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Graeme Black

Showing results (1-10 of 38) with videos related to

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BMJ Quality Improvement Reports|December 10, 2016
Improving diagnosis for congenital cataract by introducing NGS genetic testingMohammud Musleh, Jane Ashworth, Graeme Black, et al.
Journal of Community Genetics|January 26, 2019
The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophiesEleanor McVeigh, Harriet Jones, Graeme Black, et al.
BMJ Case Reports|February 14, 2018
Unique case of gyrate atrophy with a well-preserved electroretinogram (ERG)Kirti M Jasani, Neil R A Parry, Graeme Black, et al.
Case Reports in Ophthalmology|November 26, 2019
Unique Case of Bilateral Exudative Retinal Detachment following Creatine Supplementation in a Patient with Autosomal Dominant BestrophinopathyKonstantinos Kopsidas, Hedayat Javidi, Simon P Kelly, et al.
Retina (Philadelphia, Pa.)|May 8, 2023
ReplyEmma Linton, Assad Jalil, Panagiotis Sergouniotis, et al.
Retina (Philadelphia, Pa.)|September 27, 2022
LASER PROPHYLAXIS IN STICKLER SYNDROME: The Manchester ProtocolEmma Linton, Assad Jalil, Panagiotis Sergouniotis, et al.
Orphanet Journal of Rare Diseases|December 15, 2021
Genetic testing and diagnosis of inherited retinal diseasesByron L Lam, Bart P Leroy, Graeme Black, et al.
Plastic and Reconstructive Surgery|February 3, 2011
A clinical characterization of familial keloid disease in unique African tribes reveals distinct keloid phenotypesHusam Bella, Marco Heise, Khalid I Yagi, et al.
Clinical Dysmorphology|February 24, 2010
De-novo duplication of 5(q13.3q21.1) in a child with vitreo-retinal dysplasia and learning disabilitySiddharth Banka, I Chris Lloyd, Graeme Black, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 7, 2020
Hearing Loss in Enlarged Vestibular Aqueduct: A Prognostic Factor Systematic Review of the LiteratureHaroon Shakeel Saeed, Jonny Kenth, Graeme Black, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
BMJ Quality Improvement Reports|December 10, 2016
Improving diagnosis for congenital cataract by introducing NGS genetic testingMohammud Musleh, Jane Ashworth, Graeme Black, et al.
Journal of Community Genetics|January 26, 2019
The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophiesEleanor McVeigh, Harriet Jones, Graeme Black, et al.
BMJ Case Reports|February 14, 2018
Unique case of gyrate atrophy with a well-preserved electroretinogram (ERG)Kirti M Jasani, Neil R A Parry, Graeme Black, et al.
Case Reports in Ophthalmology|November 26, 2019
Unique Case of Bilateral Exudative Retinal Detachment following Creatine Supplementation in a Patient with Autosomal Dominant BestrophinopathyKonstantinos Kopsidas, Hedayat Javidi, Simon P Kelly, et al.
Retina (Philadelphia, Pa.)|May 8, 2023
ReplyEmma Linton, Assad Jalil, Panagiotis Sergouniotis, et al.
Retina (Philadelphia, Pa.)|September 27, 2022
LASER PROPHYLAXIS IN STICKLER SYNDROME: The Manchester ProtocolEmma Linton, Assad Jalil, Panagiotis Sergouniotis, et al.
Orphanet Journal of Rare Diseases|December 15, 2021
Genetic testing and diagnosis of inherited retinal diseasesByron L Lam, Bart P Leroy, Graeme Black, et al.
Plastic and Reconstructive Surgery|February 3, 2011
A clinical characterization of familial keloid disease in unique African tribes reveals distinct keloid phenotypesHusam Bella, Marco Heise, Khalid I Yagi, et al.
Clinical Dysmorphology|February 24, 2010
De-novo duplication of 5(q13.3q21.1) in a child with vitreo-retinal dysplasia and learning disabilitySiddharth Banka, I Chris Lloyd, Graeme Black, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 7, 2020
Hearing Loss in Enlarged Vestibular Aqueduct: A Prognostic Factor Systematic Review of the LiteratureHaroon Shakeel Saeed, Jonny Kenth, Graeme Black, et al.
Pageof 4