Shtilbans A - Search Results

1

A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regression.

Shtilbans A, El-Schahawi M, Malkin E, Shanske S, Musumeci O, DiMauro S. Shtilbans A, et al. J Child Neurol. 1999 Sep;14(9):610-3. doi: 10.1177/088307389901400910. J Child Neurol. 1999. PMID: 10488907

2

Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.

Andreu AL, Bruno C, Shanske S, Shtilbans A, Hirano M, Krishna S, Hayward L, Systrom DS, Brown RH Jr, DiMauro S. Andreu AL, et al. Among authors: shtilbans a. Neurology. 1998 Nov;51(5):1444-7. doi: 10.1212/wnl.51.5.1444. Neurology. 1998. PMID: 9818877

3

A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria.

Andreu AL, Bruno C, Dunne TC, Tanji K, Shanske S, Sue CM, Krishna S, Hadjigeorgiou GM, Shtilbans A, Bonilla E, DiMauro S. Andreu AL, et al. Among authors: shtilbans a. Ann Neurol. 1999 Jan;45(1):127-30. doi: 10.1002/1531-8249(199901)45:1<127::aid-art20>3.0.co;2-y. Ann Neurol. 1999. PMID: 9894887

4

G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.

Shtilbans A, Shanske S, Goodman S, Sue CM, Bruno C, Johnson TL, Lava NS, Waheed N, DiMauro S. Shtilbans A, et al. J Child Neurol. 2000 Nov;15(11):759-61. doi: 10.1177/088307380001501109. J Child Neurol. 2000. PMID: 11108511

5

Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes.

Hirano M, Shtilbans A, Mayeux R, Davidson MM, DiMauro S, Knowles JA, Schon EA. Hirano M, et al. Among authors: shtilbans a. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14894-9. doi: 10.1073/pnas.94.26.14894. Proc Natl Acad Sci U S A. 1997. PMID: 9405710 Free PMC article.

6

Differential gene expression in patients with amyotrophic lateral sclerosis.

Shtilbans A, Choi SG, Fowkes ME, Khitrov G, Shahbazi M, Ting J, Zhang W, Sun Y, Sealfon SC, Lange DJ. Shtilbans A, et al. Amyotroph Lateral Scler. 2011 Jul;12(4):250-6. doi: 10.3109/17482968.2011.560946. Epub 2011 Mar 4. Amyotroph Lateral Scler. 2011. PMID: 21375368

7

Quantitative susceptibility mapping of the motor cortex in amyotrophic lateral sclerosis and primary lateral sclerosis.

Schweitzer AD, Liu T, Gupta A, Zheng K, Seedial S, Shtilbans A, Shahbazi M, Lange D, Wang Y, Tsiouris AJ. Schweitzer AD, et al. Among authors: shtilbans a. AJR Am J Roentgenol. 2015 May;204(5):1086-92. doi: 10.2214/AJR.14.13459. AJR Am J Roentgenol. 2015. PMID: 25905946 Free PMC article.

8

Quantitative evaluation of brain iron accumulation in different stages of Parkinson's disease.

Li KR, Avecillas-Chasin J, Nguyen TD, Gillen KM, Dimov A, Chang E, Skudin C, Kopell BH, Wang Y, Shtilbans A. Li KR, et al. Among authors: shtilbans a. J Neuroimaging. 2022 Mar;32(2):363-371. doi: 10.1111/jon.12957. Epub 2021 Dec 14. J Neuroimaging. 2022. PMID: 34904328

9

Clinical quantitative susceptibility mapping (QSM): Biometal imaging and its emerging roles in patient care.

Wang Y, Spincemaille P, Liu Z, Dimov A, Deh K, Li J, Zhang Y, Yao Y, Gillen KM, Wilman AH, Gupta A, Tsiouris AJ, Kovanlikaya I, Chiang GC, Weinsaft JW, Tanenbaum L, Chen W, Zhu W, Chang S, Lou M, Kopell BH, Kaplitt MG, Devos D, Hirai T, Huang X, Korogi Y, Shtilbans A, Jahng GH, Pelletier D, Gauthier SA, Pitt D, Bush AI, Brittenham GM, Prince MR. Wang Y, et al. Among authors: shtilbans a. J Magn Reson Imaging. 2017 Oct;46(4):951-971. doi: 10.1002/jmri.25693. Epub 2017 Mar 10. J Magn Reson Imaging. 2017. PMID: 28295954 Free PMC article. Review.

10

Biomarkers in Parkinson's disease: an update.

Shtilbans A, Henchcliffe C. Shtilbans A, et al. Curr Opin Neurol. 2012 Aug;25(4):460-5. doi: 10.1097/WCO.0b013e3283550c0d. Curr Opin Neurol. 2012. PMID: 22772875 Review.

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