A review of psychiatric co-morbidity described in genetic and immune mediated movement disorders
Open accessAbstract
Psychiatric symptoms are an increasingly recognised feature of movement disorders. Recent identification of causative genes and autoantibodies has allowed detailed analysis of aetiologically homogenous subgroups, thereby enabling determination of the spectrum of psychiatric symptoms in these disorders. This review evaluates the incidence and type of psychiatric symptoms encountered in patients with movement disorders. A broad spectrum of psychiatric symptoms was identified across all subtypes of movement disorder, with depression, generalised anxiety disorder and obsessive-compulsive disorder being most common. Psychosis, schizophrenia and attention deficit hyperactivity disorder were also identified, with the psychiatric symptoms often predating onset of the motor disorder. The high incidence of psychiatric symptoms across such a wide range of movement disorders suggests a degree of common or overlapping pathogenic mechanisms. Our review demonstrates the need for increased clinical awareness of such co-morbidities, which should facilitate early neuropsychiatric intervention and allied specialist treatment for patients.
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Non-motor symptoms, notably psychiatric disorders, are well recognised comorbid features of dystonia.
“There is also increasing recognition that non-motor symptoms form an important part of the disorder [1, 2].”
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Cites
α-Synuclein Locus Triplication Causes Parkinson's Disease
Singleton, A. B., Farrer, M., Johnson, J., Singleton, A., Hague, S., Kachergus, J., Hulihan, M., Peuralinna, T., Dutra, A., Nussbaum, R., et al. (2003) · Science · doi:10.1126/science.1090278 · Cited by 4,383 · see citing works
Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies
Dalmau, J., Gleichman, A. J., Hughes, E. G., Rossi, J. E., Peng, X., Lai, M., Dessain, S. K., Rosenfeld, M. R., Balice-Gordon, R., & Lynch, D. R. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70224-2 · Cited by 3,488 · see citing works
Titulaer, M. J., McCracken, L., Gabilondo, I., Armangué, T., Glaser, C., Iizuka, T., Honig, L. S., Benseler, S. M., Kawachi, I., Martinez-Hernandez, E., et al. (2013) · The Lancet Neurology · doi:10.1016/s1474-4422(12)70310-1 · Cited by 3,165 · see citing works
Swedo, S. E., Leonard, H. L., Garvey, M., Mittleman, B., Allen, A. J., Perlmutter, S., Dow, S., Zamkoff, J., Dubbert, B. K., & Lougee, L. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.2.264 · Cited by 1,534 · see citing works
Parent, A., & Hazrati, L. (1995) · Brain Research Reviews · doi:10.1016/0165-0173(94)00008-d · Cited by 1,351 · see citing works
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis in children and adolescents
Florance, N. R., Davis, R. L., Lam, C., Szperka, C., Zhou, L., Ahmad, S., Campen, C. J., Moss, H., Peter, N., Gleichman, A. J., et al. (2009) · Annals of Neurology · doi:10.1002/ana.21756 · Cited by 1,090 · see citing works
Irani, S. R., Bera, K., Waters, P., Zuliani, L., Maxwell, S., Zandi, M. S., Friese, M. A., Galea, I., Kullmann, D. M., Beeson, D., et al. (2010) · Brain · doi:10.1093/brain/awq113 · Cited by 1,035 · see citing works
Genetic, Clinical, and Radiographic Delineation of Hallervorden–Spatz Syndrome
Hayflick, S. J., Westaway, S. K., Levinson, B., Zhou, B., Johnson, M., Ching, K. H. L., & Gitschier, J. M. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa020817 · Cited by 713 · see citing works
PINK1 mutations are associated with sporadic early‐onset parkinsonism
Valente, E. M., Salvi, S., Ialongo, T., Marongiu, R., Elia, A. E., Caputo, V., Romito, L. M., Albanese, A., Dallapiccola, B., & Bentivoglio, A. R. (2004) · Annals of Neurology · doi:10.1002/ana.20256 · Cited by 506 · see citing works
Kayser, M. S., Titulaer, M. J., Gresa‐Arribas, N., & Dalmau, J. O. (2013) · JAMA Neurology · doi:10.1001/jamaneurol.2013.3216 · Cited by 419 · see citing works
Antibodies to surface dopamine-2 receptor in autoimmune movement and psychiatric disorders
Dale, R. C., Merheb, V., Pillai, S. C., Wang, D., Cantrill, L. C., Murphy, T. K., Ben‐Pazi, H., Varadkar, S., Aumann, T. D., Horne, M. K., et al. (2012) · Brain · doi:10.1093/brain/aws256 · Cited by 387 · see citing works
Self-citationThe adult form of Niemann-Pick disease type C
Sevin, M., Lesca, G., Baumann, N., Millat, G., Lyon‐Caen, O., Vanier, M. T., & Sedel, F. (2006) · Brain · doi:10.1093/brain/awl260 · Cited by 385 · see citing works
Parkin disease: a phenotypic study of a large case series
Khan, N. L., Graham, E., Critchley, P., Schrag, A. E., Wood, N. W., Lees, A. J., Bhatia, K. P., & Quinn, N. P. (2003) · Brain · doi:10.1093/brain/awg142 · Cited by 352 · see citing works
Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity
Dale, R. C. (2003) · Brain · doi:10.1093/brain/awh008 · Cited by 344 · see citing works
Self-citationMurphy, M. L., & Pichichero, M. E. (2002) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.156.4.356 · Cited by 328 · see citing works
How much phenotypic variation can be attributed to parkin genotype?
