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Items: 1 to 50 of 319

1.

Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia.

Gu S, Chen CA, Rosenfeld JA, Cope H, Launay N, Flanigan K, Waldrop M, Schrader R, Juusola J; Undiagnosed Diseases Network, Goker-Alpan O, Milunsky A, Schlüter A, Troncoso M, Pujol A, Tan QKG, Schaaf CP, Meng L.

Hum Mutat. 2019 Nov 7. doi: 10.1002/humu.23950. [Epub ahead of print]

PMID:
31696996
2.

Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia.

Verdura E, Fons C, Schlüter A, Ruiz M, Fourcade S, Casasnovas C, Castellano A, Pujol A.

J Med Genet. 2019 Oct 5. pii: jmedgenet-2019-106373. doi: 10.1136/jmedgenet-2019-106373. [Epub ahead of print]

PMID:
31586945
3.

Brain activity during traditional textbook and audiovisual-3D learning.

Pujol J, Blanco-Hinojo L, Martínez-Vilavella G, Canu-Martín L, Pujol A, Pérez-Sola V, Deus J.

Brain Behav. 2019 Oct;9(10):e01427. doi: 10.1002/brb3.1427. Epub 2019 Sep 30.

4.

Parkinsonism and spastic paraplegia type 7: Expanding the spectrum of mitochondrial Parkinsonism.

De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, Ruiz M, Schlüter A, Spinazzola A, Muñoz-Blanco JL, Grandas F, Holt I, Álvarez V, López de Munaín A.

Mov Disord. 2019 Aug 21. doi: 10.1002/mds.27812. [Epub ahead of print]

PMID:
31433872
5.

Clinical presentation and proteomic signature of patients with TANGO2 mutations.

Mingirulli N, Pyle A, Hathazi D, Alston CL, Kohlschmidt N, O'Grady G, Waddell L, Evesson F, Cooper SBT, Turner C, Duff J, Topf A, Yubero D, Jou C, Nascimento A, Ortez C, García-Cazorla A, Gross C, O'Callaghan M, Santra S, Preece MA, Champion M, Korenev S, Chronopoulou E, Anirban M, Pierre G, McArthur D, Thompson K, Navas P, Ribes A, Tort F, Schlüter A, Pujol A, Montero R, Sarquella G, Lochmüller H, Jiménez-Mallebrera C, Taylor RW, Artuch R, Kirschner J, Grünert SC, Roos A, Horvath R.

J Inherit Metab Dis. 2019 Jul 24. doi: 10.1002/jimd.12156. [Epub ahead of print]

PMID:
31339582
6.

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R.

Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102.

PMID:
31135052
7.

Comparison of two different oocyte vitrification methods: a prospective, paired study on the same genetic background and stimulation protocol.

Pujol A, Zamora MJ, Obradors A, Garcia D, Rodriguez A, Vassena R.

Hum Reprod. 2019 Jun 4;34(6):989-997. doi: 10.1093/humrep/dez045.

PMID:
31116386
8.

Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot Study.

Casasnovas C, Ruiz M, Schlüter A, Naudí A, Fourcade S, Veciana M, Castañer S, Albertí A, Bargalló N, Johnson M, Raymond GV, Fatemi A, Moser AB, Villarroya F, Portero-Otín M, Artuch R, Pamplona R, Pujol A.

Neurotherapeutics. 2019 May 10. doi: 10.1007/s13311-019-00735-2. [Epub ahead of print]

PMID:
31077039
9.

A novel mutation in the GFAP gene expands the phenotype of Alexander disease.

Casasnovas C, Verdura E, Vélez V, Schlüter A, Pons-Escoda A, Homedes C, Ruiz M, Fourcade S, Launay N, Pujol A.

J Med Genet. 2019 Apr 19. pii: jmedgenet-2018-105959. doi: 10.1136/jmedgenet-2018-105959. [Epub ahead of print]

PMID:
31004048
10.

Deoxynivalenol inhibits the expression of trefoil factors (TFF) by intestinal human and porcine goblet cells.

Graziani F, Pinton P, Olleik H, Pujol A, Nicoletti C, Sicre M, Quinson N, Ajandouz EH, Perrier J, Pasquale ED, Oswald IP, Maresca M.

