Suchergebnisse - "Yoshimi, A"

PubPharm (85)

1

Plasma MMP-9 Levels as the Future Risk of Conversion to Dementia in ApoE4-Positive MCI Patients: Investigation Based on the Alzheimer’s Disease Neuroimaging Initiative Database

enthalten in: The journal of prevention of Alzheimer's disease | 2022

von Abe, K. | Chiba, Y. | Ide, K. | +5

2

Plasma MMP-9 Levels as the Future Risk of Conversion to Dementia in ApoE4-Positive MCI Patients: Investigation Based on the Alzheimer’s Disease Neuroimaging Initiative Database

enthalten in: The journal of prevention of Alzheimer's disease | 2022

von Abe, K. | Chiba, Y. | Ide, K. | +5

3

Plasma MMP-9 Levels as the Future Risk of Conversion to Dementia in ApoE4-Positive MCI Patients : Investigation Based on the Alzheimer's Disease Neuroimaging Initiative Database

enthalten in: The journal of prevention of Alzheimer's disease | 2022

von Abe, K. | Chiba, Y. | Ide, K. | +5

4

Fast x-ray detector system with simultaneous measurement of timing and energy for a single photon

enthalten in: The Review of scientific instruments | 2017

von Masuda, T. | Okubo, S. | Hara, H. | +12

5

Mutational landscape in children with myelodysplastic syndromes is distinct from adults : specific somatic drivers and novel germline variants

enthalten in: Leukemia | 2017

von Pastor, V. | Hirabayashi, S. | Karow, A. | +16

6

High-resolution copy number variation analysis of schizophrenia in Japan

enthalten in: Molecular psychiatry | 2017

von Kushima, I. | Aleksic, B. | Nakatochi, M. | +46

7

High-resolution copy number variation analysis of schizophrenia in Japan

enthalten in: Molecular psychiatry | 2017

von Kushima, I. | Aleksic, B. | Nakatochi, M. | +46

8

Spectrum of clinical and genetic features of patients with inherited platelet disorder with suspected predisposition to hematological malignancies : a nationwide survey in Japan

enthalten in: Annals of oncology : official journal of the European Society for Medical Oncology | 2016

von Yoshimi, A. | Toya, T. | Nannya, Y. | +13

9

Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

enthalten in: Blood cancer journal | 2016

von Sakurai, M. | Kasahara, H. | Yoshida, K. | +15

10

Spectrum of clinical and genetic features of patients with inherited platelet disorder with suspected predisposition to hematological malignancies: a nationwide survey in Japan

enthalten in: Annals of oncology | 2016

von Yoshimi, A. | Toya, T. | Nannya, Y. | +13

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