Lohmann, E., Periquet, M., Bonifati, V., Wood, N. W., Michele, G. D., Bonnet, A., Fraix, V., Broussolle, E., Horstink, M. W. I. M., Vidailhet, M., et al. (2003) · Annals of Neurology · doi:10.1002/ana.10613 · Cited by 300 · see citing works
Neurodegeneration associated with genetic defects in phospholipase A 2
Gregory, A., Westaway, S. K., Holm, I. E., Kotzbauer, P. T., Hogarth, P., Sonek, S., Coryell, J. C., Nguyen, T. M., Nardocci, N., Zorzi, G. S., et al. (2008) · Neurology · doi:10.1212/01.wnl.0000327094.67726.28 · Cited by 269 · see citing works
Hacohen, Y., Wright, S. K., Waters, P. J., Agrawal, S., Carr, L., Cross, J. H., de Sousa, C., DeVile, C. J., Fallon, P., Gupta, R., et al. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-303807 · Cited by 268 · see citing works
GBA-associated PD presents with nonmotor characteristics
Brockmann, K., Srulijes, K., Hauser, A. ‐., Schulte, C., Csóti, I., Gasser, T., & Berg, D. (2011) · Neurology · doi:10.1212/wnl.0b013e318225ab77 · Cited by 267 · see citing works
Cognitive performance of GBA mutation carriers with early-onset PD
Alcalay, R. N., Caccappolo, E., Mejia‐Santana, H., Tang, M. X., Rosado, L., Reilly, M. O., Ruiz, D., Ross, B., Verbitsky, M., Kisselev, S., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e318253d54b · Cited by 266 · see citing works
PINK1-linked parkinsonism is associated with Lewy body pathology
Samaranch, L., Lorenzo‐Betancor, O., Arbelo, J. M., Ferrer, I., Lorenzo, E., Irigoyen, J., Pastor, M. A., Marrero, C., Isla, C., Herrera-Henriquez, J., et al. (2010) · Brain · doi:10.1093/brain/awq051 · Cited by 256 · see citing works
Novel PINK1 mutations in early‐onset parkinsonism
Hatano, Y., Li, Y., Sato, K., Asakawa, S., Yamamura, Y., Tomiyama, H., Yoshino, H., Asahina, M., Kobayashi, S. S., Hassin‐Baer, S., et al. (2004) · Annals of Neurology · doi:10.1002/ana.20251 · Cited by 246 · see citing works
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
Meyer, E., Study, D. D. D., Carss, K., Rankin, J., Nichols, J. M. E., Grozeva, D., Joseph, A. P., Mencacci, N. E., Papandreou, A., Ng, J., et al. (2016) · Nature Genetics · doi:10.1038/ng.3740 · Cited by 243 · see citing works
Self-citationDening, T. R. (1989) · Archives of General Psychiatry · doi:10.1001/archpsyc.1989.01810120068011 · Cited by 232 · see citing works
Novel PINK1 mutations in early-onset parkinsonism
波田野, 靖. (2005) · Medical Entomology and Zoology · Cited by 227 · see citing works
Psychiatric disorders in preclinical Huntington's disease
Julien, C. L., Thompson, J. C., Wild, S., Yardumian, P., Snowden, J. S., Turner, G., & Craufurd, D. (2006) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2006.103309 · Cited by 219 · see citing works
N‐methyl‐ D ‐aspartate receptor antibodies in pediatric dyskinetic encephalitis lethargica
Dale, R. C., Irani, S. R., Brilot, F., Pillai, S. C., Webster, R., Gill, D. S., Lang, B., & Vincent, A. C. (2009) · Annals of Neurology · doi:10.1002/ana.21807 · Cited by 218 · see citing works
Self-citationObserving Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY
Orth, M., Handley, O., Schwenke, C., Dunnett, S. B., Craufurd, D., Ho, A. K., Wild, E. J., Tabrizi, S. J., & Landwehrmeyer, G. B. (2010) · PLoS Currents · doi:10.1371/currents.rrn1184 · Cited by 217 · see citing works
Neuroepidemiologic Trends in 105 US Cases of Pediatric Opsoclonus-Myoclonus Syndrome
Tate, E. D., Allison, T. J., Pranzate, M. R., & Verhu, S. J. (2004) · Journal of Pediatric Oncology Nursing · doi:10.1177/1043454204272560 · Cited by 191 · see citing works
Hogarth, P., Gregory, A., Kruer, M. C., Sanford, L., Wagoner, W., Natowicz, M. R., Egel, R. T., Subramony, S. H., Goldman, J. G., Berry‐Kravis, E., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e31827e07be · Cited by 179 · see citing works
Trender‐Gerhard, I., Sweeney, M. G., Schwingenschuh, P., Mir, P., Edwards, M. J., Gerhard, A., Polke, J. M., Hanna, M. G., Davis, M. B., Wood, N. W., et al. (2009) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2008.155861 · Cited by 178 · see citing works
