Hayflick SJ - Search Results

1

Neurodegeneration associated with genetic defects in phospholipase A(2).

Gregory A, Westaway SK, Holm IE, Kotzbauer PT, Hogarth P, Sonek S, Coryell JC, Nguyen TM, Nardocci N, Zorzi G, Rodriguez D, Desguerre I, Bertini E, Simonati A, Levinson B, Dias C, Barbot C, Carrilho I, Santos M, Malik I, Gitschier J, Hayflick SJ. Gregory A, et al. Among authors: hayflick sj. Neurology. 2008 Oct 28;71(18):1402-9. doi: 10.1212/01.wnl.0000327094.67726.28. Epub 2008 Sep 17. Neurology. 2008. PMID: 18799783 Free PMC article.

2

Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13.

Taylor TD, Litt M, Kramer P, Pandolfo M, Angelini L, Nardocci N, Davis S, Pineda M, Hattori H, Flett PJ, Cilio MR, Bertini E, Hayflick SJ. Taylor TD, et al. Among authors: hayflick sj. Nat Genet. 1996 Dec;14(4):479-81. doi: 10.1038/ng1296-479. Nat Genet. 1996. PMID: 8944032

3

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome.

Zhou B, Westaway SK, Levinson B, Johnson MA, Gitschier J, Hayflick SJ. Zhou B, et al. Among authors: hayflick sj. Nat Genet. 2001 Aug;28(4):345-9. doi: 10.1038/ng572. Nat Genet. 2001. PMID: 11479594

4

hGFRalpha-4: a new member of the GDNF receptor family and a candidate for NBIA.

Zhou B, Bae SK, Malone AC, Levinson BB, Kuo YM, Cilio MR, Bertini E, Hayflick SJ, Gitschier JM. Zhou B, et al. Among authors: hayflick sj. Pediatr Neurol. 2001 Aug;25(2):156-61. doi: 10.1016/s0887-8994(00)00277-0. Pediatr Neurol. 2001. PMID: 11551746

5

Cranial MRI changes may precede symptoms in Hallervorden-Spatz syndrome.

Hayflick SJ, Penzien JM, Michl W, Sharif UM, Rosman NP, Wheeler PG. Hayflick SJ, et al. Pediatr Neurol. 2001 Aug;25(2):166-9. doi: 10.1016/s0887-8994(01)00296-x. Pediatr Neurol. 2001. PMID: 11551748

6

HARP syndrome is allelic with pantothenate kinase-associated neurodegeneration.

Ching KH, Westaway SK, Gitschier J, Higgins JJ, Hayflick SJ. Ching KH, et al. Among authors: hayflick sj. Neurology. 2002 Jun 11;58(11):1673-4. doi: 10.1212/wnl.58.11.1673. Neurology. 2002. PMID: 12058097

7

In reference to the Short Communication published by Ni et al.

Westaway SK, Hayflick SJ, Zhou B, Gitschier JD. Westaway SK, et al. Among authors: hayflick sj. Int J Biochem Cell Biol. 2002 Dec;34(12):1629. doi: 10.1016/s1357-2725(02)00125-5. Int J Biochem Cell Biol. 2002. PMID: 12379284 No abstract available.

8

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.

Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J. Hayflick SJ, et al. N Engl J Med. 2003 Jan 2;348(1):33-40. doi: 10.1056/NEJMoa020817. N Engl J Med. 2003. PMID: 12510040 Free article.

9

Progressive dystonia in a 12-year-old boy.

Klepper J, Schaper J, Raca G, Coryell J, Das S, Hayflick SJ, Voit T. Klepper J, et al. Among authors: hayflick sj. Eur J Paediatr Neurol. 2003;7(2):85-8. doi: 10.1016/s1090-3798(03)00019-9. Eur J Paediatr Neurol. 2003. PMID: 12697433

10

Unraveling the Hallervorden-Spatz syndrome: pantothenate kinase-associated neurodegeneration is the name.

Hayflick SJ. Hayflick SJ. Curr Opin Pediatr. 2003 Dec;15(6):572-7. doi: 10.1097/00008480-200312000-00005. Curr Opin Pediatr. 2003. PMID: 14631201 Review.

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