
in English
| MEDLINE | ID: mdl-38684250
5.
The effect of Functional Electrical Stimulation-assisted posture-shifting in bone mineral density: case series-pilot study.
Spinal Cord Ser Cases
; 8(1): 60, 2022 06 10.
Article
in English
| MEDLINE | ID: mdl-35680785
6.
Novel instrumented frame for standing exercising of users with complete spinal cord injuries.
Sci Rep
; 9(1): 13003, 2019 09 10.
Article
in English
| MEDLINE | ID: mdl-31506460
7.
A clinical and molecular characterisation of CRB1-associated maculopathy.
Eur J Hum Genet
; 26(5): 687-694, 2018 05.
Article
in English
| MEDLINE | ID: mdl-29391521
8.
A Design Method for FES Bone Health Therapy in SCI.
Eur J Transl Myol
; 26(4): 6419, 2016 Sep 15.
Article
in English
| MEDLINE | ID: mdl-28078075
9.
Inhomogeneous Response of Articular Cartilage: A Three-Dimensional Multiphasic Heterogeneous Study.
PLoS One
; 11(6): e0157967, 2016.
Article
in English
| MEDLINE | ID: mdl-27327166
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