Moroziewicz DN - Search Results

1

Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses.

Zhong NA, Wisniewski KE, Ju W, Moroziewicz DN, Jurkiewicz A, McLendon L, Jenkins EC, Brown WT. Zhong NA, et al. Among authors: moroziewicz dn. Genet Test. 2000;4(3):243-8. doi: 10.1089/10906570050501452. Genet Test. 2000. PMID: 11142754

2

Genotype-phenotype analyses of classic neuronal ceroid lipofuscinosis (NCLs): genetic predictions from clinical and pathological findings.

Ju W, Wronska A, Moroziewicz DN, Zhong R, Wisniewski N, Jurkiewicz A, Fiory M, Wisniewski KE, Johnston L, Brown WT, Zhong N. Ju W, et al. Among authors: moroziewicz dn. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):41-8. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415965 Free article.

3

Prenatal diagnostic testing for infantile and late-infantile neuronal ceroid lipofusinoses (NCL) using allele specific primer extension (ASPE).

Zhong N, Ju W, Moroziewicz D, Wronska A, Li M, Wisniewski K, Brooks SS, Jenkins E, Brown WT. Zhong N, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2005 Feb 18;37(1):20-5. Beijing Da Xue Xue Bao Yi Xue Ban. 2005. PMID: 15719035 Free article.

4

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. Among authors: moroziewicz dn. Clin Genet. 1998 Sep;54(3):234-8. doi: 10.1111/j.1399-0004.1998.tb04291.x. Clin Genet. 1998. PMID: 9788728

5

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: moroziewicz dn. Mol Genet Metab. 1999 Apr;66(4):248-52. doi: 10.1006/mgme.1999.2814. Mol Genet Metab. 1999. PMID: 10191110

6

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: moroziewicz dn. Mol Genet Metab. 1999 Jun;67(2):162-8. doi: 10.1006/mgme.1999.2853. Mol Genet Metab. 1999. PMID: 10356316

7

CLN-encoded proteins do not interact with each other.

Zhong NA, Moroziewicz DN, Ju W, Wisniewski KE, Jurkiewicz A, Brown WT. Zhong NA, et al. Among authors: moroziewicz dn. Neurogenetics. 2000 Sep;3(1):41-4. doi: 10.1007/pl00022978. Neurogenetics. 2000. PMID: 11085596

8

Heterogeneity of late-infantile neuronal ceroid lipofuscinosis.

Zhong N, Moroziewicz DN, Ju W, Jurkiewicz A, Johnston L, Wisniewski KE, Brown WT. Zhong N, et al. Among authors: moroziewicz dn. Genet Med. 2000 Nov-Dec;2(6):312-8. doi: 10.1097/00125817-200011000-00002. Genet Med. 2000. PMID: 11339651 Free article.

9

N-terminal segments are the functional domains of CLN3-encoded battenin for protein interactions.

Moroziewicz DN, Ju W, Zhong R, Zhong N. Moroziewicz DN, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2006 Feb 18;38(1):38-40. Beijing Da Xue Xue Bao Yi Xue Ban. 2006. PMID: 16415964 Free article.

10

New mutations in the neuronal ceroid lipofuscinosis genes.

Mole SE, Zhong NA, Sarpong A, Logan WP, Hofmann S, Yi W, Franken PF, van Diggelen OP, Breuning MH, Moroziewicz D, Ju W, Salonen T, Holmberg V, Järvelä I, Taschner PE. Mole SE, et al. Eur J Paediatr Neurol. 2001;5 Suppl A:7-10. doi: 10.1053/ejpn.2000.0427. Eur J Paediatr Neurol. 2001. PMID: 11589012 Review.

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