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A case of a hereditary, late progressing sensory autonomic neuropathy

dc.contributor.authorInce, B
dc.contributor.authorOnganer, E
dc.contributor.authorCinar, Y
dc.contributor.authorHekimoglu, F
dc.contributor.authorInce, U
dc.date.accessioned2021-03-03T20:14:18Z
dc.date.available2021-03-03T20:14:18Z
dc.date.issued1998
dc.identifier.citationCinar Y., Hekimoglu F., Ince B., Ince U., Onganer E., "A case of a hereditary, late progressing sensory autonomic neuropathy", CLINICAL NEUROPATHOLOGY, cilt.17, sa.1, ss.12-14, 1998
dc.identifier.issn0722-5091
dc.identifier.othervv_1032021
dc.identifier.otherav_58df9f2a-e114-4b8f-ba11-5b3a87224030
dc.identifier.urihttp://hdl.handle.net/20.500.12627/62548
dc.description.abstractA case of a hereditary sensory autonomic neuropathy (HSAN) with severe medical complications that had been reported as nonprogressive HSAN typo II has been followed and treated for a period of 10 years, and is now considered to be progressive HSAN type III, is presented, Current difficulties in the present form of the classification of HSAN, the necessity to observe these cases for longer periods and possible prolongation of survival with appropriate supportive treatment are emphasized.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectDahili Tıp Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleA case of a hereditary, late progressing sensory autonomic neuropathy
dc.typeMakale
dc.relation.journalCLINICAL NEUROPATHOLOGY
dc.contributor.department, ,
dc.identifier.volume17
dc.identifier.issue1
dc.identifier.startpage12
dc.identifier.endpage14
dc.contributor.firstauthorID19941


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