Serotonin and Mental Disorders: A Concise Review on Molecular Neuroimaging Evidence
Lin, S., Lee, L.-T., & Yang, Y. K. (2014) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2014.12.3.196 · Cited by 177 · see citing works
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers
Marras, C., Schüle, B., Munhoz, R. P., Rogaeva, E. A., Langston, J. W., Kasten, M., Meaney, C. A., Klein, C., Wadia, P. M., Lim, S., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e318227042d · Cited by 171 · see citing works
Longitudinal Psychiatric Symptoms in Prodromal Huntington’s Disease: A Decade of Data
Epping, E. A., Kim, J., Craufurd, D., Brashers-Krug, T. M., Anderson, K. E., McCusker, E. A., Luther, J., Long, J. D., Paulsen, J. S., & PREDICT-HD Investigators and Coordinators of the Huntington Study Group (2015) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2015.14121551 · Cited by 169 · see citing works
Ikeuchi, T., Koide, R., Tanaka, H., Onodera, O., Igarashi, S., Takahashi, H., Kondo, R., Ishikawa, A., Tomoda, A., Miike, T., et al. (1995) · Annals of Neurology · doi:10.1002/ana.410370610 · Cited by 168 · see citing works
A heterozygous effect for PINK1 mutations in Parkinson's disease?
Abou‐Sleiman, P. M., Muqit, M. M. K., McDonald, N. Q., Yang, Y. X., Gandhi, S., Healy, D. G., Harvey, K., Harvey, R. J., Deas, E., Bhatia, K. P., et al. (2006) · Annals of Neurology · doi:10.1002/ana.20960 · Cited by 166 · see citing works
The Psychiatric Symptoms of Rheumatic Fever
Mercadante, M. T., Busatto, G. F., Lombroso, P. J., Prado, L. G., do Rosário, M. C., do Valle, R., Marques‐Dias, M. J., Kiss, M. H., Leckman, J. F., & Miguel, E. C. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.12.2036 · Cited by 159 · see citing works
Leckman, J. F., King, R. A., Gilbert, D. L., Coffey, B. J., Singer, H. S., Dure, L. S., Grantz, H., Katsovich, L., Lin, H., & Lombroso, P. J. (2011) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2010.10.011 · Cited by 159 · see citing works
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood
Ng, J., Zhen, J., Meyer, E., Erreger, K., Li, Y., Kakar, N., Ahmad, J., Thiele, H., Kubisch, C., Rider, N. L., et al. (2014) · Brain · doi:10.1093/brain/awu022 · Cited by 157 · see citing works
Self-citationMissense dopamine transporter mutations associate with adult parkinsonism and ADHD
Herborg, F., Skjørringe, T., Yasmeen, S., Arends, N. V., Sahai, M. A., Erreger, K., Andreassen, T. F., Holy, M., Hamilton, P. J., Neergheen, V., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci73778 · Cited by 145 · see citing works
Lougee, L., Perlmutter, S., Nicolson, R., Garvey, M. A., & Swedo, S. E. (2000) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-200009000-00011 · Cited by 140 · see citing works
Murphy, T. K., Storch, E. A., Lewin, A. B., Edge, P. J., & Goodman, W. K. (2012) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2011.07.012 · Cited by 138 · see citing works
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY
Orth, M., & The European Huntington 's Disease Network (2010) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2010.209668 · Cited by 136 · see citing works
Expanding the clinical phenotype of SNCA duplication carriers
Nishioka, K., Ross, O. A., Ishii, K., Kachergus, J. M., Ishiwata, K., Kitagawa, M., Kono, S., Obi, T., Mizoguchi, K., Inoue, Y., et al. (2009) · Movement Disorders · doi:10.1002/mds.22682 · Cited by 135 · see citing works
Hedrich, K., Hagenah, J. M., Djarmati, A., Hiller, A., Lohnau, T., Lasek, K., Grünewald, A., Hilker, R., Steinlechner, S., Boston, H., et al. (2006) · Archives of Neurology · doi:10.1001/archneur.63.6.833 · Cited by 133 · see citing works
Gras, D., Jonard, L., Roze, E. F., Chantot‐Bastaraud, S., Koht, J. A., Motte, J. E., Rodriguez, D., Louha, M., Caubel, I., Kemlin, I., et al. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2012-302505 · Cited by 129 · see citing works
