Neurosciences

Molecular Physiology of the Synapse

2020
Revista Internacional

A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy

Cabrera-Serrano, M; Coote, DJ; Azmanov, D; Goullee, H; Andersen, E; McLean, C; Davis, M; Ishimura, R; Stark, Z; Vallat, JM; Komatsu, M; Kornberg, A; Ryan, M; Laing, NG; Ravenscroft, G

Vol: JOURNAL OF MEDICAL GENETICS Revista Internacional
Revista Internacional

Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy

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, SG; Blazquez-Bermejo, C; Camara, Y; Marti, R; Mavillard, F; Martin, MA; Montoya, J; Ruiz-Pesini, E; Villarroya, J; Montero, R; Villarroya, F; Artuch, R; Hirano, M; Nascimento, A; Jimenez-Mallebrera, C

Vol: SCIENTIFIC REPORTS Revista Internacional
Revista Internacional

HeterozygousCAPN3missense variants causing autosomal-dominant calpainopathy in seven unrelated families

Gonzalez-Mera, L; Ravenscroft, G; Cabrera-Serrano, M; Ermolova, N; Dominguez-Gonzalez, C; Arteche-Lopez, A; Soltanzadeh, P; Evesson, F; Navas, C; Mavillard, F; Clayton, J; Rodrigo, P; Servian-Morilla, E; Cooper, ST; Waddell, L; Reardon, K; Corbett, A; Hernandez-Lain, A; Sanchez, A; Perez, JE; Paradas-Lopez, C; Rivas-Infante, E; Spencer, M; Laing, N; Olive, M

Vol: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY Revista Internacional
Revista Internacional

POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, alpha-dystroglycan hypoglycosylation and a distinctive radiological pattern

Servian-Morilla, E; Cabrera-Serrano, M; Johnson, K; Pandey, A; Ito, A; Rivas, E; Chamova, T; Muelas, N; Mongini, T; Nafissi, S; Claeys, KG; Grewal, RP; Takeuchi, M; Hao, H; Bonnemann, C; Neto, OLA; Medne, L; Brandsema, J; Topf, A; Taneva, A; Vilchez, JJ; Tournev, I; Haltiwanger, RS; Takeuchi, H; Jafar-Nejad, H; Straub, V; Paradas, C

Vol: ACTA NEUROPATHOLOGICA Revista Internacional
Revista Internacional

Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience

Beecroft, SJ; Yau, KS; Allcock, RJN; Mina, K; Gooding, R; Faiz, F; Atkinson, VJ; Wise, C; Sivadorai, P; Trajanoski, D; Kresoje, N; Ong, R; Duff, RM; Cabrera-Serrano, M; Nowak, KJ; Pachter, N; Ravenscroft, G; Lamont, PJ; Davis, MR; Laing, NG

Vol: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY Revista Internacional
2019
Revista Internacional

240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands.

Morgan J, Butler-Browne G, Muntoni F, Patel K; skeletal muscle stem cells involvement in pathology study group

Vol: Neuromuscul Disord. Revista Internacional
Revista Internacional

Altered myogenesis and premature senescence underlie human TRIM32-related myopathy.

Servián-Morilla E, Cabrera-Serrano M, Rivas-Infante E, Carvajal A, Lamont PJ, Pelayo-Negro AL, Ravenscroft G, Junckerstorff R, Dyke JM, Fletcher S, Adams AM, Mavillard F, Fernández-García MA, Nieto-González JL, Laing NG, Paradas C

Vol: Acta Neuropathol Commun. Revista Internacional
Revista Internacional

Assessment of disease progression in dysferlinopathy: A 1-year cohort study.