Arch Toxicol. 2019 Apr;93(4):1039-1049. doi: 10.1007/s00204-019-02425-6. Epub 2019 Mar 11.

PMID:
30854615
11.

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy.

Pant DC, Dorboz I, Schluter A, Fourcade S, Launay N, Joya J, Aguilera-Albesa S, Yoldi ME, Casasnovas C, Willis MJ, Ruiz M, Ville D, Lesca G, Siquier-Pernet K, Desguerre I, Yan H, Wang J, Burmeister M, Brady L, Tarnopolsky M, Cornet C, Rubbini D, Terriente J, James KN, Musaev D, Zaki MS, Patterson MC, Lanpher BC, Klee EW, Pinto E Vairo F, Wohler E, Sobreira NLM, Cohen JS, Maroofian R, Galehdari H, Mazaheri N, Shariati G, Colleaux L, Rodriguez D, Gleeson JG, Pujades C, Fatemi A, Boespflug-Tanguy O, Pujol A.

J Clin Invest. 2019 Mar 1;129(3):1240-1256. doi: 10.1172/JCI123959. Epub 2019 Feb 11.

12.

Novel Double Factor PGT strategy analyzing blastocyst stage embryos in a single NGS procedure.

Del Rey J, Vidal F, Ramírez L, Borràs N, Corrales I, Garcia I, Martinez-Pasarell O, Fernandez SF, Garcia-Cruz R, Pujol A, Plaja A, Salaverria I, Oliver-Bonet M, Benet J, Navarro J.

PLoS One. 2018 Oct 17;13(10):e0205692. doi: 10.1371/journal.pone.0205692. eCollection 2018.

13.

"EspaiJove.net"- a school-based intervention programme to promote mental health and eradicate stigma in the adolescent population: study protocol for a cluster randomised controlled trial.

Casañas R, Arfuch VM, Castellví P, Gil JJ, Torres M, Pujol A, Castells G, Teixidó M, San-Emeterio MT, Sampietro HM, Caussa A, Alonso J, Lalucat-Jo L.

BMC Public Health. 2018 Jul 31;18(1):939. doi: 10.1186/s12889-018-5855-1.

14.

Aberrant regulation of the GSK-3β/NRF2 axis unveils a novel therapy for adrenoleukodystrophy.

Ranea-Robles P, Launay N, Ruiz M, Calingasan NY, Dumont M, Naudí A, Portero-Otín M, Pamplona R, Ferrer I, Beal MF, Fourcade S, Pujol A.

EMBO Mol Med. 2018 Aug;10(8). pii: e8604. doi: 10.15252/emmm.201708604.

15.

Copper(I)-USY as a Ligand-Free and Recyclable Catalyst for Ullmann-Type O-, N-, S-, and C-Arylation Reactions: Scope and Application to Total Synthesis.

Garnier T, Danel M, Magné V, Pujol A, Bénéteau V, Pale P, Chassaing S.

J Org Chem. 2018 Jun 15;83(12):6408-6422. doi: 10.1021/acs.joc.8b00620. Epub 2018 May 29.

PMID:
29790337
16.

Inhibition of Gsk3b Reduces Nfkb1 Signaling and Rescues Synaptic Activity to Improve the Rett Syndrome Phenotype in Mecp2-Knockout Mice.

Jorge-Torres OC, Szczesna K, Roa L, Casal C, Gonzalez-Somermeyer L, Soler M, Velasco CD, Martínez-San Segundo P, Petazzi P, Sáez MA, Delgado-Morales R, Fourcade S, Pujol A, Huertas D, Llobet A, Guil S, Esteller M.

Cell Rep. 2018 May 8;23(6):1665-1677. doi: 10.1016/j.celrep.2018.04.010.

17.

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Guissart C, Latypova X, Rollier P, Khan TN, Stamberger H, McWalter K, Cho MT, Kjaergaard S, Weckhuysen S, Lesca G, Besnard T, Õunap K, Schema L, Chiocchetti AG, McDonald M, de Bellescize J, Vincent M, Van Esch H, Sattler S, Forghani I, Thiffault I, Freitag CM, Barbouth DS, Cadieux-Dion M, Willaert R, Guillen Sacoto MJ, Safina NP, Dubourg C, Grote L, Carré W, Saunders C, Pajusalu S, Farrow E, Boland A, Karlowicz DH, Deleuze JF, Wojcik MH, Pressman R, Isidor B, Vogels A, Van Paesschen W, Al-Gazali L, Al Shamsi AM, Claustres M, Pujol A, Sanders SJ, Rivier F, Leboucq N, Cogné B, Sasorith S, Sanlaville D, Retterer K, Odent S, Katsanis N, Bézieau S, Koenig M, Davis EE, Pasquier L, Küry S.

