A case of congenital Horner syndrome from the 16th century.

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Bibliographic Details
Title: A case of congenital Horner syndrome from the 16th century.
Authors: Bianucci R; Warwick Medical School, Biomedical Sciences, University of Warwick, Coventry CV4 7AL, UK; Legal Medicine Section, Department of Public Health and Paediatric Sciences, University of Turin, Turin, Italy; UMR 7268, Laboratoire d'Anthropologie bio-culturelle, Droit, Etique & Santé (Adés), Faculté de Médecine, Marseille, France. Electronic address: r.bianucci@warwick.ac.uk., Kirkpatrick CL; Paleo-oncology Research Organization, Minneapolis, MN, USA; Department of Anthropology, University of Western Ontario, London, ON, Canada., Perciaccante A; Azienda Sanitaria Universitaria Giuliano Isontina, Department of Medicine 'San Giovanni di Dio' Hospital, Gorizia, Italy., Galassi FM; Archaeology, College of Humanities, Arts and Social Sciences, Flinders University, Adelaide, SA, Australia; FAPAB Research Center, Avola, Italy., Lippi D; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy., Appenzeller O; New Mexico Health Enhancement and Marathon Clinics Research Foundation, Albuquerque, NM, USA; New Mexico Museum of Natural History and Science, Albuquerque, NM, USA., Nerlich AG; Institute of Pathology, Academic Clinic Munich-Bogenhausen, Munich, Germany.
Source: The Lancet. Neurology [Lancet Neurol] 2020 Aug; Vol. 19 (8), pp. 646-647.
Publication Type: Historical Article; Letter; Portrait
Journal Info: Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Internet ISSN: 1474-4465 (Electronic) Linking ISSN: 14744422 NLM ISO Abbreviation: Lancet Neurol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1474-4465
DOI:10.1016/S1474-4422(20)30214-3