Malalties Neuromusculars

Almodóvar-Payá A, Villarreal-Salazar M, de Luna N, Nogales-Gadea G, Real-Martínez A, Andreu AL, Martín MA, Arenas J, Lucia A, Vissing J, Krag T, Pinós T. Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models. INT J MOL SCI. 2020 Dec 17;21(24):9621. doi: 10.3390/ijms21249621. PMID: 33348688.

IF: 5,9230

Alonso-Perez J., Segovia S., Dominguez-Gonzalez C., Olive M., Mendoza Grimon M.D., Fernandez-Torron R., Lopez de Munain A., Munoz-Blanco J.L., Ramos-Fransi A., Almendrote M., Illa I., Diaz-Manera J. (2020) Spanish Pompe registry: Baseline characteristics of first 49 patients with adult onset of Pompe disease Registro español de la enfermedad de Pompe: análisis de los primeros 49 pacientes con enfermedad de Pompe del adulto. MED CLIN-BARCELONA, 154 (3), 80-85.

IF: 1,7250

Alonso-Perez J., Gonzalez-Quereda L., Bello L., Guglieri M., Straub V., Gallano P., Semplicini C., Pegoraro E., Zangaro V., Nascimento A., Ortez C., Comi G.P., Dam L.T., De Visser M., van der Kooi A.J., Garrido C., Santos M., Schara U., Gangfuss A., Lokken N., Storgaard J.H., Vissing J., Schoser B., Dekomien G., Udd B., Palmio J., D'Amico A., Politano L., Nigro V., Bruno C., Panicucci C., Sarkozy A., Abdel-Mannan O., Alonso-Jimenez A., Claeys K.G., Gomez-Andres D., Munell F., Costa-Comellas L., Haberlova J., Rohlenova M., Elke V., De Bleecker J.L., Dominguez-Gonzalez C., Tasca G., Weiss C., Deconinck N., Fernandez-Torron R., Lopez de Munain A., Camacho-Salas A., Melegh B., Hadzsiev K., Leonardis L., Koritnik B., Garibaldi M., de Leon-Hernandez J.C., Malfatti E., Fraga-Bau A., Richard I., Illa I., Diaz-Manera J. (2020) New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy. BRAIN, 143 (9), 2696-2708.

IF: 13,5010

Athanasopoulos D., Motte J., Fisse A.L., Grueter T., Trampe N., Sturm D., Tegenthoff M., Sgodzai M., Klimas R., Querol L., Gold R., Pitarokoili K. (2020) Longitudinal study on nerve ultrasound and corneal confocal microscopy in NF155 paranodopathy. ANN CLIN TRANSL NEUR, 7 (6), 1061-1068.

IF: 4,5110

Barp A., Laforet P., Bello L., Tasca G., Vissing J., Monforte M., Ricci E., Choumert A., Stojkovic T., Malfatti E., Pegoraro E., Semplicini C., Stramare R., Scheidegger O., Haberlova J., Straub V., Marini-Bettolo C., Lokken N., Diaz-Manera J., Urtizberea J.A., Mercuri E., Kyncl M., Walter M.C., Carlier R.Y. (2020) European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A). J NEUROL, 267 (1), 45-56.

IF: 4,8490

Cortes-Vicente E., Alvarez-Velasco R., Segovia S., Paradas C., Casasnovas C., Guerrero-Sola A., Pardo J., Ramos-Fransi A., Sevilla T., Lopez de Munain A., Gomez M.T., Jerico I., Gutierrez-Gutierrez G., Pelayo-Negro A.L., Martin M.A., Mendoza M.D., Moris G., Rojas-Garcia R., Diaz-Manera J., Querol L., Gallardo E., Velez B., Alberti M.A., Galan L., Garcia-Sobrino T., Martinez-Pineiro A., Lozano-Veintimilla A., Fernandez-Torron R., Cano-Abascal A., Illa I. (2020) Clinical and therapeutic features of myasthenia gravis in adults based on age at onset. NEUROLOGY, 94 (11), e1171-e1180.

IF: 9,9100

Cortes-Vicente E., Gallardo E., Alvarez-Velasco R., Illa I. (2020) Myasthenia Gravis Treatment Updates. CURR TREAT OPTION NE, 22 (8), -.

IF: 3,5980

De Luna N., Turon-Sans J., Cortes-Vicente E., Carrasco-Rozas A., Illan-Gala I., Dols-Icardo O., Clarimon J., Lleo A., Gallardo E., Illa I., Rojas-Garcia R. (2020) Downregulation of miR-335-5P in Amyotrophic Lateral Sclerosis Can Contribute to Neuronal Mitochondrial Dysfunction and Apoptosis. SCI REP-UK, 10 (1), -.