Obsessive compulsive behavior, hyperactivity, and attention deficit disorder in Sydenham chorea
Maia, D. P., Teixeira, A. L., Cunningham, M. C. Q., & Cardoso, F. (2005) · Neurology · doi:10.1212/01.wnl.0000161840.62090.0e · Cited by 128 · see citing works
Chen, D., Méneret, A., Friedman, J., Korvatska, O., Gad, A., Bonkowski, E. S., Stessman, H. A. F., Doummar, D., Mignot, C., Anheim, M., et al. (2015) · Neurology · doi:10.1212/wnl.0000000000002058 · Cited by 123 · see citing works
Dopa-Responsive Dystonia Revisited
Tadić, V., Kasten, M., Brüggemann, N., Stiller, S., Hagenah, J. M., & Klein, C. (2012) · Archives of Neurology · doi:10.1001/archneurol.2012.574 · Cited by 120 · see citing works
Increased risk for recurrent major depression in DYT1 dystonia mutation carriers
Heiman, G. A., Ottman, R., Saunders-Pullman, R. J., Ozelius, L. J., RISCH, N. J., & Bressman, S. (2004) · Neurology · doi:10.1212/01.wnl.0000137113.39225.fa · Cited by 118 · see citing works
The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration
Pellecchia, M. T., Valente, E. M., Cif, L., Salvi, S., Albanese, A., Scarano, V., Bonuccelli, U., Bentivoglio, A. R., D’Amico, A., Marelli, C., et al. (2005) · Neurology · doi:10.1212/01.wnl.0000161843.52641.ec · Cited by 117 · see citing works
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
Peall, K. J., Smith, D. J., Kurian, M. A., Wardle, M., Waite, A. J., Hedderly, T., Lin, J.-P., Smith, M., Whone, A., Pall, H., et al. (2013) · Brain · doi:10.1093/brain/aws308 · Cited by 116 · see citing works
Self-citationAsbahr, F. R., Negrão, A. B., Gentil, V., Zanetta, D. M. T., da Paz, J. A., Marques‐Dias, M. J., & Kiss, M. H. (1998) · American Journal of Psychiatry · doi:10.1176/ajp.155.8.1122 · Cited by 113 · see citing works
Outcome and Prognostic Features in Opsoclonus-Myoclonus Syndrome From Infancy to Adult Life
Brunklaus, A., Pohl, K., Zuberi, S. M., & de Sousa, C. (2011) · PEDIATRICS · doi:10.1542/peds.2010-3114 · Cited by 113 · see citing works
AromaticL-amino acid decarboxylase deficiency: Overview of clinical features and outcomes
Swoboda, K. J., Saul, J. P., McKenna, C. E., Speller, N. B., & Hyland, Κ. (2003) · Annals of Neurology · doi:10.1002/ana.10631 · Cited by 112 · see citing works
Hove, J. L. K. V. (2005) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2004.051664 · Cited by 112 · see citing works
The role of immune mechanisms in Tourette syndrome
Martino, D., Zis, P., & Buttiglione, M. (2014) · Brain Research · doi:10.1016/j.brainres.2014.04.027 · Cited by 108 · see citing works
Goldwurm, S., Zini, M., Fonzo, A. D., Gaspari, D. D., Siri, C., Simons, E. J., van Doeselaar, M., Tesei, S., Antonini, A., Canesi, M., et al. (2006) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2006.04.001 · Cited by 108 · see citing works
Anti-N-Methyl-D-Aspartate Receptor Encephalitis in Korea: Clinical Features, Treatment, and Outcome
Lim, J., Lee, S., Jung, K., Kim, S., Shin, J.-W., Moon, J., Byun, J., Kim, T., Shin, Y., Lee, K., et al. (2014) · Journal of Clinical Neurology · doi:10.3988/jcn.2014.10.2.157 · Cited by 106 · see citing works
van Duijn, E., Kingma, E. M., Timman, R., Zitman, F. G., Tibben, A., Roos, R. A. C., & van der Mast, R. C. (2008) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v69n1116 · Cited by 102 · see citing works
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers
Hess, C. W., Raymond, D., Aguiar, P. D. C., Frucht, S. J., Shriberg, J., Heiman, G. A., Kurlan, R., Klein, C., Bressman, S., Ozelius, L. J., et al. (2007) · Neurology · doi:10.1212/01.wnl.0000253188.76092.06 · Cited by 99 · see citing works
Bernstein, G. A., Victor, A. M., Pipal, A. J., & Williams, K. A. (2010) · Journal of Child and Adolescent Psychopharmacology · doi:10.1089/cap.2010.0034 · Cited by 98 · see citing works
