Ro LS - Search Results

1

The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.

Germain DP, Moiseev S, Suárez-Obando F, Al Ismaili F, Al Khawaja H, Altarescu G, Barreto FC, Haddoum F, Hadipour F, Maksimova I, Kramis M, Nampoothiri S, Nguyen KN, Niu DM, Politei J, Ro LS, Vu Chi D, Chen N, Kutsev S. Germain DP, et al. Among authors: ro ls. Mol Genet Genomic Med. 2021 May;9(5):e1666. doi: 10.1002/mgg3.1666. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33835733 Free PMC article. Review.

2

Fabry's disease: report of a case.

Chang HS, Ro LS, Chen ST, Tang LM, Hsiao KJ. Chang HS, et al. Among authors: ro ls. J Formos Med Assoc. 1995 Jun;94(6):346-50. J Formos Med Assoc. 1995. PMID: 7549555

3

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease.

Wu YR, Lin HY, Chen CM, Gwinn-Hardy K, Ro LS, Wang YC, Li SH, Hwang JC, Fang K, Hsieh-Li HM, Li ML, Tung LC, Su MT, Lu KT, Lee-Chen GJ. Wu YR, et al. Among authors: ro ls. Clin Genet. 2004 Mar;65(3):209-14. doi: 10.1111/j.0009-9163.2004.00213.x. Clin Genet. 2004. PMID: 14756671

4

Current perception threshold testing in Fabry's disease.

Ro LS, Chen ST, Tang LM, Hsu WC, Chang HS, Huang CC. Ro LS, et al. Muscle Nerve. 1999 Nov;22(11):1531-7. doi: 10.1002/(sici)1097-4598(199911)22:11<1531::aid-mus7>3.0.co;2-o. Muscle Nerve. 1999. PMID: 10514230

5

The correlation of small fiber neuropathy with pain intensity and age in patients with Fabry's disease: A cross sectional study within a large Taiwanese family.

Liao MF, Hsu JL, Fung HC, Kuo HC, Chu CC, Chang HS, Lyu RK, Ro LS. Liao MF, et al. Among authors: ro ls. Biomed J. 2022 Apr;45(2):406-413. doi: 10.1016/j.bj.2021.04.011. Epub 2021 May 3. Biomed J. 2022. PMID: 35595648 Free PMC article.

6

Comparison of two PCR-based molecular methods in the diagnosis of CMT 1A and HNPP diseases in Chinese.

Chen SR, Lin KP, Kuo HC, Chen CM, Hsieh ST, Lee MJ, Yang CC, Liu CS, Huang CC, Lyu RK, Ro LS. Chen SR, et al. Among authors: ro ls. Clin Neurol Neurosurg. 2008 May;110(5):466-71. doi: 10.1016/j.clineuro.2008.02.002. Epub 2008 Mar 18. Clin Neurol Neurosurg. 2008. PMID: 18353535

7

Neurofibromatosis 2 with peripheral neuropathies: Electrophysiological, pathological and genetic studies of a Taiwanese family.

Kuo HC, Chen SR, Jung SM, Wu Chou YH, Huang CC, Chuang WL, Wei KC, Ro LS. Kuo HC, et al. Among authors: ro ls. Neuropathology. 2010 Oct;30(5):515-23. doi: 10.1111/j.1440-1789.2009.01099.x. Neuropathology. 2010. PMID: 20113402

8

Association between PARK16 and Parkinson's disease in the Han Chinese population: a meta-analysis.

Chang KH, Chen CM, Chen YC, Lyu RK, Chang HS, Ro LS, Lee-Chen GJ, Wu YR. Chang KH, et al. Among authors: ro ls. Neurobiol Aging. 2013 Oct;34(10):2442.e5-9. doi: 10.1016/j.neurobiolaging.2013.04.028. Epub 2013 Jun 5. Neurobiol Aging. 2013. PMID: 23747047

9

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis.

Hsu HC, Liao MF, Hsu JL, Lee YL, Ro LS. Hsu HC, et al. Among authors: ro ls. J Vis Exp. 2018 Jun 9;(136):57743. doi: 10.3791/57743. J Vis Exp. 2018. PMID: 29939164 Free PMC article.

10

Glucocerebrosidase gene mutation is a risk factor for early onset of Parkinson disease among Taiwanese.

Wu YR, Chen CM, Chao CY, Ro LS, Lyu RK, Chang KH, Lee-Chen GJ. Wu YR, et al. Among authors: ro ls. J Neurol Neurosurg Psychiatry. 2007 Sep;78(9):977-9. doi: 10.1136/jnnp.2006.105940. J Neurol Neurosurg Psychiatry. 2007. PMID: 17702778 Free PMC article.

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