Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Akgun Olmez Turker"'
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:
Chihiro Ohba, Akgun Olmez Turker, Burcu Albuz, Fabio Benfenati, Kazuhiro Ogata, Naomichi Matsumoto, Ashley L. Siniard, Keri Ramsey, Alessandro Esposito, Davide Mei, Carla Marini, Mitsuhiro Kato, Chris Balak, C Nur Semerci Gündüz, Renzo Guerrini, Vinodh Narayanan, Keiko Yanagihara, Elisa Belmonte, Mitsuko Nakashima, Valerio Conti, Masaaki Shiina, Anna Fassio, Nobuhiko Okamoto, Luca Maragliano, Hirotomo Saitsu
Publikováno v:
Brain
Using whole exome sequencing, Fassio et al. identify de novo mutations in ATP6V1A, encoding the A subunit of v-ATPase, in four patients with developmental encephalopathies and epilepsy. Functional and expression studies demonstrate impaired lysosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0005eadc19e8dd317cbba9f60a0d1691
https://pubmed.ncbi.nlm.nih.gov/29668857
https://pubmed.ncbi.nlm.nih.gov/29668857
