dc.contributor.author | Aydinlar, Elif Ilgaz | |
dc.contributor.author | Ertas, Mustafa | |
dc.date.accessioned | 2023-02-21T10:07:36Z | |
dc.date.available | 2023-02-21T10:07:36Z | |
dc.identifier.citation | Aydinlar E. I., Ertas M., "Case series of HaNDL syndrome responding to valproic acid", Cephalalgia Reports, cilt.5, 2022 | |
dc.identifier.issn | 2515-8163 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_3cf6eda5-5e90-402c-a2a1-afd6e8d21940 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/188124 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85126576757&origin=inward | |
dc.identifier.uri | https://doi.org/10.1177/25158163221084274 | |
dc.description.abstract | © The Author(s) 2022.Objective: We report a case series of patients diagnosed with the syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis (HaNDL) responding to high dose Valproic acid. Background: HaNDL syndrome is an infrequent entity, presenting with neurological impairment episodes and severe headache. A treatment to prevent the attacks has not been proposed yet. Results: We describe 6 patients with a definite diagnosis of HaNDL, responding to Valproic acid 1000–1500 mg/day. Conclusion: Although HaNDL’s self-limiting nature, episodes may cause important disability and can last up to 3 months. Valproic acid may be a good choice to prevent attacks due to its effect on cortical depression and fast titration. | |
dc.language.iso | eng | |
dc.subject | Nöroloji | |
dc.subject | Nöroloji (klinik) | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıp | |
dc.subject | KLİNİK NÖROLOJİ | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.title | Case series of HaNDL syndrome responding to valproic acid | |
dc.type | Makale | |
dc.relation.journal | Cephalalgia Reports | |
dc.contributor.department | Acıbadem Mehmet Ali Aydınlar Üniversitesi , , | |
dc.identifier.volume | 5 | |
dc.contributor.firstauthorID | 4185225 | |