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Year | Number of Results |
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2003 | 1 |
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2018 | 1 |
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Page 1
Erythropoietin Upregulates Brain Hemoglobin Expression and Supports Neuronal Mitochondrial Activity.
Mol Neurobiol. 2018 Oct;55(10):8051-8058. doi: 10.1007/s12035-018-0971-6. Epub 2018 Mar 1.
Mol Neurobiol. 2018.
PMID: 29498007
Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
Traboulsi EI, Al-Khayer K, Matsumoto M, Kimak MA, Crowe S, Wilson SE, Finegold DN, Ferrell RE, Meisler DM.
Traboulsi EI, et al.
Am J Ophthalmol. 2002 Oct;134(4):592-6. doi: 10.1016/s0002-9394(02)01642-2.
Am J Ophthalmol. 2002.
PMID: 12383817
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Betaine restores epigenetic control and supports neuronal mitochondria in the cuprizone mouse model of multiple sclerosis.
Singhal NK, Sternbach S, Fleming S, Alkhayer K, Shelestak J, Popescu D, Weaver A, Clements R, Wasek B, Bottiglieri T, Freeman EJ, McDonough J.
Singhal NK, et al. Among authors: alkhayer k.
Epigenetics. 2020 Aug;15(8):871-886. doi: 10.1080/15592294.2020.1735075. Epub 2020 Mar 9.
Epigenetics. 2020.
PMID: 32096676
Free PMC article.
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Neuronal Hemoglobin Expression and Its Relevance to Multiple Sclerosis Neuropathology.
Brown N, Alkhayer K, Clements R, Singhal N, Gregory R, Azzam S, Li S, Freeman E, McDonough J.
Brown N, et al. Among authors: alkhayer k.
J Mol Neurosci. 2016 May;59(1):1-17. doi: 10.1007/s12031-015-0711-6. Epub 2016 Jan 25.
J Mol Neurosci. 2016.
PMID: 26809286
Free PMC article.
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Changes in Methionine Metabolism and Histone H3 Trimethylation Are Linked to Mitochondrial Defects in Multiple Sclerosis.
Singhal NK, Li S, Arning E, Alkhayer K, Clements R, Sarcyk Z, Dassanayake RS, Brasch NE, Freeman EJ, Bottiglieri T, McDonough J.
Singhal NK, et al. Among authors: alkhayer k.
J Neurosci. 2015 Nov 11;35(45):15170-86. doi: 10.1523/JNEUROSCI.4349-14.2015.
J Neurosci. 2015.
PMID: 26558787
Free PMC article.
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A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.
Yazdani A, et al.
Am J Ophthalmol. 2003 Nov;136(5):861-5. doi: 10.1016/s0002-9394(03)00891-2.
Am J Ophthalmol. 2003.
PMID: 14597037
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Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations.
Al-Khayer K, Hagstrom S, Pauer G, Zegarra H, Sears J, Traboulsi EI.
Al-Khayer K, et al.
Am J Ophthalmol. 2004 Feb;137(2):375-7. doi: 10.1016/S0002-9394(03)00913-9.
Am J Ophthalmol. 2004.
PMID: 14962443
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