# Neurological diseases and metabolism

**Type:** Topics  
**Canonical URL:** https://scholariq.org/topics/neurological-diseases-and-metabolism/

## Facts

| Field | Value |
| --- | --- |
| Description | This cluster of papers focuses on neurodegenerative disorders associated with brain iron accumulation, particularly emphasizing the genetic mutations in genes such as Pantothenate Kinase (PANK2), Coenzyme A biosynthesis, and Phospholipase A2 (PLA2G6). The research also explores the clinical, radiographic, and neuroimaging features of these disorders. |
| Domain | Life Sciences |
| Field | Neuroscience |
| OpenAlex ID | t13481 |
| Works | 113 |

## Topic papers all

Showing 15 of 113.

- [MDS clinical diagnostic criteria for Parkinson's disease](https://scholariq.org/papers/mds-clinical-diagnostic-criteria-for-parkinson-s-disease/)
- [Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis](https://scholariq.org/papers/ubiquitinated-tdp-43-in-frontotemporal-lobar-degeneration-and-amyotrophic/)
- [El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis](https://scholariq.org/papers/el-escorial-revisited-revised-criteria-for-the-diagnosis-of-amyotrophic-lateral/)
- [A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD](https://scholariq.org/papers/a-hexanucleotide-repeat-expansion-in-c9orf72-is-the-cause-of-chromosome-9p21/)
- [The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease.](https://scholariq.org/papers/the-relevance-of-the-lewy-body-to-the-pathogenesis-of-idiopathic-parkinson-s/)
- [Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology](https://scholariq.org/papers/mutations-in-lrrk2-cause-autosomal-dominant-parkinsonism-with-pleomorphic/)
- [Clinical diagnostic criteria for dementia associated with Parkinson's disease](https://scholariq.org/papers/clinical-diagnostic-criteria-for-dementia-associated-with-parkinson-s-disease/)
- [Mutations in the <i>DJ-1</i> Gene Associated with Autosomal Recessive Early-Onset Parkinsonism](https://scholariq.org/papers/mutations-in-the-i-dj-1-i-gene-associated-with-autosomal-recessive-early-onset/)
- [Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease](https://scholariq.org/papers/cloning-of-the-gene-containing-mutations-that-cause-park8-linked-parkinson-s/)
- [The Emerging Evidence of the Parkinson Pandemic](https://scholariq.org/papers/the-emerging-evidence-of-the-parkinson-pandemic/)
- [Progressive Supranuclear Palsy](https://scholariq.org/papers/progressive-supranuclear-palsy/)
- [State of play in amyotrophic lateral sclerosis genetics](https://scholariq.org/papers/state-of-play-in-amyotrophic-lateral-sclerosis-genetics/)
- [TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis](https://scholariq.org/papers/tardbp-mutations-in-individuals-with-sporadic-and-familial-amyotrophic-lateral/)
- [Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS](https://scholariq.org/papers/exome-sequencing-reveals-vcp-mutations-as-a-cause-of-familial-als/)
- [Epidemiology and etiology of Parkinson’s disease: a review of the evidence](https://scholariq.org/papers/epidemiology-and-etiology-of-parkinson-s-disease-a-review-of-the-evidence/)

## Topic primary papers

- [The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease.](https://scholariq.org/papers/the-relevance-of-the-lewy-body-to-the-pathogenesis-of-idiopathic-parkinson-s/)
- [Progressive Supranuclear Palsy](https://scholariq.org/papers/progressive-supranuclear-palsy/)
- [Coenzyme A: Back in action](https://scholariq.org/papers/coenzyme-a-back-in-action/)
- [Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture](https://scholariq.org/papers/genome-sequencing-analysis-identifies-new-loci-associated-with-lewy-body/)
- [<i>Purkinje cell degeneration</i> ( <i>pcd</i> ) Phenotypes Caused by Mutations in the Axotomy-Induced Gene, <i>Nna1</i>](https://scholariq.org/papers/i-purkinje-cell-degeneration-i-i-pcd-i-phenotypes-caused-by-mutations-in-the/)
- [Disrupted iron homeostasis causes dopaminergic neurodegeneration in mice](https://scholariq.org/papers/disrupted-iron-homeostasis-causes-dopaminergic-neurodegeneration-in-mice/)
- [Primary progressive aphasia with focal neuronal achromasia](https://scholariq.org/papers/primary-progressive-aphasia-with-focal-neuronal-achromasia/)
- [Crystal Structure of a Type III Pantothenate Kinase: Insight into the Mechanism of an Essential Coenzyme A Biosynthetic Enzyme Universally Distributed in Bacteria](https://scholariq.org/papers/crystal-structure-of-a-type-iii-pantothenate-kinase-insight-into-the-mechanism/)
- [NAXE gene mutation-related progressive encephalopathy](https://scholariq.org/papers/naxe-gene-mutation-related-progressive-encephalopathy/)
- [Atypical idiopathic <scp>NBIA</scp> (neurodegeneration with brain iron accumulation) associated with treatment‐resistant bipolar mania responding to clozapine](https://scholariq.org/papers/atypical-idiopathic-scp-nbia-scp-neurodegeneration-with-brain-iron-accumulation/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.