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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: ferrer i. 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
Somatic mosaicism in a case of apparently sporadic Creutzfeldt-Jakob disease carrying a de novo D178N mutation in the PRNP gene.
Alzualde A, Moreno F, Martínez-Lage P, Ferrer I, Gorostidi A, Otaegui D, Blázquez L, Atares B, Cardoso S, Martínez de Pancorbo M, Juste R, Rodríguez-Martínez AB, Indakoetxea B, López de Munain A. Alzualde A, et al. Among authors: ferrer i. Am J Med Genet B Neuropsychiatr Genet. 2010 Oct 5;153B(7):1283-91. doi: 10.1002/ajmg.b.31099. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20872767
Severe adenovirus infection: presentation of 3 cases.
García ACG, Ferrer ITB, Pelegay PC, Romero RG, de Vicente CM. García ACG, et al. Among authors: ferrer itb. An Pediatr (Engl Ed). 2024 May 28:S2341-2879(24)00144-3. doi: 10.1016/j.anpede.2024.05.005. Online ahead of print. An Pediatr (Engl Ed). 2024. PMID: 38811334 No abstract available.
Putting the brakes on axonal branching.
Ferrer I, Sanyal C, Moutin MJ, Lorenzo DN. Ferrer I, et al. Trends Neurosci. 2024 May 16:S0166-2236(24)00081-X. doi: 10.1016/j.tins.2024.05.001. Online ahead of print. Trends Neurosci. 2024. PMID: 38760194
1,336 results