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1.

Publisher Correction: Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T; GERAD1 Consortium; CRESTAR Consortium, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR.

Nat Genet. 2019 Jul;51(7):1193. doi: 10.1038/s41588-019-0450-7.

2.

Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis.

Rees E, Carrera N, Morgan J, Hambridge K, Escott-Price V, Pocklington AJ, Richards AL, Pardiñas AF; GROUP Investigators, McDonald C, Donohoe G, Morris DW, Kenny E, Kelleher E, Gill M, Corvin A, Kirov G, Walters JTR, Holmans P, Owen MJ, O'Donovan MC.

Biol Psychiatry. 2019 Apr 1;85(7):554-562. doi: 10.1016/j.biopsych.2018.08.022. Epub 2018 Oct 1.

3.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.

Pardiñas AF, Holmans P, Pocklington AJ, Escott-Price V, Ripke S, Carrera N, Legge SE, Bishop S, Cameron D, Hamshere ML, Han J, Hubbard L, Lynham A, Mantripragada K, Rees E, MacCabe JH, McCarroll SA, Baune BT, Breen G, Byrne EM, Dannlowski U, Eley TC, Hayward C, Martin NG, McIntosh AM, Plomin R, Porteous DJ, Wray NR, Caballero A, Geschwind DH, Huckins LM, Ruderfer DM, Santiago E, Sklar P, Stahl EA, Won H, Agerbo E, Als TD, Andreassen OA, Bækvad-Hansen M, Mortensen PB, Pedersen CB, Børglum AD, Bybjerg-Grauholm J, Djurovic S, Durmishi N, Pedersen MG, Golimbet V, Grove J, Hougaard DM, Mattheisen M, Molden E, Mors O, Nordentoft M, Pejovic-Milovancevic M, Sigurdsson E, Silagadze T, Hansen CS, Stefansson K, Stefansson H, Steinberg S, Tosato S, Werge T; GERAD1 Consortium; CRESTAR Consortium, Collier DA, Rujescu D, Kirov G, Owen MJ, O'Donovan MC, Walters JTR.

Nat Genet. 2018 Mar;50(3):381-389. doi: 10.1038/s41588-018-0059-2. Epub 2018 Feb 26. Erratum in: Nat Genet. 2019 Jul;51(7):1193.

4.

Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples.

Rodríguez-López J, Sobrino B, Amigo J, Carrera N, Brenlla J, Agra S, Paz E, Carracedo Á, Páramo M, Arrojo M, Costas J.

Eur Arch Psychiatry Clin Neurosci. 2018 Sep;268(6):585-592. doi: 10.1007/s00406-017-0799-5. Epub 2017 Apr 18.

PMID:
28421333
5.

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.