Am J Hum Genet. 2018 May 3;102(5):744-759. doi: 10.1016/j.ajhg.2018.02.021. Epub 2018 Apr 12.

18.

Is there a relation between the time to ICSI and the reproductive outcomes?

Pujol A, García D, Obradors A, Rodríguez A, Vassena R.

Hum Reprod. 2018 May 1;33(5):797-806. doi: 10.1093/humrep/dey067.

PMID:
29635450
19.

SIRT2 in age-related neurodegenerative disorders.

Fourcade S, Outeiro TF, Pujol A.

Aging (Albany NY). 2018 Mar 3;10(3):295-296. doi: 10.18632/aging.101397. No abstract available.

20.

Deletion of the RabGAP TBC1D1 Leads to Enhanced Insulin Secretion and Fatty Acid Oxidation in Islets From Male Mice.

Stermann T, Menzel F, Weidlich C, Jeruschke K, Weiss J, Altenhofen D, Benninghoff T, Pujol A, Bosch F, Rustenbeck I, Ouwens DM, Thoresen GH, de Wendt C, Lebek S, Schallschmidt T, Kragl M, Lammert E, Chadt A, Al-Hasani H.

Endocrinology. 2018 Apr 1;159(4):1748-1761. doi: 10.1210/en.2018-00087.

PMID:
29481597
21.

Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation.

Schlüter A, Sandoval J, Fourcade S, Díaz-Lagares A, Ruiz M, Casaccia P, Esteller M, Pujol A.

Brain Pathol. 2018 Nov;28(6):902-919. doi: 10.1111/bpa.12595. Epub 2018 Apr 10.

PMID:
29476661
22.

Mercury Trithiolate Binding (HgS3) to a de Novo Designed Cyclic Decapeptide with Three Preoriented Cysteine Side Chains.

Sénèque O, Rousselot-Pailley P, Pujol A, Boturyn D, Crouzy S, Proux O, Manceau A, Lebrun C, Delangle P.

Inorg Chem. 2018 Mar 5;57(5):2705-2713. doi: 10.1021/acs.inorgchem.7b03103. Epub 2018 Feb 14.

PMID:
29443519
23.

Evaluation of afferent pain pathways in adrenomyeloneuropathic patients.

Yagüe S, Veciana M, Casasnovas C, Ruiz M, Pedro J, Valls-Solé J, Pujol A.

Clin Neurophysiol. 2018 Mar;129(3):507-515. doi: 10.1016/j.clinph.2017.12.011. Epub 2017 Dec 24.

PMID:
29367165
24.

Vancomycin and tobramycin impregnated mineralized allograft for the surgical regenerative treatment of peri-implantitis: a 1-year follow-up case series.

Nart J, de Tapia B, Pujol À, Pascual A, Valles C.

Clin Oral Investig. 2018 Jul;22(6):2199-2207. doi: 10.1007/s00784-017-2310-0. Epub 2017 Dec 24.

PMID:
29275491
25.

Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder.

Falkenberg KD, Braverman NE, Moser AB, Steinberg SJ, Klouwer FCC, Schlüter A, Ruiz M, Pujol A, Engvall M, Naess K, van Spronsen F, Körver-Keularts I, Rubio-Gozalbo ME, Ferdinandusse S, Wanders RJA, Waterham HR.

Am J Hum Genet. 2017 Dec 7;101(6):965-976. doi: 10.1016/j.ajhg.2017.11.007.

26.

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.