IF: 4,3790

De Simoni D, Ricken G, Winklehner M, Koneczny I, Karenfort M, Hustedt U, Seidel U, Abdel-Mannan O, Munot P, Rinaldi S, Steen C, Freilinger M, Breu M, Seidl R, Reindl M, Wanschitz J, Lleixà C, Bernert G, Wandinger KP, Junker R, Querol L, Leypoldt F, Rostásy K, Höftberger R. Antibodies to nodal/paranodal proteins in paediatric immune-mediated neuropathy. NEUROL-NEUROIMMUNOL. 2020 Jun 2;7(4):e763. PMID: 32487720.

IF: 8,4850

Delaby C., Alcolea D., Carmona-Iragui M., Illan-Gala I., Morenas-Rodriguez E., Barroeta I., Altuna M., Estelles T., Santos-Santos M., Turon-Sans J., Munoz L., Ribosa-Nogue R., Sala-Matavera I., Sanchez-Saudinos B., Subirana A., Videla L., Benejam B., Sirisi S., Lehmann S., Belbin O., Clarimon J., Blesa R., Pagonabarraga J., Rojas-Garcia R., Fortea J., Lleo A. (2020) Differential levels of Neurofilament Light protein in cerebrospinal fluid in patients with a wide range of neurodegenerative disorders. SCI REP-UK, 10 (1), -.

IF: 4,3790

Dols-Icardo O., Montal V., Sirisi S., Lopez-Pernas G., Cervera-Carles L., Querol-Vilaseca M., Munoz L., Belbin O., Alcolea D., Molina-Porcel L., Pegueroles J., Turon-Sans J., Blesa R., Lleo A., Fortea J., Rojas-Garcia R., Clarimon J. (2020) Motor cortex transcriptome reveals microglial key events in amyotrophic lateral sclerosis. NEUROL-NEUROIMMUNOL, 7 (5), -.

IF: 8,4850

Dominguez-Gonzalez C., Badosa C., Madruga-Garrido M., Marti I., Paradas C., Ortez C., Diaz-Manera J., Berardo A., Alonso-Perez J., Trifunov S., Cuadras D., Kalko S.G., Blazquez-Bermejo C., Camara Y., Marti R., Mavillard F., Martin M.A., Montoya J., Ruiz-Pesini E., Villarroya J., Montero R., Villarroya F., Artuch R., Hirano M., Nascimento A., Jimenez-Mallebrera C. (2020) Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy. SCI REP-UK, 10 (1), -.

IF: 4,3790

Eftimov F, Lucke IM, Querol LA, Rajabally YA, Verhamme C. Diagnostic challenges in chronic inflammatory demyelinatingpolyradiculoneuropathy. BRAIN. 2020 Dec 5;143(11):3214-3224. PMID: 33155018.

IF: 13,5010

Fernandez-Eulate G., Fernandez-Torron R., Guisasola A., Gaspar M.T.I., Diaz-Manera J., Maneiro M., Zulaica M., Olasagasti V., Formica A.F., Espinal J.B., Ruiz M., Schluter A., Pujol A., Poza J.J., Lopez de Munain A. (2020) Phenotypic correlations in a large single-center cohort of patients with BSCL2 nerve disorders: a clinical, neurophysiological and muscle magnetic resonance imaging study. EUR J NEUROL, (), -.

IF: 6,0890

Fernández-Simón E, Lleixà C, Suarez-Calvet X, Diaz-Manera J, Illa I, Gallardo E, de Luna N. Proteasome inhibitors reduce thrombospondin-1 release in human dysferlin-deficient myotubes. BMC MUSCULOSKEL DIS. 2020 Nov 27;21(1):784. doi: 10.1186/s12891-020-03756-7. PMID: 33246442.

IF: 2,3620

Fionda L, Turon-Sans J, Fuentes Prior P, Bernal Noguera S, Cortés-Vicente E, López-Pérez MA, Gallardo E, Rojas-García R. A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular junction dysfunction? J PERIPHER NERV SYST. 2020 Dec 15. doi: 10.1111/jns.12425. Online ahead of print. PMID: 33320396.

