Suchergebnisse - "Özdemir, Taha Reşid"

PubPharm (49)

1

JAKCalc : A machine-learning approach to rationalized JAK2 testing in patients with elevated hemoglobin levels

enthalten in: Medicine | 2024

von Koseoglu, F. | Keklik Karadag, F. | Bulbul, H. | +3

2

Association between fetal fraction of cell-free DNA and adverse pregnancy outcomes

enthalten in: Archives of gynecology and obstetrics | 2024

von Golbasi, H. | Bayraktar, B. | Golbasi, C. | +7

3

Prognostic and predictive role of liquid biopsy in lung cancer patients

enthalten in: Frontiers in oncology | 2023

von Goksel, T. | Özgür, S. | Vardarlı, A. | +13

4

Gilbert Syndrome and Genetic Findings in Children : A Tertiary-Center Experience from Turkey

enthalten in: Turkish archives of pediatrics | 2022

von Çağan Appak, Y. | Aksoy, B. | Özyılmaz, B. | +2

5

The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

enthalten in: Journal of pediatric endocrinology & metabolism : JPEM | 2021

von Kose, M. | Isik, E. | Aykut, A. | +14

6

Neuronal ceroid lipofuscinosis : genetic and phenotypic spectrum of 14 patients from Turkey

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2021

von Kose, M. | Kose, E. | Ünalp, A. | +8

7

The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

enthalten in: The journal of pediatric endocrinology and metabolism | 2021

von Kose, M. | Isik, E. | Aykut, A. | +14

8

The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

enthalten in: The journal of pediatric endocrinology and metabolism | 2021

von Kose, M. | Isik, E. | Aykut, A. | +14

9

Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey

enthalten in: Neurological sciences | 2021

von Kose, M. | Kose, E. | Ünalp, A. | +8

10

Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey

enthalten in: Neurological sciences | 2021

von Kose, M. | Kose, E. | Ünalp, A. | +8

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