Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Atilla Ersen"'
Autor:
Sefer Kumandaş, Akgun Olmez Turker, Dilek Cavusoglu, Atilla Ersen, Rojan İpek, Serkan Kirik, Selcan Ozturk, Kursat Bora Carman, Betül Kılıç, Hakan Gümüş, Dilek Yilmaz-Ciftdogan, Hande Gazeteci-Tekin, Çetin Okuyaz, Neslihan Ozcan, Ceren Günbey, Gülen Gül Mert, Hülya İnce, Eda Karadag-Oncel, Pinar Arican, Meryem Karaca, Hüseyin Per, Mustafa Kömür, Ebru Arhan, Mustafa Calik, Merve Feyza Yüksel, Gürkan Gürbüz, Pinar Gencpinar, Sema Bozkaya-Yilmaz, Berrak Sarioglu, Nihal Olgaç-Dündar, Mehmet Canpolat, Ömer Bektaş, Coskun Yarar, Serap Teber, Pınar Ozbudak
© 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::815dbe1241a34f622426c960dd562671
https://avesis.kayseri.edu.tr/publication/details/766a9ee4-cb90-4a41-884a-fe2bc61bc151/oai
https://avesis.kayseri.edu.tr/publication/details/766a9ee4-cb90-4a41-884a-fe2bc61bc151/oai
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:
Deepika Chandrasekaran, R. Padmavathi, Sandhya Sundaram, N. Kathiresan, Fernanda Cardia Martins Ribeiro, Larissa Alves Ruas, Aluysio Leal Júnior, Adriana Andrade de Sousa, Adriana Farias Araújo, Jonathan Mwambire, Ana Luísa Conceição de Jesus, Renata Maksoud Bussuan, Larissa Bianca Cunha de Sá, Alberto Krayyem Arbex, Duzgun Yildirim, Onur Tutar, Deniz Alis, Gokhan Kuyumcu, Selim Bakan, Özlem Güngör, Nupura Vibhute, Aniket Vibhute, Komalpreet Kaur, Ramninder Kaur, E. Mboloko, M. Fataki, E. Nzau-Ngoma, L. D. Lokengo, A. Ingala, B. C. J. Bikuelo, A. N. Apangwa, M. M. M. Kapend, M. Mboloko, N. Mumba, A. S. Sabnis, Y. Bhosale, E. L. Kotingo, D. O. Allagoa, Cesur Samanci, Fethi Emre Ustabasioğlu, Atilla Ersen, Shobha Misra, Bhakti Sharma, V. Coulic, Robin A. Bernhoft, Jordan Amanyire, Mathias Tumwebaze, Mauda Kamatenesi Mugisha, Labani Waswa Bright, Rania M. Khashaba, Mervet Moussa, Christopher Koch, Arthur R. Jurgensen, David M. Missimer, Ronny L. Rutherford, Norman B. Chutkan, James L. Borke, O. Psenak, A. Studnicka-Benke, H. Haufe, R. Greil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a63539c14e040c2f4879a20ad366281
https://doi.org/10.9734/bpi/ctmamr/v9
https://doi.org/10.9734/bpi/ctmamr/v9
Publikováno v:
İstanbul Kanuni Sultan Süleyman Tıp Dergisi.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffdf8ebe677a9403dc341fba6f9904cb
https://doi.org/10.5222/iksstd.2020.33866
https://doi.org/10.5222/iksstd.2020.33866
Autor:
Pinar Gencpinar, Atilla Ersen, Nargiz Aliyeva, Nihal Olgaç Dündar, Pinar Arican, Sema Bozkaya Yılmaz, Taha Reşid Özdemir, Ozgur Oztekin
Publikováno v:
Clinical Neuropharmacology. 43:121-122
Hereditary spastic paraplegia (HSP) is group of a rare neurodegenerative disorder with both genetically and clinically diverse neurologic features. Indeed, disease progression is varying greatly within the different forms and current treatment modali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5d79f6fc347a535bed164aa85ec31f4
https://doi.org/10.1097/wnf.0000000000000392
https://doi.org/10.1097/wnf.0000000000000392
Autor:
Nihal Olgaç Dündar, Atilla Ersen, Pinar Gencpinar, Pinar Arican, Sema Bozkaya Yılmaz, Ozgur Oztekin, Ozgur Kirbiyik
Publikováno v:
Pediatric neurology. 99
Background We explored the clinical and molecular characteristics of molybdenum cofactor deficiency due to MOCS2 muations. Methods We summarize the genetic and clinical findings of previously reported patients with a MOCS2 mutation. We also present a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44acb26f0d48562cfbce8aa949798039
https://pubmed.ncbi.nlm.nih.gov/31201073
https://pubmed.ncbi.nlm.nih.gov/31201073
Autor:
Canan Tanidir, Esra Kutlu, Banu Kucukemre Aydin, Hasan Önal, Dilara Pirhan, Nihat Sayın, Neval Topal, Erdal Adal, Hilal Doktur, Hatice Güneş, Atilla Ersen
Objective To investigate the relationship between brain masculinization and retinal thickness in children with congenital adrenal hyperplasia (CAH). Methods Forty-five patients with CAH aged between 4 and 18 years and 30 age-matched healthy controls
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2d635d1944164602963ba6ad86da9e1
https://hdl.handle.net/20.500.12511/1398
https://hdl.handle.net/20.500.12511/1398
Autor:
Fethi Emre Ustabasioglu, Atilla Ersen, Cesur Samanci, Duzgun Yildirim, Deniz Alis, Onur Tutar
Publikováno v:
Open Journal of Medical Imaging. :93-101
Objective: Thanks to fast developing technology, visualization of fiber tracts at brain is possible. But with the new developments, data processing and interpretation are becoming more difficult. Actually interpretations in these fields are mostly in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88af788b4773654dce7bdf53dd05f415
https://doi.org/10.4236/ojmi.2016.63009
https://doi.org/10.4236/ojmi.2016.63009
Autor:
Dilek Cavusoglu, Pinar Gencpinar, Sema Bozkaya Yılmaz, Nihal Olgaç Dündar, Atilla Ersen, Pinar Arican, Ozgur Oztekin
Publikováno v:
The Turkish Journal of Pediatrics. 62:343
Background Hypertrophic olivary degeneration (HOD) is a rare degenerative disorder that is thought to occur subsequent to a disruption of the dentate-rubro-olivary pathway. Case We report a pediatric case of unilateral HOD presented with persistent h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf9b5f659c761489a86a1b527533f123
https://doi.org/10.24953/turkjped.2020.02.025
https://doi.org/10.24953/turkjped.2020.02.025
Autor:
Serdar Sander, Erdal Adal, Sait Albayram, Hakan Gemici, Atilla Ersen, Serhat Guler, Hasan Önal
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Spontaneous intracranial hypotension (SIH) is a rare and potentially serious condition in childhood. Cerebrospinal fluid (CSF) volume depletion is thought to be the main causative feature for intracranial hypotension and results from a spontaneous CS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a8ba4242c32e174e7d9623b69b2b0b
https://pubmed.ncbi.nlm.nih.gov/29513222
https://pubmed.ncbi.nlm.nih.gov/29513222