D N Moroziewicz
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Explore the profile of D N Moroziewicz including associated specialties, affiliations and a list of published articles.
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6
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38
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Recent Articles
1.
Zhong N, Moroziewicz D, Ju W, Jurkiewicz A, Johnston L, Wisniewski K, et al.
Genet Med
. 2001 May;
2(6):312-8.
PMID: 11339651
Purpose: Late-infantile neuronal ceroid lipofuscinosis (LINCL), an autosomal recessively inherited lysosomal storage disorder characterized by autofluorescent inclusions and rapid progression of neurodegeneration, is due to CLN2 gene mutations. However, CLN2...
2.
Zhong N, Wisniewski K, Ju W, Moroziewicz D, Jurkiewicz A, McLendon L, et al.
Genet Test
. 2001 Jan;
4(3):243-8.
PMID: 11142754
The neuronal ceroid lipofuscinoses (NCLs) are a large group of autosomal recessive lysosomal storage disorders with both enzymatic deficiency and structural protein dysfunction. Three typical forms, the infantile (INCL), late-infantile...
3.
Zhong N, Moroziewicz D, Ju W, Wisniewski K, Jurkiewicz A, Brown W
Neurogenetics
. 2000 Nov;
3(1):41-4.
PMID: 11085596
The lysosomal storage of lipofuscins is the common pathological feature that characterizes the infantile, late-infantile, juvenile (Batten's disease), and Finnish-variant neuronal ceroid lipofuscinosis (INCL, LINCL, JNCL and FNCL), which are...
4.
Hartikainen J, Ju W, Wisniewski K, Moroziewicz D, Kaczmarski A, McLendon L, et al.
Mol Genet Metab
. 1999 Jun;
67(2):162-8.
PMID: 10356316
Late infantile neuronal ceroid lipofuscinosis, LINCL, is one of the most common pediatric neurodegenerative disorders. It is caused by mutations in the CLN2 gene, which encodes a lysosomal pepstatin-insensitive peptidase...
5.
Wisniewski K, Kaczmarski A, Kida E, Connell F, Kaczmarski W, Michalewski M, et al.
Mol Genet Metab
. 1999 Apr;
66(4):248-52.
PMID: 10191110
This study describes the phenotype/genotype analyses of 56 probands with a juvenile onset, some of which had atypical features of neuronal ceroid lipofuscinosis, collected at the New York State Institute...
6.
Zhong N, Wisniewski K, Hartikainen J, Ju W, Moroziewicz D, McLendon L, et al.
Clin Genet
. 1998 Oct;
54(3):234-8.
PMID: 9788728
Late infantile neuronal ceroid lipofuscinosis (LINCL) is one of the most common pediatric neuronal degenerative disorders. A candidate gene underlying this disease, designated CLN2, was recently cloned and the gene...