352 related articles for article (PubMed ID: 25914049)
1. Favourable response to ketogenic dietary therapies: undiagnosed glucose 1 transporter deficiency syndrome is only one factor.
Schoeler NE; Cross JH; Drury S; Lench N; McMahon JM; MacKay MT; Scheffer IE; Sander JW; Sisodiya SM
Dev Med Child Neurol; 2015 Oct; 57(10):969-76. PubMed ID: 25914049
[TBL] [Abstract][Full Text] [Related]
2. 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; 13(3):. PubMed ID: 33806661
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [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]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. 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]
8. 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
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. GLUT1 deficiency syndrome and ketogenic diet therapies: missing rare but treatable diseases?
Klepper J
Dev Med Child Neurol; 2015 Oct; 57(10):896-7. PubMed ID: 25997718
[No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome.
Gumus H; Bayram AK; Kardas F; Canpolat M; Çağlayan AO; Kumandas S; Kendirci M; Per H
Neuropediatrics; 2015 Oct; 46(5):313-20. PubMed ID: 26267703
[TBL] [Abstract][Full Text] [Related]
15. Clinical reasoning: novel GLUT1-DS mutation: refractory seizures and ataxia.
Sen S; Keough K; Gibson J
Neurology; 2015 Apr; 84(15):e111-4. PubMed ID: 25870456
[TBL] [Abstract][Full Text] [Related]
16. Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome.
Ivanova N; Peycheva V; Kamenarova K; Kancheva D; Tsekova I; Aleksandrova I; Hristova D; Litvinenko I; Todorova D; Sarailieva G; Dimova P; Tomov V; Bozhinova V; Mitev V; Kaneva R; Jordanova A
Seizure; 2018 Jan; 54():41-44. PubMed ID: 29223885
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C.
Çolak R; Alkan Özdemir S; Yangın Ergon E; Kağnıcı M; Çalkavur Ş
Balkan Med J; 2017 Dec; 34(6):580-583. PubMed ID: 28443597
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
