A citation-based method for searching scientific literature

Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.
Dong Wang, Juan M Pascual, Hong Yang, Kristin Engelstad, Sarah Jhung, Ruo Peng Sun, Darryl C De Vivo. Ann Neurol 2005
Times Cited: 194






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List of co-cited articles
522 articles co-cited >1



Times Cited
  Times     Co-cited
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Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay.
D C De Vivo, R R Trifiletti, R I Jacobson, G M Ronen, R A Behmand, S I Harik. N Engl J Med 1991
482
55
55

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Wilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, Maike Leferink, Tom Hofste, Baziel G van Engelen, Ron A Wevers, Todd Arthur, Nadia Bahi-Buisson, Diana Ballhausen,[...]. Brain 2010
223
42
42

GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier.
G Seidner, M G Alvarez, J I Yeh, K R O'Driscoll, J Klepper, T S Stump, D Wang, N B Spinner, M J Birnbaum, D C De Vivo. Nat Genet 1998
264
36
36

Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.
Arvid Suls, Peter Dedeken, Karolien Goffin, Hilde Van Esch, Patrick Dupont, David Cassiman, Judith Kempfle, Thomas V Wuttke, Yvonne Weber, Holger Lerche,[...]. Brain 2008
208
26
26

The expanding phenotype of GLUT1-deficiency syndrome.
Knut Brockmann. Brain Dev 2009
148
26
26

GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak.
Yvonne G Weber, Alexander Storch, Thomas V Wuttke, Knut Brockmann, Judith Kempfle, Snezana Maljevic, Lucia Margari, Christoph Kamm, Susanne A Schneider, Stephan M Huber,[...]. J Clin Invest 2008
234
25
25

Phenotypic spectrum of glucose transporter type 1 deficiency syndrome (Glut1 DS).
Toni S Pearson, Cigdem Akman, Veronica J Hinton, Kristin Engelstad, Darryl C De Vivo. Curr Neurol Neurosci Rep 2013
118
24
24

The spectrum of movement disorders in Glut-1 deficiency.
Roser Pons, Abbie Collins, Michael Rotstein, Kristin Engelstad, Darryl C De Vivo. Mov Disord 2010
96
22
22

GLUT1 deficiency syndrome--2007 update.
Joerg Klepper, Baerbel Leiendecker. Dev Med Child Neurol 2007
150
21
21

Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency.
S A Mullen, A Suls, P De Jonghe, S F Berkovic, I E Scheffer. Neurology 2010
117
19
19

Imaging the metabolic footprint of Glut1 deficiency on the brain.
Juan M Pascual, Ronald L Van Heertum, Dong Wang, Kristin Engelstad, Darryl C De Vivo. Ann Neurol 2002
97
19
19

Seizure characterization and electroencephalographic features in Glut-1 deficiency syndrome.
Linda D Leary, Dong Wang, Douglas R Nordli, Kristin Engelstad, Darryl C De Vivo. Epilepsia 2003
89
19
21

Glut1 deficiency syndrome and erythrocyte glucose uptake assay.
Hong Yang, Dong Wang, Kristin Engelstad, Leslie Bagay, Ying Wei, Michael Rotstein, Vimla Aggarwal, Brynn Levy, Lijiang Ma, Wendy K Chung,[...]. Ann Neurol 2011
57
18
31

GLUT1 deficiency syndrome 2013: current state of the art.
Valentina De Giorgis, Pierangelo Veggiotti. Seizure 2013
116
18
18

Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.
K Brockmann, D Wang, C G Korenke, A von Moers, Y Y Ho, J M Pascual, K Kuang, H Yang, L Ma, P Kranz-Eble,[...]. Ann Neurol 2001
114
17
17

Glut1 deficiency: inheritance pattern determined by haploinsufficiency.
Michael Rotstein, Kristin Engelstad, Hong Yang, Dong Wang, Brynn Levy, Wendy K Chung, Darryl C De Vivo. Ann Neurol 2010
57
17
29

Glucose transporter type I deficiency syndrome: epilepsy phenotypes and outcomes.
Amanda W Pong, Brianna R Geary, Kris M Engelstad, Ashwini Natarajan, Hong Yang, Darryl C De Vivo. Epilepsia 2012
85
17
20