Moore U, Jacobs M, James MK, Mayhew AG, Fernandez-Torron R, Feng J, Cnaan A, Eagle M, Bettinson K, Rufibach LE, Lofra RM, Blamire AM, Carlier PG, Mittal P, Lowes LP, Alfano L, Rose K, Duong T, Berry KM, Montiel-Morillo E, Pedrosa-Hernández I, Holsten S, Sanjak M, Ashida A, Sakamoto C, Tateishi T, Yajima H, Canal A, Ollivier G, Decostre V, Mendez JB, Sánchez-Aguilera Praxedes N, Thiele S, Siener C, Shierbecker J, Florence JM, Vandevelde B, DeWolf B, Hutchence M, Gee R, Prügel J, Maron E, Hilsden H, Lochmüller H, Grieben U, Spuler S, Tesi Rocha C, Day JW, Jones KJ, Bharucha-Goebel DX, Salort-Campana E, Harms M, Pestronk A, Krause S, Schreiber-Katz O, Walter MC, Paradas C, Hogrel JY, Stojkovic T, Takeda S, Mori-Yoshimura M, Bravver E, Sparks S, Díaz-Manera J, Bello L, Semplicini C, Pegoraro E, Mendell JR, Bushby K, Straub V, Jain COS Consortium

Vol: Neurology. Revista Internacional
Revista Internacional

Combined HIIT and Resistance Training in Very Long-Chain Acyl-CoA Dehydrogenase Deficiency: A Case Report.

Herrera-Olivares AM, Fernández-Luque JA, Paradas C, Lucia A, Santalla A

Vol: Front Physiol. Revista Internacional
Revista Internacional

Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient Myopathy.

Domínguez-González C, Madruga-Garrido M, Mavillard F, Garone C, Aguirre-Rodríguez FJ, Donati MA, Kleinsteuber K, Martí I, Martín-Hernández E, Morealejo-Aycinena JP, Munell F, Nascimento A, Kalko SG, Sardina MD, Álvarez Del Vayo C, Serrano O, Long Y, Tu Y, Levin B, Thompson JLP, Engelstad K, Uddin J, Torres-Torronteras J, Jimenez-Mallebrera C, Martí R, Paradas C, Hirano M

Vol: Ann Neurol. Revista Internacional
Revista Internacional

Editorial on the Special Issue on SNARE Proteins: A Long Journey of Science in Brain Health and Disease.

Matteoli M, Menna E, Honer WG, Fernández-Chacón R

Vol: Neuroscience Revista Internacional
Revista Internacional

Identification of serum microRNAs as potential biomarkers in Pompe disease.

Carrasco-Rozas A, Fernández-Simón E, Lleixà MC, Belmonte I, Pedrosa-Hernandez I, Montiel-Morillo E, Nuñez-Peralta C, Llauger Rossello J, Segovia S, De Luna N, Suarez-Calvet X, Illa I, Pompe Spanish Study group, Díaz-Manera J, Gallardo E

Vol: Ann Clin Transl Neurol. Revista Internacional
Revista Internacional

Late-onset thymidine kinase 2 deficiency: a review of 18 cases.

Domínguez-González C, Hernández-Laín A, Rivas E, Hernández-Voth A, Sayas Catalán J, Fernández-Torrón R, Fuiza-Luces C, García García J, Morís G, Olivé M, Miralles F, Díaz-Manera J, Caballero C, Méndez-Ferrer B, Martí R, García Arumi E, Badosa MC, Esteban J, Jimenez-Mallebrera C, Encinar AB, Arenas J, Hirano M, Martin MÁ, Paradas C

Vol: Orphanet J Rare Dis. Revista Internacional
Revista Internacional

Loss of postnatal quiescence of neural stem cells through mTOR activation upon genetic removal of cysteine string protein-α.

Nieto-González JL, Gómez-Sánchez L, Mavillard F, Linares-Clemente P, Rivero MC, Valenzuela-Villatoro M, Muñoz-Bravo JL, Pardal R, Fernández-Chacón R

Vol: Proc Natl Acad Sci U S A. Revista Internacional
Revista Internacional

Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy.

Alonso-Jimenez A, Kroon RHMJM, Alejaldre-Monforte A, Nuñez-Peralta C, Horlings CGC, van Engelen BGM, Olivé M, González L, Verges-Gil E, Paradas C, Márquez C, Garibaldi M, Gallano P, Rodriguez MJ, Gonzalez-Quereda L, Dominguez Gonzalez C, Vissing J, Fornander F, Eisum AV, García-Sobrino T, Pardo J, García-Figueiras R, Muelas N, Vilchez JJ, Kapetanovic S, Tasca G, Monforte M, Ricci E, Gomez MT, Bevilacqua JA, Diaz-Jara J, Zamorano II, Carlier RY, Laforet P, Pelayo-Negro A, Ramos-Fransi A, Martínez A, Marini-Bettolo C, Straub V, Gutiérrez G, Stojkovic T, Martín MA, Morís G, Fernández-Torrón R, Lopez De Munaín A, Cortes-Vicente E, Querol L, Rojas-García R, Illa I, Diaz-Manera J

Vol: J Neurol Neurosurg Psychiatry. Revista Internacional
Revista Internacional

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.

