336 related articles for article (PubMed ID: 25353328)
1. [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]
2. [Exercise and fasting induced movement disorder in children: think of the GLUT1 deficiency syndrome].
van Kan KEM; Panis B
Ned Tijdschr Geneeskd; 2018 Jul; 162():. PubMed ID: 30040286
[TBL] [Abstract][Full Text] [Related]
3. 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; 50(12):1025-6. PubMed ID: 25440161
[TBL] [Abstract][Full Text] [Related]
4. GLUT1 deficiency syndrome in clinical practice.
Klepper J
Epilepsy Res; 2012 Jul; 100(3):272-7. PubMed ID: 21382692
[TBL] [Abstract][Full Text] [Related]
5. Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
Klepper J
Epilepsia; 2008 Nov; 49 Suppl 8():46-9. PubMed ID: 19049586
[TBL] [Abstract][Full Text] [Related]
6. Towards a more palatable treatment for Glut1 deficiency syndrome.
Brockmann K
Dev Med Child Neurol; 2011 Jul; 53(7):580-1. PubMed ID: 21585366
[No 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. The glucose transporter type 1 (Glut1) syndromes.
Koch H; Weber YG
Epilepsy Behav; 2019 Feb; 91():90-93. PubMed ID: 30076047
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. [GLUT-1 deficiency syndrome].
Zavala M; Castillo V; Gonzalez M; Castillo S
Rev Neurol; 2019 Aug; 69(4):178-179. PubMed ID: 31334562
[TBL] [Abstract][Full Text] [Related]
12. GLUT1 deficiency syndrome 2013: current state of the art.
De Giorgis V; Veggiotti P
Seizure; 2013 Dec; 22(10):803-11. PubMed ID: 23890838
[TBL] [Abstract][Full Text] [Related]
13. Does ketogenic diet improve cognitive function in patients with GLUT1-DS? A 6- to 17-month follow-up study.
Ramm-Pettersen A; Stabell KE; Nakken KO; Selmer KK
Epilepsy Behav; 2014 Oct; 39():111-5. PubMed ID: 25240122
[TBL] [Abstract][Full Text] [Related]
14. 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;
Epilepsy Res; 2019 Aug; 154():39-41. PubMed ID: 31035243
[TBL] [Abstract][Full Text] [Related]
15. Long-term clinical course of Glut1 deficiency syndrome.
Alter AS; Engelstad K; Hinton VJ; Montes J; Pearson TS; Akman CI; De Vivo DC
J Child Neurol; 2015 Feb; 30(2):160-9. PubMed ID: 24789115
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Use of modified Atkins diet in glucose transporter type 1 deficiency syndrome.
Amalou S; Gras D; Ilea A; Greneche MO; Francois L; Bellavoine V; Delanoe C; Auvin S
Dev Med Child Neurol; 2016 Nov; 58(11):1193-1199. PubMed ID: 27273526
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. Intermittent Ataxia with Early Onset Absence Epilepsy in Glucose Transporter Type 1 Deficiency Syndrome.
Gowda VK; Sheshu S
Indian Pediatr; 2015 Nov; 52(11):997. PubMed ID: 26615362
[No Abstract] [Full Text] [Related]
[Next] [New Search]
