Neurodegeneration With Brain Iron Accumulation
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Last Posted: Apr 14, 2024
- Clinical, neuroimaging and genetic findings in Brazilian patients with neurodegeneration with brain iron accumulation.
Rubens Paulo Araújo Salomão, et al. Parkinsonism & related disorders 2024 0 106103 - A systematic analysis of genotype-phenotype associations with PLA2G6.
Jian Xue, et al. Parkinsonism & related disorders 2023 0 105477 - Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.
Alvarez Jerez Pilar, et al. NPJ Parkinson's disease 2023 0 (1) 54 - Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement.
Lan Min-Yu, et al. Frontiers in neurology 2022 0 1005670 - Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulation.
Tschentscher Anne, et al. Journal of the neurological sciences 2015 0 (1-2) 105-9 - Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases.
Kolarova Hana, et al. EBioMedicine 2022 0 103869 - PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran.
Jafarzadeh Esfehani Reza, et al. Iranian journal of basic medical sciences 2022 0 (9) 1190-1195 - Management of rare movement disorders in Europe: outcome of surveys of the European Reference Network for Rare Neurological Diseases.
Painous C et al. European journal of neurology 2020 May - The relevance of gene panels in movement disorders diagnosis: A lab perspective.
Reale Chiara et al. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2018 Jan - Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force.
Marras Connie et al. Movement disorders : official journal of the Movement Disorder Society 2016 Apr 31(4) 436-57
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
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- Phenylketonuria
- Retinitis Pigmentosa
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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