IF: 3,4940

Giacomucci G., Monforte M., Diaz-Manera J., Mul K., Fernandez Torron R., Maggi L., Marini Bettolo C., Dahlqvist J.R., Haberlova J., Camano P., Gros M., Tartaglione T., Cristiano L., Gerevini S., Calandra P., Deidda G., Giardina E., Sacconi S., Straub V., Vissing J., Van Engelen B., Ricci E., Tasca G. (2020) Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging. EUR J NEUROL, 27 (12), 2604-2615.

IF: 6,0890

Gonzalez-Quereda L, Rodriguez MJ, Diaz-Manera J, Alonso-Perez J, Gallardo E, Nascimento A, Ortez C, Natera-de Benito D, Olive M, Gonzalez-Mera L, Munain AL, Zulaica M, Poza JJ, Jerico I, Torne L, Riera P, Milisenda J, Sanchez A, Garrabou G, Llano I, Madruga-Garrido M, Gallano P. Targeted Next-Generation Sequencing in a Large Cohort of Genetically Undiagnosed Patients with Neuromuscular Disorders in Spain. GENES-BASEL. 2020 May 11;11(5):539. doi: 10.3390/genes11050539. PMID: 32403337.

IF: 4,0960

Gutierrez Gutierrez G., Diaz-Manera J., Almendrote M., Azriel S., Eulalio Barcena J., Cabezudo Garcia P., Camacho Salas A., Casanova Rodriguez C., Cobo A.M., Diaz Guardiola P., Fernandez-Torron R., Gallano Petit M.P., Garcia Pavia P., Gomez Gallego M., Gutierrez Martinez A.J., Jerico I., Kapetanovic Garcia S., Lopez de Munain Arregui A., Martorell L., Moris de la Tassa G., Moreno Zabaleta R., Munoz-Blanco J.L., Olivar Roldan J., Pascual Pascual S.I., Peinado Peinado R., Perez H., Poza Aldea J.J., Rabasa M., Ramos A., Rosado Bartolome A., Rubio Perez M.A., Urtizberea J.A., Zapata-Wainberg G., Gutierrez-Rivas E. (2020) Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert. NEUROLOGIA, 35 (3), 185-206.

IF: 3,1090

Illán-Gala I, Montal V, Pegueroles J, Vilaplana E, Alcolea D, Dols-Icardo O, de Luna N, Turón-Sans J, Cortés-Vicente E, Martinez-Roman L, Sánchez-Saudinós MB, Subirana A, Videla L, Sala I, Barroeta I, Valldeneu S, Blesa R, Clarimón J, Lleó A, Fortea J, Rojas-García R. Cortical microstructure in the amyotrophic lateral sclerosis-frontotemporal dementia continuum. NEUROLOGY. 2020 Nov 3;95(18):e2565-e257. PMID: 32913016.

IF: 9,9100

Jacob S., Muppidi S., Guidon A., Guptill J., Hehir M., Howard J.F., Illa I., Mantegazza R., Murai H., Utsugisawa K., Vissing J., Wiendl H., Nowak R.J. (2020) Guidance for the management of myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) during the COVID-19 pandemic. J NEUROL SCI, 412 (), -.

IF: 3,1810

Martel-Duguech L., Alonso-Jimenez A., Bascunana H., Diaz-Manera J., Llauger J., Nunez-Peralta C., Biagetti B., Montesinos P., Webb S.M., Valassi E. (2020) Thigh muscle fat infiltration is associated with impaired physical performance despite remission in Cushing’s syndrome. J CLIN ENDOCR METAB, 105 (5), -.

IF: 5,9580

Martín-Aguilar L, Camps-Renom P, Lleixà C, Pascual-Goñi E, Díaz-Manera J, Rojas-García R, De Luna N, Gallardo E, Cortés-Vicente E, Muñoz L, Alcolea D, Lleó A, Casasnovas C, Homedes C, Gutiérrez-Gutiérrez G, et al. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barré syndrome patients. J NEUROL NEUROSUR PS. 2020 Nov 5:jnnp-2020-323899. doi: 10.1136/jnnp-2020-323899. Online ahead of print. PMID: 33154183.

IF: 10,1540

Martin-Aguilar L., Pascual-Goni E., Lleixa C., Frasquet M., Argente H., Cano-Abascal A., Diaz-Manera J., Cortes-Vicente E., Pelayo-Negro A.L., Sevilla T., Rojas-Garcia R., Querol L. (2020) Antibodies against nodo-paranodal proteins are not present in genetic neuropathies. NEUROLOGY, 95 (4), E427-E433.

