A citation-based method for searching scientific literature

C Tranchant, M Anheim. Rev Neurol (Paris) 2016
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease.
Mika H Martikainen, Yi Shiau Ng, Gráinne S Gorman, Charlotte L Alston, Emma L Blakely, Andrew M Schaefer, Patrick F Chinnery, David J Burn, Robert W Taylor, Robert McFarland,[...]. JAMA Neurol 2016
44
19

Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, Fernando Scaglia, Gregory M Enns, Russell Saneto, Irina Anselm, Bruce H Cohen, Marni J Falk, Carol Greene,[...]. Genet Med 2015
221
12

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.
Gráinne S Gorman, Andrew M Schaefer, Yi Ng, Nicholas Gomez, Emma L Blakely, Charlotte L Alston, Catherine Feeney, Rita Horvath, Patrick Yu-Wai-Man, Patrick F Chinnery,[...]. Ann Neurol 2015
428
12

Mitochondrial diseases.
Gráinne S Gorman, Patrick F Chinnery, Salvatore DiMauro, Michio Hirano, Yasutoshi Koga, Robert McFarland, Anu Suomalainen, David R Thorburn, Massimo Zeviani, Douglass M Turnbull. Nat Rev Dis Primers 2016
522
12

Phenomenology and classification of dystonia: a consensus update.
Alberto Albanese, Kailash Bhatia, Susan B Bressman, Mahlon R Delong, Stanley Fahn, Victor S C Fung, Mark Hallett, Joseph Jankovic, Hyder A Jinnah, Christine Klein,[...]. Mov Disord 2013
12

Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.
Maria Andrea Desbats, Giada Lunardi, Mara Doimo, Eva Trevisson, Leonardo Salviati. J Inherit Metab Dis 2015
125
12

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.
Niccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, Friedrich Asmus, Marthe H R Ludtmann, Mina Ryten, Vincent Plagnol, Ann-Kathrin Hauser, Sara Bandres-Ciga, Conceição Bettencourt,[...]. Am J Hum Genet 2015
69
12

[A case of MELAS presenting juvenile-onset hyperglycemic chorea-ballism].
Hideaki Nakagaki, Jun-ichiro Furuya, Yo Santa, Sukehisa Nagano, Eiichi Araki, Takeshi Yamada. Rinsho Shinkeigaku 2005
13
23

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.
Matthew G D Bates, John P Bourke, Carla Giordano, Giulia d'Amati, Douglass M Turnbull, Robert W Taylor. Eur Heart J 2012
125
9

Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.
M A Grönlund, A K Seyedi Honarvar, S Andersson, A R Moslemi, A Oldfors, E Holme, M Tulinius, N Darin. Br J Ophthalmol 2010
55
9

Mitochondrial Cardiomyopathies.
Ayman W El-Hattab, Fernando Scaglia. Front Cardiovasc Med 2016
86
9

Sleep disorders associated with primary mitochondrial diseases.
Ryan J Ramezani, Peter W Stacpoole. J Clin Sleep Med 2014
21
14

A randomized placebo-controlled trial of idebenone in Leber's hereditary optic neuropathy.
Thomas Klopstock, Patrick Yu-Wai-Man, Konstantinos Dimitriadis, Jacinthe Rouleau, Suzette Heck, Maura Bailie, Alaa Atawan, Sandip Chattopadhyay, Marion Schubert, Aylin Garip,[...]. Brain 2011
267
9

Mitochondrial respiratory-chain diseases.
Salvatore DiMauro, Eric A Schon. N Engl J Med 2003
9

Ophthalmological findings in 74 patients with mitochondrial disease.
Cheng-Cheng Zhu, Elias I Traboulsi, Sumit Parikh. Ophthalmic Genet 2017
27
11

Familial parkinsonism and ophthalmoplegia from a mutation in the mitochondrial DNA helicase twinkle.
Robert H Baloh, Ezequiel Salavaggione, Jeffrey Milbrandt, Alan Pestronk. Arch Neurol 2007
72
9

