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 *

217 related articles for article (PubMed ID: 20063428)

  • 1. The spectrum of movement disorders in Glut-1 deficiency.
    Pons R; Collins A; Rotstein M; Engelstad K; De Vivo DC
    Mov Disord; 2010 Feb; 25(3):275-81. PubMed ID: 20063428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The expanding phenotype of GLUT1-deficiency syndrome.
    Brockmann K
    Brain Dev; 2009 Aug; 31(7):545-52. PubMed ID: 19304421
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Glucose transporter type 1 (GLUT-1) deficiency].
    Cano A; Ticus I; Chabrol B
    Rev Neurol (Paris); 2008 Nov; 164(11):896-901. PubMed ID: 18808765
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
    Leen WG; Klepper J; Verbeek MM; Leferink M; Hofste T; van Engelen BG; Wevers RA; Arthur T; Bahi-Buisson N; Ballhausen D; Bekhof J; van Bogaert P; Carrilho I; Chabrol B; Champion MP; Coldwell J; Clayton P; Donner E; Evangeliou A; Ebinger F; Farrell K; Forsyth RJ; de Goede CG; Gross S; Grunewald S; Holthausen H; Jayawant S; Lachlan K; Laugel V; Leppig K; Lim MJ; Mancini G; Marina AD; Martorell L; McMenamin J; Meuwissen ME; Mundy H; Nilsson NO; Panzer A; Poll-The BT; Rauscher C; Rouselle CM; Sandvig I; Scheffner T; Sheridan E; Simpson N; Sykora P; Tomlinson R; Trounce J; Webb D; Weschke B; Scheffer H; Willemsen MA
    Brain; 2010 Mar; 133(Pt 3):655-70. PubMed ID: 20129935
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Glucose transporter type 1 deficiency: ketogenic diet in three patients with atypical phenotype.
    Veggiotti P; Teutonico F; Alfei E; Nardocci N; Zorzi G; Tagliabue A; De Giorgis V; Balottin U
    Brain Dev; 2010 May; 32(5):404-8. PubMed ID: 19515520
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rett syndrome and associated movement disorders.
    FitzGerald PM; Jankovic J; Percy AK
    Mov Disord; 1990; 5(3):195-202. PubMed ID: 2388636
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Atypical GLUT1 deficiency with prominent movement disorder responsive to ketogenic diet.
    Friedman JR; Thiele EA; Wang D; Levine KB; Cloherty EK; Pfeifer HH; De Vivo DC; Carruthers A; Natowicz MR
    Mov Disord; 2006 Feb; 21(2):241-5. PubMed ID: 16149086
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
    Leen WG; Mewasingh L; Verbeek MM; Kamsteeg EJ; van de Warrenburg BP; Willemsen MA
    Mov Disord; 2013 Sep; 28(10):1439-42. PubMed ID: 23801573
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [GLUT-1 deficiency syndrome or De Vivo disease: a case report].
    Ticus I; Cano A; Villeneuve N; Milh M; Mancini J; Chabrol B
    Arch Pediatr; 2008 Aug; 15(8):1296-9. PubMed ID: 18556184
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glucose transporter type I deficiency syndrome: epilepsy phenotypes and outcomes.
    Pong AW; Geary BR; Engelstad KM; Natarajan A; Yang H; De Vivo DC
    Epilepsia; 2012 Sep; 53(9):1503-10. PubMed ID: 22812641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.
    Temudo T; Ramos E; Dias K; Barbot C; Vieira JP; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Fonseca M; Cabral A; Cabral P; Monteiro JP; Borges L; Gomes R; Santos M; Sequeiros J; Maciel P
    Mov Disord; 2008 Jul; 23(10):1384-90. PubMed ID: 18512755
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Glucose transporter type 1 deficiency syndrome with carbohydrate-responsive symptoms but without epilepsy.
    Koy A; Assmann B; Klepper J; Mayatepek E
    Dev Med Child Neurol; 2011 Dec; 53(12):1154-6. PubMed ID: 21838819
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The adult form of Niemann-Pick disease type C.
    Sévin M; Lesca G; Baumann N; Millat G; Lyon-Caen O; Vanier MT; Sedel F
    Brain; 2007 Jan; 130(Pt 1):120-33. PubMed ID: 17003072
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Milder phenotypes of glucose transporter type 1 deficiency syndrome.
    Anand G; Padeniya A; Hanrahan D; Scheffer H; Zaiwalla Z; Cox D; Mann N; Hewertson J; Price S; Nemeth A; Arsov T; Scheffer I; Jayawant S; Pike M; McShane T
    Dev Med Child Neurol; 2011 Jul; 53(7):664-8. PubMed ID: 21649651
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Adding video recording increases the diagnostic yield of routine electroencephalograms in children with frequent paroxysmal events.
    Watemberg N; Tziperman B; Dabby R; Hasan M; Zehavi L; Lerman-Sagie T
    Epilepsia; 2005 May; 46(5):716-9. PubMed ID: 15857438
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Movement disorders in multiple sclerosis.
    Tranchant C; Bhatia KP; Marsden CD
    Mov Disord; 1995 Jul; 10(4):418-23. PubMed ID: 7565820
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Modified Atkins diet therapy for a case with glucose transporter type 1 deficiency syndrome.
    Ito S; Oguni H; Ito Y; Ishigaki K; Ohinata J; Osawa M
    Brain Dev; 2008 Mar; 30(3):226-8. PubMed ID: 17869467
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.
    Klepper J; Scheffer H; Leiendecker B; Gertsen E; Binder S; Leferink M; Hertzberg C; Näke A; Voit T; Willemsen MA
    Neuropediatrics; 2005 Oct; 36(5):302-8. PubMed ID: 16217704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
    Mullen SA; Marini C; Suls A; Mei D; Della Giustina E; Buti D; Arsov T; Damiano J; Lawrence K; De Jonghe P; Berkovic SF; Scheffer IE; Guerrini R
    Arch Neurol; 2011 Sep; 68(9):1152-5. PubMed ID: 21555602
    [TBL] [Abstract][Full Text] [Related]  

  • 20. "Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiency.
    Gaspard N; Suls A; Vilain C; De Jonghe P; Van Bogaert P
    Epileptic Disord; 2011 Sep; 13(3):300-3. PubMed ID: 21865127
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.