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Items: 1 to 50 of 68

1.

Milder forms of α-sarcoglicanopathies diagnosed in adulthood by NGS analysis.

Cantero D, Hernández-Laín A, Martínez JFG, Pérez MR, Ruano Y, Lleixà C, Gallardo E, Domínguez-González C.

J Neurol Sci. 2018 Nov 15;394:63-67. doi: 10.1016/j.jns.2018.08.026. Epub 2018 Sep 5.

PMID:
30218921
2.

Perfusion MRI grading diffuse gliomas: Impact of permeability parameters on molecular biomarkers and survival.

Hilario A, Hernandez-Lain A, Sepulveda JM, Lagares A, Perez-Nuñez A, Ramos A.

Neurocirugia (Astur). 2018 Aug 21. pii: S1130-1473(18)30067-8. doi: 10.1016/j.neucir.2018.06.004. [Epub ahead of print] English, Spanish.

PMID:
30143443
3.

Tumor cell vanishing with radiological changes suggesting progression in IDH-mutated diffuse astrocytoma treated only with surgery.

Hernandez-Lain A, Hilario A, Sepulveda JM, Cantero D, Ramos A, Perez-Nuñez A.

Clin Neuropathol. 2018 Sep/Oct;37(5):217-220. doi: 10.5414/NP301116.

PMID:
30079885
4.

Molecular Study of Long-Term Survivors of Glioblastoma by Gene-Targeted Next-Generation Sequencing.

Cantero D, Rodríguez de Lope Á, Moreno de la Presa R, Sepúlveda JM, Borrás JM, Castresana JS, D'Haene N, García JF, Salmon I, Mollejo M, Rey JA, Hernández-Laín A, Meléndez B.

J Neuropathol Exp Neurol. 2018 Aug 1;77(8):710-716. doi: 10.1093/jnen/nly048.

PMID:
30010995
5.

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, Diaz-Manera J, Davis M, Ávila R, Domínguez C, Romero NB, Vílchez JJ, Comas D, Laing NG, Laporte J, Kalaydjieva L, Paradas C.

Neurology. 2018 Jul 24;91(4):e339-e348. doi: 10.1212/WNL.0000000000005862. Epub 2018 Jun 27.

PMID:
29950440
6.

Author Correction: STAT3 labels a subpopulation of reactive astrocytes required for brain metastasis.

Priego N, Zhu L, Monteiro C, Mulders M, Wasilewski D, Bindeman W, Doglio L, Martínez L, Martínez-Saez E, Ramón Y Cajal S, Megías D, Hernández-Encinas E, Blanco-Aparicio C, Martínez L, Zarzuela E, Muñoz J, Fustero-Torre C, Piñeiro-Yáñez E, Hernández-Laín A, Bertero L, Poli V, Sanchez-Martinez M, Menendez JA, Soffietti R, Bosch-Barrera J, Valiente M.

Nat Med. 2018 Sep;24(9):1481. doi: 10.1038/s41591-018-0108-5.

PMID:
29921958
7.

STAT3 labels a subpopulation of reactive astrocytes required for brain metastasis.

Priego N, Zhu L, Monteiro C, Mulders M, Wasilewski D, Bindeman W, Doglio L, Martínez L, Martínez-Saez E, Cajal SRY, Megías D, Hernández-Encinas E, Blanco-Aparicio C, Martínez L, Zarzuela E, Muñoz J, Fustero-Torre C, Piñeiro-Yáñez E, Hernández-Laín A, Bertero L, Poli V, Sanchez-Martinez M, Menendez JA, Soffietti R, Bosch-Barrera J, Valiente M.

Nat Med. 2018 Jul;24(7):1024-1035. doi: 10.1038/s41591-018-0044-4. Epub 2018 Jun 11. Erratum in: Nat Med. 2018 Jun 19;:.

PMID:
29892069
8.

Correction to: SEOM clinical guidelines for anaplastic gliomas (2017).

Balañá C, Alonso M, Hernandez-Lain A, Perez-Segura P, Pineda E, Ramos A, Sanchez AR, Teixidor P, Verger E, Benavides M.