Spectrum of mutations in Chinese children with steroid-resistant nephrotic syndrome.
Fang Wang, Yanqin Zhang, Jianhua Mao, Zihua Yu, Zhuwen Yi, Li Yu, Jun Sun, Xiuxiu Wei, Fangrui Ding, Hongwen Zhang,[...]. Pediatr Nephrol 2017
53
9

Early-onset of ADCK4 glomerulopathy with renal failure: a case report.
Ksenija Lolin, Benedetta D Chiodini, Elise Hennaut, Brigitte Adams, Karin Dahan, Khalid Ismaili. BMC Med Genet 2017
12
25

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.
Shazia Ashraf, Heon Yung Gee, Stephanie Woerner, Letian X Xie, Virginia Vega-Warner, Svjetlana Lovric, Humphrey Fang, Xuewen Song, Daniel C Cattran, Carmen Avila-Casado,[...]. J Clin Invest 2013
206
9

Mutations causing mitochondrial disease: What is new and what challenges remain?
Robert N Lightowlers, Robert W Taylor, Doug M Turnbull. Science 2015
179
9

ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS.
Emine Korkmaz, Beata S Lipska-Ziętkiewicz, Olivia Boyer, Olivier Gribouval, Cecile Fourrage, Mansoureh Tabatabaei, Sven Schnaidt, Safak Gucer, Figen Kaymaz, Mustafa Arici,[...]. J Am Soc Nephrol 2016
50
9

Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society.
Kailash P Bhatia, Peter Bain, Nin Bajaj, Rodger J Elble, Mark Hallett, Elan D Louis, Jan Raethjen, Maria Stamelou, Claudia M Testa, Guenther Deuschl. Mov Disord 2018
434
9

Movement disorders in mitochondrial disease.
Roula Ghaoui, Carolyn M Sue. J Neurol 2018
21
14

Movement disorders and inborn errors of metabolism in adults: a diagnostic approach.
F Sedel, J-M Saudubray, E Roze, Y Agid, M Vidailhet. J Inherit Metab Dis 2008
46
9


Movement Disorders in Treatable Inborn Errors of Metabolism.
Darius Ebrahimi-Fakhari, Clara Van Karnebeek, Alexander Münchau. Mov Disord 2019
24
12

Myoclonus in mitochondrial disorders.
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Michela Catteruccia, Elena Pegoraro, Valerio Carelli, Maria L Valentino, Giacomo P Comi, Carlo Minetti,[...]. Mov Disord 2014
27
7

The genetics and pathology of mitochondrial disease.
Charlotte L Alston, Mariana C Rocha, Nichola Z Lax, Doug M Turnbull, Robert W Taylor. J Pathol 2017
194
6

MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins.
Sarah E Calvo, Karl R Clauser, Vamsi K Mootha. Nucleic Acids Res 2016
786
6

Prevalence of mitochondrial DNA disease in adults.
Andrew M Schaefer, Robert McFarland, Emma L Blakely, Langping He, Roger G Whittaker, Robert W Taylor, Patrick F Chinnery, Douglass M Turnbull. Ann Neurol 2008
386
6


Diagnosis and treatment of chronic intestinal pseudo-obstruction in children: report of consensus workshop.
C D Rudolph, P E Hyman, S M Altschuler, J Christensen, R B Colletti, S Cucchiara, C Di Lorenzo, A F Flores, A C Hillemeier, R W McCallum,[...]. J Pediatr Gastroenterol Nutr 1997
115
6

Predisposition to infection and SIRS in mitochondrial disorders: 8 years' experience in an academic center.
Melissa A Walker, Nancy Slate, Alexandra Alejos, Stefano Volpi, Rajashri S Iyengar, David Sweetser, Katherine B Sims, Jolan E Walter. J Allergy Clin Immunol Pract 2014
22
9

