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Journal Abstract Search

482 related items for PubMed ID: 23890838

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  • 2. From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
    Hully M, Vuillaumier-Barrot S, Le Bizec C, Boddaert N, Kaminska A, Lascelles K, de Lonlay P, Cances C, des Portes V, Roubertie A, Doummar D, LeBihannic A, Degos B, de Saint Martin A, Flori E, Pedespan JM, Goldenberg A, Vanhulle C, Bekri S, Roubergue A, Heron B, Cournelle MA, Kuster A, Chenouard A, Loiseau MN, Valayannopoulos V, Chemaly N, Gitiaux C, Seta N, Bahi-Buisson N.
    Eur J Med Genet; 2015 Sep; 58(9):443-54. PubMed ID: 26193382
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  • 3. Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
    Klepper J.
    Epilepsia; 2008 Nov; 49 Suppl 8():46-9. PubMed ID: 19049586
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  • 4. Sporadic and familial glut1ds Italian patients: A wide clinical variability.
    De Giorgis V, Teutonico F, Cereda C, Balottin U, Bianchi M, Giordano L, Olivotto S, Ragona F, Tagliabue A, Zorzi G, Nardocci N, Veggiotti P.
    Seizure; 2015 Jan; 24():28-32. PubMed ID: 25564316
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  • 10. The many faces of Glut1 deficiency syndrome.
    Tzadok M, Nissenkorn A, Porper K, Matot I, Marcu S, Anikster Y, Menascu S, Bercovich D, Ben Zeev B.
    J Child Neurol; 2014 Mar; 29(3):349-59. PubMed ID: 23340081
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  • 11. [Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].
    Liu YY, Bao XH, Wang S, Fu N, Liu XY, Song FY, Yang YL, Wu Y, Zhang YH, Wu JX, Jiang YW, Qin J, Wu XR.
    Zhonghua Er Ke Za Zhi; 2013 Jun; 51(6):443-7. PubMed ID: 24120063
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  • 12. GLUT1 deficiency syndrome: an update.
    Gras D, Roze E, Caillet S, Méneret A, Doummar D, Billette de Villemeur T, Vidailhet M, Mochel F.
    Rev Neurol (Paris); 2014 Feb; 170(2):91-9. PubMed ID: 24269118
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  • 19. A 23 years follow-up study identifies GLUT1 deficiency syndrome initially diagnosed as complicated hereditary spastic paraplegia.
    Diomedi M, Gan-Or Z, Placidi F, Dion PA, Szuto A, Bengala M, Rouleau GA, Gigli GL.
    Eur J Med Genet; 2016 Nov; 59(11):564-568. PubMed ID: 27725288
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  • 20. Phenotypic and Genotypic Spectrum of Glucose Transporter-1 Deficiency Syndrome.
    Bourque DK, Cordeiro D, Nimmo GAM, Kobayashi J, Mercimek-Andrews S.
    Can J Neurol Sci; 2021 Nov; 48(6):826-830. PubMed ID: 33431108
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