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 *

109 related articles for article (PubMed ID: 34303586)

  • 21. GLUT-1 deficiency syndrome in Norway--yet another piece of the puzzle.
    Klepper J
    Dev Med Child Neurol; 2013 May; 55(5):400-1. PubMed ID: 23448598
    [No Abstract]   [Full Text] [Related]  

  • 22. Paroxysmal ocular movements - an early sign in Glut1 deficiency Syndrome.
    Reis S; Matias J; Machado R; Monteiro JP
    Metab Brain Dis; 2018 Aug; 33(4):1381-1383. PubMed ID: 29730803
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Nanotechnology may provide hope for patients with glucose transporter type 1 deficiency syndrome.
    Asadi-Pooya AA; Mirzaei E
    Epileptic Disord; 2022 Jun; 24(3):630-632. PubMed ID: 35653086
    [No Abstract]   [Full Text] [Related]  

  • 24. [Glucose transporter 1 deficiency syndrome: features of movement disorders, diagnosis and treatment].
    Ji XN; Xu CJ; Gao ZJ; Chen SH; Xu KM; Chen Q
    Zhongguo Dang Dai Er Ke Za Zhi; 2018 Mar; 20(3):209-213. PubMed ID: 29530121
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Atypical Manifestations in Glut1 Deficiency Syndrome.
    De Giorgis V; Varesio C; Baldassari C; Piazza E; Olivotto S; Macasaet J; Balottin U; Veggiotti P
    J Child Neurol; 2016 Aug; 31(9):1174-80. PubMed ID: 27250207
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain-- a review.
    Klepper J; Voit T
    Eur J Pediatr; 2002 Jun; 161(6):295-304. PubMed ID: 12029447
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Somatic mosaicism for a SLC2A1 mutation: implications for genetic counseling for GLUT1 deficiency syndrome.
    Takahashi S; Matsufuji M; Yonee C; Tsuru H; Sano N; Oguni H
    Clin Genet; 2017 Jun; 91(6):932-933. PubMed ID: 28124377
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome.
    Willemsen MA; Vissers LE; Verbeek MM; van Bon BW; Geuer S; Gilissen C; Klepper J; Kwint MP; Leen WG; Pennings M; Wevers RA; Veltman JA; Kamsteeg EJ
    Eur J Hum Genet; 2017 Jun; 25(6):771-774. PubMed ID: 28378819
    [TBL] [Abstract][Full Text] [Related]  

  • 29. EEG features of glut-1 deficiency syndrome.
    von Moers A; Brockmann K; Wang D; Korenke CG; Huppke P; De Vivo DC; Hanefeld F
    Epilepsia; 2002 Aug; 43(8):941-5. PubMed ID: 12181017
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Anemia in Glucose Transporter Type 1 Deficiency Syndrome: Often Expected, Rarely Encountered, and with a Fascinating Explanation.
    Willemsen MA
    Neuropediatrics; 2017 Oct; 48(5):327-328. PubMed ID: 28582793
    [No Abstract]   [Full Text] [Related]  

  • 31. Inborn errors of organic acid metabolism.
    Green A
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
    Wang D; Pascual JM; Yang H; Engelstad K; Jhung S; Sun RP; De Vivo DC
    Ann Neurol; 2005 Jan; 57(1):111-8. PubMed ID: 15622525
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.
    Wang D; Kranz-Eble P; De Vivo DC
    Hum Mutat; 2000 Sep; 16(3):224-31. PubMed ID: 10980529
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Refractory absence epilepsy associated with GLUT-1 deficiency syndrome.
    Byrne S; Kearns J; Carolan R; Mc Menamin J; Klepper J; Webb D
    Epilepsia; 2011 May; 52(5):1021-4. PubMed ID: 21366555
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect.
    Hainque E; Gras D; Meneret A; Atencio M; Luton MP; Barbier M; Doulazmi M; Habarou F; Ottolenghi C; Roze E; Mochel F
    J Neurol Neurosurg Psychiatry; 2019 Nov; 90(11):1291-1293. PubMed ID: 30948626
    [No Abstract]   [Full Text] [Related]  

  • 36. Genetic mimics of cerebral palsy.
    Pearson TS; Pons R; Ghaoui R; Sue CM
    Mov Disord; 2019 May; 34(5):625-636. PubMed ID: 30913345
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Glucose transporter-1 deficiency syndrome can cause various clinical symptoms].
    Larsen J; Stubbings V; Møller RS; Hjalgrim H
    Ugeskr Laeger; 2013 Dec; 175(50A):V04130248. PubMed ID: 25353328
    [TBL] [Abstract][Full Text] [Related]  

  • 38. New Paradigm for the Treatment of Glucose Transporter 1 Deficiency Syndrome: Low Glycemic Index Diet and Modified High Amylopectin Cornstarch.
    Almuqbil M; Go C; Nagy LL; Pai N; Mamak E; Mercimek-Mahmutoglu S
    Pediatr Neurol; 2015 Sep; 53(3):243-6. PubMed ID: 26216499
    [TBL] [Abstract][Full Text] [Related]  

  • 39. GLUT-1 deficiency presenting with seizures and reversible leukoencephalopathy on MRI imaging.
    Ismayilova N; Hacohen Y; MacKinnon AD; Elmslie F; Clarke A
    Eur J Paediatr Neurol; 2018 Nov; 22(6):1161-1164. PubMed ID: 30115503
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Intermittent Alternating Eye-Head Synkinesia in GLUT1 Deficiency Syndrome.
    Ribeiro Reis AP; Gerber-Hollbach N; Weber P; Palmowski-Wolfe A
    Klin Monbl Augenheilkd; 2022 Jun; 239(6):812-813. PubMed ID: 33607684
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.