Renal pathology in children with mitochondrial diseases.
Elena Martín-Hernández, M Teresa García-Silva, Julia Vara, Yolanda Campos, Ana Cabello, Rafael Muley, Pilar Del Hoyo, Miguel Angel Martín, Joaquín Arenas. Pediatr Nephrol 2005
73
6

"Mitochondrial neuropathies": A survey from the large cohort of the Italian Network.
Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, Enrico Bertini, Valerio Carelli, Giacomo Pietro Comi, Antonio Federico, Carlo Minetti, Maurizio Moggio, Tiziana Mongini,[...]. Neuromuscul Disord 2016
31
6

Characteristic cardiac phenotypes are detected by cardiovascular magnetic resonance in patients with different clinical phenotypes and genotypes of mitochondrial myopathy.
Anca Florian, Anna Ludwig, Bianca Stubbe-Dräger, Matthias Boentert, Peter Young, Johannes Waltenberger, Sabine Rösch, Udo Sechtem, Ali Yilmaz. J Cardiovasc Magn Reson 2015
33
6

Mitochondrial disease--an important cause of end-stage renal failure.
Shamima Rahman, Andrew M Hall. Pediatr Nephrol 2013
20
10

Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease.
Manoj P Menezes, Shamima Rahman, Kaustuv Bhattacharya, Damian Clark, John Christodoulou, Carolyn Ellaway, Michelle Farrar, Matthew Pitt, Hugo Sampaio, Tyson L Ware,[...]. Mitochondrion 2016
8
25

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
Ayman W El-Hattab, Adekunle M Adesina, Jeremy Jones, Fernando Scaglia. Mol Genet Metab 2015
250
6

Treatment for mitochondrial disorders.
Gerald Pfeffer, Kari Majamaa, Douglass M Turnbull, David Thorburn, Patrick F Chinnery. Cochrane Database Syst Rev 2012
221
6


Mitochondrial diseases and epilepsy.
Laurence A Bindoff, Bernt A Engelsen. Epilepsia 2012
60
6

Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases.
Karim Wahbi, Wulfran Bougouin, Anthony Béhin, Tanya Stojkovic, Henri Marc Bécane, Claude Jardel, Nawal Berber, Fanny Mochel, Anne Lombès, Bruno Eymard,[...]. Eur Heart J 2015
43
6

Endocrine disorders in mitochondrial disease.
Andrew M Schaefer, Mark Walker, Douglass M Turnbull, Robert W Taylor. Mol Cell Endocrinol 2013
57
6

Mitochondrial neuropathy: considerations on pathogenesis.
M Luigetti, D Sauchelli, G Primiano, C Cuccagna, D Bernardo, M Lo Monaco, S Servidei. Eur J Neurol 2016
3
66

Mitochondrial disease and epilepsy.
Shamima Rahman. Dev Med Child Neurol 2012
90
6

Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
Judith Altmann, Boriana Büchner, Aleksandra Nadaj-Pakleza, Jochen Schäfer, Sandra Jackson, Diana Lehmann, Marcus Deschauer, Robert Kopajtich, Ronald Lautenschläger, Klaus A Kuhn,[...]. J Neurol 2016
48
6

Pseudo-obstruction, stroke, and mitochondrial dysfunction: A lethal combination.
Yi Shiau Ng, Catherine Feeney, Andrew M Schaefer, Carol Ellen Holmes, Paula Hynd, Charlotte L Alston, John P Grady, Mark Roberts, Mellisa Maguire, Alexandra Bright,[...]. Ann Neurol 2016
18
11

Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathy.
T Klopstock, G Metz, P Yu-Wai-Man, B Büchner, C Gallenmüller, M Bailie, N Nwali, P G Griffiths, B von Livonius, L Reznicek,[...]. Brain 2013
110
6

Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation.
Ayman W El-Hattab, Lisa T Emrick, Jean W Hsu, Sirisak Chanprasert, Farook Jahoor, Fernando Scaglia, William J Craigen. Mitochondrion 2014
25
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.