Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Eser Bulus"'
Publikováno v:
Haseki Tıp Bülteni, Vol 62, Iss 4, Pp 250-254 (2024)
Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive neurometabolic disease caused by a mutation in the CYP27A1 gene and deficiency of the mitochondrial 27-sterol hydroxylase enzyme. Deficiency of this enzyme leads to the accumulation o
Externí odkaz:
https://doaj.org/article/8c286111781c4c2b832dcb710bb28982
Autor:
Sinem Iliaz, Gulshan Yunisova, Ozgur Oztop Cakmak, Ozlem Celebi, Eser Bulus, Arda Duman, Mesut Bayraktaroglu, Piraye Oflazer
Publikováno v:
Respiratory medicine. 200
The patients with neuromuscular diseases (NMD) are very fragile and it is hard to evaluate respiratory involvement of the primary disease in this group. Therefore, our study aimed to reveal the relationship between pulmonary function tests (PFT) and
Publikováno v:
The neurologist. 27(3)
Introduction: In the midst of the coronavirus disease of 2019 pandemic, active immunization by effective vaccination gained utmost importance in terms of global health. The messenger RNA (mRNA) vaccines are novel strategies requiring clinical surveil
Autor:
Eser Bulus
Publikováno v:
Journal of the Turkish Epilepsi Society.
Autor:
Eser Bulus
Publikováno v:
Journal of the Turkish Epilepsi Society.
Publikováno v:
Medical Bulletin of Haseki / Haseki Tip Bulteni. Sep2024, Vol. 62 Issue 4, p250-254. 5p.
Publikováno v:
Genomics & Genetics Weekly; 11/29/2024, p1292-1292, 1p
Publikováno v:
Neurologist; May2022, Vol. 27 Issue 3, p147-150, 4p
Autor:
BULUS, Eser1, NALBANTOGLU, Mecbure1, GOZUBATIK-CELIK, Gokcen1, GUNDUZ, Aysegul1, UZUN, Nurten1 nurtenzn@yahoo.com
Publikováno v:
Journal of Neurological Sciences. 2014, Vol. 31 Issue 3, p601-603. 3p.
Publikováno v:
Epileptic Disorders; Sep2013, Vol. 15 Issue 3, p311-313, 3p