IF: 9,9100

Moore U, Jacobs M, Fernandez-Torron R, LLauger Rossello J, Smith FE, James M, Mayhew A, Rufibach L, Carlier PG, Blamire AM, Day JW, Jones KJ, Bharucha-Goebel DX, Salort-Campana E, Pestronk A, Walter MC, Paradas C, Stojkovic T, Mori-Yoshimura M, Bravver E, Pegoraro E, Mendell JR, Bushby K, Straub V, Diaz-Manera J. Intensive Teenage Activity Is Associated With Greater Muscle Hyperintensity on T1W Magnetic Resonance Imaging in Adults With Dysferlinopathy. FRONT NEUROL. 2020 Dec 16;11:613446. PMID: 33391171.

IF: 4,0030

Muppidi S, Guptill JT, Jacob S, Li Y, Farrugia ME, Guidon AC, Tavee JO, Kaminski H, Howard JF Jr, Cutter G, Wiendl H, Maas MB, Illa I, Mantegazza R, Murai H, Utsugisawa K, Nowak RJ; CARE-MG Study Group. COVID-19-associated risks and effects in myasthenia gravis (CARE-MG). LANCET NEUROL. 2020 Dec;19(12):970-971. PMID: 33212055.

IF: 44,1820

Nunez-Peralta C., Alonso-Perez J., Llauger J., Segovia S., Montesinos P., Belmonte I., Pedrosa I., Montiel E., Alonso-Jimenez A., Sanchez-Gonzalez J., Martinez-Noguera A., Illa I., Diaz-Manera J. (2020) Follow-up of late-onset Pompe disease patients with muscle magnetic resonance imaging reveals increase in fat replacement in skeletal muscles. J CACHEXIA SARCOPENI, (), -.

IF: 12,9100

Nunez-Peralta C., Alonso-Perez J., Diaz-Manera J. (2020) The increasing role of muscle MRI to monitor changes over time in untreated and treated muscle diseases. CURR OPIN NEUROL, 33 (5), 611-620.

IF: 5,7100

Pascual-Goñi E, Fortea J, Martínez-Domeño A, Rabella N, Tecame M, Gómez-Oliva C, Querol L, Gómez-Ansón B. COVID-19-associated ophthalmoparesis and hypothalamic involvement. NEUROL-NEUROIMMUNOL. 2020 Jun 25;7(5):e823. PMID: 32587102.

IF: 8,4850

Previtali S.C., Gidaro T., Diaz-Manera J., Zambon A., Carnesecchi S., Roux-Lombard P., Spitali P., Signorelli M., Szigyarto C.A.-K., Johansson C., Gray J., Labolle D., Porte Thome F., Pitchforth J., Domingos J., Muntoni F. (2020) Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy. PHARMACOL RES, 159 (), -.

IF: 7,6580

Querol L., Crabtree M., Herepath M., Priedane E., Viejo Viejo I., Agush S., Sommerer P., Systematic literature review of burden of illness in chronic inflammatory demyelinating polyneuropathy (CIDP) (2020) J NEUROL.

IF: 4,8490

Querol L, Crabtree M, Herepath M, Priedane E, Viejo-Viejo I, Agush S, Sommerer P. Burden of illness in chronic inflammatory demyelinating polyneuropathy: some clarifications. J NEUROL. 2020 Oct;267(10):3094-3095. PMID: 32728947.

IF: 4,8490

Savarese M., Vihola A., Oates E.C., Barresi R., Fiorillo C., Tasca G., Jokela M., Sarkozy A., Luo S., Diaz-Manera J., Ehrstedt C., Rojas-Garcia R., Saenz A., Muelas N., Lonardo F., Fodstad H., Qureshi T., Johari M., Valipakka S., Luque H., Petiot P., de Munain A.L., Pane M., Mercuri E., Torella A., Nigro V., Astrea G., Santorelli F.M., Bruno C., Kuntzer T., Illa I., Vilchez J.J., Julien C., Ferreiro A., Malandrini A., Zhao C.-B., Casar-Borota O., Davis M., Muntoni F., Hackman P., Udd B. (2020) Genotype–phenotype correlations in recessive titinopathies. GENET MED, 22 (12), 2029-2040.

IF: 8,8220

Suarez-Calvet X., Alonso-Perez J., Castellvi I., Carrasco-Rozas A., Fernandez-Simon E., Zamora C., Martinez-Martinez L., Alonso-Jimenez A., Rojas-Garcia R., Turon J., Querol L., de Luna N., Milena-Millan A., Corominas H., Castillo D., Cortes-Vicente E., Illa I., Gallardo E., Diaz-Manera J. (2020) Thrombospondin-1 mediates muscle damage in brachio-cervical inflammatory myopathy and systemic sclerosis. NEUROL-NEUROIMMUNOL, 7 (3), -.

