Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Timucin, Dogan A."'
Autor:
Dorche, Ali Eshaghian, Timucin, Dogan, Thyagarajan, Krishnan, Wunderer, Thomas, Johnson, Noble, Schwartz, David
A systematic dispersion engineering approach is presented toward designing a III-Nitride micro-resonator for a blue/UV frequency comb. The motivation for this endeavor is to fill the need for compact, coherent, multi-wavelength photon sources that ca
Externí odkaz:
http://arxiv.org/abs/2006.07391
Autor:
Leckey, Cara A.C., Wheeler, Kevin R., Hafiychuk, Vasyl N., Hafiychuk, Halyna, Timuçin, Doğan A.
Publikováno v:
In Ultrasonics March 2018 84:187-200
We have developed a general technique to study the dynamics of the quantum adiabatic evolution algorithm applied to random combinatorial optimization problems in the asymptotic limit of large problem size $n$. We use as an example the NP-complete Num
Externí odkaz:
http://arxiv.org/abs/quant-ph/0202155
Autor:
Fatma Duksal, Melih Timucin Dogan
Background Chest pain is one of the important reasons for hospital admissions among children. However, it is known that the cause of chest pain is mostly not because of cardiac origin Objectives It was aimed to investigate asthma and other atopic dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99eaef2b423370d7bc6a18be97be21cc
https://doi.org/10.21203/rs.3.rs-1987478/v1
https://doi.org/10.21203/rs.3.rs-1987478/v1
Publikováno v:
Intractable & Rare Diseases Research. 10:220-222
Centronuclear myopathies (CNMs) are a subgroup of congenital myopathies (CMs) characterized by muscle weakness, genetic heterogeneity, and predominant type 1 fibers and increased central nuclei in muscle biopsy. Mutations in CNM-causing genes such as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b28bfbc5dad275f0b50147b3b7ba3580
https://doi.org/10.5582/irdr.2021.01034
https://doi.org/10.5582/irdr.2021.01034
Publikováno v:
J Pediatr Genet
PHACE syndrome is an acronym that describes a neurocutaneous condition, consisting of posterior fossa malformations that coexist with large facial hemangiomas, eye anomalies, and cardiac/aortic defects. The prognosis of the disease has not been clear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85af8b5da7ad8d125969cbea25f6f4ff
https://doi.org/10.1055/s-0040-1714066
https://doi.org/10.1055/s-0040-1714066
Publikováno v:
Cardiology in the Young. 29:1272-1277
Background:The aim of this study is to investigate the prevalence of subclinical rheumatic heart disease in schoolchildren aged 5–18 by using portable echocardiography in Ankara, Turkey.Methods:The portable echocardiography screening was performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e518c2934d42077e3bed853c7a285f45
https://doi.org/10.1017/s1047951119002075
https://doi.org/10.1017/s1047951119002075
Publikováno v:
Turk Arch Pediatr
Mutations in protein O-mannosyltransferase 2 can cause a wide spectrum of clinical phenotypes from severe congenital muscular dystrophy such as Walker-Warburg syndrome to milder limb-girdle muscular dystrophy 2N. We aimed to describe the clinical and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cb5c6c43842ef62f04a6428068a463
https://europepmc.org/articles/PMC8114593/
https://europepmc.org/articles/PMC8114593/
Platelet activation plays a key part in the process of atherosclerosis. The risk of atherosclerosis increased in familial Mediterranean fever (FMF). Mean platelet volume (MPV), platelet distribution width (PDW) and platelet counts are important in pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d687d2b0f015c9900d7b7cfbe42f2e0
http://hdl.handle.net/11452/12748
http://hdl.handle.net/11452/12748
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