OpenAlex topic

Legal Cases and Commentary

This page lists works and academicians tagged with an OpenAlex topic. It is not a YÖKSİS primary or secondary field.

OpenAlex 598 works 6 author topics

Works

598 works

Recombinant factor VIII half life using a bayesian model in patients with severe haemophilia A on prophylaxis in Turkey 2019
YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.5%
No abstract yet.
- CANAN ALBAYRAK
Haemophilia A genotype-phenotype analysis in Turkey 2019
YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.5%
No abstract yet.
- CANAN ALBAYRAK
Sacrococcygeal Pilonidal Sinus Surgery In Two Patients With Haemophilia 2019
YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.5%
No abstract yet.
- CANAN ALBAYRAK
Clinical Features and HSCT Outcome for SCID in Turkey 2019
YÖKSİS SJR Q1 JCR Q1 OpenAlex 86.5%
No abstract yet.
- OSMAN ALPHAN KÜPESİZ
- SERAP AKSOYLAR
Pharmacokinetic-guided prophylaxis based on bayesian model with myPKFiT® in hemophilia A: Turkish experience 2019
YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.5%
No abstract yet.
Poster Presentations 2019
YÖKSİS SJR Q1 JCR Q2 OpenAlex 86.5%
No abstract yet.
- AYŞEGÜL ÜNÜVAR
Subject Index Vol. 12, 2002–2003 2005

Background noise 119 Bell's palsy 132 Blank gun 270 Cancer 33 Causal illness beliefs 300 Central venous catheter 145 Cerebrospinal fluid 91 Cervical lymphadenitis 97 Chemokines 52, 63 Chronic sinusitis 48, 52, 63,71 -vertigo 77 Cochlea 109 Contact blank 270 Cryosurgery 103 Cytokines 52, 63 Different cultures, dysphoni…
Evaluation of Urban Spaces from the Perspective of Universal Design Principles The Case of Konya Turkey 2016
YÖKSİS OpenAlex 46.8%
During the process of accessing services provided within urban interior and outer spaces the elderly and disabled individuals encounter with a myriad of problems due to the limitations posed by structured environments. This limitation hinders elderly and disabled individuals from mobility without assistance, which in…
- HAVVA FİLİZ MEŞHUR
Congenital macrothrombocytopenia: is it misdiagnosed? 2018
YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.1%
SCI-Expanded | YÖK-Özgeçmiş
- DİDEM ÖZKAN
- TÜLİN TIRAJE CELKAN
A case of congenital fibrinogen deficiency complicated with acute lymphoblastic leukemia 2018
YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.1%
SCI-Expanded | YÖK-Özgeçmiş
- EKREM ÜNAL
Mutation spectrum of F8 gene in Turkish hemophilia A patients: identification of 14 novel mutations 2018
YÖKSİS SJR Q1 JCR Q2 OpenAlex 89.1%
SCI-Expanded | YÖK-Özgeçmiş
Contributing Authors 2011
OpenAlex 62.0%
No abstract yet.

Academicians

6 academicians