Ngā hua rapu kaituhi :: APM

1

The ocular features of the mucopolysaccharidoses mā Jane Ashworth, Susmito Biswas, Ed Wraith, I. Christopher Lloyd

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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2

Advances in the management of congenital and infantile cataract mā I. Christopher Lloyd, Jane Ashworth, Susmito Biswas, R V Abadi

I whakaputaina 2007

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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3

A mutation in the RIEG1 gene associated with Peters’ anomaly mā W Doward, Rahat Perveen, I. Christopher Lloyd, A E Ridgway, Laura C. Wilson, Graeme Black

I whakaputaina 1999

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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4

Neonatal cataract: Aetiology, pathogenesis and management mā I. Christopher Lloyd, Mark Goss‐Sampson, Brett G. Jeffrey, A Kriss, I Russell‐Eggitt, David Taylor

I whakaputaina 1992

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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5

Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis mā Graeme Black, Rahat Perveen, Richard Bonshek, Mark Cahill, Jill Clayton-Smith, I. Christopher Lloyd, David McLeod

I whakaputaina 1999

Whiwhi kuputuhi katoa
Artigo

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6

Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach mā Mahmoud Musleh, Georgina Hall, I. Christopher Lloyd, Rachel Gillespie, S. Waller, Sofia Douzgou, Jill Clayton‐Smith, Elias Kehdi, Graeme Black, Jane Ashworth

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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7

Next-generation Sequencing in the Diagnosis of Metabolic Disease Marked by Pediatric Cataract mā Rachel Gillespie, Jill Urquhart, Beverley Anderson, Simon G. Williams, Sarah Waller, Jane Ashworth, Susmito Biswas, Simon Jones, Fiona Stewart, I. Christopher Lloyd, Jill Clayton‐Smith, Graeme Black

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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8

Cataract management in children: a review of the literature and current practice across five large UK centres mā Jay Self, Rachel L. Taylor, Ameenat Lola Solebo, Susmito Biswas, Manoj Parulekar, Arundhati Dev Borman, Jane Ashworth, Rory McClenaghan, Joseph Abbott, Elizabeth O’Flynn, Darius Hildebrand, I. Christopher Lloyd

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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9

Molecular findings from 537 individuals with inherited retinal disease mā Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, James O’Sullivan, Simon G. Williams, Janine A. Lamb, Binay Panda, Panagiotis I. Sergouniotis, Rachel Gillespie, Stephen P. Daiger, Georgina Hall, Theodora Gale, I. Christopher Lloyd, Paul N. Bishop, Simon Ramsden, Graeme Black

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Mutations in<i>SIPA1L3</i>cause eye defects through disruption of cell polarity and cytoskeleton organization mā Rebecca Greenlees, Marija Mihelec, Saira Yousoof, Daniel Speidel, Selwin K. Wu, Silke Rinkwitz, Ivan Prokudin, Rahat Perveen, Anson Cheng, Alan Ma, Benjamin M. Nash, Rachel Gillespie, David A.F. Loebel, Jill Clayton‐Smith, I. Christopher Lloyd, John Grigg, Patrick Tam, Alpha S. Yap, Thomas Becker, Graeme Black, Elena V. Semina, Robyn V. Jamieson

I whakaputaina 2015

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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