Zhong N - Search Results

1

Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosis.

Zhong N, Wisniewski KE, Hartikainen J, Ju W, Moroziewicz DN, McLendon L, Sklower Brooks SS, Brown WT. Zhong N, et al. Clin Genet. 1998 Sep;54(3):234-8. doi: 10.1111/j.1399-0004.1998.tb04291.x. Clin Genet. 1998. PMID: 9788728

2

Atypical late infantile and juvenile forms of neuronal ceroid lipofuscinosis and their diagnostic difficulties.

Wiśniewski KE, Zhong N, Kida E, Kaczmarski W, Kaczmarski A, Connell F, Brooks SS, Brown WT. Wiśniewski KE, et al. Among authors: zhong n. Folia Neuropathol. 1997;35(2):73-9. Folia Neuropathol. 1997. PMID: 9377079 Review.

3

Compound heterozygous genotype is associated with protracted juvenile neuronal ceroid lipofuscinosis.

Wisniewski KE, Zhong N, Kaczmarski W, Kaczmarski A, Kida E, Brown WT, Schwarz KO, Lazzarini AM, Rubin AJ, Stenroos ES, Johnson WG, Wisniewski TM. Wisniewski KE, et al. Among authors: zhong n. Ann Neurol. 1998 Jan;43(1):106-10. doi: 10.1002/ana.410430118. Ann Neurol. 1998. PMID: 9450775

4

Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene.

Zhong N, Wisniewski KE, Kaczmarski AL, Ju W, Xu WM, Xu WW, Mclendon L, Liu B, Kaczmarski W, Sklower Brooks SS, Brown WT. Zhong N, et al. Hum Genet. 1998 Jan;102(1):57-62. doi: 10.1007/s004390050654. Hum Genet. 1998. PMID: 9490299

5

Studies of atypical JNCL suggest overlapping with other NCL forms.

Wisniewski KE, Zhong N, Kaczmarski W, Kaczmarski A, Sklower-Brooks S, Brown WT. Wisniewski KE, et al. Among authors: zhong n. Pediatr Neurol. 1998 Jan;18(1):36-40. doi: 10.1016/s0887-8994(97)00188-4. Pediatr Neurol. 1998. PMID: 9492089 Clinical Trial.

6

Reevaluation of neuronal ceroid lipofuscinoses: atypical juvenile onset may be the result of CLN2 mutations.

Wisniewski KE, Kaczmarski A, Kida E, Connell F, Kaczmarski W, Michalewski MP, Moroziewicz DN, Zhong N. Wisniewski KE, et al. Among authors: zhong n. Mol Genet Metab. 1999 Apr;66(4):248-52. doi: 10.1006/mgme.1999.2814. Mol Genet Metab. 1999. PMID: 10191110

7

Late infantile neuronal ceroid lipofuscinosis is due to splicing mutations in the CLN2 gene.

Hartikainen JM, Ju W, Wisniewski KE, Moroziewicz DN, Kaczmarski AL, McLendon L, Zhong D, Suarez CT, Brown WT, Zhong N. Hartikainen JM, et al. Among authors: zhong d, zhong n. Mol Genet Metab. 1999 Jun;67(2):162-8. doi: 10.1006/mgme.1999.2853. Mol Genet Metab. 1999. PMID: 10356316

8

Neuronal ceroid lipofuscinoses: research update.

Wisniewski KE, Kida E, Connell F, Zhong N. Wisniewski KE, et al. Among authors: zhong n. Neurol Sci. 2000;21(3 Suppl):S49-56. doi: 10.1007/s100720070040. Neurol Sci. 2000. PMID: 11073228 Review.

9

Neuronal ceroid lipofuscinoses: classification and diagnosis.

Wisniewski KE, Kida E, Golabek AA, Kaczmarski W, Connell F, Zhong N. Wisniewski KE, et al. Among authors: zhong n. Adv Genet. 2001;45:1-34. doi: 10.1016/s0065-2660(01)45002-4. Adv Genet. 2001. PMID: 11332767 Review.

10

Outlook for future treatment.

Zhong N, Wisniewski KE. Zhong N, et al. Adv Genet. 2001;45:217-24. doi: 10.1016/s0065-2660(01)45013-9. Adv Genet. 2001. PMID: 11332775 Review.

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