Belarbi, S., Hecham, N., Lesage, S., Kediha, M. I., Smail, N., Benhassine, T., Ysmail-Dahlouk, F., Lohman, E., Benhabyles, B., Hamadouche, T., et al. (2010) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2010.09.003 · Cited by 94 · see citing works
A multidisciplinary study of patients with early-onset PD with and without parkin mutations
Lohmann, E., Thobois, S., Lesage, S., Broussolle, E., du Montcel, S. T., Ribeiro, M.-J., Rémy, P., Pélissolo, A., Dubois, B., Mallet, L., et al. (2008) · Neurology · doi:10.1212/01.wnl.0000327098.86861.d4 · Cited by 90 · see citing works
Aromatic l-amino acid decarboxylase deficiency in Taiwan
Lee, H.-F., Tsai, C., Chi, C.-S., Chang, T., & Lee, H. (2008) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2008.03.008 · Cited by 89 · see citing works
Bipolar disorders and Wilson’s disease
Carta, M. G., Sorbello, O., Moro, M. F., Bhat, K. M., Demelia, E., Serra, A., Mura, G., Sancassiani, F., Piga, M., & Demelia, L. (2012) · BMC Psychiatry · doi:10.1186/1471-244x-12-52 · Cited by 71 · see citing works
Psychiatric disorders in rapid-onset dystonia-parkinsonism
Brashear, A., Cook, J., Hill, D. F., Amponsah, A., Snively, B. M., Light, L. S., Boggs, N., Suerken, C. K., Stacy, M. A., Ozelius, L. J., et al. (2012) · Neurology · doi:10.1212/wnl.0b013e3182698d6c · Cited by 68 · see citing works
Defects in the striatal neuropeptide Y system in X-linked dystonia-parkinsonism
Goto, S., Kawarai, T., Morigaki, R., Okita, S., Koizumi, H., Nagahiro, S., Muñoz, E. L., Lee, L. V., & Kaji, R. (2013) · Brain · doi:10.1093/brain/awt084 · Cited by 68 · see citing works
Familial Aggregation of Psychotic Symptoms in Huntington’s Disease
Tsuang, D. W., Almqvist, E. W., Lipe, H., Strgar, F., DiGiacomo, L., Hoff, D., Eugenio, C. J., Hayden, M. R., & Bird, T. D. (2000) · American Journal of Psychiatry · doi:10.1176/appi.ajp.157.12.1955 · Cited by 68 · see citing works
Cognitive Correlates of Obsessive and Compulsive Symptoms in Huntington’s Disease
Anderson, K. E., Louis, E. D., Stern, Y., & Marder, K. S. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.5.799 · Cited by 68 · see citing works
Dystonia: a disorder often misdiagnosed as a conversion reaction
Lesser, R. P., & Fahn, S. (1978) · American Journal of Psychiatry · doi:10.1176/ajp.135.3.349 · Cited by 65 · see citing works
Effect of CAG repeat length on psychiatric disorders in Huntington’s disease
Vassos, E., Πάνας, Μ., Kladi, A., & Vassilopoulos, D. (2007) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2007.05.008 · Cited by 65 · see citing works
Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations
Steinlechner, S., Stahlberg, J., Volkel, B., Djarmati, A., Hagenah, J., Hiller, A., Hedrich, K., König, I. R., Klein, C., & Lencer, R. (2006) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2006.105676 · Cited by 65 · see citing works
Cognition and psychopathology in myoclonus-dystonia
van Tricht, M. J., Dreissen, Y. E. M., Cath, D. C., Dijk, J. M., Contarino, M. F., der Salm, S. M. A. V., Foncke, E. M. J., Groen, J. L., Schmand, B. A., & Tijssen, M. A. J. (2012) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2011-301386 · Cited by 65 · see citing works
Self-citationWilson′s disease: An Indian perspective
Taly, A., Kukkle, P. L., & Sinha, S. (2009) · Neurology India · doi:10.4103/0028-3886.57789 · Cited by 65 · see citing works
Obsessive and Compulsive Symptoms in Prediagnosed Huntington's Disease
Beglinger, L. J., Paulsen, J. S., Watson, D. B., Wang, C., Duff, K., Langbehn, D. R., Moser, D. J., Paulson, H. L., Alyward, E. H., Carlozzi, N. E., et al. (2008) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.v69n1111 · Cited by 65 · see citing works
Neuropsychiatric characteristics of GBA-associated Parkinson disease
Swan, M. C., Doan, N., Ortega, R., Barrett, M. J., Nichols, W. C., Ozelius, L. J., Soto‐Valencia, J., Boschung, S., Deik, A., Sarva, H., et al. (2016) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2016.08.059 · Cited by 64 · see citing works
