Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4)

Management of Hereditary Spastic Paraplegia: A Systematic Review of the Literature

(2019) Marta Bellofatto et al.   Frontiers in Neurology

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications

(2019) Tim W Rattay et al.   BRAIN

Is fatigue a disease-specific or generic symptom in chronic medical conditions?

(2018) Juliane Menting et al.   HEALTH PSYCHOLOGY

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex

(2018) Livia Parodi et al.   BRAIN

Perspectives on the Genomics of HSP Beyond Mendelian Inheritance

(2018) Dana M. Bis-Brewer et al.   Frontiers in Neurology

Truncating mutations inSPASTpatients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia

(2017) Viorica Chelban et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients

(2016) Rebecca Schüle et al.   ANNALS OF NEUROLOGY

Cognitive Impairment Involving Social Cognition in SPG4 Hereditary Spastic Paraplegia

(2016) Ludivine Chamard et al.   BEHAVIOURAL NEUROLOGY

Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations

(2016) K. R. Servelhere et al.   EUROPEAN JOURNAL OF NEUROLOGY

Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations

(2015) Tobias Lindig et al.   JOURNAL OF NEUROLOGY

Dalfampridine in hereditary spastic paraplegia: a prospective, open study

(2015) Matthieu Béreau et al.   JOURNAL OF NEUROLOGY

ACG Clinical Guideline: Management of Benign Anorectal Disorders

(2014) Arnold Wald et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Restless legs syndrome/Willis–Ekbom disease diagnostic criteria: updated International Restless Legs Syndrome Study Group (IRLSSG) consensus criteria – history, rationale, description, and significance

(2014) Richard P. Allen et al.   SLEEP MEDICINE

Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)

(2013) Kathrin N Karle et al.   Orphanet Journal of Rare Diseases

Retinal nerve fibre layer loss in hereditary spastic paraplegias is restricted to complex phenotypes

(2012) Sarah Wiethoff et al.   BMC Neurology

The neurological and ophthalmological manifestations of SPG4-related hereditary spastic paraplegia

(2012) Grant Guthrie et al.   JOURNAL OF NEUROLOGY

Disease severity affects quality of life of hereditary spastic paraplegia patients

(2011) S. Klimpe et al.   EUROPEAN JOURNAL OF NEUROLOGY

Health-related quality of life in patients with hereditary spastic paraplegia in Estonia

(2010) M Braschinsky et al.   SPINAL CORD

The prevalence of depression in hereditary spastic paraplegia

(2009) L. Vahter et al.   CLINICAL REHABILITATION

Dementia in SPG4 hereditary spastic paraplegia: Clinical, genetic, and neuropathologic evidence

(2009) S. Murphy et al.   NEUROLOGY