Olivé M, Engvall M, Ravenscroft G, Cabrera-Serrano M, Jiao H, Bortolotti CA, Pignataro M, Lambrughi M, Jiang H, Forrest ARR, Benseny-Cases N, Hofbauer S, Obinger C, Battistuzzi G, Bellei M, Borsari M, Di Rocco G, Viola HM, Hool LC, Cladera J, Lagerstedt-Robinson K, Xiang F, Wredenberg A, Miralles F, Baiges JJ, Malfatti E, Romero NB, Streichenberger N, Vial C, Claeys KG, Straathof CSM, Goris A, Freyer C, Lammens M, Bassez G, Kere J, Clemente P, Sejersen T, Udd B, Vidal N, Ferrer I, Edström L, Wedell A, Laing NG

Vol: Nat Commun. Revista Internacional
Revista Internacional

NOVEL intronic CAPN3 Roma mutation alters splicing causing RNA mediated decay.

Mavillard F, Madruga-Garrido M, Rivas E, Servián-Morilla E, Ávila-Polo R, Marcos I, Morón FJ, Paradas C, Cabrera-Serrano M

Vol: Ann Clin Transl Neurol. Revista Internacional
Revista Internacional

PDGF-BB serum levels are decreased in adult onset Pompe patients.

Fernández-Simón E, Carrasco-Rozas A, Gallardo E, Figueroa-Bonaparte S, Belmonte I, Pedrosa I, Montiel E, Suárez-Calvet X, Alonso-Pérez J, Segovia S, Nuñez-Peralta C, Llauger J, Mayos M, Illa I, Spanish Pompe Study Group, Díaz-Manera J

Vol: Sci Rep. Revista Internacional
Revista Internacional

State-Dependent Subnetworks of Parvalbumin-Expressing Interneurons in Neocortex.

Garcia-Junco-Clemente P, Tring E, Ringach DL, Trachtenberg JT

Vol: Cell Rep. Revista Internacional
Revista Internacional

Study of the effect of anti-rhGAA antibodies at low and intermediate titers in late onset Pompe patients treated with ERT.

Fernández-Simón E, Carrasco-Rozas A, Gallardo E, González-Quereda L, Alonso-Pérez J, Belmonte I, Pedrosa-Hernández I, Montiel E, Segovia S, Suárez-Calvet X, Llauger J, Mayos M, Illa I, Barba-Romero MA, Barcena J, Paradas C, Carzorla MR, Creus C, Coll-Cantí J, Díaz M, Domínguez C, Fernández-Torrón R, García-Antelo MJ, Grau JM, López de Munáin A, Martínez-García FA, Morgado Y, Moreno A, Morís G, Muñoz-Blanco MA, Nascimento A, Parajuá-Pozo JL, Querol L, Rojas R, Robledo-Strauss A, Rojas-Marcos Í, Salazar JA, Usón M, Díaz-Manera J

Vol: Mol Genet Metab. Revista Internacional
2018
Revista Internacional

A Roma founder BIN1 mutation causes a novel phenotype of centronuclear myopathy with rigid spine

. Cabrera-Serrano M, Mavillard F, Biancalana V, Rivas E, Morar B, Hernández-Laín A, Olive M, Muelas N, Khan E, Carvajal A, Quiroga P, Díaz-Manera J, Davis M, Ávila R, Domínguez C, Romero NB, Vílchez JJ, Comas D, Laing NG, Laporte J, Kalaydjieva L, Paradas C.

Vol: Neurology. Revista Internacional
Revista Internacional

A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain.

Carbonell-Corvillo P, Tristán-Clavijo E, Cabrera-Serrano M, Servián-Morilla E, García-Martín G, Villarreal-Pérez L, Rivas-Infante E, Area-Gómez E, Chamorro-Muñoz MI, Gil-Gálvez A, Miranda-Vizuete A, Martínez-Mir A, Laing N, Paradas C.

