Hayflick SJ - Search Results

1

PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.

Morgan NV, Westaway SK, Morton JE, Gregory A, Gissen P, Sonek S, Cangul H, Coryell J, Canham N, Nardocci N, Zorzi G, Pasha S, Rodriguez D, Desguerre I, Mubaidin A, Bertini E, Trembath RC, Simonati A, Schanen C, Johnson CA, Levinson B, Woods CG, Wilmot B, Kramer P, Gitschier J, Maher ER, Hayflick SJ. Morgan NV, et al. Among authors: hayflick sj. Nat Genet. 2006 Jul;38(7):752-4. doi: 10.1038/ng1826. Epub 2006 Jun 18. Nat Genet. 2006. PMID: 16783378 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

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

6

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.

7

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.

8

Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration.

Johnson MA, Kuo YM, Westaway SK, Parker SM, Ching KH, Gitschier J, Hayflick SJ. Johnson MA, et al. Among authors: hayflick sj. Ann N Y Acad Sci. 2004 Mar;1012:282-98. doi: 10.1196/annals.1306.023. Ann N Y Acad Sci. 2004. PMID: 15105273

9

Deficiency of pantothenate kinase 2 (Pank2) in mice leads to retinal degeneration and azoospermia.

Kuo YM, Duncan JL, Westaway SK, Yang H, Nune G, Xu EY, Hayflick SJ, Gitschier J. Kuo YM, et al. Among authors: hayflick sj. Hum Mol Genet. 2005 Jan 1;14(1):49-57. doi: 10.1093/hmg/ddi005. Epub 2004 Nov 3. Hum Mol Genet. 2005. PMID: 15525657 Free PMC article.

10

Neuro-ophthalmologic and electroretinographic findings in pantothenate kinase-associated neurodegeneration (formerly Hallervorden-Spatz syndrome).

Egan RA, Weleber RG, Hogarth P, Gregory A, Coryell J, Westaway SK, Gitschier J, Das S, Hayflick SJ. Egan RA, et al. Among authors: hayflick sj. Am J Ophthalmol. 2005 Aug;140(2):267-74. doi: 10.1016/j.ajo.2005.03.024. Am J Ophthalmol. 2005. PMID: 16023068 Free PMC article.

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