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/vufind/Search/Results?lookfor=%22Demir%2C+Gizem%22&type=Person&sort=year
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PubPharm (44)
1
Enhancing systematic reviews in orthodontics : a comparative examination of GPT-3.5 and GPT-4 for generating PICO-based queries with tailored prompts and configurations
enthalten in:
European journal of orthodontics
| 2024
von
Demir, G.
|
Süküt, Y.
|
Duran, G.
| +2
Wird geladen...
2
Elastography findings in acne scar patients who were treated with microneedling
enthalten in:
International journal of dermatology
| 2024
von
Demir, G.
|
Aksoy, F.
|
Buğdaycı, O.
| +1
Wird geladen...
3
Early diagnostic clues of mucolipidosis type II : Significance of radiological findings
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Burgac, E.
|
Kaplan, .
|
Köseci, B.
| +9
Wird geladen...
4
Clinical Evaluation of Pediatric Patients with Hereditary Angioedema
enthalten in:
The Tohoku journal of experimental medicine
| 2024
von
Kırmızıtaş Aydoğdu, A.
|
Ürel Demir, G.
Wird geladen...
5
Elastography findings in acne scar patients who were treated with microneedling
enthalten in:
International Journal of Dermatology
| 2024
von
Demir, G.
|
Aksoy, F.
|
Buğdaycı, O.
| +1
Wird geladen...
6
White Blood Cell/Mean Platelet Volume Ratio as a Predictor of Long-Term Outcomes but Not Coronary Artery Disease Severity in Non-ST Elevation Myocardial Infarction Patients
enthalten in:
Cureus
| 2023
von
Demir, G.
|
Karaca, G.
|
Ekmekci, A.
| +3
Wird geladen...
7
EXTL3-Associated Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities : A Lethal Phenotype
enthalten in:
Pediatric allergy, immunology, and pulmonology
| 2023
von
Demir, E.
|
Adım, F.
|
Döğen, M.
| +5
Wird geladen...
8
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand abnormal calcification type : Further expanding the mutational spectrum and dental findings of three new patients
enthalten in:
European journal of medical genetics
| 2023
von
Akalın, A.
|
Özşin, C.
|
Koç, N.
| +6
Wird geladen...
9
Neonatal ichthyosis-sclerosing cholangitis syndrome : report of a novel mutation and a review of the literature
enthalten in:
Clinical dysmorphology
| 2023
von
Demir, E.
|
Tuna Kirsaçlioğlu, C.
|
Saltik-Temizel, .
| +7
Wird geladen...
10
Novel sphingosine-1-phosphate lyase mutation causes multisystemic diseases : case report
enthalten in:
The Turkish journal of pediatrics
| 2023
von
Büyükyılmaz, G.
|
Adıgüzel, K.
|
Aksoy, .
| +6
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immunodeficiency
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420K487FSG
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5-chloro-2-methyl-4-isothiazolin-3-one
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