IF: 8,4850

Tarraso G., Real-Martinez A., Pares M., Romero-Cortadellas L., Puigros L., Moya L., de Luna N., Brull A., Martin M.A., Arenas J., Lucia A., Andreu A.L., Barquinero J., Vissing J., Krag T.O., Pinos T. (2020) Absence of p.R50X Pygm read-through in McArdle disease cellular models. DIS MODEL MECH, 13 (1), -.

IF: 5,7580

Topf A., Johnson K., Bates A., Phillips L., Chao K.R., England E.M., Laricchia K.M., Mullen T., Valkanas E., Xu L., Bertoli M., Blain A., Casasus A.B., Duff J., Mroczek M., Specht S., Lek M., Ensini M., MacArthur D.G., Akay E., Alonso-Perez J., Baets J., Barisic N., Bastian A., Borell S., Chamova T., Claeys K., Colomer J., Coppens S., Deconinck N., de Ridder W., Diaz-Manera J., Dominguez-Gonzalez C., Duncan A., Durmus H., Fahmy N.A., Farrugia M.E., Fernandez-Torron R., Gonzalez-Quereda L., Haberlova J., von der Hagen M., Hahn A., Jakovcevic A., JericoPascual I., Kapetanovic S., Kenina V., Kirschner J., Klein A., Kolbel H., Kostera-Pruszczyk A., Kulshrestha R., Lahdetie J., Layegh M., Longman C., Lopezde Munain A., Loscher W., Lusakowska A., Maddison P., Magot A., Majumdar A., Marti P., MartinezArroyo A., Mazanec R., Mercier S., Mongini T., Muelas N., Nascimento A., Nafissi S., Omidi S., Ortez C., Paquay S., Pereon Y., Peric S., Ponzalino V., Rakocevic Stojanovic V., Remiche G., RodriguezSainz A., Rudnik S., SanchezAlbisua I., Santos M., Schara U., Shatillo A., Sertic J., Stephani U., Strang-Karlsson S., Sznajer Y., Tanev A., Tournev I., Van den Bergh P., Van Parijs V., Vilchez J., Vill K., Vissing J., Wallgren-Pettersson C., Wanschitz J., Willis T., Witting N., Zulaica M., Straub V. (2020) Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness. GENET MED, 22 (9), 1478-1488.

IF: 8,8220

Van den Bergh P.Y.K., van Doorn P.A., Jacobs B.C., Querol L., Bunschoten C., Cornblath D.R. (2020) Boundaries of chronic inflammatory demyelinating polyradiculoneuropathy. J PERIPHER NERV SYST, 25 (1), 4-8.

IF: 3,4940

Verdu-Diaz J., Alonso-Perez J., Nunez-Peralta C., Tasca G., Vissing J., Straub V., Fernandez-Torron R., Llauger J., Illa I., Diaz-Manera J. (2020) Accuracy of a machine learning muscle MRI-based tool for the diagnosis of muscular dystrophies. NEUROLOGY, 94 (10), e1094-e1102.

