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Results: 1-17 |
Results: 17
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
Authors: Zhang, K Kniazeva, M Han, M Li, W Yu, ZY Yang, ZL Li, Y Metzker, ML Allikmets, R Zack, DJ Kakuk, LE Lagali, PS Wong, PW MacDonald, IM Sieving, PA Figueroa, DJ Austin, CP Gould, RJ Ayyagari, R Petrukhin, K
Citation: K. Zhang et al., A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy, NAT GENET, 27(1), 2001, pp. 89-93
September 11, 2001
Authors: MacDonald, IM
Citation: Im. Macdonald, September 11, 2001, CAN J OPHTH, 36(6), 2001, pp. 305-305
The only difference between men and boys is the price of their toys
Authors: MacDonald, IM
Citation: Im. Macdonald, The only difference between men and boys is the price of their toys, CAN J OPHTH, 36(5), 2001, pp. 241-241
What are you reading?
Authors: MacDonald, IM
Citation: Im. Macdonald, What are you reading?, CAN J OPHTH, 36(4), 2001, pp. 171-172
How to be a successful ophthalmologist
Authors: MacDonald, IM
Citation: Im. Macdonald, How to be a successful ophthalmologist, CAN J OPHTH, 36(1), 2001, pp. 1-1
Autosomal dominant Stargardt-like macular dystrophy - Founder effect and reassessment of genetic heterogeneity
Authors: Donoso, LA Frost, AT Stone, EM Weleber, RG MacDonald, IM Hageman, GS Cibis, GW Ritter, R Edwards, AO
Citation: La. Donoso et al., Autosomal dominant Stargardt-like macular dystrophy - Founder effect and reassessment of genetic heterogeneity, ARCH OPHTH, 119(4), 2001, pp. 564-570
Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms
Authors: Tran, M Bhargava, R MacDonald, IM
Citation: M. Tran et al., Leber hereditary optic neuropathy, progressive visual loss, and multiple-sclerosis-like symptoms, AM J OPHTH, 132(4), 2001, pp. 591-593
Going solo
Authors: MacDonald, IM
Citation: Im. Macdonald, Going solo, CAN J OPHTH, 35(7), 2000, pp. 359-359
What's our Journal all about?
Authors: MacDonald, IM
Citation: Im. Macdonald, What's our Journal all about?, CAN J OPHTH, 35(6), 2000, pp. 299-299
Autosomal dominant Stargardt-like macular dystrophy segregating in a largeCanadian family
Authors: Lagali, PS MacDonald, IM Griesinger, IB Chambers, ML Ayyagari, R Wong, PW
Citation: Ps. Lagali et al., Autosomal dominant Stargardt-like macular dystrophy segregating in a largeCanadian family, CAN J OPHTH, 35(6), 2000, pp. 315-324
New guidelines or old?
Authors: MacDonald, IM
Citation: Im. Macdonald, New guidelines or old?, CAN J OPHTH, 35(5), 2000, pp. 245-245
Do they have to take the eye out?
Authors: MacDonald, IM
Citation: Im. Macdonald, Do they have to take the eye out?, CAN J OPHTH, 35(3), 2000, pp. 123-123
Back to the future
Authors: MacDonald, IM
Citation: Im. Macdonald, Back to the future, CAN J OPHTH, 35(1), 2000, pp. 1-1
Isolated sulfite oxidase deficiency - Review of two cases in one family
Authors: Edwards, MC Johnson, JL Marriage, B Graf, TN Coyne, KE Rajagopalan, KV MacDonald, IM
Citation: Mc. Edwards et al., Isolated sulfite oxidase deficiency - Review of two cases in one family, OPHTHALMOL, 106(10), 1999, pp. 1957-1961
The years ahead
Authors: MacDonald, IM
Citation: Im. Macdonald, The years ahead, CAN J OPHTH, 34(6), 1999, pp. 315-315
Update in genetics: genetic eye diseases and the ophthalmologist
Authors: MacDonald, IM
Citation: Im. Macdonald, Update in genetics: genetic eye diseases and the ophthalmologist, CAN J OPHTH, 34(2), 1999, pp. 69-73
Choroideremia
Authors: MacDonald, IM
Citation: Im. Macdonald, Choroideremia, OX MG MED G, (36), 1998, pp. 397-405
Risultati: 1-17 |