Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Sefer Kumandas"'
Autor:
Hamit Acer, Gül Demet Özçora, Mehmet Canpolat, Muhammet Ensar Doğan, Zehra Filiz Kahraman, Sefer Kumandaş
Publikováno v:
The Journal of Pediatric Academy, Vol 5, Iss 3, Pp 93-98 (2024)
Cockayne syndrome (CS) is a rare, severe, genetic neurodegenerative disorder. To better understand the condition, this article aimed to discuss the clinical manifestations and prognosis of CS. This clinical study was a retrospective review of the med
Externí odkaz:
https://doaj.org/article/0339ff09e8e446eba93d577fdbea35ca
Autor:
Fatih Bayrakli, Mehmet Canpolat, Huseyin Per, Hakan Gumus, Sefer Kumandas, Ugur Kartal, Hatice Balaban
Publikováno v:
Case Reports in Neurology, Vol 6, Iss 1, Pp 18-22 (2014)
Background: Cerebellar hypoplasia (CH) is a rare malformation caused by various etiologies, usually manifesting clinically as nonprogressive cerebellar ataxia with or without mental retardation. The molecular pathogenesis of the autosomal recessive c
Externí odkaz:
https://doaj.org/article/33b61200e3bd40dca72ce2ea1fc92629
Autor:
Sema BOZKAYA YILMAZ, Eda KARADAG ONCEL, Nihal OLGAC DUNDAR, Pinar GENCPINAR, Berrak SARIOGLU, Pinar ARICAN, Atilla ERSEN, Dilek YILMAZ CIFTDOGAN, Merve Feyza YUKSEL, Omer BEKTAS, Serap TEBER, Betul KILIC, Mustafa CALIK, Meryem KARACA, Mehmet CANPOLAT, Sefer KUMANDAS, Huseyin PER, Hakan GUMUS, Selcan OZTURK, Cetin OKUYAZ, Mustafa KOMUR, Rojan IPEK, Pinar OZBUDAK, Ebru ARHAN, Hulya INCE, Gurkan GURBUZ, Gulen GUL MERT, Neslihan OZCAN, Akgun OLMEZ TURKER, Hande GAZETECI TEKIN, Serkan KIRIK, Ceren GUNBEY, Kursat Bora CARMAN, Coskun YARAR, Dilek CAVUSOGLU
Children with chronic neurological diseases,including cerebral palsy(CP)are especially susceptible to vaccine-preventable infections and face an increased risk of severe respiratory infections and decompensation of their disease.This study aims to ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c802ede368e90afdaa580ad571dc1fa1
https://doi.org/10.21203/rs.3.rs-288533/v1
https://doi.org/10.21203/rs.3.rs-288533/v1
Autor:
Huseyin Per, Munis Dundar, Ali Yikilmaz, Selim Doganay, Kenan Yilmaz, Hatice Poyrazoglu, Sibel Yel, Sefer Kumandas, Ruhan Dusunsel, Zubeyde Gunduz, Hakan Gumus, Mehmet Canpolat, Ayşe Bayram
Publikováno v:
Neuropediatrics. 48:402-402
Autor:
Huseyin, Per, Mehmet, Canpolat, Ugur, Sahin, Hakan, Gumus, Bahadir, Konuskan, Sefer, Kumandas
Publikováno v:
Saudi medical journal. 33(9)
To determine the role of serum and urine selenium, and boron levels in children with resistant epilepsy.Serum and urine boron and selenium levels were studied in 53 cases (32 boys and 21 girls) diagnosed with resistant epilepsy between April 2006 and
Autor:
Mehmet, Canpolat, Sefer, Kumandas, Ali, Yikilmaz, Hakan, Gumus, Emel, Koseoglu, Hatice Gamze, Poyrazoğlu, Mehmet, Kose, Huseyin, Per
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 55(6)
Guillain-Barré syndrome is a rapidly progressive symmetrical muscle weakness associated with acute inflammatory disease. Transverse myelitis (TM) is the inflammation of the spinal cord characterized by rapidly evolving muscle weakness in the lower e
Autor:
Recep, Aksu, Sefer, Kumandas, Aynur, Akin, Cihangir, Bicer, Hakan, Gümüş, Gülen, Güler, Hüseyin, Per, Adnan, Bayram, Adem, Boyaci
Publikováno v:
Paediatric anaesthesia. 21(4)
When electroencephalogram (EEG) activity is recorded for diagnostic purposes, the effects of sedative drugs on EEG activity should be minimal. This study compares the sedative efficacy and EEG effects of dexmedetomidine and midazolam.EEG recordings o
Autor:
Sefer, Kumandas, Esad, Koklu, Hakan, Gümüs, Selmin, Koklu, Selim, Kurtoglu, Musa, Karakukcu, Mehmet, Keskin
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 19(4)
To examine the effect of carbamezapine and valproate on bone mineral density (BMD), IGF-I and IGFBP-3 levels in children.The effects of at least 2 years valproic acid and carbamazepine therapy on BMD were evaluated in a cross-sectional and retrospect
Publikováno v:
Haematologica. 89(9)
We describe the case of a 12-year old boy with Hoyeraal-Hreidarsson Syndrome (HHS). This syndrome includes intrauterine growth retardation, microcephaly, mental retardation, cerebellar malformation, and pancytopenia. HHS is a severe multisystem disor