Novel mutation in ATP13A2 widens the spectrum of Kufor‐Rakeb syndrome (PARK9)
Eiberg, H., Hansen, L. H., Korbo, L., Nielsen, I., Svenstrup, K., Bech, S., Pinborg, L. H., Friberg, L., Hjermind, L. E., Olsen, O., et al. (2011) · Clinical Genetics · doi:10.1111/j.1399-0004.2011.01745.x · Cited by 62 · see citing works
Obsessive-compulsive symptoms among patients with Sydenham chorea
Asbahr, F. R., Garvey, M. A., Snider, L. A., Zanetta, D. M. T., Elkis, H., & Swedo, S. E. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.01.037 · Cited by 62 · see citing works
Benign Hereditary Chorea of Early Onset Maps to Chromosome 14q
Vries, B. B. A. D., ARTS, W. F. M., Breedveld, G. J., Hoogeboom, J. J. M., Niermeijer, M. F., & Heutink, P. (2000) · The American Journal of Human Genetics · doi:10.1086/302725 · Cited by 61 · see citing works
Psychiatric disorders, myoclonus dystonia and SGCE : an international study
Peall, K. J., Dijk, J. M., Saunders-Pullman, R. J., Dreissen, Y. E. M., van Loon, I., Cath, D. C., Kurian, M. A., Owen, M. J., Foncke, E. M. J., Morris, H. R., et al. (2015) · Annals of Clinical and Translational Neurology · doi:10.1002/acn3.263 · Cited by 61 · see citing works
Self-citationLong-term outcome of ten children with opsoclonus-myoclonus syndrome
Klein, A., Schmitt, B., & Boltshauser, E. (2006) · European Journal of Pediatrics · doi:10.1007/s00431-006-0247-4 · Cited by 59 · see citing works
Phenotypic variability of PINK1 expression: 12 Years' clinical follow‐up of two Italian families
Ricciardi, L., Petrucci, S., Guidubaldi, A., Ialongo, T., Serra, L., Ferraris, A., Spanò, B., Bozzali, M., Valente, E. M., & Bentivoglio, A. R. (2014) · Movement Disorders · doi:10.1002/mds.25994 · Cited by 57 · see citing works
Benign hereditary chorea related to NKX 2.1: expansion of the genotypic and phenotypic spectrum
Peall, K. J., Lumsden, D. E., Kneen, R., Madhu, R., Peake, D., Gibbon, F. M., Lewis, H., Hedderly, T. J., Meyer, E., Robb, S. A., et al. (2013) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.12323 · Cited by 56 · see citing works
Self-citationSprengelmeyer, R., Orth, M., Müller, H., Wolf, R. C., Grön, G., Depping, M. S., Kassubek, J., Justo, D., Rees, E. M., Haider, S., et al. (2013) · Psychological Medicine · doi:10.1017/s003329171300247x · Cited by 54 · see citing works
Probability of Obsessive and Compulsive Symptoms in Huntington’s Disease
Beglinger, L. J., Langbehn, D. R., Duff, K., Stierman, L., Black, D. W., Nehl, C., Anderson, K. E., Penziner, E., & Paulsen, J. S. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.04.034 · Cited by 53 · see citing works
Psychopathology in treated Wilson's disease determined by means of CPRS expert and self‐ratings
Portala, K., Westermark, K., von Knorring, L., & Ekselius, L. (2000) · Acta Psychiatrica Scandinavica · doi:10.1034/j.1600-0447.2000.90085.x · Cited by 52 · see citing works
Structural imaging in the presymptomatic stage of genetically determined parkinsonism
Reetz, K., Tadić, V., Kasten, M., Brüggemann, N., Schmidt, A., Hagenah, J. M., Pramstaller, P. P., Ramı́rez, A., Behrens, M. I., Siebner, H. R., et al. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.05.006 · Cited by 51 · see citing works
Molecular and clinical findings in a family with dentatorubral‐pallidoluysian atrophy
Potter, N. T., Meyer, M. A., Zimmerman, A. W., Eisenstadt, M. L., & Anderson, I. J. (1995) · Annals of Neurology · doi:10.1002/ana.410370220 · Cited by 50 · see citing works
The relation between depression and parkin genotype: The CORE-PD study
Srivastava, A., Tang, M. X., Mejia‐Santana, H., Rosado, L., Louis, E. D., Caccappolo, E., Comella, C. L., Colcher, A., Siderowf, A. D., Jennings, D. L., et al. (2011) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2011.07.008 · Cited by 48 · see citing works
