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Disease

Heredodegenerative Disorders, Nervous System

Clinical development underwayEmerging research
2
Publications
2
Clinical trials
2023
Latest publication
Latest activity
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Recent clinical, regulatory, research and industry developments relating to this disease.

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Clinical trials

2 sponsors · 0 new · 1 completed in the last 12 months (net +0)

The current development programme across all trial phases.

Research activity

2 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Publications over time
20122023
Major themes4
  • Heredodegenerative Disorders, Nervous System1
  • Mixed Function Oxygenases1
  • Neurogenesis1
  • Spastic Paraplegia, Hereditary1
Leading journals2
  • Genes1
  • Genes & development1
Leading researchers8
  • Abicht A1
  • Arnold P1
  • Barres BA1
  • Deneen B1
  • German A1
  • Jukic J1
  • Krencik R1
  • Laner A1
Affiliations (unnormalised)5
  • Center for Rare Diseases (ZSEER)1
  • Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research1
  • Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)1
  • Institute of Functional and Clinical Anatomy1
  • Institute of Neuroradiology1

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.