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Page 1
Heritable and non-heritable uncommon causes of stroke.
J Neurol. 2021 Aug;268(8):2780-2807. doi: 10.1007/s00415-020-09836-x. Epub 2020 Apr 21.
J Neurol. 2021.
PMID: 32318851
Review.
Advancing low vision services: a plan for Australian optometry.
Bentley SA, Jackson AJ, Johnston AW, Napper GA, Hodgson M, Soong GP, Oberstein SL, Chong MF, Baggoley G; Optometrists Association Australia Low Vision Working Group.
Bentley SA, et al. Among authors: oberstein sl.
Clin Exp Optom. 2014 May;97(3):214-20. doi: 10.1111/cxo.12139.
Clin Exp Optom. 2014.
PMID: 24766509
Free article.
Review.
No abstract available.
Item in Clipboard
Correction to: Heritable and non-heritable uncommon causes of stroke.
Bersano A, Kraemer M, Burlina A, Mancuso M, Finsterer J, Sacco S, Salvarani C, Caputi L, Chabriat H, Oberstein SL, Federico A, Tournier-Lasserve E, Hunt D, Dichgans M, Arnold M, Debette S, Markus HS.
Bersano A, et al. Among authors: oberstein sl.
J Neurol. 2021 Aug;268(8):2808-2809. doi: 10.1007/s00415-020-09948-4.
J Neurol. 2021.
PMID: 32556534
No abstract available.
Item in Clipboard
An unusual corneal injury.
Newsom RS, Oberstein SL, Falcon MG.
Newsom RS, et al. Among authors: oberstein sl.
Br J Ophthalmol. 1996 Dec;80(12):1112-3. doi: 10.1136/bjo.80.12.1112.
Br J Ophthalmol. 1996.
PMID: 9059284
Free PMC article.
No abstract available.
Item in Clipboard
Ranibizumab is a potential prophylaxis for proliferative vitreoretinopathy, a nonangiogenic blinding disease.
Pennock S, Kim D, Mukai S, Kuhnle M, Chun DW, Matsubara J, Cui J, Ma P, Maberley D, Samad A, Van Geest RJ, Oberstein SL, Schlingemann RO, Kazlauskas A.
Pennock S, et al. Among authors: oberstein sl.
Am J Pathol. 2013 May;182(5):1659-70. doi: 10.1016/j.ajpath.2013.01.052. Epub 2013 Apr 9.
Am J Pathol. 2013.
PMID: 23582767
Free PMC article.
Item in Clipboard
Views and practices of Australian optometrists regarding driving for patients with central visual impairment.
Oberstein SL, Boon MY, Chu BS, Wood JM.
Oberstein SL, et al.
Clin Exp Optom. 2016 Sep;99(5):476-83. doi: 10.1111/cxo.12398. Epub 2016 Aug 18.
Clin Exp Optom. 2016.
PMID: 27539055
Free article.
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Characterization of missense mutations and large deletions in the ALPL gene by sequencing and quantitative multiplex PCR of short fragments.
Spentchian M, Brun-Heath I, Taillandier A, Fauvert D, Serre JL, Simon-Bouy B, Carvalho F, Grochova I, Mehta SG, Müller G, Oberstein SL, Ogur G, Sharif S, Mornet E.
Spentchian M, et al. Among authors: oberstein sl.
Genet Test. 2006 Winter;10(4):252-7. doi: 10.1089/gte.2006.10.252.
Genet Test. 2006.
PMID: 17253930
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