Suchergebnisse - "Khanahmad, Hossein"

PubPharm (222)

1

Prospective Prediction of Treatment Response in High-Grade Glioma Patients using Pre-Treatment Tumor ADC Value and miR-222 and miR-205 Expression Levels in Plasma

enthalten in: Journal of biomedical physics & engineering | 2024

von Heidari, M. | Amouheidari, A. | Hemati, S. | +4

2

In-Utero exposure to potential sources of indoor air pollution and umbilical cord blood leukocyte telomere length

enthalten in: Environmental research | 2024

von Dehdashti, B. | Miri, M. | Khanahmad, H. | +4

3

Expression of Matrix Metalloproteinases in Human Cystic Echinococcosis

enthalten in: Current molecular medicine | 2024

von Hasanzadeh, A. | Beiromvand, M. | Rafiei, A. | +3

4

Unmasking the complex roles of hypocalcemia in cancer, COVID-19, and sepsis : Engineered nanodelivery and diagnosis

enthalten in: Environmental research | 2023

von Ghafouri, E. | Bigdeli, M. | Khalafiyan, A. | +6

5

Unraveling the potential of M13 phages in biomedicine : Advancing drug nanodelivery and gene therapy

enthalten in: Environmental research | 2023

von Fadaie, M. | Dianat-Moghadam, H. | Ghafouri, E. | +6

6

Four families with X-linked intellectual disability affected males: Novel deleterious variants and clinical features with the review of literature

enthalten in: ResearchSquare.com | 2023

von Mir, A. | Song, Y. | Lee, H. | +4

7

Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families : novel deleterious variants and clinical features with the review of literature

enthalten in: BMC medical genomics | 2023

von Mir, A. | Song, Y. | Lee, H. | +4

8

Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature

enthalten in: BMC medical genomics | 2023

von Mir, A. | Song, Y. | Lee, H. | +4

9

Phage based vaccine : A novel strategy in prevention and treatment

enthalten in: Heliyon | 2023

von Mohammad Hasani, S. | Ghafouri, E. | Kouhpayeh, S. | +4

10

A novel METTL5 variant disrupting a donor splice site leads to primary microcephaly-related intellectual disability in an Iranian family: clinical features and literature review

enthalten in: Journal of genetics | 2023

von Shakarami, F. | Nouri, Z. | Khanahmad, H. | +2

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