Marshall CR, Howrigan DP, Merico D, Thiruvahindrapuram B, Wu W, Greer DS, Antaki D, Shetty A, Holmans PA, Pinto D, Gujral M, Brandler WM, Malhotra D, Wang Z, Fajarado KVF, Maile MS, Ripke S, Agartz I, Albus M, Alexander M, Amin F, Atkins J, Bacanu SA, Belliveau RA Jr, Bergen SE, Bertalan M, Bevilacqua E, Bigdeli TB, Black DW, Bruggeman R, Buccola NG, Buckner RL, Bulik-Sullivan B, Byerley W, Cahn W, Cai G, Cairns MJ, Campion D, Cantor RM, Carr VJ, Carrera N, Catts SV, Chambert KD, Cheng W, Cloninger CR, Cohen D, Cormican P, Craddock N, Crespo-Facorro B, Crowley JJ, Curtis D, Davidson M, Davis KL, Degenhardt F, Del Favero J, DeLisi LE, Dikeos D, Dinan T, Djurovic S, Donohoe G, Drapeau E, Duan J, Dudbridge F, Eichhammer P, Eriksson J, Escott-Price V, Essioux L, Fanous AH, Farh KH, Farrell MS, Frank J, Franke L, Freedman R, Freimer NB, Friedman JI, Forstner AJ, Fromer M, Genovese G, Georgieva L, Gershon ES, Giegling I, Giusti-Rodríguez P, Godard S, Goldstein JI, Gratten J, de Haan L, Hamshere ML, Hansen M, Hansen T, Haroutunian V, Hartmann AM, Henskens FA, Herms S, Hirschhorn JN, Hoffmann P, Hofman A, Huang H, Ikeda M, Joa I, Kähler AK, Kahn RS, Kalaydjieva L, Karjalainen J, Kavanagh D, Keller MC, Kelly BJ, Kennedy JL, Kim Y, Knowles JA, Konte B, Laurent C, Lee P, Lee SH, Legge SE, Lerer B, Levy DL, Liang KY, Lieberman J, Lönnqvist J, Loughland CM, Magnusson PKE, Maher BS, Maier W, Mallet J, Mattheisen M, Mattingsdal M, McCarley RW, McDonald C, McIntosh AM, Meier S, Meijer CJ, Melle I, Mesholam-Gately RI, Metspalu A, Michie PT, Milani L, Milanova V, Mokrab Y, Morris DW, Müller-Myhsok B, Murphy KC, Murray RM, Myin-Germeys I, Nenadic I, Nertney DA, Nestadt G, Nicodemus KK, Nisenbaum L, Nordin A, O'Callaghan E, O'Dushlaine C, Oh SY, Olincy A, Olsen L, O'Neill FA, Van Os J, Pantelis C, Papadimitriou GN, Parkhomenko E, Pato MT, Paunio T; Psychosis Endophenotypes International Consortium, Perkins DO, Pers TH, Pietiläinen O, Pimm J, Pocklington AJ, Powell J, Price A, Pulver AE, Purcell SM, Quested D, Rasmussen HB, Reichenberg A, Reimers MA, Richards AL, Roffman JL, Roussos P, Ruderfer DM, Salomaa V, Sanders AR, Savitz A, Schall U, Schulze TG, Schwab SG, Scolnick EM, Scott RJ, Seidman LJ, Shi J, Silverman JM, Smoller JW, Söderman E, Spencer CCA, Stahl EA, Strengman E, Strohmaier J, Stroup TS, Suvisaari J, Svrakic DM, Szatkiewicz JP, Thirumalai S, Tooney PA, Veijola J, Visscher PM, Waddington J, Walsh D, Webb BT, Weiser M, Wildenauer DB, Williams NM, Williams S, Witt SH, Wolen AR, Wormley BK, Wray NR, Wu JQ, Zai CC, Adolfsson R, Andreassen OA, Blackwood DHR, Bramon E, Buxbaum JD, Cichon S, Collier DA, Corvin A, Daly MJ, Darvasi A, Domenici E, Esko T, Gejman PV, Gill M, Gurling H, Hultman CM, Iwata N, Jablensky AV, Jönsson EG, Kendler KS, Kirov G, Knight J, Levinson DF, Li QS, McCarroll SA, McQuillin A, Moran JL, Mowry BJ, Nöthen MM, Ophoff RA, Owen MJ, Palotie A, Pato CN, Petryshen TL, Posthuma D, Rietschel M, Riley BP, Rujescu D, Sklar P, St Clair D, Walters JTR, Werge T, Sullivan PF, O'Donovan MC, Scherer SW, Neale BM, Sebat J; CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium.

Nat Genet. 2017 Jan;49(1):27-35. doi: 10.1038/ng.3725. Epub 2016 Nov 21. Erratum in: Nat Genet. 2017 Mar 30;49(4):651. Nat Genet. 2017 Sep 27;49(10 ):1558.

6.

Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia.

Costas J, Carrera N, Alonso P, Gurriarán X, Segalàs C, Real E, López-Solà C, Mas S, Gassó P, Domènech L, Morell M, Quintela I, Lázaro L, Menchón JM, Estivill X, Carracedo Á.

Transl Psychiatry. 2016 Mar 29;6:e768. doi: 10.1038/tp.2016.34.

7.

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Tsuang MT, Glatt SJ, Chen WJ, Hwu HG; Taiwanese Trios Exome Sequencing Consortium, Neale BM, Palotie A, Sklar P, Purcell SM, McCarroll SA, Holmans P, Owen MJ, O'Donovan MC.

Transl Psychiatry. 2015 Jul 21;5:e607. doi: 10.1038/tp.2015.99.

8.

An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders.

Rodriguez-Lopez J, Carrera N, Arrojo M, Amigo J, Sobrino B, Páramo M, Paz E, Agra S, Ramos-Ríos R, Brenlla J, Carracedo Á, Costas J.

Clin Chim Acta. 2015 May 20;445:34-40. doi: 10.1016/j.cca.2015.03.013. Epub 2015 Mar 20.

PMID:
25797897
9.

De novo mutations in schizophrenia implicate synaptic networks.

Fromer M, Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S, Gormley P, Georgieva L, Rees E, Palta P, Ruderfer DM, Carrera N, Humphreys I, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Grant SG, Hannon E, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Kirov G, Palotie A, McCarroll SA, Holmans P, Sklar P, Owen MJ, Purcell SM, O'Donovan MC.