Clin Transl Oncol. 2018 Jul;20(7):937. doi: 10.1007/s12094-018-1904-6.

PMID:
29858734
9.

Concurrent progressive multifocal leukoencephalopathy and central nervous system infiltration by multiple myeloma: A case report.

Ruiz-Heredia Y, Sanchez-Vega B, Barrio S, Linares M, Rapado I, Braggio E, Stewart K, Folgueira MD, Ramos A, Collado L, Ruiz J, Toldos O, Hernandez-Lain A, Martinez-Lopez J.

J Oncol Pharm Pract. 2018 Jan 1:1078155218769367. doi: 10.1177/1078155218769367. [Epub ahead of print]

PMID:
29690814
10.

Correction to: SEOM clinical guideline of diagnosis and management of low-grade glioma (2017).

Sepúlveda-Sánchez JM, Muñoz Langa J, Arráez MÁ, Fuster J, Hernández Laín A, Reynés G, Rodríguez González V, Vicente E, Vidal Denis M, Gallego Ó.

Clin Transl Oncol. 2018 Jan;20(1):108-109. doi: 10.1007/s12094-017-1814-z.

PMID:
29209952
11.

SEOM clinical guideline of diagnosis and management of low-grade glioma (2017).

Sepúlveda-Sánchez JM, Muñoz Langa J, Arráez MÁ, Fuster J, Hernández Laín A, Reynés G, Rodríguez González V, Vicente E, Vidal Denis M, Gallego Ó.

Clin Transl Oncol. 2018 Jan;20(1):3-15. doi: 10.1007/s12094-017-1790-3. Epub 2017 Nov 9. Erratum in: Clin Transl Oncol. 2017 Dec 5;:.

12.

[Assessment of the correlation between histological degeneration and radiological and clinical parameters in a series of patients who underwent lumbar disc herniation surgery].

Munarriz PM, Paredes I, Alén JF, Castaño-Leon AM, Cepeda S, Hernandez-Lain A, Lagares A.

Neurocirugia (Astur). 2018 Mar - Apr;29(2):79-85. doi: 10.1016/j.neucir.2017.07.003. Epub 2017 Sep 28. Spanish.

PMID:
28967575
13.

Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene.

Martín-Hernández E, García-Silva MT, Quijada-Fraile P, Rodríguez-García ME, Rivera H, Hernández-Laín A, Coca-Robinot D, Fernández-Toral J, Arenas J, Martín MA, Martínez-Azorín F.

Pediatr Dev Pathol. 2017 Sep-Oct;20(5):416-420. doi: 10.1177/1093526616686439. Epub 2017 Jan 25.

PMID:
28812460
14.

Enteroviral T-cell encephalitis related to immunosuppressive therapy including rituximab.

Garzo-Caldas N, Ruiz-Sainz E, Vila-Bedmar S, Llamas-Velasco S, Hernández-Lain A, Ruiz-Morales J, Folgueira-López D, Villarejo-Galende A.

Neurology. 2017 Jul 25;89(4):408-409. doi: 10.1212/WNL.0000000000004148. Epub 2017 Jun 23. No abstract available.

15.

Phase II trial of dacomitinib, a pan-human EGFR tyrosine kinase inhibitor, in recurrent glioblastoma patients with EGFR amplification.

Sepúlveda-Sánchez JM, Vaz MÁ, Balañá C, Gil-Gil M, Reynés G, Gallego Ó, Martínez-García M, Vicente E, Quindós M, Luque R, Ramos A, Ruano Y, Pérez-Segura P, Benavides M, Sánchez-Gómez P, Hernández-Laín A.

Neuro Oncol. 2017 Oct 19;19(11):1522-1531. doi: 10.1093/neuonc/nox105.

16.

Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome.

Bellusci M, Quijada-Fraile P, Barrio-Carreras D, Martin-Hernandez E, Garcia-Silva M, Merinero B, Perez B, Hernandez-Lain A.

