Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Ayse Caglar Sarilar"'
Autor:
Ayse Caglar Sarilar, Duygu Kurt Gök
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 38, Iss 4, Pp 245-249 (2021)
Objectives: The Boston Carpal Tunnel Questionnaire (BCTQ) is a patient-based outcome measure that has been developed for patients with Carpal tunnel syndrome (CTS). The purpose of this study was to investigate the association between BCTQ scores and
Externí odkaz:
https://doaj.org/article/8548743d6a634654a506262219f912d8
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim: The use of complementary and alternative medicine (CAM) is common in patients with primary headache. However, no study has been reported in which standardized modalities were questioned in a Turkish population. The aim of the present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01914120e541b4aab10515940ec78d64
https://doi.org/10.3906/sag-2102-234
https://doi.org/10.3906/sag-2102-234
Publikováno v:
Sleep Medicine. 77:256-260
Objective Electroencephalographic (EEG) changes in patients with NREM parasomnias (NRP) occur in sleep architecture as changes in slow wave sleep or cyclic pattern, which are not considered abnormal. However, abnormalities in EEG in these patients ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65d42206438b6cb8b6ef3005505f1566
https://doi.org/10.1016/j.sleep.2019.05.009
https://doi.org/10.1016/j.sleep.2019.05.009
Autor:
Nilgun Karasu, Hamit Acer, Hilal Akalin, Mikail Demir, Izem Olcay Sahin, Nuriye Gokce, Ayten Gulec, Asli Ciplakligil, Ayse Caglar Sarilar, Isa Cuce, Hakan Gumus, Huseyin Per, Mehmet Canpolat, Munis Dundar
SMA (spinal muscular atrophy) is an autosomal recessive neuromuscular disease that causes muscle atrophy and weakness. SMA is diagnosed by homozygous deletion in exon 7 of the SMN1 gene. However, mutations in other genes in the SMA region may contrib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9a4fb5184ae8c68b181b6881a5e87eb
https://doi.org/10.21203/rs.3.rs-1442537/v1
https://doi.org/10.21203/rs.3.rs-1442537/v1
HaNDL sendromu, migren benzeri orta siddette veya cok siddetli bas agrisi epizodlari ile beraber gecici norolojik defisitin goruldugu, beyin omurilik sivisinda (BOS) lenfositoz saptanan inme ve aurali migreni taklit edebilen, nadir bir sendromdur. Bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6506556b604f7dd8ad282076d21b314b
https://avesis.erciyes.edu.tr/publication/details/d5b7d44c-2c86-4a6b-b9f8-d782fc4076d2/oai
https://avesis.erciyes.edu.tr/publication/details/d5b7d44c-2c86-4a6b-b9f8-d782fc4076d2/oai
Autor:
Recep Baydemir, Elif Gülşen Köse, Ayse Caglar Sarilar, Kemal Erol, Ulfet Zehra Erbay, Murat Kendirci, Soner Senel, Murat Gultekin, Sule Ketenci Ertas, Sevda Ismailogullari, Meral Mirza, Mehmet Fatih Yetkin, Merve Akcakoyunlu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5cfe7d436c5c20c14066beab605786a
https://avesis.erciyes.edu.tr/publication/details/44f0db1d-77da-4385-983f-d4f0ea4710cc/oai
https://avesis.erciyes.edu.tr/publication/details/44f0db1d-77da-4385-983f-d4f0ea4710cc/oai
Publikováno v:
Bozok Tıp Dergisi.
Fabry hastalığı (FH), alfa galaktosidaz A (GLA) genindeki mutasyon nedeniyle oluşan, X’e bağlı kalıtılan lizozomal depo hastalığıdır. Hastalığın atipik formunda klinik semptomlar daha geç yaşlarda ortaya çıkar ve en sık görüle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06becfc94af172f30a6d75d4f9ead9b4
https://doi.org/10.16919/bozoktip.673653
https://doi.org/10.16919/bozoktip.673653
Autor:
Mehmet Canpolat, Ayse Caglar Sarilar, Mehmet Fatih Yetkin, Murat Gultekin, Recep Baydemir, Hüseyin Per, Meral Mirza
Publikováno v:
Noro Psikiyatr Ars
Friedreich's Ataxia (FRDA) is the most common form of autosomal recessive ataxia. The disease primarily results from a GAA trinucleotide repeat expansion within the FXN gene in up to 97% of patients. The clinical presentation begins approximately bet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecc0fb7a38b1dc51be772553b2190157
https://doi.org/10.29399/npa.25047
https://doi.org/10.29399/npa.25047
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Parkinson's Disease
Parkinson's Disease
Introduction. Only a few studies have been conducted to determine the level of knowledge among caregivers about Parkinson’s disease (PD). The aim of the current study was to determine the knowledge of PD among caregivers at a movement disorder clin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ac92cbc07676ad87342b3f4384deab0
https://doaj.org/article/377bc7d233c14854ade6e226b87f127d
https://doaj.org/article/377bc7d233c14854ade6e226b87f127d
Publikováno v:
Gülhane Tıp Dergisi, Vol 64, Iss 1, Pp 84-88 (2022)
Aims:The prevalence of Restless legs syndrome (RLS) in migraine patients is estimated to be 8.7-39.0%. In this study, we set out to compare the frequency of RLS in patients diagnosed with migraine with headache free participants.Methods:We included 2
Externí odkaz:
https://doaj.org/article/8f2f1b5114674da899fd80e9d4061cd3