Küry S, van Woerden GM, Besnard T, Proietti Onori M, Latypova X, Towne MC, Cho MT, Prescott TE, Ploeg MA, Sanders S, Stessman HAF, Pujol A, Distel B, Robak LA, Bernstein JA, Denommé-Pichon AS, Lesca G, Sellars EA, Berg J, Carré W, Busk ØL, van Bon BWM, Waugh JL, Deardorff M, Hoganson GE, Bosanko KB, Johnson DS, Dabir T, Holla ØL, Sarkar A, Tveten K, de Bellescize J, Braathen GJ, Terhal PA, Grange DK, van Haeringen A, Lam C, Mirzaa G, Burton J, Bhoj EJ, Douglas J, Santani AB, Nesbitt AI, Helbig KL, Andrews MV, Begtrup A, Tang S, van Gassen KLI, Juusola J, Foss K, Enns GM, Moog U, Hinderhofer K, Paramasivam N, Lincoln S, Kusako BH, Lindenbaum P, Charpentier E, Nowak CB, Cherot E, Simonet T, Ruivenkamp CAL, Hahn S, Brownstein CA, Xia F, Schmitt S, Deb W, Bonneau D, Nizon M, Quinquis D, Chelly J, Rudolf G, Sanlaville D, Parent P, Gilbert-Dussardier B, Toutain A, Sutton VR, Thies J, Peart-Vissers LELM, Boisseau P, Vincent M, Grabrucker AM, Dubourg C; Undiagnosed Diseases Network, Tan WH, Verbeek NE, Granzow M, Santen GWE, Shendure J, Isidor B, Pasquier L, Redon R, Yang Y, State MW, Kleefstra T, Cogné B; GEM HUGO; Deciphering Developmental Disorders Study, Petrovski S, Retterer K, Eichler EE, Rosenfeld JA, Agrawal PB, Bézieau S, Odent S, Elgersma Y, Mercier S.

Am J Hum Genet. 2017 Nov 2;101(5):768-788. doi: 10.1016/j.ajhg.2017.10.003.

27.

Oxidative stress and mitochondrial dynamics malfunction are linked in Pelizaeus-Merzbacher disease.

Ruiz M, Bégou M, Launay N, Ranea-Robles P, Bianchi P, López-Erauskin J, Morató L, Guilera C, Petit B, Vaurs-Barriere C, Guéret-Gonthier C, Bonnet-Dupeyron MN, Fourcade S, Auwerx J, Boespflug-Tanguy O, Pujol A.

Brain Pathol. 2018 Sep;28(5):611-630. doi: 10.1111/bpa.12571. Epub 2017 Dec 26.

PMID:
29027761
28.

Loss of SIRT2 leads to axonal degeneration and locomotor disability associated with redox and energy imbalance.

Fourcade S, Morató L, Parameswaran J, Ruiz M, Ruiz-Cortés T, Jové M, Naudí A, Martínez-Redondo P, Dierssen M, Ferrer I, Villarroya F, Pamplona R, Vaquero A, Portero-Otín M, Pujol A.

Aging Cell. 2017 Dec;16(6):1404-1413. doi: 10.1111/acel.12682. Epub 2017 Oct 5.

29.

A Nucleophilic Gold(III) Carbene Complex.

Pujol A, Lafage M, Rekhroukh F, Saffon-Merceron N, Amgoune A, Bourissou D, Nebra N, Fustier-Boutignon M, Mézailles N.

Angew Chem Int Ed Engl. 2017 Sep 25;56(40):12264-12267. doi: 10.1002/anie.201706197. Epub 2017 Aug 24.

PMID:
28782276
30.

Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes.

Rotroff DM, Pijut SS, Marvel SW, Jack JR, Havener TM, Pujol A, Schluter A, Graf GA, Ginsberg HN, Shah HS, Gao H, Morieri ML, Doria A, Mychaleckyi JC, McLeod HL, Buse JB, Wagner MJ, Motsinger-Reif AA; ACCORD/ACCORDion Investigators.

Clin Pharmacol Ther. 2018 Apr;103(4):712-721. doi: 10.1002/cpt.798. Epub 2017 Nov 3.

31.

Surgical options in benign parotid tumors: a proposal for classification.

Quer M, Vander Poorten V, Takes RP, Silver CE, Boedeker CC, de Bree R, Rinaldo A, Sanabria A, Shaha AR, Pujol A, Zbären P, Ferlito A.

Eur Arch Otorhinolaryngol. 2017 Nov;274(11):3825-3836. doi: 10.1007/s00405-017-4650-4. Epub 2017 Jun 21. Review.

PMID:
28639060
32.

Double Diastereoselective Approach to Chiral syn- and anti-1,3-Diol Analogues through Consecutive Catalytic Asymmetric Borylations.

