Nocturnal normobaric hyperoxia treatment in a case of chronic diabetic macular edema von Song, Soobin, Lemire, Colin A., Seto, Brendan, Arroyo, Jorge G.

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Normobaric hyperoxia rapidly reduces diabetic macular oedema von Lemire, Colin A., Seto, Brendan, Yamada, Keiko, Arroyo, Jorge G.

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GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome von Doherty, Dan, Chudley, Albert E., Coghlan, Gail, Ishak, Gisele E., Innes, A. Micheil, Lemire, Edmond G., Rogers, R. Curtis, Mhanni, Aizeddin A., Phelps, Ian G., Jones, Steven J.M., Zhan, Shing H., Fejes, Anthony P., Shahin, Hashem, Kanaan, Moien, Akay, Hatice, Tekin, Mustafa, Triggs-Raine, Barbara, Zelinski, Teresa

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Sotos syndrome: Antenatal presentation von Thomas, Aidan, Lemire, Edmond G.

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Clinical and radiologic findings in an adult male with dysosteosclerosis von Lemire, Edmond G., Wiebe, Sheldon

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Congenital anterolateral tibial bowing and polydactyly: a case report von Lemire, Edmond G

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A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population von Lamont, Ryan E., Beaulieu, Chandree L., Bernier, Francois P., Sparkes, Rebecca, Innes, A. Micheil, Jackel‐Cram, Candice, Ober, Carole, Parboosingh, Jillian S., Lemire, Edmond G.

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Endoscope-Assisted Sutureless Intrascleral Haptic Fixation of a Posterior Chamber Intraocular Lens von Tandias, Rachel, Lemire, Colin A., Yu, Gina, Seto, Brendan, Arroyo, Jorge G.

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Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series von Bygarski, Elizabeth, Paterson, Melanie, Lemire, Edmond G

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CFPCLearn: anytime, anywhere, by FPs, for FPs von Lemire, Francine, Sisler, Jeff, Allan, G. Michael

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Discordant intrauterine environment may explain discordance in monozygotic twins von Lemire, Edmond G.

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Saskatchewan continues breast cancer screening von Lemire, Edmond G

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Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation von Metcalfe, KA, Foulkes, WD, Kim-Sing, C, Ainsworth, P, Rosen, B, Armel, S, Poll, A, Eisen, A, Gilchrist, D, Chudley, A, Ghadirian, P, Maugard, C, Lemire, EG, Sun, P, Narod, SA

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Spondylocarpotarsal synostosis syndrome: MRI evaluation of vertebral and disk malformation von Breitling, Magnus, Lemire, Edmond G, Rabin, Michael

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Leri-Weill dyschondrosteosis: An under-recognised cause of short stature von Lemire, E G, Wiebe, S

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Hereditary nonpolyposis colon cancer von Lemire, E G

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Harvey, P.-L. & Lemire, G. (2001) . La nouvelle education, NTIC, transdiscip/inarite et communautique. Quebec: Les Presses de l 'universite Laval, (softcover), 258 pages von Ouellet, Micheline

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Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis von Chibbar, Rajni, Shih, Francis, Baga, Monica, Torlakovic, Emina, Ramlall, Kumar, Skomro, Robert, Cockcroft, Donald W, Lemire, Edmond G

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Novel mutations and polymorphisms in genes causing hereditary hemorrhagic telangiectasia von Abdalla, Salma A., Cymerman, Urszula, Rushlow, Diane, Chen, Ning, Stoeber, Gwendolyn P., Lemire, Edmond G., Letarte, Michelle

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Peripheral Neuropathy in a Child With Cree Leukodystrophy von Huntsman, R.J., Seshia, S., Lowry, N., Lemire, E.G., Harder, S.L.

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