Zobrazeno 1 - 10
of 58
pro vyhledávání: '"C. Foguem"'
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Randall disease is an unusual cause of extraocular motor nerve (VI) palsy. A 35-year-old woman was hospitalized for sicca syndrome. The physical examination showed general weakness, weight loss, diplopia related to a left VIth nerve palsy, hypertroph
Externí odkaz:
https://doaj.org/article/b035f885f4d946039b6657ebee9ebd3a
Publikováno v:
Clinical Rheumatology. 42:1-14
Primary Sjögren's syndrome is an autoimmune exocrinopathy related to lymphocytic infiltration of the exocrine glandular epithelia (such as salivary, lacrimal, nasal, and sebaceous glands or vaginal mucosa) with systemic manifestations of an immuno-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc6d2f4d1744ce11d103f59e47b9868
https://doi.org/10.1007/s10067-022-06359-w
https://doi.org/10.1007/s10067-022-06359-w
Nasal chemosensory tests: biomarker between dementia with Lewy bodies and Parkinson disease dementia
Publikováno v:
Rhinology, Vol. 58, no. 6, p. 605-609 (2020)
BACKGROUND: Dementia with Lewy bodies (DLB) and Parkinson disease dementia (PDD) are progressive and disabling neurodegenerative disorders, which are often misdiagnosed due to theirs overlapping clinical and paraclinical features. Nevertheless, their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88fd289bfcea6bcea41df7028213daa9
https://pubmed.ncbi.nlm.nih.gov/32830809
https://pubmed.ncbi.nlm.nih.gov/32830809
Akademický článek
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Publikováno v:
Rhinology, Vol. 56, no. 2, p. 127-132 (2018)
BACKGROUND: Human nasal chemosensation is mediated by two separate, though interacting sensory pathways: the trigeminal and olfactory systems. Trigeminal sensitivity and olfacto-trigeminal interactions have not yet been well studied in idiopathic Par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88fdc63a4060fde026a1b1682be2dd6e
https://pubmed.ncbi.nlm.nih.gov/29550854
https://pubmed.ncbi.nlm.nih.gov/29550854
Publikováno v:
La Revue de Médecine Interne. 30:165-169
Resume Introduction De tres nombreuses pathologies peuvent etre responsables de granulomes, decouverts parfois fortuitement sur un prelevement anatomopathologique, et de ce fait entrent dans le vaste cadre des granulomatoses. La presentation clinique
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b241b9bff3bde02a5db29bb8e4ea835
https://doi.org/10.1016/j.revmed.2008.09.007
https://doi.org/10.1016/j.revmed.2008.09.007
Autor:
C. Hafsaoui, Bernadette Kantelip, C. Foguem, Nadine Magy-Bertrand, Eric Deconinck, Jean-Louis Dupond, H. Gil, Nadine Meaux-Ruault
Publikováno v:
La Revue de Médecine Interne. 30:49-52
Resume Introduction La maladie de Randall ou maladie par depot de chaines legeres d’immunoglobulines est une affection systemique caracterisee par la deposition de chaines legeres monoclonales libres, n’ayant pas de caracteristiques tinctoriales
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e69f52435db209109e64a2410a80a392
https://doi.org/10.1016/j.revmed.2008.08.003
https://doi.org/10.1016/j.revmed.2008.08.003
Autor:
Martin F. Lambert, Thomas Quemeneur, Benoit Wallaert, P.Y. Hatron, D. Launay, C. Foguem, E. Hachulla
Publikováno v:
La Revue de Médecine Interne. 27:620-624
Resume Introduction La maladie kystique pulmonaire se caracterise iconographiquement par des images pulmonaires hypodenses a paroi bien definie et fine ( Exegese Nous rapportons deux cas de maladie kystique pulmonaire associee au syndrome de Gougerot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2a4a44fc75079b3c99f73fed278bb92
https://doi.org/10.1016/j.revmed.2006.04.011
https://doi.org/10.1016/j.revmed.2006.04.011
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Case Reports in Medicine
Case Reports in Medicine
Randall disease is an unusual cause of extraocular motor nerve (VI) palsy. A 35-year-old woman was hospitalized for sicca syndrome. The physical examination showed general weakness, weight loss, diplopia related to a left VIth nerve palsy, hypertroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e1a78425b6eedcf46b9fd1f4b366f4f
https://doaj.org/article/b035f885f4d946039b6657ebee9ebd3a
https://doaj.org/article/b035f885f4d946039b6657ebee9ebd3a
Autor:
C, Foguem, B, Kantelip, E, Deconinck, C, Hafsaoui, N, Méaux-Ruault, H, Gil, N, Magy-Bertrand, J-L, Dupond
Publikováno v:
La Revue de Médecine Interne
La Revue de Médecine Interne, Elsevier, 2009, 30 (1), pp.49-52. ⟨10.1016/j.revmed.2008.08.003⟩
La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2009, 30 (1), pp.49-52. ⟨10.1016/j.revmed.2008.08.003⟩
La Revue de Médecine Interne, Elsevier, 2009, 30 (1), pp.49-52. ⟨10.1016/j.revmed.2008.08.003⟩
La Revue De Médecine Interne
La Revue De Médecine Interne, Elsevier, 2009, 30 (1), pp.49-52. ⟨10.1016/j.revmed.2008.08.003⟩
International audience; INTRODUCTION: Light chain deposition disease is a systemic disorder characterised by tissue deposition of monoclonal immunoglobulin light chains without tinctorial properties. It has been exceptionally reported with salivary i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::49b2b6f43568123fd09e611ef6d6f216
https://www.hal.inserm.fr/inserm-00484589
https://www.hal.inserm.fr/inserm-00484589
