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Journal Abstract Search

255 related items for PubMed ID: 34573360

  • 1. GLUT1 Deficiency Syndrome-Early Treatment Maintains Cognitive Development? (Literature Review and Case Report).
    Kolic I, Radic Nisevic J, Vlasic Cicvaric I, Butorac Ahel I, Lah Tomulic K, Segulja S, Baraba Dekanic K, Serifi S, Ovuka A, Prpic I.
    Genes (Basel); 2021 Aug 31; 12(9):. PubMed ID: 34573360
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  • 3. GLUT1 deficiency syndrome 2013: current state of the art.
    De Giorgis V, Veggiotti P.
    Seizure; 2013 Dec 31; 22(10):803-11. PubMed ID: 23890838
    [Abstract] [Full Text] [Related]

  • 4. 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 31; 58(9):443-54. PubMed ID: 26193382
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  • 5. 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 31; 24():28-32. PubMed ID: 25564316
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  • 6. Classic Ketogenic Diet and Modified Atkins Diet in SLC2A1 Positive and Negative Patients with Suspected GLUT1 Deficiency Syndrome: A Single Center Analysis of 18 Cases.
    Ruiz Herrero J, Cañedo Villarroya E, González Gutiérrez-Solana L, García Alcolea B, Gómez Fernández B, Puerta Macfarland LA, Pedrón-Giner C.
    Nutrients; 2021 Mar 04; 13(3):. PubMed ID: 33806661
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  • 7. A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet.
    Tornese G, Patti G, Pellegrin MC, Costa P, Faletra F, Faleschini E, Barbi E.
    Ital J Pediatr; 2020 Aug 26; 46(1):119. PubMed ID: 32847563
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  • 8. Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes.
    Castellotti B, Ragona F, Freri E, Solazzi R, Ciardullo S, Tricomi G, Venerando A, Salis B, Canafoglia L, Villani F, Franceschetti S, Nardocci N, Gellera C, DiFrancesco JC, Granata T.
    J Neurol; 2019 Jun 26; 266(6):1439-1448. PubMed ID: 30895386
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  • 9. First report of GLUT1 deficiency syndrome in Chinese patients with novel and hot spot mutations in SLC2A1 gene.
    Fung EL, Ho YY, Hui J, Wong JH, Ng TB, Fong NY, Klepper J, Tsui KW.
    Brain Dev; 2011 Feb 26; 33(2):170-3. PubMed ID: 20417043
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  • 10. 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 26; 48(6):826-830. PubMed ID: 33431108
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  • 11. Occurrence of GLUT1 deficiency syndrome in patients treated with ketogenic diet.
    Ramm-Pettersen A, Nakken KO, Haavardsholm KC, Selmer KK.
    Epilepsy Behav; 2014 Mar 26; 32():76-8. PubMed ID: 24508593
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  • 12. Glucose transporter 1 deficiency syndrome and hemiplegic migraines as a dominant presenting clinical feature.
    Mohammad SS, Coman D, Calvert S.
    J Paediatr Child Health; 2014 Dec 26; 50(12):1025-6. PubMed ID: 25440161
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  • 14. [Clinical characteristics and ketogenic diet therapy of glucose transporter type 1 deficiency syndrome in children: a multicenter clinical study].
    Yu LF, Zhang YQ, Duan J, Ni Y, Gong XY, Lu ZY, Liao JX, Lu XP, Shi ZN, Lei MF, Zhong JM, Zha J, Zhou SZ.
    Zhonghua Er Ke Za Zhi; 2020 Nov 02; 58(11):881-886. PubMed ID: 33120458
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  • 15. Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features.
    Soto-Insuga V, López RG, Losada-Del Pozo R, Rodrigo-Moreno M, Cayuelas EM, Giráldez BG, Díaz-Gómez E, Sánchez-Martín G, García LO, Serratosa JM, Grupo Español de Genética de las Epilepsias de la Infancia (GEGEI)Department of Pediatrics, Hospital Universitario Fundación Jiménez Díaz, UAM, Madrid, Spain; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Madrid, Spain; Neurology Lab and Epilepsy Unit, Department of Neurology, IIS- Fundación Jiménez Díaz, UAM, Madrid, Spain..
    Epilepsy Res; 2019 Aug 02; 154():39-41. PubMed ID: 31035243
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  • 16. Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
    Klepper J.
    Epilepsia; 2008 Nov 02; 49 Suppl 8():46-9. PubMed ID: 19049586
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  • 18. 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 02; 29(3):349-59. PubMed ID: 23340081
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  • 19. [GLUT-1 deficiency syndrome].
    Zavala M, Castillo V, Gonzalez M, Castillo S.
    Rev Neurol; 2019 Aug 16; 69(4):178-179. PubMed ID: 31334562
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  • 20. [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 16; 51(6):443-7. PubMed ID: 24120063
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