Vol: NeuromusculDisord. Revista Internacional
Revista Internacional

Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.

Parras A, Anta H, Santos-Galindo M, Swarup V, Elorza A, Nieto-González JL, Picó S, Hernández IH, Díaz-Hernández JI, Belloc E, Rodolosse A, Parikshak NN, Peñagarikano O, Fernández-Chacón R, Irimia M, Navarro P, Geschwind DH, Méndez R, Lucas JJ.

Vol: Nature. Revista Internacional
Revista Internacional

CUGC for Duchenne muscular dystrophy (DMD).

Coote DJ, Davis MR, Cabrera M, Needham M, Laing NG, Nowak KJ.

Vol: Eur J Hum Genet. Revista Internacional
Revista Internacional

Clinical Utility Gene Card for: Becker muscular dystrophy.

Coote D, Davis MR, Cabrera M, Needham M, Laing NG, Nowak KJ.

Vol: Eur J HumGenet. Revista Internacional
Revista Internacional

Clinical Utility Gene Card for: autosomal dominant myotoniacongenita (Thomsen Disease).

Coote DJ, Davis MR, Cabrera M, Needham M, Laing NG, Nowak KJ.

Vol: Eur J HumGenet Revista Internacional
Revista Internacional

Clinical utility gene card for McArdle disease.

Taylor RL, Davis M, Turner E, Brull A, Pinos T, Cabrera M, Nowak KJ.

Vol: Eur J Hum Genet. Revista Internacional
Revista Internacional

Core-rod myopathy due to a novel mutation in BTB/POZ domain of KBTBD13 manifesting as late onset LGMD.

Garibaldi M, Fattori F, Bortolotti CA, Brochier G, Labasse C, Verardo M, Servián-Morilla E, Gibellini L, Pinti M, Di Rocco G, Raffa S, Pennisi EM, Bertini ES, Paradas C, Romero NB, Antonini G.

Vol: ActaNeuropatholCommun. Revista Internacional
Revista Internacional

Muscle MRI in patients with dysferlinopathy: pattern recognition and implications for clinical trials.

Díaz-Manera J, Fernández-Torrón R, LLauger J, James MK, Mayhew A, Smith FE, Moore UR, Blamire AM, Carlier PG, Rufibach L, Mittal P, Eagle M, Jacobs M, Hodgson T, Wallace D, Ward L, Smith M, Stramare R, Rampado A, Sato N, Tamaru T, Harwick B, Rico Gala S, Turk S, Coppenrath EM, Foster G, Bendahan D, Le Fur Y, Fricke ST, Otero H, Foster SL, Peduto A, Sawyer AM, Hilsden H, Lochmuller H, Grieben U, Spuler S, Tesi Rocha C, Day JW, Jones KJ, Bharucha-Goebel DX, Salort-Campana E, Harms M, Pestronk A, Krause S, Schreiber-Katz O, Walter MC, Paradas C, Hogrel JY, Stojkovic T, Takeda S, Mori-Yoshimura M, Bravver E, Sparks S, Bello L, Semplicini C, Pegoraro E, Mendell JR, Bushby K, Straub V, Jain COS Consortium.

Vol: J NeurolNeurosurgPsychiatry Revista Internacional
Revista Internacional

Muscle imaging in laminopathies: Synthesis study identifies meaningful muscles for follow-up

Gómez-Andrés D, Díaz-Manera J, Alejaldre A, Pulido-Valdeolivas I, GonzáLez-Mera L, Olivé M, Vilchez JJ, De Munain AL, Paradas C, Muelas N, Sánchez-Montáñez Á, Alonso-Jiménez A, De la Banda MGG, Dabaj I, Bonne G, Munell F, Carlier RY, Quijano-Roy S.

Vol: MuscleNerve Revista Internacional
Revista Internacional

Proteolytic Processing of Neurexins by Presenilins Sustains Synaptic Vesicle Release

Servián-Morilla E, Robles-Lanuza E, Sánchez-Hidalgo AC, Camacho-García RJ, Páez-Gómez JA, Mavillard F, Saura CA, Martínez-Mir A, Scholl FG.