Nature. 2014 Feb 13;506(7487):179-84. doi: 10.1038/nature12929. Epub 2014 Jan 22.

10.

Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs.

Costas J, Suárez-Rama JJ, Carrera N, Paz E, Páramo M, Agra S, Brenlla J, Ramos-Ríos R, Arrojo M.

Ann Hum Genet. 2013 Nov;77(6):504-12. doi: 10.1111/ahg.12037. Epub 2013 Jul 30.

11.

[Subcutaneously inserted central intravascular devices in the pediatric oncology patient: can we minimize their infection].

Tardáguila AR, Del Cañizo A, Santos MM, Fanjul M, Corona C, Zornoza M, Parente A, Carrera N, Beléndez C, Cerdá J, Saavedra J, Molina E, García-Casillas MA, Peláez D.

Cir Pediatr. 2011 Oct;24(4):208-13. Spanish.

PMID:
23155633
12.

[Cold-knife retrograde endoscopic endopyelotomy (Cutting-Balloon) in children with ureteropelvic junction obstruction: early results].

Carrera N, Parente A, Rivas S, Romero R, Angulo JM.

Cir Pediatr. 2011 Oct;24(4):192-5. Spanish.

PMID:
23155630
13.

[Response to treatment with corticoids in a case of inflammatory amyloid angiopathy without performing a biopsy].

de la Riva P, Moreno F, Carrera N, Barandiarán M, Arruti M, Martí-Massó JF.

Rev Neurol. 2012 Oct 1;55(7):408-12. Spanish.

14.

[Role of peritoneal drainage in necrotizing enterocolitis in critical infants with extremely low birth weight].

Zornoza M, Peláez D, Romero R, Corona C, Tardáguila A, Rojo R, Carrera N, Cañizo A, Molina E, García-Casillas MA, Cerdá J.

Cir Pediatr. 2011 Aug;24(3):146-50. Spanish.

PMID:
22295655
15.

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia.

Carrera N, Arrojo M, Sanjuán J, Ramos-Ríos R, Paz E, Suárez-Rama JJ, Páramo M, Agra S, Brenlla J, Martínez S, Rivero O, Collier DA, Palotie A, Cichon S, Nöthen MM, Rietschel M, Rujescu D, Stefansson H, Steinberg S, Sigurdsson E, St Clair D, Tosato S, Werge T, Stefansson K, González JC, Valero J, Gutiérrez-Zotes A, Labad A, Martorell L, Vilella E, Carracedo Á, Costas J.

Biol Psychiatry. 2012 Jan 15;71(2):169-77. doi: 10.1016/j.biopsych.2011.09.032. Epub 2011 Nov 10.

PMID:
22078303
16.

[Hypertrophic pyloric stenosis: comparison between transversal and supraumbilical incision].

Carrera N, Cerdá JA, Cañizo A, Parente A, Laín A, Fanjul M, Corona C, Molina E, de Tomás E, Vázquez J.

Cir Pediatr. 2010 Apr;23(2):77-81. Spanish.

PMID:
21298914
17.

[Phimosis: dorsal slit or circumcision?].

Corona C, Cañizo A, Cerda J, Fanjul M, Carrera N, Tardáguila A, Zornoza M, Parente A, Angulo JM, De Tomás E, Molina E, Peláez D, García Casillas MA, Rivas S, Romero R, Marín MC.

Cir Pediatr. 2011 Jan;24(1):51-4. Spanish.

PMID:
23155652
18.

Syntheses and structures of thermally stable diketiminato complexes of gold and copper.

Carrera N, Savjani N, Simpson J, Hughes DL, Bochmann M.

Dalton Trans. 2011 Feb 7;40(5):1016-9. doi: 10.1039/c0dt01422b. Epub 2010 Dec 9.

PMID:
21152532
19.

[Percutaneous gastrostomy: when should antireflux surgery be associated?].

Corona C, Cañizo A, Cerda J, Laín A, Fanjul M, Carrera N, Tardáguila A, García-Casillas MA, Parente A, Molina E, Matute JA, Peláez D.

Cir Pediatr. 2010 Jul;23(3):189-92. Spanish.

PMID:
23155668
20.

Testing the antagonistic pleiotropy model of schizophrenia susceptibility by analysis of DAOA, PPP1R1B, and APOL1 genes.

Carrera N, Arrojo M, Paz E, Ramos-Ríos R, Agra S, Páramo M, Brenlla J, Costas J.

Psychiatry Res. 2010 Sep 30;179(2):126-9. doi: 10.1016/j.psychres.2009.05.014. Epub 2010 May 18.

