iseases and Disorders
33
G. Fiedorowicz, J. A. Mills, A. Ruggle, et al., “Suicidal behavior
prodromal huntington disease,” Neurodegenerative Diseases, vol. 8,
p. 483–490, 2011.
J. Sadock and V. A. Sadock, “Kaplan and sadock’s comprehensive
xtbook of psychiatry,” 2017.
E. Anderson, E. van Duijn, D. Craufurd, et al., “Clinical manage-
ent of neuropsychiatric symptoms of huntington disease: Expert-based
nsensus guidelines on agitation, anxiety, apathy, psychosis and sleep
sorders,” Journal of Huntington’s Disease, vol. 7, pp. 355–366, 2018.
J. Hughes, S. E. Daniel, Y. Ben-Shlomo, et al., “The accuracy of
agnosis of parkinsonian syndromes in a specialist movement disorder
rvice,” Brain: a journal of neurology, vol. 125 Pt 4, pp. 861–70, 2002.
S. Paulsen, “Functional imaging in huntington’s disease,” Experimen-
l Neurology, vol. 216, pp. 272–277, 2009.
S. Ishihara, D. Oliveri, and E. J. Wild, “Neuropsychiatric comor-
dities in huntington’s and parkinson’s disease: A united states claims
tabase analysis,” Annals of Clinical and Translational Neurology,
l. 8, pp. 126–137, 2020.
. Groves, “The highly anxious individual presenting for huntington
sease-predictive genetic testing: the psychiatrist’s role in assessment
d counseling,” Handbook of clinical neurology, vol. 144, pp. 99–105,
17.
-B. R. Wahlin, “To know or not to know: a review of behaviour and
icidal ideation in preclinical huntington’s disease,” Patient education
nd counseling, vol. 65 3, pp. 279–87, 2007.
Goldstein, O. Nayshool, B. Nefussy, et al., “Optn 691_692insag is a
under mutation causing recessive als and increased risk in heterozy-
tes,” Neurology, vol. 86, pp. 446–453, 2016.
. H. Hastings and M. Goedert, “Circadian clocks and neurodegener-
ive diseases: time to aggregate?,” Current Opinion in Neurobiology,
l. 23, pp. 880–887, 2013.
M. Ahmed, R. E. A. Newcombe, A. J. Piper, et al., “Sleep disorders
d respiratory function in amyotrophic lateral sclerosis,” Sleep medicine
views, vol. 26, pp. 33–42, 2016.
Byrne, C. Walsh, C. Lynch, et al., “Rate of familial amyotrophic lat-
al sclerosis: a systematic review and meta-analysis,” Journal of Neu-
logy, Neurosurgery & Psychiatry, vol. 82, pp. 623–627, 2010.
. Agrawal and A. Biswas, “Molecular diagnostics of neurodegenerative
sorders,” Frontiers in Molecular Biosciences, vol. 2, 2015.