Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nesibe Gevher Eroglu‐Ertugrul"'
Autor:
Ceren Günbey, Bahadır Konuşkan, Mehmet Ceyhan, Sevgen Tanır Basaranoglu, Yasemin Cosgun, Gulay Korukluoglu, Banu Anlar, Ali Bülent Cengiz, Nesibe Gevher Eroglu Ertugrul, Yasemin Ozsurekci
Publikováno v:
Neuropediatrics. 52:448-454
Encephalitis is a serious neurological syndrome caused by inflammation of the brain. The diagnosis can be challenging and etiology remains unidentified in about half of the pediatric cases. We aimed to investigate demographic, clinical, laboratory, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e07d3717747dd10f5b0b578ab364c253
https://doi.org/10.1055/s-0041-1723954
https://doi.org/10.1055/s-0041-1723954
Autor:
Nur Berna Celik, Ekim Z. Taskiran, Gülen Eda Utine, E. Nazli Gonc, Ayfer Alikasifoglu, Nurgun Kandemir, Goknur Haliloglu, Busra Aydin, Mehmet Alikasifoglu, Pelin Özlem Şimşek Kiper, Nesibe Gevher Eroglu‐Ertugrul, Dilek Yalnizoglu, Kader Karli Oguz, Beren Karaosmanoglu, Z. Alev Ozon
Publikováno v:
Pediatric Diabetes. 21:1176-1182
Background A number of inborn errors of metabolism caused by abnormal protein trafficking that lead to endoplasmic reticulum storage diseases (ERSD) have been defined in the last two decades. One such disorder involves biallelic mutations in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::156a4725e147144a1726ce6acd5a117d
https://doi.org/10.1111/pedi.13098
https://doi.org/10.1111/pedi.13098
Autor:
Nesibe Gevher Eroglu-Ertugrul, Mohammadreza Yousefi, Faruk Pekgül, Tansu Doran, Ceren Günbey, Meral Topcu, Kader K. Oguz, Hatice Asuman Ozkara, Atay Vural, Banu Anlar
Publikováno v:
Journal of neuroimmunology. 369
Accumulation of intermediate metabolites due to enzyme deficiencies and demyelination can provoke inflammation in genetic leukodystrophies. Thirty patients with genetic leukodystrophy and 48 healthy control sera were tested for anti-myelin oligodendr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4f29c2f78011ef07061e6ec86e6e046
https://pubmed.ncbi.nlm.nih.gov/35752102
https://pubmed.ncbi.nlm.nih.gov/35752102
Autor:
Can Ebru Bekircan-Kurt, Faruk Pekgül, Sevim Erdem-Ozdamar, Nurten A. Akarsu, Ersin Tan, Hatice Asuman Özkara, Bahadır Konuşkan, Meral Topçu, Arda Cetinkaya, Nesibe Gevher Eroglu‐Ertugrul, Banu Anlar, Kader Karli Oguz, Ergun Karaagaoglu
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100688-(2020)
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100688-(2020)
Metachromatic leukodystrophy (MLD) is a glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ASA) or its activator protein saposin B. MLD can affect all age groups in severity varying from a severe fatal for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a133dc9e73ee634fad59bb70b2a39463
http://europepmc.org/articles/PMC7734308
http://europepmc.org/articles/PMC7734308
Autor:
Ekim Taskiran, Mehmet Alikasifoglu, PelinOzlem Kiper, Gülen Eda Utine, Nesibe Gevher Eroglu‐Ertugrul, Kader Karli Oguz, Dilek Yalnizoglu, Goknur Haliloglu, Ayfer Alikasifoglu, E. Nazli Gonc, Nurgun Kandemir, Busra Aydin, Z. Alev Ozon, Beren Karaosmanoglu, Nur Berna Celik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ff36a63b5eb7907d03551d98050ee9
https://doi.org/10.1111/pedi.13098/v2/response1
https://doi.org/10.1111/pedi.13098/v2/response1
Autor:
Nesibe Gevher Eroglu‐Ertugrul, Ugur Ozcelik, Turgay Öcal, Berna Oguz, Baris Kuskonmaz, Ilhan Tezcan, Nural Kiper, Nagehan Emiralioglu, Deniz Doğru-Ersöz, Ebru Yalcin
Publikováno v:
The Clinical Respiratory Journal
Objectives: To demonstrate the value of flexible bronchoscopy (FB) and bronchoalveolar lavage (BAL) when determining causes of lung infection in immunocompromised children;to investigate differences in causes and radiological features of lung infecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e1c9395e9a556e91039221e6f447a15
Autor:
Faruk Pekgül, Nesibe Gevher Eroğlu-Ertuğrul, Can Ebru Bekircan-Kurt, Sevim Erdem-Ozdamar, Arda Çetinkaya, Ersin Tan, Bahadır Konuşkan, Ergun Karaağaoğlu, Meral Topçu, Nurten Ayşe Akarsu, Kader K. Oguz, Banu Anlar, Hatice Asuman Özkara
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100688- (2020)
Metachromatic leukodystrophy (MLD) is a glycosphingolipid storage disease caused by deficiency of the lysosomal enzyme arylsulfatase A (ASA) or its activator protein saposin B. MLD can affect all age groups in severity varying from a severe fatal for
Externí odkaz:
https://doaj.org/article/04adf75434bf4fb083408a4e29032740