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Author/Creator Branham, Kari

12. Reliability of kinetic visual field testing in children with mutation-proven retinal dystrophies: Implications for therapeutic clinical trials. (2nd January 2018)

Authors:
Dedania, Vaidehi S.; Liu, Jerry Y.; Schlegel, Dana; Andrews, Chris A.; Branham, Kari; Khan, Naheed W.; Musch, David C.; Heckenlively, John R.; Jayasundera, K. Thiran
Journal:
Ophthalmic genetics
Issue:
Volume 39:Number 1(2018)
Page Start:
22
Record Type:
Journal Article
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13. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations. Issue 1 (30th October 2013)

Authors:
Mackay, Donna S.; Borman, Arundhati Dev; Sui, Ruifang; van den, L. Ingeborgh; Berson, Eliot L.; Ocaka, Louise A.; Davidson, Alice E.; Heckenlively, John R.; Branham, Kari; Ren, Huanan; Lopez, Irma; Maria, Maleeha; Azam, Maleeha; Henkes, Arjen; Blokland, Ellen; Andreasson, [Sten; de, Elfride; Benn...
Journal:
Human mutation
Issue:
Volume 35:Issue 1(2014:Jan.)
Page Start:
150
Record Type:
Journal Article
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14. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations. Issue 11 (17th September 2013)

Authors:
Mackay, Donna S.; Borman, Arundhati Dev; Sui, Ruifang; van den, L. Ingeborgh; Berson, Eliot L.; Ocaka, Louise A.; Davidson, Alice E.; Heckenlively, John R.; Branham, Kari; Ren, Huanan; Lopez, Irma; Maria, Maleeha; Azam, Maleeha; Henkes, Arjen; Blokland, Ellen; Andreasson, Sten; de, Elfride; Benne...
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1537
Record Type:
Journal Article
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15. Screening of a Large Cohort of Leber Congenital Amaurosis and Retinitis Pigmentosa Patients Identifies Novel LCA5 Mutations and New Genotype–Phenotype Correlations. Issue 11 (17th September 2013)

Authors:
Mackay, Donna S.; Borman, Arundhati Dev; Sui, Ruifang; van den Born, L. Ingeborgh; Berson, Eliot L.; Ocaka, Louise A.; Davidson, Alice E.; Heckenlively, John R.; Branham, Kari; Ren, Huanan; Lopez, Irma; Maria, Maleeha; Azam, Maleeha; Henkes, Arjen; Blokland, Ellen; Andreasson, Sten; de Baere, Elf...
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1537
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

16. Tissue‐specific genotype–phenotype correlations among USH2A‐related disorders in the RUSH2A study. Issue 5 (21st March 2022)

Authors:
Hufnagel, Robert B.; Liang, Wendi; Duncan, Jacque L.; Brewer, Carmen C.; Audo, Isabelle; Ayala, Allison R.; Branham, Kari; Cheetham, Janet K.; Daiger, Stephen P.; Durham, Todd A.; Guan, Bin; Heon, Elise; Hoyng, Carel B.; Iannaccone, Alessandro; Kay, Christine N.; Michaelides, Michel; Pennesi, Mar...
Journal:
Human mutation
Issue:
Volume 43:Issue 5(2022)
Page Start:
613
Record Type:
Journal Article
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17. Worldwide Argus II implantation: recommendations to optimize patient outcomes. Issue 1 (December 2016)

Authors:
Ghodasra, Devon; Chen, Adrienne; Arevalo, J.; Birch, David; Branham, Kari; Coley, Brian; Dagnelie, Gislin; de Juan, Eugene; Devenyi, Robert; Dorn, Jessy; Fisher, Andy; Geruschat, Duane; Gregori, Ninel; Greenberg, Robert; Hahn, Paul; Ho, Allen; Howson, Ashley; Huang, Suber; Iezzi, Raymond; Khan, N...
Journal:
BMC ophthalmology
Issue:
Volume 16:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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18. Worldwide Argus II implantation: recommendations to optimize patient outcomes. Issue 1 (December 2016)

Authors:
Ghodasra, Devon; Chen, Adrienne; Arevalo, J.; Birch, David; Branham, Kari; Coley, Brian; Dagnelie, Gislin; de Juan, Eugene; Devenyi, Robert; Dorn, Jessy; Fisher, Andy; Geruschat, Duane; Gregori, Ninel; Greenberg, Robert; Hahn, Paul; Ho, Allen; Howson, Ashley; Huang, Suber; Iezzi, Raymond; Khan, N...
Journal:
BMC ophthalmology
Issue:
Volume 16:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