Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Nihan Hande Akcakaya"'
Autor:
Nihan Hande Akcakaya, Muhammed Selman Colak, Abdulvahap Sevin, Kagan Gurpinar, Hizir Asliyuksek, Elif Kocasoy Orhan
Publikováno v:
Haseki Tıp Bülteni, Vol 59, Iss 5, Pp 388-392 (2021)
Aim:Obstetrical brachial plexopathy (OBP) is the loss of function of the brachial plexus due to a traumatic, idiopathic, or iatrogenic reason since birth. OBP mostly occurs with a traumatic background that is secondary to a difficult birth. In this s
Externí odkaz:
https://doaj.org/article/2435c52f19e34d7db11fa7f2139e1fc3
Publikováno v:
Türk Nöroloji Dergisi, Vol 25, Iss 2, Pp 63-70 (2019)
Objective: Motor development is at the forefront of evaluation of neurodevelopmental functions in the first 6 months of life. Significant spontaneous movement patterns of infants are called general movements. General movements are rough and complex m
Externí odkaz:
https://doaj.org/article/892294ca91bf4d269a14e3f13255229c
Autor:
Nihan Hande Akcakaya
Publikováno v:
Türk Nöroloji Dergisi, Vol 25, Iss 2, Pp 98-99 (2019)
Externí odkaz:
https://doaj.org/article/c78114798355496f84dc9b98900a22f2
Autor:
Sevcan Mercan, Nihan Hande Akcakaya, Baris Salman, Zuhal Yapici, Ugur Ozbek, Sibel Aylin Ugur Iseri
Publikováno v:
Genes & Genomics. 45:13-21
Syndromic intellectual disability (ID) with accompanying primary microcephaly is a group of rare neurodevelopmental disorders exhibiting extreme genetic and clinical heterogeneity. This layered heterogeneity can partially be resolved by unbiased gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d93d401970aafd2096f0f2ef8d92ab
https://doi.org/10.1007/s13258-022-01344-8
https://doi.org/10.1007/s13258-022-01344-8
Autor:
Kagan Gurpinar, Nihan Hande Akcakaya, Elif Kocasoy Orhan, Abdulvahap Sevin, Muhammed Selman Colak, Hızır Aslıyüksek
Publikováno v:
Haseki Tıp Bülteni, Vol 59, Iss 5, Pp 388-392 (2021)
Aim:Obstetrical brachial plexopathy (OBP) is the loss of function of the brachial plexus due to a traumatic, idiopathic, or iatrogenic reason since birth. OBP mostly occurs with a traumatic background that is secondary to a difficult birth. In this s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000f2a4fa29f78982753d7624447bd3c
https://doaj.org/article/2435c52f19e34d7db11fa7f2139e1fc3
https://doaj.org/article/2435c52f19e34d7db11fa7f2139e1fc3
Autor:
Sevcan Mercan, Sibel Aylin Ugur Iseri, Remzi Yigiter, Nihan Hande Akcakaya, Esen Saka, Zuhal Yapici
Mitochondrial membrane protein-associated neurodegeneration (MPAN) is a rare neurological disease with childhood or adult onset. It is a subtype of clinically and genetically heterogeneous group of disorders, collectively known as neurodegeneration w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76654f43106cb6387cd777e7f3cb2ad8
Autor:
Nihan Hande Akcakaya, Salman, B., Arguden, Y. Tarkan, Gormez, Z., Donmez, R., Colakoglu, B., Yapici, Z., Hacihanefioglu, S., Ozbek, U., Iseri, S. A. Ugur
Publikováno v:
Web of Science
Gormez, Zeliha (isu author) 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) -- JUN 16-19, 2018 -- Milan, ITALY … European Soc Human Genet Scientif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2578047de3fa8c90240abc9a03689dd9
https://avesis.deu.edu.tr/publication/details/da26f80d-ceb5-4e53-8457-ffc523d91d67/oai
https://avesis.deu.edu.tr/publication/details/da26f80d-ceb5-4e53-8457-ffc523d91d67/oai
Autor:
Turgay Altunalan, Zübeyir Sarı, Tuba Derya Doğan, Nilüfer Eldeş Hacıfazlıoğlu, İpek Akman, Tuğba Altıntaş, Sevil Uzer, Nihan Hande Akçakaya
Publikováno v:
Brain and Behavior, Vol 13, Iss 11, Pp n/a-n/a (2023)
Abstract Introduction Preterm infants are at high risk for developmental disabilities, and their parents are at increased risk for high stress. Early intervention programs are applied to reduce these adverse outcomes. The primary aim is to compare th
Externí odkaz:
https://doaj.org/article/63ad1bcec785456ea4703619a82ce6d2
Autor:
Nihan Hande Akçakaya
Publikováno v:
Haseki Tıp Bülteni, Vol 58, Iss 4, Pp 351-358 (2020)
Aim:Cerebral palsy (CP), with its comprehensive definition, is the most common cause of disability in children under the age of 18 years. In rehabilitation-oriented approach, many diseases with different etiologies that cause physical disability are
Externí odkaz:
https://doaj.org/article/1864ec7a3469433082d39c63e1902542
Publikováno v:
Türk Nöroloji Dergisi, Vol 23, Iss 2, Pp 43-50 (2017)
Idiopathic intracranial hypertension (IIH) is a condition of increased intracranial pressure without a secondary etiology. IIH is seen frequently in young and obese women. Headache, vision problems, and pulsatile tinnitus are the most common symptoms
Externí odkaz:
https://doaj.org/article/6296f439ecf7428aa51afbc86e42793f