Phenomenology and classification of dystonia: a consensus update.

Albanese A, Bhatia K, Bressman SB, Delong MR, Fahn S, Fung VS, Hallett M, Jankovic J, Jinnah HA, Klein C, Lang AE, Mink JW, Teller JK.

Mov Disord. 2013 Jun 15;28(7):863-73. doi: 10.1002/mds.25475. Review.

Molybdenum cofactor deficiency presenting with a parkinsonism-dystonia syndrome.

Alkufri F, Harrower T, Rahman Y, Hughes E, Mundy H, Knibb JA, Moriarty J, Connor S, Samuel M.

Mov Disord. 2013 Mar;28(3):399-401. doi: 10.1002/mds.25276. No abstract available.

Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus.

Cacciagli P, Sutera-Sardo J, Borges-Correia A, Roux JC, Dorboz I, Desvignes JP, Badens C, Delepine M, Lathrop M, Cau P, Lévy N, Girard N, Sarda P, Boespflug-Tanguy O, Villard L.

Am J Hum Genet. 2013 Sep 5;93(3):579-86. doi: 10.1016/j.ajhg.2013.07.023.

Special concerns in defining, studying, and treating dystonia in children.

Mink JW.

Mov Disord. 2013 Jun 15;28(7):921-5. doi: 10.1002/mds.25548. Review.

When the levator scapulae becomes a rotator capitis": implications for cervical dystonia."

Erro R, Bhatia KP, Catania S, Shields K, Cordivari C.

Parkinsonism Relat Disord. 2013 Jul;19(7):705-6. doi: 10.1016/j.parkreldis.2013.03.012. No abstract available.

The syndrome of deafness-dystonia: clinical and genetic heterogeneity.

Kojovic M, Pareés I, Lampreia T, Pienczk-Reclawowicz K, Xiromerisiou G, Rubio-Agusti I, Kramberger M, Carecchio M, Alazami AM, Brancati F, Slawek J, Pirtosek Z, Valente EM, Alkuraya FS, Edwards MJ, Bh

Mov Disord. 2013 Jun;28(6):795-803. doi: 10.1002/mds.25394.

Impulse control disorder in a patient with X-linked dystonia-parkinsonism after bilateral pallidal deep brain stimulation.

Piano AN, Tan LC.

Parkinsonism Relat Disord. 2013 Nov;19(11):1069-70. doi: 10.1016/j.parkreldis.2013.07.012. No abstract available.

Writer's cramp: is focal dystonia the best explanation?

Pritchard MH.

JRSM Short Rep. 2013 Jun 5;4(7):1-7. doi: 10.1177/2042533313480071.

Kinematic analysis of grasping in focal dystonia of the face and neck.

Nowak DA, Dafotakis M, Fink GR.

Neuroscience. 2013 May 1;237:216-22. doi: 10.1016/j.neuroscience.2013.01.065.

Fluvoxamine induced oculogyric dystonia and manic switch in a patient with obsessive compulsive disorder.

Tikka SK, Garg S, Das B.

Indian J Pharmacol. 2013 Sep-Oct;45(5):532-3. doi: 10.4103/0253-7613.117760.

Acute focal dystonia induced by a tricyclic antidepressant in a patient with Wilson disease: a case report.

Litwin T, Chabik G, Członkowska A.

Neurol Neurochir Pol. 2013 Sep-Oct;47(5):502-6.

The role of a dentist in managing patients with dystonia.

Watt E, Sangani I, Crawford F, Gillgrass T.

Dent Update. 2013 Dec;40(10):846-8.

Dystonia, facial dysmorphism, intellectual disability and breast cancer associated with a chromosome 13q34 duplication and overexpression of TFDP1: case report.

Moscovich M, LeDoux MS, Xiao J, Rampon GL, Vemula SR, Rodriguez RL, Foote KD, Okun MS.

BMC Med Genet. 2013 Jul 13;14:70. doi: 10.1186/1471-2350-14-70.

Pallidal somatotopy suggested by deep brain stimulation in a patient with dystonia.

Joint C, Thevathasan W, Green AL, Aziz T.

Neurology. 2013 Feb 12;80(7):685-6. doi: 10.1212/WNL.0b013e318281cbfe. No abstract available.

Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.

Lohmann K, Wilcox RA, Winkler S, Ramirez A, Rakovic A, Park JS, Arns B, Lohnau T, Groen J, Kasten M, Brüggemann N, Hagenah J, Schmidt A, Kaiser FJ, Kumar KR, Zschiedrich K, Alvarez-Fischer D, Altenmül

Ann Neurol. 2013 Apr;73(4):537-45. doi: 10.1002/ana.23829.