A citation-based method for searching scientific literature

D C De Vivo, R R Trifiletti, R I Jacobson, G M Ronen, R A Behmand, S I Harik. N Engl J Med 1991
Times Cited: 482







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



Times Cited
  Times     Co-cited
Similarity


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
24

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
23

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
194
20

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
27

GLUT1 deficiency syndrome in clinical practice.
Joerg Klepper. Epilepsy Res 2012
92
18

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
17

GLUT1 deficiency syndrome--2007 update.
Joerg Klepper, Baerbel Leiendecker. Dev Med Child Neurol 2007
150
17

Use of dietary therapies amongst patients with GLUT1 deficiency syndrome.
Hannah R Kass, S Parrish Winesett, Stacey K Bessone, Zahava Turner, Eric H Kossoff. Seizure 2016
60
25

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
14

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
14

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
14

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
13

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
12

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
17


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
14

GLUT1 deficiency syndrome 2013: current state of the art.
Valentina De Giorgis, Pierangelo Veggiotti. Seizure 2013
116
12

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group.
Joerg Klepper, Cigdem Akman, Marisa Armeno, Stéphane Auvin, Mackenzie Cervenka, Helen J Cross, Valentina De Giorgis, Adela Della Marina, Kristin Engelstad, Nicole Heussinger,[...]. Epilepsia Open 2020
39
30

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
11

The glucose transporter type 1 (Glut1) syndromes.
Henner Koch, Yvonne G Weber. Epilepsy Behav 2019
49
22

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
19

Failure of ketogenic diet therapy in GLUT1 deficiency syndrome.
Yvonne A C Bekker, Danielle A Lambrechts, Judith S Verhoeven, Jessy van Boxtel, Caroline Troost, Erik-Jan Kamsteeg, Michèl A Willemsen, Hilde M H Braakman. Eur J Paediatr Neurol 2019
14
78

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
11

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
10

Paroxysmal eye-head movements in Glut1 deficiency syndrome.
Toni S Pearson, Roser Pons, Kristin Engelstad, Steven A Kane, Michael E Goldberg, Darryl C De Vivo. Neurology 2017
22
45

From splitting GLUT1 deficiency syndromes to overlapping phenotypes.
Marie Hully, Sandrine Vuillaumier-Barrot, Christiane Le Bizec, Nathalie Boddaert, Anna Kaminska, Karine Lascelles, Pascale de Lonlay, Claude Cances, Vincent des Portes, Agathe Roubertie,[...]. Eur J Med Genet 2015
31
32

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
10

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
23

Clinical Aspects of Glucose Transporter Type 1 Deficiency: Information From a Global Registry.
Jian Hao, Dorothy I Kelly, Jianzhong Su, Juan M Pascual. JAMA Neurol 2017
13
76

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
12

Pericytes are required for blood-brain barrier integrity during embryogenesis.
Richard Daneman, Lu Zhou, Amanuel A Kebede, Ben A Barres. Nature 2010
9

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
15

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

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
19

Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group.
Eric H Kossoff, Beth A Zupec-Kania, Stéphane Auvin, Karen R Ballaban-Gil, A G Christina Bergqvist, Robyn Blackford, Jeffrey R Buchhalter, Roberto H Caraballo, J Helen Cross, Maria G Dahlin,[...]. Epilepsia Open 2018
203
9

Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.
Maoxue Tang, Guangping Gao, Carlos B Rueda, Hang Yu, David N Thibodeaux, Tomoyuki Awano, Kristin M Engelstad, Maria-Jose Sanchez-Quintero, Hong Yang, Fanghua Li,[...]. Nat Commun 2017
57
15

Pericytes regulate the blood-brain barrier.
Annika Armulik, Guillem Genové, Maarja Mäe, Maya H Nisancioglu, Elisabet Wallgard, Colin Niaudet, Liqun He, Jenny Norlin, Per Lindblom, Karin Strittmatter,[...]. Nature 2010
8

Evaluation of non-coding variation in GLUT1 deficiency.
Yu-Chi Liu, Jia Wei Audrey Lee, Susannah T Bellows, John A Damiano, Saul A Mullen, Samuel F Berkovic, Melanie Bahlo, Ingrid E Scheffer, Michael S Hildebrand. Dev Med Child Neurol 2016
16
50

The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.
Jan Larsen, Katrine Marie Johannesen, Jakob Ek, Shan Tang, Carla Marini, Susanne Blichfeldt, Maria Kibaek, Sarah von Spiczak, Sarah Weckhuysen, Mimoza Frangu,[...]. Epilepsia 2015
44
18

Atypical Manifestations in Glut1 Deficiency Syndrome.
V De Giorgis, C Varesio, C Baldassari, E Piazza, S Olivotto, J Macasaet, U Balottin, P Veggiotti. J Child Neurol 2016
19
42


Glut1 deficiency: when to suspect and how to diagnose?
A Verrotti, C D'Egidio, S Agostinelli, G Gobbi. Eur J Paediatr Neurol 2012
43
18

Outcome of ketogenic diets in GLUT1 deficiency syndrome in Japan: A nationwide survey.
Tatsuya Fujii, Yasushi Ito, Satoru Takahashi, Kuriko Shimono, Jun Natsume, Keiko Yanagihara, Hirokazu Oguni. Brain Dev 2016
25
32

Topography of brain glucose hypometabolism and epileptic network in glucose transporter 1 deficiency.
Cigdem Inan Akman, Frank Provenzano, Dong Wang, Kristin Engelstad, Veronica Hinton, Julia Yu, Ronald Tikofsky, Masonari Ichese, Darryl C De Vivo. Epilepsy Res 2015
20
40

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
23

Therapeutic strategies for glucose transporter 1 deficiency syndrome.
Maoxue Tang, Sarah H Park, Darryl C De Vivo, Umrao R Monani. Ann Clin Transl Neurol 2019
20
40

Structure and function of the blood-brain barrier.
N Joan Abbott, Adjanie A K Patabendige, Diana E M Dolman, Siti R Yusof, David J Begley. Neurobiol Dis 2010
7

Stepwise recruitment of transcellular and paracellular pathways underlies blood-brain barrier breakdown in stroke.
Daniel Knowland, Ahmet Arac, Kohei J Sekiguchi, Martin Hsu, Sarah E Lutz, John Perrino, Gary K Steinberg, Ben A Barres, Axel Nimmerjahn, Dritan Agalliu. Neuron 2014
303
7

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009.
Anne T Berg, Samuel F Berkovic, Martin J Brodie, Jeffrey Buchhalter, J Helen Cross, Walter van Emde Boas, Jerome Engel, Jacqueline French, Tracy A Glauser, Gary W Mathern,[...]. Epilepsia 2010
7

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
7


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.