PMID:
20483474
21.

[Long-term results of patients with congenital diaphragmatic hernia].

Menéndez C, Fariñas M, Parente A, Laín A, Fanjul M, Chimenti P, Carrera N, Huerga A, Corona C, Marsinyach I, Cañizo A, Villar S, Sánchez-Luna M, Vázquez J.

Cir Pediatr. 2009 Oct;22(4):205-9. Spanish.

PMID:
20405656
22.

[Is it correct to use neonatal intensive care units as operating rooms?].

Parente A, Cañizo A, Huerga A, Laín A, Fanjul M, Carrera N, Corona C, Fariñas M, Menéndez C, Cerdá J, Molina E, Vázquez J.

Cir Pediatr. 2009 Apr;22(2):61-4. Spanish.

PMID:
19715126
23.
24.

[Characteristics of the anorectal atresia without fistula. Based on 12 cases].

Fanjul M, Molina E, Cerdá J, Parente A, Laín A, Cañizo A, Carrera N.

Cir Pediatr. 2009 Jan;22(1):45-8. Spanish.

PMID:
19323083
25.

A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia.

Costas J, Carrera N, Domínguez E, Vilella E, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A.

Hum Genet. 2009 Jan;124(6):607-13. doi: 10.1007/s00439-008-0584-7. Epub 2008 Nov 6.

PMID:
18987889
26.

Stannylated polynorbornenes as new reagents for a clean Stille reaction.

Carrera N, Gutiérrez E, Benavente R, Villavieja MM, Albéniz AC, Espinet P.

Chemistry. 2008;14(32):10141-8. doi: 10.1002/chem.200800558.

PMID:
18816555
27.

[Tracheal stenosis: outcome analysis of the last 14 years].

Laín A, García-Casillas MA, Matute JA, Cañizo A, Parente A, Fanjul M, Carrera N, Vázquez J.

Cir Pediatr. 2008 Jul;21(3):138-42. Spanish.

PMID:
18756866
28.

[Is immediate prophylactic thyroidectomy indispensable in familiar medullary thyroid carcinoma?].

Cañizo A, Fanjul M, Cerdá J, Menárguez J, Parente A, Laín A, Carrera N, Rodríguez-Arnao MD, Rodríguez-Sánchez A, Polo JR, Vázquez J.

Cir Pediatr. 2008 Apr;21(2):100-3. Spanish.

PMID:
18624279
29.

Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia.

Carrera N, Sanjuán J, Moltó MD, Carracedo A, Costas J.

Am J Med Genet B Neuropsychiatr Genet. 2009 Apr 5;150B(3):369-74. doi: 10.1002/ajmg.b.30823.

PMID:
18553363
30.

Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.

López de Munain A, Alzualde A, Gorostidi A, Otaegui D, Ruiz-Martínez J, Indakoetxea B, Ferrer I, Pérez-Tur J, Sáenz A, Bergareche A, Barandiarán M, Poza JJ, Zabalza R, Ruiz I, Urtasun M, Fernández-Manchola I, Olasagasti B, Espinal JB, Olaskoaga J, Ruibal M, Moreno F, Carrera N, Martí Massó JF.

Biol Psychiatry. 2008 May 15;63(10):946-52. Epub 2007 Oct 22.

PMID:
17950702
31.

Trimetazidine induces parkinsonism, gait disorders and tremor.

Martí Massó JF, Martí I, Carrera N, Poza JJ, López de Munain A.

Therapie. 2005 Jul-Aug;60(4):419-22.

PMID:
16268443
32.

Phenotypic variability in familial prion diseases due to the D178N mutation.

Zarranz JJ, Digon A, Atarés B, Rodríguez-Martínez AB, Arce A, Carrera N, Fernández-Manchola I, Fernández-Martínez M, Fernández-Maiztegui C, Forcadas I, Galdos L, Gómez-Esteban JC, Ibáñez A, Lezcano E, López de Munain A, Martí-Massó JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, de Pancorbo MM.

J Neurol Neurosurg Psychiatry. 2005 Nov;76(11):1491-6.

33.

Familial prion diseases in the Basque Country (Spain).

Zarranz JJ, Digon A, Atarés B, Arteagoitia JM, Carrera N, Fernández-Manchola I, Fernández-Martínez M, Fernández-Maiztegui C, Forcadas I, Galdos L, Ibáñez A, Lezcano E, Martí-Massó JF, Mendibe MM, Urtasun M, Uterga JM, Saracibar N, Velasco F, González de Galdeano L.