Pujol A, Whiting A.

J Org Chem. 2017 Jul 21;82(14):7265-7279. doi: 10.1021/acs.joc.7b00854. Epub 2017 Jun 30.

PMID:
28628323
33.

Strategies for reducing the risk of transfusion-transmitted leishmaniasis in an area endemic for Leishmania infantum: a patient- and donor-targeted approach.

Jimenez-Marco T, Riera C, Girona-Llobera E, Guillen C, Iniesta L, Alcover M, Berenguer D, Pujol A, Tomás-Pérez M, Cancino-Faure B, Serra T, Mascaró M, Gascó J, Fisa R.

Blood Transfus. 2018 Feb;16(2):130-136. doi: 10.2450/2017.0201-16. Epub 2017 Mar 15.

34.

Use of the ROLL technique for lumpectomy in non-palpable breast lesions.

Carrera D, Martín L, Flor M, Guspí F, Picas J, Izquierdo V, Martínez S, Jordà C, Siurana R, Martínez-Casals M, Jaén JM, Pujol A, Benítez A.

Rev Esp Med Nucl Imagen Mol. 2017 Sep - Oct;36(5):285-291. doi: 10.1016/j.remn.2017.02.004. Epub 2017 Mar 22. English, Spanish.

PMID:
28341228
35.

Disease correction by AAV-mediated gene therapy in a new mouse model of mucopolysaccharidosis type IIID.

Roca C, Motas S, Marcó S, Ribera A, Sánchez V, Sánchez X, Bertolin J, León X, Pérez J, Garcia M, Villacampa P, Ruberte J, Pujol A, Haurigot V, Bosch F.

Hum Mol Genet. 2017 Apr 15;26(8):1535-1551. doi: 10.1093/hmg/ddx058.

PMID:
28334745
36.

A multi-faceted strategy to reduce ventilation-associated mortality in brain-injured patients. The BI-VILI project: a nationwide quality improvement project.

Asehnoune K, Mrozek S, Perrigault PF, Seguin P, Dahyot-Fizelier C, Lasocki S, Pujol A, Martin M, Chabanne R, Muller L, Hanouz JL, Hammad E, Rozec B, Kerforne T, Ichai C, Cinotti R, Geeraerts T, Elaroussi D, Pelosi P, Jaber S, Dalichampt M, Feuillet F, Sebille V, Roquilly A; BI-VILI study group.

Intensive Care Med. 2017 Jul;43(7):957-970. doi: 10.1007/s00134-017-4764-6. Epub 2017 Mar 18.

PMID:
28315940
37.

Bicomponent Supramolecular Architectures at the Vacuum-Solid Interface.

Bouju X, Mattioli C, Franc G, Pujol A, Gourdon A.

Chem Rev. 2017 Feb 8;117(3):1407-1444. doi: 10.1021/acs.chemrev.6b00389. Epub 2017 Jan 18. Review.

PMID:
28097870
38.

Tauroursodeoxycholic bile acid arrests axonal degeneration by inhibiting the unfolded protein response in X-linked adrenoleukodystrophy.

Launay N, Ruiz M, Grau L, Ortega FJ, Ilieva EV, Martínez JJ, Galea E, Ferrer I, Knecht E, Pujol A, Fourcade S.

Acta Neuropathol. 2017 Feb;133(2):283-301. doi: 10.1007/s00401-016-1655-9. Epub 2016 Dec 21.

39.

Mutations in Histone Acetylase Modifier BRPF1 Cause an Autosomal-Dominant Form of Intellectual Disability with Associated Ptosis.

Mattioli F, Schaefer E, Magee A, Mark P, Mancini GM, Dieterich K, Von Allmen G, Alders M, Coutton C, van Slegtenhorst M, Vieville G, Engelen M, Cobben JM, Juusola J, Pujol A, Mandel JL, Piton A.

Am J Hum Genet. 2017 Jan 5;100(1):105-116. doi: 10.1016/j.ajhg.2016.11.010. Epub 2016 Dec 8.

40.

Residual craniofacial growth: A cephalometric study of 50 cases.

Oualalou Y, Antouri MA, Pujol A, Zaoui F, Azaroual MF.

