Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gultekin Kutluk"'
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 5, Pp 694-696 (2020)
Megaconial congenital muscular dystrophy (OMIM 602541) is defined by early-onset hypotonia, mildly elevated serum creatine kinase (CK) levels, muscle wasting, cardiomyopathy, psychomotor developmental delay and intellectual disability. The disease is
Externí odkaz:
https://doaj.org/article/77a2af28383c4e3d91a5bfeccdc1d8ca
Publikováno v:
Acta Neurologica Belgica. 121:1807-1814
Although cerebral palsy (CP), which affects the quality of life of many children and their families, is the most common cause of motor dysfunction in children, no comprehensive bibliometric study has holistically evaluated the publications on CP. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac3aef3904144c9632f74c812180b621
https://doi.org/10.1007/s13760-020-01549-2
https://doi.org/10.1007/s13760-020-01549-2
Publikováno v:
Child's Nervous System. 37:617-626
Childhood epilepsy is one of the disease groups with the highest disease burden in society. This study aimed to guide researchers for new studies by determining the most compelling studies and current issues through a bibliometric analysis of scienti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41975ad7ded424a402eb628ec7406668
https://doi.org/10.1007/s00381-020-04897-9
https://doi.org/10.1007/s00381-020-04897-9
Autor:
Ömer Bektaş, Gökçen Öz Tunçer, M Gultekin Kutluk, Nadide Cemre Randa, Serap Teber, Pelin Albayrak, Tuba F. Eminoglu, Naz Kadem
Publikováno v:
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fced6e7610be2c646a7381644a78694d
http://europepmc.org/articles/PMC8232516
http://europepmc.org/articles/PMC8232516
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 5, Pp 694-696 (2020)
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology
Megaconial congenital muscular dystrophy (OMIM 602541) is defined by early-onset hypotonia, mildly elevated serum creatine kinase (CK) levels, muscle wasting, cardiomyopathy, psychomotor developmental delay and intellectual disability. The disease is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c3471ce3b1242aa94fd8c8354c5110
http://www.annalsofian.org/article.asp?issn=0972-2327
http://www.annalsofian.org/article.asp?issn=0972-2327
Autor:
M Gultekin Kutluk, E Naz Kadem
Publikováno v:
Archivos Argentinos de Pediatria. 119
Influenza is mostly associated with the respiratory tract system, especially in the winter season. Various neurological complications could occur due to influenza infection. Pediatric patients who had severe neurological manifestations due to influen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e95f1fcbab09ae8beb9128d204bf0385
https://doi.org/10.5546/aap.2021.eng.e142
https://doi.org/10.5546/aap.2021.eng.e142
Autor:
Afagh Alavi, Yalda Nilipour, Luca Bello, Jorge Alonso-Pérez, Shahriar Nafissi, Muhammad Umair, Lidia Gonzalez-Quereda, Mario Emilio Dourado, Chiara Marini-Bettolo, Chiara Panicucci, Xavier Suárez-Calvet, Gultekin Kutluk, Kinga Hadzsiev, Lucas Michielon de Augusto Isihi, Edmar Zanoteli, Jordi Díaz-Manera, Thomas O. Crawford, Muhammad Younus, Ana Töpf, Naz Kadem, Elena Pegorano, Juan José Vilchez, Claudio Bruno, Pia Gallano, Béla Melegh, Michela Guglieri, Nuria Muelas, Volker Straub
Publikováno v:
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Universitat Autònoma de Barcelona
Sarcoglycanopathies include four subtypes of autosomal recessive limb-girdle muscular dystrophies (LGMDR3, LGMDR4, LGMDR5 and LGMDR6) that are caused, respectively, by mutations in the SGCA, SGCB, SGCG and SGCD genes. Delta-sarcoglycanopathy (LGMDR6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73651a42bdeaee241f06acea9ddd79f9
https://ddd.uab.cat/record/258072
https://ddd.uab.cat/record/258072
Publikováno v:
Cureus
Background and aim Infantile spasm (IS) is a common epileptic syndrome of childhood epilepsies. The most effective treatment for IS is adrenocorticotropic hormone (ACTH). We hypothesized that ACTH treatment might change myocardial systolic and diasto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01d2d4640f2622e51ec5b9bb4735457b
https://pubmed.ncbi.nlm.nih.gov/32257667
https://pubmed.ncbi.nlm.nih.gov/32257667
Akademický článek
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Autor:
M Gultekin Kutluk, Naz Kadem, Omer Bektas, Nadide Cemre Randa, Gökcen O Z Tuncer, Pelin Albayrak, Tuba Eminoglu, Serap Tiras Teber
Publikováno v:
Annals of Indian Academy of Neurology, Vol 24, Iss 2, Pp 280-282 (2021)
Externí odkaz:
https://doaj.org/article/8d171ea81d474ee1b49da4d9f1020518