Four siblings with Hallervorden–Spatz disease-Reference-Cited by-同舟云学术

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Four siblings with Hallervorden–Spatz disease

Published:2001-07 Issue:4 Volume:23 Page:236-239
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Vaher Ulvi,Napa Aita,Nurmiste Andres,Piirsoo Andres,Sibul Hiljar,Talvik Tiina

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference8 articles.

1. Naming of syndromes and unethical activities: the case of Hallervorden and Spatz;Harper;Lancet,1996

2. Hallervorden–Spatz syndrome and brain iron metabolism;Swaiman;Arch Neurol,1991

3. Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3-p13;Taylor;Nat Genet,1996

4. Stereotactic pallidotomy in a child with Hallervorden–Spatz disease. Case report;Justesen;Neurosurgery,1999

5. Optic atrophy as the first symptom in Hallervorden–Spatz syndrome;Battistella;Child's Nerv Syst,1998

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mecp2 Deficiency Alters M1/M2 Gene Expresion in Bone Marrow-Derived Macrophages Upon Stimulation;2020-08-18

2. Optic Atrophy in Children;Pediatric Neuro-Ophthalmology;2009-12-09

3. Enhanced Hypoxia Susceptibility in Hippocampal Slices From a Mouse Model of Rett Syndrome;Journal of Neurophysiology;2009-02

4. Touretismo, hemibalismo y parkinsonismo juvenil: expandiendo el espectro clínico de la neurodegeneración asociada a deficiencia de pantotenato cinasa (síndrome de HallervordenSpatz);Revista de Neurología;2004

5. Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration;Movement Disorders;2003-10-28

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