Reetz, K., Lencer, R., Steinlechner, S., Christian Gaser, B., Hagenah, J. M., Büchel, C., Petersen, D., Kock, N., Djarmati, A., Siebner, H. R., et al. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.12.010 · Cited by 47 · see citing works
Sleep Disturbance and Rage Attacks in Opsoclonus-Myoclonus Syndrome: Response to Trazodone
Pranzatelli, M. R., Tate, E. D., Dukart, W. S., Flint, M. J., Hoffman, M. T., & Oksa, A. E. (2005) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2005.05.016 · Cited by 47 · see citing works
Mood and Behavioral Dysfunction With Opsoclonus-Myoclonus Ataxia
Turkel, S. B., Brumm, V. L., Mitchell, W. G., & Tavaré, C. J. (2006) · Journal of Neuropsychiatry · doi:10.1176/jnp.2006.18.2.239 · Cited by 45 · see citing works
Munoz, E., Milà, M., Sánchez, A., Latorre, P., Ariza, A., Codina, M., Ballesta, F., & TOLOSA, E. S. (1999) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.67.6.811 · Cited by 42 · see citing works
Mood and cognition in leucine‐rich repeat kinase 2 G2019S Parkinson's disease
Shanker, V., Groves, M., Heiman, G. A., Palmese, C. A., Saunders-Pullman, R. J., Ozelius, L. J., Raymond, D., & Bressman, S. (2011) · Movement Disorders · doi:10.1002/mds.23746 · Cited by 40 · see citing works
Edwards, M. J., Dale, R. C., Church, A. J., Trikouli, E., Quinn, N. P., Lees, A. J., Giovannoni, G., & Bhatia, K. P. (2004) · Movement Disorders · doi:10.1002/mds.20126 · Cited by 39 · see citing works
Self-citationPsychiatric disorders in persistent and remitted Sydenham's chorea
Moreira, J. M., Kümmer, A., Harsányi, E., Cardoso, F., & Teixeira, A. L. (2013) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2013.10.029 · Cited by 37 · see citing works
Cognitive impairment in carriers of glucocerebrosidase gene mutation in Parkinson disease patients
Malec‐Litwinowicz, M., Rudzińska, M., Szubiga, M., Michalski, M., Tomaszewski, T., & Szczudlik, A. (2014) · Neurologia i Neurochirurgia Polska · doi:10.1016/j.pjnns.2014.07.005 · Cited by 36 · see citing works
The Prevalence of Neuropsychiatric Disorders in Sydenham's Chorea
Ridel, K. R., Lipps, T. D., & Gilbert, D. L. (2010) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2009.12.004 · Cited by 33 · see citing works
Clinical correlates of depressive symptoms in familial Parkinson's disease
Pankratz, N., Marder, K. S., Halter, C. A., Rudolph, A., Shults, C. W., Nichols, W. C., & Foroud, T. (2008) · Movement Disorders · doi:10.1002/mds.22285 · Cited by 32 · see citing works
Non-motor phenotype of dopa-responsive dystonia and quality of life assessment
Brüggemann, N., Stiller, S., Tadić, V., Kasten, M., Münchau, A. M., Gräf, J., Klein, C., & Hagenah, J. M. (2014) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2013.12.014 · Cited by 31 · see citing works
Kim, H. J., Kim, H., Lee, J., Yun, J. Y., Kim, S. Y., Park, S. S., & Jeon, B. S. (2011) · Journal of Neurology · doi:10.1007/s00415-011-6110-1 · Cited by 28 · see citing works
Papapetropoulos, S., Ellul, J., Paschalis, C., Athanassiadou, A., Papadimitriou, A., & Papapetropoulos, T. (2003) · European Journal of Neurology · doi:10.1046/j.1468-1331.2003.00576.x · Cited by 27 · see citing works
Caccappolo, E., Alcalay, R. N., Mejia‐Santana, H., Tang, M., Rakitin, B. C., Rosado, L., Louis, E. D., Comella, C. L., Colcher, A., Jennings, D. L., et al. (2010) · Journal of the International Neuropsychological Society · doi:10.1017/s1355617710001190 · Cited by 25 · see citing works
The complex genetics of Gilles de la Tourette syndrome: implications for clinical practice
Ali, F., Morrison, K. E., & Cavanna, A. E. (2013) · Neuropsychiatry · doi:10.2217/npy.13.25 · Cited by 24 · see citing works
Gregorowski, C., Löchner, C., Martin, L. I., Simmons, C., Kidd, M., Walker, K., Wilmshurst, J. M., & Seedat, S. (2015) · Metabolic Brain Disease · doi:10.1007/s11011-015-9681-1 · Cited by 21 · see citing works
Dentatorubral-Pallidoluysian Atrophy (DRPLA) Presenting With Psychosis