Seizure control and acceptance of the ketogenic diet in GLUT1 deficiency syndrome: a 2- to 5-year follow-up of 15 children enrolled prospectively.
J Klepper, H Scheffer, B Leiendecker, E Gertsen, S Binder, M Leferink, C Hertzberg, A Näke, T Voit, M A Willemsen. Neuropediatrics 2005
93
16
17

A mouse model for Glut-1 haploinsufficiency.
Dong Wang, Juan M Pascual, Hong Yang, Kristin Engelstad, Xia Mao, Jianfeng Cheng, Jong Yoo, Jeffrey L Noebels, Darryl C De Vivo. Hum Mol Genet 2006
129
16
16

GLUT1 deficiency syndrome in clinical practice.
Joerg Klepper. Epilepsy Res 2012
92
16
17

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies.
Todor Arsov, Saul A Mullen, Sue Rogers, A Marie Phillips, Kate M Lawrence, John A Damiano, Hadassa Goldberg-Stern, Zaid Afawi, Sara Kivity, Chantal Trager,[...]. Ann Neurol 2012
82
16
19

Autosomal dominant transmission of GLUT1 deficiency.
J Klepper, M Willemsen, A Verrips, E Guertsen, R Herrmann, C Kutzick, A Flörcken, T Voit. Hum Mol Genet 2001
77
15
19

Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiency.
Mathieu Anheim, Elisabeth Maillart, Sandrine Vuillaumier-Barrot, Constance Flamand-Rouvière, Fanny Pineau, Claire Ewenczyk, Florence Riant, Emmanuelle Apartis, Emmanuel Roze. J Neurol 2011
33
13
39

Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1.
Arvid Suls, Saul A Mullen, Yvonne G Weber, Kristien Verhaert, Berten Ceulemans, Renzo Guerrini, Thomas V Wuttke, Alberto Salvo-Vargas, Liesbet Deprez, Lieve R F Claes,[...]. Ann Neurol 2009
161
13
13

Atypical GLUT1 deficiency with prominent movement disorder responsive to ketogenic diet.
Jennifer R L Friedman, Elizabeth A Thiele, Dong Wang, Kara B Levine, Erin K Cloherty, Heidi H Pfeifer, Darryl C De Vivo, Anthony Carruthers, Marvin R Natowicz. Mov Disord 2006
58
12
20

GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.
Susanne A Schneider, Coro Paisan-Ruiz, Ines Garcia-Gorostiaga, Niall P Quinn, Yvonne G Weber, Holger Lerche, John Hardy, Kailash P Bhatia. Mov Disord 2009
72
12
16

Paroxysmal movement disorders in GLUT1 deficiency syndrome.
G Zorzi, B Castellotti, F Zibordi, C Gellera, N Nardocci. Neurology 2008
50
12
24

Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet.
Jörg Klepper. Epilepsia 2008
88
12
13

Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency.
Todor Arsov, Saul A Mullen, John A Damiano, Kate M Lawrence, Linda L Huh, Melinda Nolan, Helen Young, Anaïs Thouin, Hans-Henrik M Dahl, Samuel F Berkovic,[...]. Epilepsia 2012
67
12
17

Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.
D Wang, P Kranz-Eble, D C De Vivo. Hum Mutat 2000
106
11
11

GLUT-1 deficiency without epilepsy--an exceptional case.
W C G Overweg-Plandsoen, J E M Groener, D Wang, W Onkenhout, O F Brouwer, H D Bakker, D C De Vivo. J Inherit Metab Dis 2003
42
11
26

Autosomal recessive inheritance of GLUT1 deficiency syndrome.
J Klepper, H Scheffer, M F Elsaid, E-J Kamsteeg, M Leferink, T Ben-Omran. Neuropediatrics 2009
34
11
32

Glut1 deficiency: when to suspect and how to diagnose?
A Verrotti, C D'Egidio, S Agostinelli, G Gobbi. Eur J Paediatr Neurol 2012
43
11
25

Long-term clinical course of Glut1 deficiency syndrome.
Aliza S Alter, Kristin Engelstad, Veronica J Hinton, Jacqueline Montes, Toni S Pearson, Cigdem I Akman, Darryl C De Vivo. J Child Neurol 2015
47
11
23

