Urtasun M - Search Results

1

Management of an outbreak of botulism with benign clinical presentation.

Equiza J, Campo-Caballero D, Rodríguez-Antigüedad J, Iruzubieta P, Vinagre-Aragón A, Echeverria J, Imaz N, Alberdi T, López de Munain A, Urtasun M, Espinal JB. Equiza J, et al. Among authors: urtasun m. J Clin Neurosci. 2021 Jun;88:159-162. doi: 10.1016/j.jocn.2021.03.041. Epub 2021 Apr 13. J Clin Neurosci. 2021. PMID: 33992177

2

Autoimmune GFAP astrocytopathy presenting with remarkable CNS hyperexcitability and oculogyric crises.

Equiza J, Rodríguez-Antigüedad J, Campo-Caballero D, Iruzubieta P, Prada Á, Roncancio A, Fernández E, Ganzarain Oyarbide M, Arruti M, Urtasun MA, Castillo-Triviño T. Equiza J, et al. Among authors: urtasun ma. J Neuroimmunol. 2021 Oct 15;359:577695. doi: 10.1016/j.jneuroim.2021.577695. Epub 2021 Aug 14. J Neuroimmunol. 2021. PMID: 34416409

3

Description of Two Families with New Mutations in Familial Cerebral Cavernous Malformations Genes.

Iruzubieta P, Campo-Caballero D, Equiza J, Albajar I, Sulibarría N, Sáez R, Andrés N, Mondragón E, Zulaica M, de Arce A, Urtasun M, López de Munain A. Iruzubieta P, et al. Among authors: urtasun m. J Stroke Cerebrovasc Dis. 2021 Dec;30(12):106130. doi: 10.1016/j.jstrokecerebrovasdis.2021.106130. Epub 2021 Sep 29. J Stroke Cerebrovasc Dis. 2021. PMID: 34597987

4

Clinical response to thalidomide in the treatment of intracranial tuberculomas: case report.

de la Riva P, Urtasun M, Castillo-Trivino T, Camino X, Arruti M, Mondragón E, Lopez de Munain A. de la Riva P, et al. Among authors: urtasun m. Clin Neuropharmacol. 2013 Mar-Apr;36(2):70-2. doi: 10.1097/WNF.0b013e318285caa1. Clin Neuropharmacol. 2013. PMID: 23503553 Review.

5

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. López de Munain A, et al. Among authors: urtasun m. Biol Psychiatry. 2008 May 15;63(10):946-52. doi: 10.1016/j.biopsych.2007.08.015. Epub 2007 Oct 22. Biol Psychiatry. 2008. PMID: 17950702

6

A common haplotype associated with the Basque 2362AG --> TCATCT mutation in the muscular calpain-3 gene.

Cobo AM, Sáenz A, Poza JJ, Urtasun M, Indakoetxea B, Urtizberea JA, López de Munain A, Calafell F. Cobo AM, et al. Among authors: urtasun m. Hum Biol. 2004 Oct;76(5):731-41. doi: 10.1353/hub.2005.0002. Hum Biol. 2004. PMID: 15757244

7

[Limb girdle dystrophy: a syndrome clinically and genetically heterogeneous].

Urtasun M, López de Munain A. Urtasun M, et al. Neurologia. 1999 Mar;14(3):97-101. Neurologia. 1999. PMID: 10232008 Review. Spanish. No abstract available.

8

Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?

Sáenz A, Ono Y, Sorimachi H, Goicoechea M, Leturcq F, Blázquez L, García-Bragado F, Marina A, Poza JJ, Azpitarte M, Doi N, Urtasun M, Kaplan JC, López de Munain A. Sáenz A, et al. Among authors: urtasun m. Muscle Nerve. 2011 Nov;44(5):710-4. doi: 10.1002/mus.22194. Muscle Nerve. 2011. PMID: 22006685

9

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. Urtasun M, et al. Ann Pharmacother. 1992 Jan;26(1):32-3. doi: 10.1177/106002809202600108. Ann Pharmacother. 1992. PMID: 1606342

10

The validity of Hodkinson's Abbreviated Mental Test for dementia screening in Guipuzcoa, Spain.

Sarasqueta C, Bergareche A, Arce A, Lopez de Munain A, Poza JJ, De La Puente E, Urtasun M, Emparanza JE, Martí Masso JF. Sarasqueta C, et al. Among authors: urtasun m. Eur J Neurol. 2001 Sep;8(5):435-40. doi: 10.1046/j.1468-1331.2001.00246.x. Eur J Neurol. 2001. PMID: 11554906 Clinical Trial.

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