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Page 1
Severe methylenetetrahydrofolate reductase deficiency: clinical clues to a potentially treatable cause of adult-onset hereditary spastic paraplegia.
Lossos A, Teltsh O, Milman T, Meiner V, Rozen R, Leclerc D, Schwahn BC, Karp N, Rosenblatt DS, Watkins D, Shaag A, Korman SH, Heyman SN, Gal A, Newman JP, Steiner-Birmanns B, Abramsky O, Kohn Y. Lossos A, et al. Among authors: steiner birmanns b. JAMA Neurol. 2014 Jul 1;71(7):901-4. doi: 10.1001/jamaneurol.2014.116. JAMA Neurol. 2014. PMID: 24797679
A case of probable Parkinson's disease after SARS-CoV-2 infection.
Cohen ME, Eichel R, Steiner-Birmanns B, Janah A, Ioshpa M, Bar-Shalom R, Paul JJ, Gaber H, Skrahina V, Bornstein NM, Yahalom G. Cohen ME, et al. Among authors: steiner birmanns b. Lancet Neurol. 2020 Oct;19(10):804-805. doi: 10.1016/S1474-4422(20)30305-7. Epub 2020 Sep 16. Lancet Neurol. 2020. PMID: 32949534 Free PMC article. No abstract available.
Phenotype in patients with Gaucher disease and Parkinson disease.
Chetrit EB, Alcalay RN, Steiner-Birmanns B, Altarescu G, Phillips M, Elstein D, Zimran A. Chetrit EB, et al. Among authors: steiner birmanns b. Blood Cells Mol Dis. 2013 Mar;50(3):218-21. doi: 10.1016/j.bcmd.2012.11.011. Epub 2012 Dec 20. Blood Cells Mol Dis. 2013. PMID: 23265741
22 results