Neuroepidemiology. 2005;24(1-2):103-9. Epub 2004 Sep 24.

PMID:
15459517
34.

[Clinical variability of bilateral paramedian thalamic infarcts].

Martínez Pérez-Balsa A, Martí-Massó JF, Carrera N, Urtasun M.

Rev Neurol. 1997 Sep;25(145):1353-62. Spanish.

PMID:
9377289
35.

[Benign intracranial hypertension: a new symptom and a new association].

Martí Massó JF, Carrera N, Blanco A, Martí Carrera E.

Neurologia. 1996 May;11(5):197-8. Spanish. No abstract available.

PMID:
8754636
36.

[Corticobasal ganglionic degeneration: a report of 7 clinically diagnosed cases].

Martí Massó JF, López de Munain A, Poza JJ, Urtasun M, Carrera N.

Neurologia. 1994 Mar;9(3):115-20. Spanish.

PMID:
8204260
37.

Clinical signs of brain death simulated by Guillain-Barré syndrome.

Martí-Massó JF, Suárez J, López de Munain A, Carrera N.

J Neurol Sci. 1993 Dec 1;120(1):115-7.

PMID:
8289072
38.

Drug-induced parkinsonism: a growing list.

Martí Massó JF, Carrera N, Urtasun M.

Mov Disord. 1993;8(1):125. No abstract available.

PMID:
8419801
39.

High-dose intravenous immune globulin in the management of severe Guillain-Barre syndrome.

Urtasun M, López de Munain A, Carrera N, Martí-Massó JF, López de Dicastillo G, Mozo C.

Ann Pharmacother. 1992 Jan;26(1):32-3.

PMID:
1606342
40.

[Paralysis of the vertical gaze caused by a hematoma of the caudate nucleus. A false localizing sign].

López de Munain A, Martí Massó JF, Carrera N, Urtasún M, Blanco A.

Neurologia. 1988 May-Jun;3(3):116-9. Spanish. No abstract available.

PMID:
3273514
41.

Aggravation of Parkinson's disease by cinnarizine.

Martí Massó JF, Obeso JA, Carrera N, Martínez-Lage JM.

J Neurol Neurosurg Psychiatry. 1987 Jun;50(6):804-5.

42.

[Vascular abnormalities in a case of tuberous sclerosis].

Martí Massó JF, Carrera N, Zabalza R.

Neurologia. 1986 Jan-Feb;1(1):36-8. Spanish. No abstract available.

PMID:
3274106
43.

[Parkinsonism possibly caused by cinnarizine].

Martí Massó JF, Carrera N, de la Puente E.

Med Clin (Barc). 1985 Nov 9;85(15):614-6. Spanish. No abstract available.

PMID:
4079549
44.

[Pseudomigraine with inflammatory cerebrospinal fluid: a benign syndrome].

Martí Massó JF, Obeso JA, Carrera N, de la Puente E.

Med Clin (Barc). 1984 Nov 17;83(16):665-7. Spanish. No abstract available.

PMID:
6513656
45.

[Eosinophilic meningitis caused by lipiodol myelography].

Martí-Massó JF, Carrera N, Zabalza R.

Med Clin (Barc). 1983 Oct 8;81(10):440-1. Spanish. No abstract available.

PMID:
6316041
46.

[Hepatotoxicity caused by diphenylhydantoin].

Martí Massó JF, Carrera N, Zabalza R, García Bengoechea M.

Med Clin (Barc). 1983 Sep 17;81(7):320-1. Spanish. No abstract available.

PMID:
6645676
47.

Pseudomigraine with CSF lymphocytosis.

Marti Masso JF, Obeso JA, Carrera N, Martiniz Lage JM.

Neurology. 1983 Apr;33(4):524-5. No abstract available.

PMID:
6682206
48.

Lithium therapy in torsion dystonia.

Marti-Masso JF, Obeso JA, Carrera N, Astudillo W, Martinez Lage JM.

Ann Neurol. 1982 Jan;11(1):106-7. No abstract available.

PMID:
7059126
49.

[Supracallosal hematoma simulating a subarachnoid hemorrhage].

Martí Massó JF, Obeso J, Carrera N, Gereka L.

Rev Clin Esp. 1981 Oct 15;163(1):55-60. Spanish. No abstract available.

PMID:
7330339
50.

[Acute polyradiculoneuritis and amyotrophic neuralgia in Addison's disease].

Martí-Massó JF, Obeso JA, de la Puente E, Carrera N, Damiano A.

Rev Clin Esp. 1981 Oct 15;163(1):53-4. Spanish. No abstract available.

PMID:
7330338

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