Tics as an initial manifestation of juvenile Huntington’s disease: case report and literature review
暂无分享,去创建一个
[1] K. Patra,et al. Childhood-onset (Juvenile) Huntington's disease: A rare case report , 2015, Journal of Pediatric Neurosciences.
[2] C. Colosimo. A Case of Atypical Adult-onset Tic Disorder , 2015, The Neurologist.
[3] W. McMahon,et al. Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome. , 2015, JAMA psychiatry.
[4] Olgu Sunumu,et al. A RARE CASE REPORT , 2015 .
[5] P. Holmans,et al. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. , 2015, Journal of Huntington's disease.
[6] Yi-Min Sun,et al. Huntington’s Disease: Relationship Between Phenotype and Genotype , 2015, Molecular Neurobiology.
[7] Zia Choudhry,et al. The mechanism of degeneration of striatal neuronal subtypes in Huntington disease , 2014, Annals of neurosciences.
[8] W. Ni,et al. Clinical features of Chinese patients with Huntington's disease carrying CAG repeats beyond 60 within HTT gene , 2014, Clinical genetics.
[9] B. P. Warrenburg,et al. Early onset dystonia and parkinsonism with abnormal globus pallidal signal in MRI: A diagnostic challenge , 2013, Movement Disorders.
[10] L. Defebvre,et al. Association between caffeine intake and age at onset in Huntington's disease , 2013, Neurobiology of Disease.
[11] P. Monrad,et al. Typical clinical findings should prompt investigation for juvenile Huntington disease. , 2013, Pediatric neurology.
[12] Chih-Chien Lin,et al. Juvenile Huntington's disease presenting as difficult-to-treat seizure and the first episode of psychosis. , 2012, General hospital psychiatry.
[13] G. Rizzo,et al. Eating disorder as a psychiatric onset of juvenile Huntington's disease. , 2011, American Journal of Psychiatry.
[14] J. Jankovic,et al. DYT 6—A novel THAP1 mutation with excellent effect on pallidal DBS , 2011, Movement disorders : official journal of the Movement Disorder Society.
[15] D. Hannequin,et al. Juvenile Huntington disease in an 18‐month‐old boy revealed by global developmental delay and reduced cerebellar volume , 2011, American journal of medical genetics. Part A.
[16] Soon-Tae Lee,et al. A Case of Juvenile Huntington Disease in a 6-Year-Old Boy , 2010, Journal of movement disorders.
[17] M. I. López-Ibor Alcocer,et al. Juvenile Huntington's disease: a case report and literature review. , 2010, Actas espanolas de psiquiatria.
[18] Audrey E Hendricks,et al. Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. , 2009, Human molecular genetics.
[19] T. Shiihara,et al. A patient with early onset Huntington disease and severe cerebellar atrophy , 2009, American journal of medical genetics. Part A.
[20] J. Zeng,et al. Excessive blinking as an initial manifestation of juvenile Huntington’s disease , 2008, Neurological Sciences.
[21] J. Waugh,et al. Juvenile Huntington Disease Exacerbated by Methylphenidate: Case Report , 2008, Journal of child neurology.
[22] N. Müller. Tourette's syndrome: clinical features, pathophysiology, and therapeutic approaches. , 2007, Dialogues in clinical neuroscience.
[23] E. Marszał,et al. Huntington Disease in a 9-Year-Old Boy: Clinical Course and Neuropathologic Examination , 2006, Journal of child neurology.
[24] W. Poewe,et al. Seminar on choreas , 2006, The Lancet Neurology.
[25] F. Cendes,et al. Clinical presentation of juvenile Huntington disease. , 2006, Arquivos de neuro-psiquiatria.
[26] C. Singer,et al. Case of maternally transmitted juvenile Huntington's disease with a very large trinucleotide repeat , 2005, Movement disorders : official journal of the Movement Disorder Society.
[27] G. Feldman,et al. Juvenile onset Huntington disease resulting from a very large maternal expansion , 2005, American journal of medical genetics. Part A.
[28] J. Jankovic,et al. Secondary tics and tourettism , 2005 .
[29] J. Jankovic,et al. Secondary tics and tourettism. , 2005, Revista brasileira de psiquiatria.
[30] M. Schulte-Markwort,et al. Huntington disease: a case study of early onset presenting as depression. , 2004, Journal of the American Academy of Child and Adolescent Psychiatry.
[31] S. Seneca,et al. Early onset Huntington disease: a neuronal degeneration syndrome , 2004, European Journal of Pediatrics.
[32] M. Schapiro,et al. MR imaging and spectroscopy in juvenile Huntington disease , 2004, Pediatric Radiology.
[33] Karen Marder,et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[34] G. Bruyn,et al. Juvenile Huntington disease , 1986, Human Genetics.
[35] M. Ito,et al. XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's disease , 2003, Clinical genetics.
[36] F. J. Carod-Artal,et al. Unusual Early-Onset Huntington's Disease , 2003, Journal of child neurology.
[37] M. Muglia,et al. Juvenile Huntington’s disease presenting as progressive myoclonic epilepsy , 2001, Neurology.
[38] E. Engelhardt,et al. Juvenile Huntington's disease confirmed by genetic examination in twins. , 1999, Arquivos de neuro-psiquiatria.
[39] M. Wick,et al. Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington’s disease , 1999, Neurology.
[40] T. Ashizawa,et al. Tourettism associated with Huntington's disease , 1995, Movement disorders : official journal of the Movement Disorder Society.
[41] E. Bianchini,et al. Neuropsychological and Neuroradiological Study of a Case of Early‐onset Huntington's Chorea , 1993, Developmental medicine and child neurology.
[42] L. Burd,et al. Huntington disease and childhood-onset Tourette syndrome. , 1991, American journal of medical genetics.
[43] P. Sethi,et al. Electro-Clinical Findings in Huntington's Chorea , 1977 .