Vol: J Neurosci. Revista Internacional
Revista Internacional

Report by the Spanish Foundation for the Brain on the social impact of amyotrophic lateral sclerosis and other neuromuscular disorders.

Camacho A, Esteban J, Paradas C.

Vol: Neurologia. Revista Internacional
Revista Internacional

Substantia nigra dopaminergic neurons and striatal interneurons are engaged in three parallel but interdependent postnatal neurotrophic circuits

Ortega-de San Luis C, Sánchez-García MA, Nieto-González JL, García-Junco-Clemente P, Montero-Sánchez A, Fernández-Chacón R, Pascual A.

Vol: AgingCell Revista Internacional
Revista Internacional

Teenage exercise is associated with earlier symptom onset in dysferlinopathy: a retrospective cohort study.

Moore UR, Jacobs M, Fernández-Torrón R, Jang J, James MK, Mayhew A, Rufibach L, Mittal P, Eagle M, Cnaan A, Carlier PG, Blamire A, Hilsden H, Lochmüller H, Grieben U, Spuler S, Tesi Rocha C, Day JW, Jones KJ, Bharucha-Goebel DX, Salort-Campana E, Harms M, Pestronk A, Krause S, Schreiber-Katz O, Walter MC, Paradas C, Hogrel JY, Stojkovic T, Takeda S, Mori-Yoshimura M, Bravver E, Sparks S, Díaz-Manera J, Bello L, Semplicini C, Pegoraro E, Mendell JR, Bushby K, Straub V.

Vol: J NeurolNeurosurg Psychiatry Revista Internacional
2017
Revista Internacional

An inhibitory pull-push circuit in frontal cortex.

García-Junco-Clemente P, Ikrar T, Tring E, Xu X, Ringach DL, Trachtenberg JT.

Vol: Nat Neurosci Revista Internacional
Revista Internacional

Cystinosis distal myopathy, novel clinical, pathological and genetic features

Cabrera-Serrano M, Junckerstorff RC, Alisheri A, Pestronk A, Laing NG, Weihl CC, Lamont PJ.

Vol: Neuromuscul Disord. Revista Internacional
Revista Internacional

Generation of an induced pluripotent stem cell line (CSCRMi001-A) from a patient with a new type of limb-girdle muscular dystrophy (LGMD) due to a missense mutation in POGLUT1 (Rumi).

Wu J, Hunt SD, Matthias N, Servián-Morilla E, Lo J, Jafar-Nejad H, Paradas C, Darabi R.

Vol: Stem Cell Res Revista Internacional
Revista Internacional

Rules of tissue packing involving different cell types: human muscle organization.

Sánchez-Gutiérrez D, Sáez A, Gómez-Gálvez P, Paradas C, Escudero LM.

Vol: Sci Rep. Revista Internacional
Revista Internacional

Toward the Inner Nanostructure of a Secretory Vesicle

Nieto-González JL, Fernández-Chacón R.

Vol: ACS Nano. Revista Internacional
2012
2011
2010
2009
2008
2007
Revista Internacional

Deletion of CASK in mice is lethal and impairs synaptic function.

Atasoy D, Schoch S, Ho A, Nadasy KA, Liu X, Zhang W, Mukherjee K, Nosyreva ED, Fernandez-Chacon R, Missler M, Kavalali ET, Südhof TC

Vol: Proceedings of the National Academy of Sciences of the United States of America 2007 Feb;104(7):2525-30 Revista Internacional
2006
Revista Internacional

CSPalpha-deficiency causes massive and rapid photoreceptor degeneration.

Schmitz F, Tabares L, Khimich D, Strenzke N, de la Villa-Polo P, Castellano-Muñoz M, Bulankina A, Moser T, Fernández-Chacón R, Südhof TC

Vol: Proceedings of the National Academy of Sciences of the United States of America 2006 Feb;103(8):2926-31 Revista Internacional
2005
Revista Internacional

Recycling and EH domain proteins at the synapse.

Montesinos ML, Castellano-Muñoz M, García-Junco-Clemente P, Fernández-Chacón R

Vol: Brain research. Brain research reviews 2005 Sep;49(2):416-28 Revista Internacional
2004