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Page 1
Actinomycotic brain abscess: CT findings.
Millán JM, Escudero L, Roger RL, de la Fuente M, Díez I. Millán JM, et al. J Comput Assist Tomogr. 1985 Sep-Oct;9(5):976-8. doi: 10.1097/00004728-198509000-00030. J Comput Assist Tomogr. 1985. PMID: 4031181
Multiple intracranial hydatid cysts.
Gordillo I, Millán JM, Escudero L, Orduna M, Roger R, de la Fuente M. Gordillo I, et al. Among authors: millan jm. Neuroradiology. 1986;28(3):285. doi: 10.1007/BF00548210. Neuroradiology. 1986. PMID: 3725020 No abstract available.
Intraventricular hemorrhage in severe head injury.
Cordobés F, de la Fuente M, Lobato RD, Roger R, Pérez C, Millán JM, Bárcena A, Lamas E. Cordobés F, et al. Among authors: millan jm. J Neurosurg. 1983 Feb;58(2):217-22. doi: 10.3171/jns.1983.58.2.0217. J Neurosurg. 1983. PMID: 6600274
Cranial fasciitis of childhood with reactive periostitis.
Mollejo M, Millán JM, Ballestin C, Serrano C. Mollejo M, et al. Among authors: millan jm. Surg Neurol. 1990 Feb;33(2):146-9. doi: 10.1016/0090-3019(90)90025-k. Surg Neurol. 1990. PMID: 2305359
Acute perfusion changes after spontaneous SAH: a perfusion CT study.
Lagares A, Cicuendez M, Ramos A, Salvador E, Alén JF, Kaen A, Jiménez-Roldán L, Millán JM. Lagares A, et al. Among authors: millan jm. Acta Neurochir (Wien). 2012 Mar;154(3):405-11; discussion 411-2. doi: 10.1007/s00701-011-1267-z. Epub 2012 Jan 12. Acta Neurochir (Wien). 2012. PMID: 22234794 Clinical Trial.
Primary hepatocellular adenoma in men.
Pulpeiro JR, Orduña M, Jimenez J, Gallego MS, Millán JM. Pulpeiro JR, et al. Among authors: millan jm. J Clin Ultrasound. 1989 May;17(4):269-74. doi: 10.1002/jcu.1870170407. J Clin Ultrasound. 1989. PMID: 2541173 No abstract available.
Giant cell reparative granuloma of the occipital bone.
Santos-Briz A, Lobato RD, Ramos A, Millán JM, Ricoy JR, Martínez-Tello FJ. Santos-Briz A, et al. Among authors: millan jm. Skeletal Radiol. 2003 Mar;32(3):151-5. doi: 10.1007/s00256-002-0563-3. Epub 2002 Dec 7. Skeletal Radiol. 2003. PMID: 12605280 Review.
Deciphering complexity: TULP1 variants linked to an atypical retinal dystrophy phenotype.
Esteve-Garcia A, Cobos E, Sau C, Padró-Miquel A, Català-Mora J, Barberán-Martínez P, Millán JM, García-García G, Aguilera C. Esteve-Garcia A, et al. Among authors: millan jm. Front Genet. 2024 Feb 21;15:1352063. doi: 10.3389/fgene.2024.1352063. eCollection 2024. Front Genet. 2024. PMID: 38450199 Free PMC article.
223 results