J Inherit Metab Dis. 2017 Sep;40(5):751-752. doi: 10.1007/s10545-017-0041-7. Epub 2017 May 2. No abstract available.

PMID:
28466427
17.

Delayed tacrolimus leukoencephalopathy, a rare and reversible cause of dementia.

Barragán-Martínez D, Simarro-Díaz A, Calleja-Castaño P, Hernández-Laín A, Ramos-González A, Villarejo-Galende A.

Neurol Neuroimmunol Neuroinflamm. 2017 Jan 10;4(2):e319. doi: 10.1212/NXI.0000000000000319. eCollection 2017 Mar. No abstract available.

18.

Glioblastoma on a microfluidic chip: Generating pseudopalisades and enhancing aggressiveness through blood vessel obstruction events.

Ayuso JM, Monge R, Martínez-González A, Virumbrales-Muñoz M, Llamazares GA, Berganzo J, Hernández-Laín A, Santolaria J, Doblaré M, Hubert C, Rich JN, Sánchez-Gómez P, Pérez-García VM, Ochoa I, Fernández LJ.

Neuro Oncol. 2017 Apr 1;19(4):503-513. doi: 10.1093/neuonc/now230.

19.

Muscle fiber type proportion and size is not altered in mcardle disease.

Henning F, Cunninghame CA, Martín MA, Rubio JC, Arenas J, Lucia A, HernáNdez-Laín A, Kohn TA.

Muscle Nerve. 2017 Jun;55(6):916-918. doi: 10.1002/mus.25472. Epub 2016 Dec 16.

PMID:
27859426
20.

Novel mutation in TCAP manifesting with asymmetric calves and early-onset joint retractions.

de Fuenmayor-Fernández de la Hoz CP, Hernández-Laín A, Olivé M, Fernández-Marmiesse A, Domínguez-González C.

Neuromuscul Disord. 2016 Nov;26(11):749-753. doi: 10.1016/j.nmd.2016.07.003. Epub 2016 Jul 16.

PMID:
27618135
21.

Myosin myopathy with external ophthalmoplegia associated with a novel homozygous mutation in MYH2.

Hernández-Laín A, Esteban-Pérez J, Montenegro DC, Domínguez-González C.

Muscle Nerve. 2017 Feb;55(2):E8-E10. doi: 10.1002/mus.25365. Epub 2016 Sep 1. No abstract available.

PMID:
27490141
22.

Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders.

Yubero D, Montero R, Martín MA, Montoya J, Ribes A, Grazina M, Trevisson E, Rodriguez-Aguilera JC, Hargreaves IP, Salviati L, Navas P, Artuch R; CoQ deficiency study group, Jou C, Jimenez-Mallebrera C, Nascimento A, Pérez-Dueñas B, Ortez C, Ramos F, Colomer J, O'Callaghan M, Pineda M, García-Cazorla A, Espinós C, Ruiz A, Macaya A, Marcé-Grau A, Garcia-Villoria J, Arias A, Emperador S, Ruiz-Pesini E, Lopez-Gallardo E, Neergheen V, Simões M, Diogo L, Blázquez A, González-Quintana A, Delmiro A, Domínguez-González C, Arenas J, García-Silva MT, Martín E, Quijada P, Hernández-Laín A, Morán M, Rivas Infante E, Ávila Polo R, Paradas Lópe C, Bautista Lorite J, Martínez Fernández EM, Cortés AB, Sánchez-Cuesta A, Cascajo MV, Alcázar M, Brea-Calvo G.

Mitochondrion. 2016 Sep;30:51-8. doi: 10.1016/j.mito.2016.06.007. Epub 2016 Jun 30.

PMID:
27374853
23.

Temozolomide induces radiologic pseudoprogression and tumor cell vanishing in oligodendroglioma.

Hernandez-Lain A, Hilario A, Sepulveda JM, Cantero D, Ramos A, Perez-Nuñez A.

Neurology. 2016 Jul 5;87(1):114-5. doi: 10.1212/WNL.0000000000002810. Epub 2016 Jun 1. No abstract available.