A modified Atkins diet is promising as a treatment for glucose transporter type 1 deficiency syndrome.
Yasushi Ito, Hirokazu Oguni, Susumu Ito, Miyako Oguni, Makiko Osawa. Dev Med Child Neurol 2011
57
10
17

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect.
Y G Weber, C Kamm, A Suls, J Kempfle, K Kotschet, R Schüle, T V Wuttke, S Maljevic, J Liebrich, T Gasser,[...]. Neurology 2011
59
10
16

Good outcome in patients with early dietary treatment of GLUT-1 deficiency syndrome: results from a retrospective Norwegian study.
Anette Ramm-Pettersen, Karl O Nakken, Inger M Skogseid, Hans Randby, Erik B Skei, Laurence A Bindoff, Kaja K Selmer. Dev Med Child Neurol 2013
42
10
23

Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.
Wilhelmina G Leen, Ron A Wevers, Erik-Jan Kamsteeg, Hans Scheffer, Marcel M Verbeek, Michèl A Willemsen. JAMA Neurol 2013
66
10
15

GLUT1 deficiency syndrome into adulthood: a follow-up study.
W G Leen, M Taher, M M Verbeek, E J Kamsteeg, B P van de Warrenburg, M A Willemsen. J Neurol 2014
47
10
21

Modified Atkins diet therapy for a case with glucose transporter type 1 deficiency syndrome.
Susumu Ito, Hirokazu Oguni, Yasushi Ito, Keiko Ishigaki, Junko Ohinata, Makiko Osawa. Brain Dev 2008
36
9
25

Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome.
Jörg Klepper, Sonja Diefenbach, Alfried Kohlschütter, Thomas Voit. Prostaglandins Leukot Essent Fatty Acids 2004
76
9
11

Glucose transporter 1 deficiency syndrome and other glycolytic defects.
Darryl C De Vivo, Linda Leary, Dong Wang. J Child Neurol 2002
66
9
13

Sequence and structure of a human glucose transporter.
M Mueckler, C Caruso, S A Baldwin, M Panico, I Blench, H R Morris, W J Allard, G E Lienhard, H F Lodish. Science 1985
1351
9
9

Brain glucose supply and the syndrome of infantile neuroglycopenia.
Juan M Pascual, Dong Wang, Veronica Hinton, Kristin Engelstad, Chitra M Saxena, Ronald L Van Heertum, Darryl C De Vivo. Arch Neurol 2007
31
9
29

Glut1 deficiency syndrome and novel ketogenic diets.
Joerg Klepper, Baerbel Leiendecker. J Child Neurol 2013
39
9
23

GLUT1 reductions exacerbate Alzheimer's disease vasculo-neuronal dysfunction and degeneration.
Ethan A Winkler, Yoichiro Nishida, Abhay P Sagare, Sanket V Rege, Robert D Bell, David Perlmutter, Jesse D Sengillo, Sara Hillman, Pan Kong, Amy R Nelson,[...]. Nat Neurosci 2015
325
9
9

Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome.
J Klepper, M Garcia-Alvarez, K R O'Driscoll, M K Parides, D Wang, Y Y Ho, D C De Vivo. J Clin Lab Anal 1999
63
8
12

Glut1 deficiency (G1D): epilepsy and metabolic dysfunction in a mouse model of the most common human phenotype.
Isaac Marin-Valencia, Levi B Good, Qian Ma, Joao Duarte, Teodoro Bottiglieri, Christopher M Sinton, Charles W Heilig, Juan M Pascual. Neurobiol Dis 2012
37
8
21

GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy.
P Striano, Y G Weber, M R Toliat, J Schubert, C Leu, R Chaimana, S Baulac, R Guerrero, E LeGuern, A-E Lehesjoki,[...]. Neurology 2012
62
8
12

Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.
Saul A Mullen, Carla Marini, Arvid Suls, Davide Mei, Elvio Della Giustina, Daniela Buti, Todor Arsov, John Damiano, Kate Lawrence, Peter De Jonghe,[...]. Arch Neurol 2011
89
8
8


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.

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