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 *

161 related articles for article (PubMed ID: 33584489)

  • 1. A Challenging Diagnosis of Atypical Glut1-DS: A Case Report and Literature Review.
    Yu M; Miao J; Lv Y; Wang X; Zhang W; Shao N; Meng H
    Front Neurol; 2020; 11():549331. PubMed ID: 33584489
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hemiplegic Migraine in Glut1 Deficiency Syndrome and Paroxysmal Dyskinesia at Ketogenic Diet Induction: Case Report and Literature Review.
    Gburek-Augustat J; Heinze A; Abou Jamra R; Merkenschlager A
    Mov Disord Clin Pract; 2020 Nov; 7(8):965-970. PubMed ID: 33163569
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and Genetic Characteristics of Chinese Children With GLUT1 Deficiency Syndrome: Case Report and Literature Review.
    Hu Q; Shen Y; Su T; Liu Y; Xu S
    Front Genet; 2021; 12():734481. PubMed ID: 34880899
    [No Abstract]   [Full Text] [Related]  

  • 4. Novel mutation in a patient with late onset GLUT1 deficiency syndrome.
    Juozapaite S; Praninskiene R; Burnyte B; Ambrozaityte L; Skerliene B
    Brain Dev; 2017 Apr; 39(4):352-355. PubMed ID: 27927575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 58(11):881-886. PubMed ID: 33120458
    [No Abstract]   [Full Text] [Related]  

  • 6. Sleep Disorder: An Overlooked Manifestation of Glucose Transporter Type-1 Deficiency Syndrome.
    Anurat K; Khongkhatithum C; Tim-Aroon T; Limwongse C; Thampratankul L
    Neuropediatrics; 2022 Apr; 53(2):129-132. PubMed ID: 34674205
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet.
    Cappuccio G; Pinelli M; Alagia M; Donti T; Day-Salvatore DL; Veggiotti P; De Giorgis V; Lunghi S; Vari MS; Striano P; Brunetti-Pierri N; Kennedy AD; Elsea SH
    PLoS One; 2017; 12(9):e0184022. PubMed ID: 28961260
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome.
    Jiménez Legido M; Cortés Ledesma C; Bernardino Cuesta B; López Marín L; Cantarín Extremera V; Pérez-Cerdá C; Pérez González B; López Martín E; González Gutiérrez-Solana L
    Neurologia (Engl Ed); 2022 Mar; 37(2):91-100. PubMed ID: 31047728
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review.
    Szczepanik E; Terczyńska I; Kruk M; Lipiec A; Dudko E; Tryfon J; Jurek M; Hoffman-Zacharska D
    Dev Period Med; 2015; 19(4):454-63. PubMed ID: 26982753
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Glut1 deficiency: when to suspect and how to diagnose?
    Verrotti A; D'Egidio C; Agostinelli S; Gobbi G
    Eur J Paediatr Neurol; 2012 Jan; 16(1):3-9. PubMed ID: 21962875
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GLUT1-deficiency syndrome: Report of a four-generation Norwegian family with a mild phenotype.
    Ramm-Pettersen A; Nakken KO; Haavardsholm KC; Selmer KK
    Epilepsy Behav; 2017 May; 70(Pt A):1-4. PubMed ID: 28407523
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome.
    Coman DJ; Sinclair KG; Burke CJ; Appleton DB; Pelekanos JT; O'Neil CM; Wallace GB; Bowling FG; Wang D; De Vivo DC; McGill JJ
    J Paediatr Child Health; 2006 May; 42(5):263-7. PubMed ID: 16712556
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acetazolamide-responsive Episodic Ataxia Without Baseline Deficits or Seizures Secondary to GLUT1 Deficiency: A Case Report and Review of the Literature.
    Tchapyjnikov D; Mikati MA
    Neurologist; 2018 Jan; 23(1):17-18. PubMed ID: 29266039
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Focal epilepsy in glucose transporter type 1 (Glut1) defects: case reports and a review of literature.
    Wolking S; Becker F; Bast T; Wiemer-Kruel A; Mayer T; Lerche H; Weber YG
    J Neurol; 2014 Oct; 261(10):1881-6. PubMed ID: 25022942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report.
    Scoppola C; Magli G; Conti M; Fadda M; Luzzu GM; Simula DM; Carta A; Sotgiu S; Casellato S
    Front Neurol; 2021; 12():679354. PubMed ID: 34135856
    [No Abstract]   [Full Text] [Related]  

  • 18. Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?
    Becker F; Schubert J; Weckhuysen S; Suls A; Grüninger S; Korn-Merker E; Hofmann-Peters A; Sperner J; Cross H; Hallmann K; Elger CE; Kunz WS; Madeleyen R; Lerche H; Weber YG
    Epilepsy Res; 2015 Aug; 114():47-51. PubMed ID: 26088884
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Occurrence of GLUT1 deficiency syndrome in patients treated with ketogenic diet.
    Ramm-Pettersen A; Nakken KO; Haavardsholm KC; Selmer KK
    Epilepsy Behav; 2014 Mar; 32():76-8. PubMed ID: 24508593
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
    Leen WG; Wevers RA; Kamsteeg EJ; Scheffer H; Verbeek MM; Willemsen MA
    JAMA Neurol; 2013 Nov; 70(11):1440-4. PubMed ID: 23999624
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.