PMID:
27251883
24.

A milder phenotype of megaconial congenital muscular dystrophy due to a novel CHKB mutation.

De Fuenmayor-Fernández De La Hoz CP, Domínguez-González C, Gonzalo-Martínez JF, Esteban-Pérez J, Fernández-Marmiesse A, Arenas J, Martín MA, Hernández-Laín A.

Muscle Nerve. 2016 Oct;54(4):806-8. doi: 10.1002/mus.25183. Epub 2016 Jun 9. No abstract available.

PMID:
27169979
25.

Calf pseudohipertrophy.

Zurita Prada PA, Faré García R, Urrego Laurín CL, Pérez Toledo R, Tabernero García C, Hernández Laín A.

Reumatol Clin. 2017 May - Jun;13(3):173-175. doi: 10.1016/j.reuma.2016.02.012. Epub 2016 Apr 18. English, Spanish.

26.

Leakage decrease detected by dynamic susceptibility-weighted contrast-enhanced perfusion MRI predicts survival in recurrent glioblastoma treated with bevacizumab.

Hilario A, Sepulveda JM, Hernandez-Lain A, Salvador E, Koren L, Manneh R, Ruano Y, Perez-Nuñez A, Lagares A, Ramos A.

Clin Transl Oncol. 2017 Jan;19(1):51-57. doi: 10.1007/s12094-016-1502-4. Epub 2016 Mar 30.

PMID:
27026567
27.

Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene.

Martín-Hernández E, García-Silva MT, Quijada-Fraile P, Rodríguez-García ME, Hernández-Laín A, Coca-Robinot D, Rivera H, Fernández-Toral J, Arenas J, Martín M, Martínez-Azorín F.

Pediatr Dev Pathol. 2016 Feb 29. [Epub ahead of print]

PMID:
26925861
28.

[Acute rhabdomyolysis in a female heterozygotic carrier of an undescribed mutation in the PNPLA2 gene].

Pinel A, Hernández-Laín A, Gil-Fournier B, Ramiro-León S.

Rev Neurol. 2015 Dec 1;61(11):525-6. Spanish. No abstract available.

29.

Pathology-confirmed cerebral arterial invasion and recurrent multiple brain metastasis from cardiac myxoma without evidence of disease after surgery and radiotherapy.

Castaño-Leon AM, Hernandez-Lain A, Maroñas L, López P, Ayuso LL, Ramos A, Pérez-Regadera J, Roldan LJ.

Clin Neuropathol. 2016 Mar-Apr;35(2):84-8. doi: 10.5414/NP300900. No abstract available.

PMID:
26413778
30.

A novel RRM2B gene variant associated with Telbivudine-induced mitochondrial myopathy.

Hernández-Laín A, Guerrero AM, Domínguez-González C, Fernández-Vázquez I, Maya DG, Delmiro A, Arenas J, Morales JR, Blázquez A, Moran M, Martín MA.

J Neurol Sci. 2015 Nov 15;358(1-2):481-3. doi: 10.1016/j.jns.2015.08.1550. Epub 2015 Sep 2. No abstract available.

PMID:
26359855
31.

Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy.

Cámara Y, Carreño-Gago L, Martín MA, Melià MJ, Blázquez A, Delmiro A, Garrabou G, Morén C, Díaz-Manera J, Gallardo E, Bornstein B, López-Gallardo E, Hernández-Lain A, San Millán B, Cancho E, Rodríguez-Vico JS, Martí R, García-Arumí E.

Neurology. 2015 Jun 2;84(22):2286-8. doi: 10.1212/WNL.0000000000001644. Epub 2015 May 6. No abstract available.

PMID:
25948719
32.

Preclinical Test of Dacomitinib, an Irreversible EGFR Inhibitor, Confirms Its Effectiveness for Glioblastoma.

Zahonero C, Aguilera P, Ramírez-Castillejo C, Pajares M, Bolós MV, Cantero D, Perez-Nuñez A, Hernández-Laín A, Sánchez-Gómez P, Sepúlveda JM.

