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Alward WLM 11

Showing records 1 to 11 | Display all abstracts from Alward WLM

80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Alward WLM
JAMA ophthalmology 2019; 137: 559-563

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80515 The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Tandon A
American Journal of Ophthalmology 2019; 202: 55-61

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80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
van der Heide C
JAMA ophthalmology 2019; 137: 559-563

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80515 The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Zhang Z; Fingert JH
American Journal of Ophthalmology 2019; 202: 55-61

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80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Khanna CL
JAMA ophthalmology 2019; 137: 559-563

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80515 The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Kwon YH
American Journal of Ophthalmology 2019; 202: 55-61

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80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Roos BR; Sivaprasad S
JAMA ophthalmology 2019; 137: 559-563

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80515 The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Wang K
American Journal of Ophthalmology 2019; 202: 55-61

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80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Kam J
JAMA ophthalmology 2019; 137: 559-563

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80515 The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma
Alward WLM
American Journal of Ophthalmology 2019; 202: 55-61

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80536 Myocilin Mutations in Patients With Normal-Tension Glaucoma
Ritch R; Lotery A; Igo RP; Cooke Bailey JN; Stone EM; Scheetz TE; Kwon YH; Pasquale LR; Wiggs JL; Fingert JH;
JAMA ophthalmology 2019; 137: 559-563

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