IF: 9,9100

Vissing J., Jacob S., Fujita K.P., O'Brien F., Howard J.F., Mazia C.G., Wilken M., Barroso F., Saba J., Rugiero M., Bettini M., Chaves M., Vidal G., Garcia A.D., DeBleecker J., Vanden Abeele G., deKoning K., DeMey K., Mercelis R., Mahieu D., Wagemaekers L., VanDamme P., Depreitere A., Schotte C., Smetcoren C., Stevens O., VanDaele S., Vandenbussche N., Vanhee A., Verjans S., Vynckier J., D'Hont A., Tilkin P., Alves deSiqueira Carvalho A., DiasBrockhausen I., Feder D., Ambrosio D., Cesar P., Melo A.P., MartinsRibeiro R., Rocha R., Rosa B.B., Veiga T., daSilva L.A., SantosEngel M., GoncalvesGeraldo J., daPenha Ananias Morita M., NogueiraCoelho E., Paiva G., Pozo M., Prando N., MartineliTorres D.D., Butinhao C.F., Duran G., SurianeFialho T.A., Gomes daSilva T.C., MaiaGoncalves L.O., Pazetto L.E., CubasVolpe L.R., SouzaDuca L., GhellerFriedrich M.A., Guerreiro A., Mohr H., PereiraMartins M., daCruz Pacheco D., Ferreira L., Macagnan A.P., Pinto G., deCassia Santos A., Souza BulleOliveira A., Amaral deAndrade A.C., Annes M., DuarteSilva L., CavalcanteLino V., Pinto W., Assis N., Carrara F., Miranda C., Souza I., Fernandes P., Siddiqi Z., Phan C., Narayan J., Blackmore D., Mallon A., Roderus R., Watt E., Vohanka S., Bednarik J., Chmelikova M., Cierny M., Toncrova S., Junkerova BarboraKurkova J., Reguliova K., Zapletalova O., Pitha J., Novakova I., Tyblova M., Jurajdova I., Wolfova M., Andersen H., Harbo T., Vinge L., Krogh S., Mogensen A., Vissing J., Hojgaard J., Witting N., Mette OstergaardAutzen A., Pedersen J., Eralinna J.-P., Laaksonen M., Oksaranta O., Harrison T., Eriksson J., Rozsa C., Horvath M., Lovas G., Matolcsi J., Szabo G., Jakab G., Szabadosne B., Vecsei L., Dezsi L., Varga E., Konyane M., Antonini G., DiPasquale A., Garibaldi M., Morino S., Troili F., Fionda L., Sacca F., previous, Filla A., sub-investigators, Costabile T., Marano E., Fasanaro A., Marsili A., Puorro G., Mantegazza R., Antozzi C., Bonanno S., Camera G., Locatelli A., Maggi L., Pasanisi M., Campanella A., Evoli A., Alboini P.E., D'Amato V., Iorio R., Inghilleri M., Frasca V., Giacomelli E., Gori M., Lopergolo D., Onesti E., Frasca V., Gabriele M., Uzawa A., Kanai T., Kawaguchi N., Mori M., Kaneko Y., Kanzaki A., Kobayashi E., Murai H., Masaki K., Matsuse D., Matsushita T., Uehara T., Shimpo M., Jingu M., Kikutake K., Nakamura Y., Sano Y., Utsugisawa K., Nagane Y., Kamegamori I., Tsuda T., Fujii Y., Futono K., Ozawa Y., Mizugami A., Saito Y., Samukawa M., Suzuki H., Morikawa M., Kamakura S., Miyawaki E., Shiraishi H., Mitazaki T., Motomura M., Mukaino A., Yoshimura S., Asada S., Yoshida S., Amamoto S., Kobashikawa T., Koga M., Maeda Y., Takada K., Takada M., Tsurumaru M., Yamashita Y., Yoshida S., Suzuki Y., Akiyama T., Narikawa K., Tano O., Tsukita K., Kurihara R., Meguro F., Fukuda Y., Sato M., Okumura M., Funaka S., Kawamura T., Makamori M., Takahashi M., Taichi N., Hasuike T., Higuchi E., Kobayashi H., Osakada K., Imai T., Tsuda E., previous, Shimohama S., Hayashi T., Hisahara S., Imai T., Kawamata J., Murahara T., Saitoh M., Shimohama S., Suzuki S., Yamamoto D., Ishiyama Y., Ishiyama N., Noshiro M., Takeyama R., Uwasa K., Yasuda I., Kim B.-J., Lee C.N., Koo Y.S., Seok H.Y., Kang H.N., Ra H.J., Kim B.J., Cho E.B., Choi M.S., Lee H.L., Min J.-H., Seok J., Lee J.E., Koh D.Y., Kwon J.Y., Park S.A., Choi E.H., Hong Y.-H., Ahn S.-H., Koo D.L., Lim J.-S., Shin C.W., Hwang J.Y., Kim M., Kim S.M., Jeong H.-N., Jung J.W., Kim Y.-H., Lee H.S., Shin H.Y., Hwang E.B., Shin M., van derKooi A., deVisser M., Gibson T., Casasnovas C., AlbertiAguilo M.A., Homedes-Pedret C., Palacios N.J., DiezPorras L., VelezSantamaria V., Lazaro A., DiezTejedor E., GomezSalcedo P., Fernandez-Fournier M., LopezRuiz P., Rodriguez deRivera F.J., Sastre M., GamezCarbonell J., Sune P., SalvadoFigueras M., Gili G., Mazuela G., Illa I., CortesVicente E., Diaz-Manera J., QuerolGutierrez L.A., RojasGarcia R., Vidal N., Arribas-Ibar E., Piehl F., Hietala A., Bjarbo L., Sengun I., Meherremova 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IF: 4,8490

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IF: 10,1540