Mol Cancer Ther. 2015 Jul;14(7):1548-58. doi: 10.1158/1535-7163.MCT-14-0736. Epub 2015 May 4.

33.

Evidence-Based Diagnostic Algorithm for Glioma: Analysis of the Results of Pathology Panel Review and Molecular Parameters of EORTC 26951 and 26882 Trials.

Kros JM, Huizer K, Hernández-Laín A, Marucci G, Michotte A, Pollo B, Rushing EJ, Ribalta T, French P, Jaminé D, Bekka N, Lacombe D, van den Bent MJ, Gorlia T.

J Clin Oncol. 2015 Jun 10;33(17):1943-50. doi: 10.1200/JCO.2014.59.0166. Epub 2015 Apr 27.

PMID:
25918297
34.

Controlled release microspheres loaded with BMP7 suppress primary tumors from human glioblastoma.

González-Gómez P, Crecente-Campo J, Zahonero C, de la Fuente M, Hernández-Laín A, Mira H, Sánchez-Gómez P, Garcia-Fuentes M.

Oncotarget. 2015 May 10;6(13):10950-63.

35.

PET-Florbetapir findings in primary cerebral amyloidoma.

Villarejo-Galende A, Sarandeses P, Penas-Prado M, Hernández-Laín A, Ramos A, Hernández-Martínez AC, Carro E, Ricoy JR, Hernández-Gallego J.

J Neurol. 2015;262(4):1052-4. doi: 10.1007/s00415-015-7643-5. Epub 2015 Jan 22. No abstract available.

PMID:
25605437
36.

LAMA2-related congenital muscular dystrophy complicated by West syndrome.

Camacho A, Núñez N, Dekomien G, Hernández-Laín A, de Aragón AM, Simón R.

Eur J Paediatr Neurol. 2015 Mar;19(2):243-7. doi: 10.1016/j.ejpn.2014.11.005. Epub 2014 Dec 2.

PMID:
25500573
37.

Mitochondrial cardiomyopathies associated with the m.3243A>G mutation in the MT-TL1 gene: two sides of the same coin.

Gallego-Delgado M, Cobo-Marcos M, Bornstein B, Hernández-Laín A, Alonso-Pulpón L, Garcia-Pavia P.

Rev Esp Cardiol (Engl Ed). 2015 Feb;68(2):153-5. doi: 10.1016/j.rec.2014.09.007. Epub 2014 Nov 28. No abstract available.

PMID:
25440178
38.

A new muscle glycogen storage disease associated with glycogenin-1 deficiency.

Malfatti E, Nilsson J, Hedberg-Oldfors C, Hernandez-Lain A, Michel F, Dominguez-Gonzalez C, Viennet G, Akman HO, Kornblum C, Van den Bergh P, Romero NB, Engel AG, DiMauro S, Oldfors A.

Ann Neurol. 2014 Dec;76(6):891-8. doi: 10.1002/ana.24284. Epub 2014 Oct 31.

39.

[Neurodevelopmental disorders as the presenting symptom of Duchenne's muscular dystrophy].

Camacho-Salas A, Núñez-Enamorado N, Zamora B, Hernández-Laín A, Simón-De Las Heras R.

Rev Neurol. 2014 Feb 16;58(4):187-8. Spanish.

40.

Spinal tanycytic ependymoma associated with neurofibromatosis type 2.

Cepeda S, Hernández-Laín A, Munarriz PM, Martínez González MA, Lagares A.

Clin Neuropathol. 2014 Jul-Aug;33(4):311-4. doi: 10.5414/NP300704. No abstract available.

PMID:
24495349
41.

A prognostic model based on preoperative MRI predicts overall survival in patients with diffuse gliomas.

Hilario A, Sepulveda JM, Perez-Nuñez A, Salvador E, Millan JM, Hernandez-Lain A, Rodriguez-Gonzalez V, Lagares A, Ramos A.

AJNR Am J Neuroradiol. 2014 Jun;35(6):1096-102. doi: 10.3174/ajnr.A3837. Epub 2014 Jan 23.

