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Boudreault K 11

Showing records 1 to 11 | Display all abstracts from Boudreault K

73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Toral MA
Molecular genetics & genomic medicine 2017; 5: 202-209

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73459 Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy
Boudreault K; Justus S
Orphanet Journal of Rare Diseases 2017; 12: 129

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73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Velez G; Boudreault K
Molecular genetics & genomic medicine 2017; 5: 202-209

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73459 Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy
Sengillo JD; Schuerch K
Orphanet Journal of Rare Diseases 2017; 12: 129

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73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Schaefer KA; Xu Y
Molecular genetics & genomic medicine 2017; 5: 202-209

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73459 Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy
Lee W
Orphanet Journal of Rare Diseases 2017; 12: 129

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73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Saffra N
Molecular genetics & genomic medicine 2017; 5: 202-209

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73459 Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy
Cabral T
Orphanet Journal of Rare Diseases 2017; 12: 129

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73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Bassuk AG
Molecular genetics & genomic medicine 2017; 5: 202-209

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73459 Efficacy of rituximab in non-paraneoplastic autoimmune retinopathy
Tsang SH
Orphanet Journal of Rare Diseases 2017; 12: 129

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73157 Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia
Tsang SH; Mahajan VB
Molecular genetics & genomic medicine 2017; 5: 202-209

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