Int Orthod. 2016 Dec;14(4):438-448. doi: 10.1016/j.ortho.2016.10.007. Epub 2016 Nov 14.

PMID:
27856378
41.

La croissance craniofaciale résiduelle : étude céphalométrique à propos de 50 cas.

Oualalou Y, Antouri MA, Pujol A, Zaoui F, Azaroual MF.

Int Orthod. 2016 Dec;14(4):438-448. doi: 10.1016/j.ortho.2016.10.008. Epub 2016 Nov 14. French. No abstract available.

PMID:
27856372
42.

De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females.

Webster R, Cho MT, Retterer K, Millan F, Nowak C, Douglas J, Ahmad A, Raymond GV, Johnson MR, Pujol A, Begtrup A, McKnight D, Devinsky O, Chung WK.

Clin Genet. 2017 May;91(5):756-763. doi: 10.1111/cge.12854. Epub 2016 Sep 29.

43.

Progressive neurologic and somatic disease in a novel mouse model of human mucopolysaccharidosis type IIIC.

Marcó S, Pujol A, Roca C, Motas S, Ribera A, Garcia M, Molas M, Villacampa P, Melia CS, Sánchez V, Sánchez X, Bertolin J, Ruberte J, Haurigot V, Bosch F.

Dis Model Mech. 2016 Sep 1;9(9):999-1013. doi: 10.1242/dmm.025171. Epub 2016 Aug 4.

44.

A view on clinical genetics and genomics in Spain: of challenges and opportunities.

Pàmpols T, Ramos FJ, Lapunzina P, Gozalo-Salellas I, Pérez-Jurado LA, Pujol A.

Mol Genet Genomic Med. 2016 Jul 18;4(4):376-91. doi: 10.1002/mgg3.232. eCollection 2016 Jul.

45.

Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families.

Soehn AS, Rattay TW, Beck-Wödl S, Schäferhoff K, Monk D, Döbler-Neumann M, Hörtnagel K, Schlüter A, Ruiz M, Pujol A, Züchner S, Riess O, Schüle R, Bauer P, Schöls L.

Neurology. 2016 Jul 12;87(2):186-91. doi: 10.1212/WNL.0000000000002843. Epub 2016 Jun 17.

46.

Transfusion-transmitted leishmaniasis: a practical review.

Jimenez-Marco T, Fisa R, Girona-Llobera E, Cancino-Faure B, Tomás-Pérez M, Berenguer D, Guillen C, Pujol A, Iniesta L, Serra T, Mascaró M, Gascó J, Riera C.

Transfusion. 2016 Mar;56 Suppl 1:S45-51. doi: 10.1111/trf.13344. Review.

PMID:
27001361
47.

Targeted activation of CREB in reactive astrocytes is neuroprotective in focal acute cortical injury.

Pardo L, Schlüter A, Valor LM, Barco A, Giralt M, Golbano A, Hidalgo J, Jia P, Zhao Z, Jové M, Portero-Otin M, Ruiz M, Giménez-Llort L, Masgrau R, Pujol A, Galea E.

Glia. 2016 May;64(5):853-74. doi: 10.1002/glia.22969. Epub 2016 Feb 16.

PMID:
26880229
48.

Ruminococcus gnavus E1 modulates mucin expression and intestinal glycosylation.

Graziani F, Pujol A, Nicoletti C, Dou S, Maresca M, Giardina T, Fons M, Perrier J.

J Appl Microbiol. 2016 May;120(5):1403-17. doi: 10.1111/jam.13095. Epub 2016 Apr 4.

49.

Novel Neuroprotective Multicomponent Therapy for Amyotrophic Lateral Sclerosis Designed by Networked Systems.

Herrando-Grabulosa M, Mulet R, Pujol A, Mas JM, Navarro X, Aloy P, Coma M, Casas C.

PLoS One. 2016 Jan 25;11(1):e0147626. doi: 10.1371/journal.pone.0147626. eCollection 2016.

50.

Oxidative stress level in fresh ejaculate is not related to semen parameters or to pregnancy rates in cycles with donor oocytes.

Pujol A, Obradors A, Esteo E, Costilla B, García D, Vernaeve V, Vassena R.

J Assist Reprod Genet. 2016 Apr;33(4):529-34. doi: 10.1007/s10815-016-0660-1. Epub 2016 Jan 22.

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