These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 32627162)

  • 61. A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH gene.
    Schottmann G; Sarpong A; Lorenz C; Weinhold N; Gill E; Teschner L; Ferdinandusse S; Wanders RJ; Prigione A; Schuelke M
    Mov Disord; 2016 Nov; 31(11):1733-1739. PubMed ID: 27400804
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Meige's syndrome: History, epidemiology, clinical features, pathogenesis and treatment.
    Pandey S; Sharma S
    J Neurol Sci; 2017 Jan; 372():162-170. PubMed ID: 28017205
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Familial dystonia and choreoathetosis in three generations associated with bilateral striatal necrosis.
    Craver RD; Duncan MC; Nelson JS
    J Child Neurol; 1996 May; 11(3):185-8. PubMed ID: 8734018
    [TBL] [Abstract][Full Text] [Related]  

  • 64. A novel
    Lu JG; Bishop J; Cheyette S; Zhulin IB; Guo S; Sobreira N; Brenner SE
    Cold Spring Harb Mol Case Stud; 2018 Feb; 4(1):. PubMed ID: 29167286
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Gait disturbance in a patient with de novo 1.0-kb SOX2 microdeletion.
    Yamada H; Okanishi T; Okazaki T; Oguri M; Fukuda H; Uchiyama Y; Mizuguchi T; Matsumoto N; Maegaki Y
    Brain Dev; 2022 Jan; 44(1):68-72. PubMed ID: 34332824
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Blepharospasm--oromandibular dystonia (Meige's syndrome) misdiagnosed as secondary hemifacial spasm.
    Gottlieb JS; May M
    Am J Otol; 1984 Jan; 5(3):206-10. PubMed ID: 6720874
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Recessive mutations in VPS13D cause childhood onset movement disorders.
    Gauthier J; Meijer IA; Lessel D; Mencacci NE; Krainc D; Hempel M; Tsiakas K; Prokisch H; Rossignol E; Helm MH; Rodan LH; Karamchandani J; Carecchio M; Lubbe SJ; Telegrafi A; Henderson LB; Lorenzo K; Wallace SE; Glass IA; Hamdan FF; Michaud JL; Rouleau GA; Campeau PM
    Ann Neurol; 2018 Jun; 83(6):1089-1095. PubMed ID: 29518281
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Family history as a clue to the diagnosis of orofacial abnormal movements in a 30-year-old man.
    Vale TC; Povoas Barsottini OG; Pedroso JL
    Parkinsonism Relat Disord; 2021 Apr; 85():146-148. PubMed ID: 33191097
    [TBL] [Abstract][Full Text] [Related]  

  • 69. DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis.
    Veenma D; Cordeiro D; Sondheimer N; Mercimek-Andrews S
    Eur J Hum Genet; 2018 Dec; 26(12):1867-1870. PubMed ID: 30139987
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Movement disorders in children: Tourette syndrome.
    Golden GS
    J Dev Behav Pediatr; 1982 Dec; 3(4):209-16. PubMed ID: 6961138
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Levetiracetam in Meige's syndrome.
    Yardimci N; Karatas M; Kilinc M; Benli S
    Acta Neurol Scand; 2006 Jul; 114(1):63-6. PubMed ID: 16774630
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Meige's Syndrome: Rare Neurological Disorder Presenting as Conversion Disorder.
    Debadatta M; Mishra AK
    Indian J Psychol Med; 2013 Jul; 35(3):317-8. PubMed ID: 24249940
    [TBL] [Abstract][Full Text] [Related]  

  • 73. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Asmus F; Langseth A; Doherty E; Nestor T; Munz M; Gasser T; Lynch T; King MD
    Mov Disord; 2009 Apr; 24(5):702-9. PubMed ID: 19117362
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Family history interview of a broad phenotype in specific language impairment and matched controls.
    Kalnak N; Peyrard-Janvid M; Sahlén B; Forssberg H
    Genes Brain Behav; 2012 Nov; 11(8):921-7. PubMed ID: 22928858
    [TBL] [Abstract][Full Text] [Related]  

  • 75.
    Kamate M; Mittal N
    Neurol India; 2018; 66(Supplement):S141-S142. PubMed ID: 29503338
    [No Abstract]   [Full Text] [Related]  

  • 76. Refractory dry eye disease associated with Meige's syndrome induced by long-term use of an atypical antipsychotic.
    Kim JE; Jung JW
    BMC Ophthalmol; 2020 Dec; 20(1):474. PubMed ID: 33267850
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Tetrabenazine therapy of dystonia, chorea, tics, and other dyskinesias.
    Jankovic J; Orman J
    Neurology; 1988 Mar; 38(3):391-4. PubMed ID: 3279337
    [TBL] [Abstract][Full Text] [Related]  

  • 78. High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders.
    Kobayashi Y; Tohyama J; Kato M; Akasaka N; Magara S; Kawashima H; Ohashi T; Shiraishi H; Nakashima M; Saitsu H; Matsumoto N
    Brain Dev; 2016 Mar; 38(3):285-92. PubMed ID: 26482601
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Chorea-acanthocytosis: A Case Report with Review of Oral Manifestations.
    Urs AB; Augustine J; Khan AA
    Contemp Clin Dent; 2021; 12(1):73-75. PubMed ID: 33967542
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Oculomotor apraxia and disrupted sleep with nocturnal ballistic bouts in ADCY5-related disease.
    Balint B; Antelmi E; Mencacci NE; Batla A; Eriksson SH; Walker MC; Bronstein AM; Bhatia KP
    Parkinsonism Relat Disord; 2018 Sep; 54():103-106. PubMed ID: 29680308
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.