A case of congenital Horner syndrome from the 16th century.
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| Title: | A case of congenital Horner syndrome from the 16th century. |
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| 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 32702330 AccessLevel: 2 PubType: Editorial & Opinion PubTypeId: editorialOpinion PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A case of congenital Horner syndrome from the 16th century. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Bianucci+R%22">Bianucci R</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Kirkpatrick+CL%22">Kirkpatrick CL</searchLink>; Paleo-oncology Research Organization, Minneapolis, MN, USA; Department of Anthropology, University of Western Ontario, London, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Perciaccante+A%22">Perciaccante A</searchLink>; Azienda Sanitaria Universitaria Giuliano Isontina, Department of Medicine 'San Giovanni di Dio' Hospital, Gorizia, Italy.<br /><searchLink fieldCode="AU" term="%22Galassi+FM%22">Galassi FM</searchLink>; Archaeology, College of Humanities, Arts and Social Sciences, Flinders University, Adelaide, SA, Australia; FAPAB Research Center, Avola, Italy.<br /><searchLink fieldCode="AU" term="%22Lippi+D%22">Lippi D</searchLink>; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.<br /><searchLink fieldCode="AU" term="%22Appenzeller+O%22">Appenzeller O</searchLink>; New Mexico Health Enhancement and Marathon Clinics Research Foundation, Albuquerque, NM, USA; New Mexico Museum of Natural History and Science, Albuquerque, NM, USA.<br /><searchLink fieldCode="AU" term="%22Nerlich+AG%22">Nerlich AG</searchLink>; Institute of Pathology, Academic Clinic Munich-Bogenhausen, Munich, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101139309%22">The Lancet. Neurology</searchLink> [Lancet Neurol] 2020 Aug; Vol. 19 (8), pp. 646-647. – Name: TypePub Label: Publication Type Group: TypPub Data: Historical Article; Letter; Portrait – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lancet+Pub%2E+Group%22">Lancet Pub. Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101139309 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1474-4465 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214744422%22">14744422 </searchLink><i>NLM ISO Abbreviation: </i>Lancet Neurol <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32702330 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/S1474-4422(20)30214-3 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 646 Titles: – TitleFull: A case of congenital Horner syndrome from the 16th century. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bianucci R – PersonEntity: Name: NameFull: Kirkpatrick CL – PersonEntity: Name: NameFull: Perciaccante A – PersonEntity: Name: NameFull: Galassi FM – PersonEntity: Name: NameFull: Lippi D – PersonEntity: Name: NameFull: Appenzeller O – PersonEntity: Name: NameFull: Nerlich AG IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 08 Text: 2020 Aug Type: published Y: 2020 Identifiers: – Type: issn-electronic Value: 1474-4465 Numbering: – Type: volume Value: 19 – Type: issue Value: 8 Titles: – TitleFull: The Lancet. Neurology Type: main |
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