Adachi, N., Arima, K., Asada, T., Kato, M., Minami, N., Goto, Y.-I., Onuma, T., Ikeuchi, T., Tsuji, S., Hayashi, M., et al. (2001) · Journal of Neuropsychiatry · doi:10.1176/jnp.13.2.258 · Cited by 20 · see citing works
Depression in X-linked dystonia-parkinsonism: A case–control study
Morigaki, R., Nakataki, M., Kawarai, T., Lee, L. V., Teleg, R. A., Tabuena, M. D., Mure, H., Sako, W., Pasco, P. M. D., Nagahiro, S., et al. (2013) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2013.04.027 · Cited by 18 · see citing works
Juvenile Huntington disease in Argentina
Gatto, E. M., Parisi, V. L., Etcheverry, J. L., Sanguinetti, A. C., Cordi, L., Binelli, A., Persi, G. G., & Squitieri, F. (2015) · Arquivos de Neuro-Psiquiatria · doi:10.1590/0004-282x20150192 · Cited by 17 · see citing works
Depressive and anxiety symptoms in Sydenham's chorea
Teixeira, A. L., Athayde, G. R. S., Sacramento, D., Maia, D. P., & Cardoso, F. (2007) · Movement Disorders · doi:10.1002/mds.21436 · Cited by 16 · see citing works
Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia
da Silva‐Júnior, F. P., dos Santos, C. O., Gomes, S. M. C. D. A. S. M. M., Barbosa, E. R., Borges, V., Ferraz, H. B., Limongi, J. C. P., Rocha, M. S. G., & Aguiar, P. D. C. (2014) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2014.06.012 · Cited by 14 · see citing works
Jj, M. (1998) · Biological Psychiatry · doi:10.1016/s0006-3223(98)00299-6 · Cited by 14 · see citing works
Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa‐responsive dystonia
Theuns, J., Crosiers, D., Debaene, L., Nuytemans, K., Meeus, B., Sleegers, K., Goossens, D., Corsmit, E., Elinck, E., Peeters, K., et al. (2012) · Movement Disorders · doi:10.1002/mds.25147 · Cited by 10 · see citing works
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- [4]Mann JJ. The role of in vivo neurotransmitter system imaging studies in understanding major depression. Biol Psychiatry. 1998;44(11):1077-8.
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- Authors
- Peall, K. J., Lorentzos, M. S., Heyman, I., Tijssen, M. A. J., Owen, M. J., Dale, R. C., & Kurian, M. A.
- Affiliations
- Cardiff University (GB)
- The University of Sydney (AU)
- Great Ormond Street Hospital (GB)
- University of Groningen (NL)
- Corresponding author
- Peall, K.J.
- Kurian, M.A.
- Venue
- Neuroscience & Biobehavioral Reviews
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 80
- Pages
- 23-35
- ISSN
- 0149-7634 (ISSN-L)
- OpenAlex
- W2614791664
- Cited by
- 14
- References
- 113
- Citations by year
- 2025: 1 · 2024: 1 · 2022: 2 · 2021: 1 · 2020: 3 · 2019: 1 · 2018: 4 · 2017: 1
- FWCI
- 0.33
- Type
- journal article
- Language
- en
- Open access
- green
- research.rug.nl
- Licence
- Locations
- Neuroscience & Biobehavioral Reviews (publishedVersion)
- PubMed (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (publishedVersion, other-oa)
- ORCA Online Research @Cardiff (Cardiff University) (acceptedVersion)
- UCL Discovery (University College London) (submittedVersion)
- ORCA Online Research @Cardiff (Cardiff University) (submittedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion, other-oa)
- Funders
- AADC Research Trust
- Academy of Medical Sciences (AMS-SGCL11-Peall)
- Rosetrees Trust (M375‐F1)
- Petre Foundation
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek
- Medical Research Council (MR/P008593/1, MR/L010305/1)
- National Health and Medical Research Council
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Neurology › Neurological disorders and treatments
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Keywords
- psychiatric comorbidity, movement disorders, hereditary movement disorders, autoantibodies, depression, generalized anxiety disorder, obsessive-compulsive disorder, psychosis, schizophrenia, attention deficit hyperactivity disorder, neuropsychiatric symptoms, pathophysiological mechanisms
- MeSH terms
- Mental Disorders, Humans, Movement Disorders, Comorbidity
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