42.

Clinical features and molecular characterization of a patient with muscle-eye-brain disease: a novel mutation in the POMGNT1 gene.

Raducu M, Cotarelo RP, Simón R, Camacho A, Rubio-Fernández M, Hernández-Laín A, Cruces J.

J Child Neurol. 2014 Feb;29(2):289-94. doi: 10.1177/0883073813509119. Epub 2013 Nov 25.

PMID:
24282183
43.

Integrated analysis of mismatch repair system in malignant astrocytomas.

Rodríguez-Hernández I, Garcia JL, Santos-Briz A, Hernández-Laín A, González-Valero JM, Gómez-Moreta JA, Toldos-González O, Cruz JJ, Martin-Vallejo J, González-Sarmiento R.

PLoS One. 2013 Sep 20;8(9):e76401. doi: 10.1371/journal.pone.0076401. eCollection 2013.

44.

Pathology of bilateral pulvinar degeneration following long duration status epilepticus.

Hernandez-Lain A, Hedley-Whyte ET, Hariri LP, Molyneaux B, Nagle KJ, Cole AJ, Kilbride R.

Seizure. 2013 Dec;22(10):901-4. doi: 10.1016/j.seizure.2013.07.012. Epub 2013 Aug 17.

45.

Codeletion of 1p and 19q determines distinct gene methylation and expression profiles in IDH-mutated oligodendroglial tumors.

Mur P, Mollejo M, Ruano Y, de Lope ÁR, Fiaño C, García JF, Castresana JS, Hernández-Laín A, Rey JA, Meléndez B.

Acta Neuropathol. 2013 Aug;126(2):277-89. doi: 10.1007/s00401-013-1130-9. Epub 2013 May 21.

PMID:
23689617
46.

Inhibition of DYRK1A destabilizes EGFR and reduces EGFR-dependent glioblastoma growth.

Pozo N, Zahonero C, Fernández P, Liñares JM, Ayuso A, Hagiwara M, Pérez A, Ricoy JR, Hernández-Laín A, Sepúlveda JM, Sánchez-Gómez P.

J Clin Invest. 2013 Jun;123(6):2475-87. doi: 10.1172/JCI63623. Epub 2013 May 1.

47.

Tumefactive multiple sclerosis requiring emergency craniotomy: case report and literature review.

Munarriz PM, Castaño-Leon AM, Martinez-Perez R, Hernandez-Lain A, Ramos A, Lagares A.

Neurocirugia (Astur). 2013 Sep-Oct;24(5):220-4. doi: 10.1016/j.neucir.2013.02.008. Epub 2013 Apr 11. Review.

PMID:
23582489
48.

Mononeuritis multiplex due to leprosy: a case of atypical presentation.

Pedraza Hueso MI, Hinojosa Mena-Bernal C, Hernández-Laín A, Guerrero Peral AL.

Neurologia. 2014 Jun;29(5):313-4. doi: 10.1016/j.nrl.2012.10.012. Epub 2012 Dec 28. English, Spanish. No abstract available.

49.

Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.

Juan-Mateu J, Rodríguez MJ, Nascimento A, Jiménez-Mallebrera C, González-Quereda L, Rivas E, Paradas C, Madruga M, Sánchez-Ayaso P, Jou C, González-Mera L, Munell F, Roig-Quilis M, Rabasa M, Hernández-Lain A, Díaz-Manera J, Gallardo E, Pascual J, Verdura E, Colomer J, Baiget M, Olivé M, Gallano P.

Orphanet J Rare Dis. 2012 Oct 23;7:82. doi: 10.1186/1750-1172-7-82.

50.

Acute neurological deterioration as a result of two synchronous hemorrhagic spinal ependymomas.

Martinez-Perez R, Hernandez-Lain A, Paredes I, Munarriz PM, Castaño-Leon AM, Lagares A.

Surg Neurol Int. 2012;3:33. doi: 10.4103/2152-7806.93865. Epub 2012 Mar 14.

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