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Items: 1 to 20 of 239

1.

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

Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, Ching KH, Gitschier J.

N Engl J Med. 2003 Jan 2;348(1):33-40.

2.

Brain MRI in neurodegeneration with brain iron accumulation with and without PANK2 mutations.

Hayflick SJ, Hartman M, Coryell J, Gitschier J, Rowley H.

AJNR Am J Neuroradiol. 2006 Jun-Jul;27(6):1230-3.

3.
5.

Siblings with the adult-onset slowly progressive type of pantothenate kinase-associated neurodegeneration and a novel mutation, Ile346Ser, in PANK2: clinical features and (99m)Tc-ECD brain perfusion SPECT findings.

Doi H, Koyano S, Miyatake S, Matsumoto N, Kameda T, Tomita A, Miyaji Y, Suzuki Y, Sawaishi Y, Kuroiwa Y.

J Neurol Sci. 2010 Mar 15;290(1-2):172-6. doi: 10.1016/j.jns.2009.11.008. Epub 2009 Dec 14.

PMID:
20006850
6.

Pantothenate kinase associated neurodegeneration (Hallervorden-Spatz syndrome).

Kapoor S, Hortnagel K, Gogia S, Paul R, Malhotra V, Prakash A.

Indian J Pediatr. 2005 Mar;72(3):261-3.

PMID:
15812126
7.

[Clinical manifestations and detection of pantothenate kinase 2 gene mutation in a patient with Hallervorden-Spatz syndrome].

Song XW, Wang YL, Shi YW, Deng WY, Chen SQ, Lin H, Yi YH, Liao WP.

Zhonghua Yi Xue Za Zhi. 2009 Dec 22;89(47):3320-3. Chinese.

PMID:
20193558
8.

Familial pediatric rapidly progressive extrapyramidal syndrome: is it Hallervorden-Spatz disease?

Chakravarty A, Mukherjee A, Sen A.

Pediatr Neurol. 2003 Aug;29(2):170-2.

PMID:
14580665
9.

Adult Hallervorden-Spatz syndrome simulating amyotrophic lateral sclerosis.

Vasconcelos OM, Harter DH, Duffy C, McDonough B, Seidman JG, Seidman CE, Campbell WW.

Muscle Nerve. 2003 Jul;28(1):118-22.

PMID:
12811783
10.
11.

Progressive dystonia in a 12-year-old boy.

Klepper J, Schaper J, Raca G, Coryell J, Das S, Hayflick SJ, Voit T.

Eur J Paediatr Neurol. 2003;7(2):85-8.

PMID:
12697433
12.

Pure akinesia: an unusual phenotype of Hallervorden-Spatz syndrome.

Molinuevo JL, Martí MJ, Blesa R, Tolosa E.

Mov Disord. 2003 Nov;18(11):1351-3.

PMID:
14639680
13.

Young-onset parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome.

Mak CM, Sheng B, Lee HH, Lau KK, Chan WT, Lam CW, Chan YW.

Int J Neurosci. 2011 Apr;121(4):224-7. doi: 10.3109/00207454.2010.542843. Epub 2011 Jan 4.

PMID:
21198414
14.

The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome.

Baumeister FA, Auer DP, Hörtnagel K, Freisinger P, Meitinger T.

Neuropediatrics. 2005 Jun;36(3):221-2.

PMID:
15944911
15.

Neurodegeneration with brain iron accumulation: clinical, radiographic and genetic heterogeneity and corresponding therapeutic options.

Clement F, Devos D, Moreau C, Coubes P, Destee A, Defebvre L.

Acta Neurol Belg. 2007 Mar;107(1):26-31.

PMID:
17569231
16.

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.

Zhang YH, Tang BS, Zhao AL, Xia K, Long ZG, Guo JF, Westaway SK, Hayflick SJ.

Mov Disord. 2005 Jul;20(7):819-21.

17.

Adult onset Hallervorden-Spatz disease with psychotic symptoms.

del Valle-López P, Pérez-García R, Sanguino-Andrés R, González-Pablos E.

Actas Esp Psiquiatr. 2011 Jul-Aug;39(4):260-2. Epub 2011 Jul 1. English, Spanish.

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19.

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Chinese.

PMID:
15793782
20.

[Hallervorden-Spatz syndrome. Differential diagnosis of early onset dementia].

Lechner C, Meisenzahl EM, Uhlemann H, Helber-Böhlen H, Fähndrich E.

Nervenarzt. 1999 May;70(5):471-5. German.

PMID:
10407844
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