Suchergebnisse - "Yılmaz, Rüstem"

PubPharm (55)

1

A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice

enthalten in: The Journal of experimental medicine | 2024

von Brenner, D. | Sieverding, K. | Srinidhi, J. | +28

2

Analysis of hematological indicators via explainable artificial intelligence in the diagnosis of acute heart failure : a retrospective study

enthalten in: Frontiers in medicine | 2024

von Yilmaz, R. | Yagin, F. | Colak, C. | +4

3

Comparison of Electrocardiographic Parameters by Gender in Heart Failure Patients with Preserved Ejection Fraction via Artificial Intelligence

enthalten in: Diagnostics (Basel, Switzerland) | 2023

von Yilmaz, R. | Öz, E.

4

Comparison of the effect of uric acid/albumin ratio on coronary colleteral circulation with other inflammation-based markers in stable coronary artery disease patients

enthalten in: Perfusion | 2023

von Toprak, K. | Yılmaz, R. | Kaplangoray, M. | +6

5

Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers

enthalten in: Amyotrophic lateral sclerosis & frontotemporal degeneration | 2023

von Yilmaz, R. | Grehl, T. | Eckrich, L. | +8

6

PSEN1/SLC20A2 double mutation causes early-onset Alzheimer's disease and primary familial brain calcification co-morbidity

enthalten in: Neurogenetics | 2023

von Hebestreit, S. | Schwahn, J. | Sandikci, V. | +11

7

PSEN1/SLC20A2 double mutation causes early-onset Alzheimer’s disease and primary familial brain calcification co-morbidity

enthalten in: Neurogenetics | 2023

von Hebestreit, S. | Schwahn, J. | Sandikci, V. | +11

8

PSEN1/SLC20A2 double mutation causes early-onset Alzheimer’s disease and primary familial brain calcification co-morbidity

enthalten in: Neurogenetics | 2023

von Hebestreit, S. | Schwahn, J. | Sandikci, V. | +11

9

The Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3cc

enthalten in: bioRxiv.org | 2022

von Ambrozkiewicz, M. | Ripamonti, S. | Borisova, E. | +15

10

ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain-of-function

enthalten in: EMBO reports | 2022

von Pant, D. | Parameswaran, J. | Rao, L. | +11

1
2
3
4
5
6
Nächster »
[6]