Suchergebnisse - "Streich, Lukas"

PubPharm (9)

1

Case Report : ASXL1, RUNX1, and IDH1 mutation in tyrosine kinase-independent resistant chronic myeloid leukemia progressing to chronic myelomonocytic leukemia-like accelerated phase

enthalten in: Frontiers in oncology | 2023

von Oyogoa, E. | Streich, L. | Raess, P. | +1

2

Inflammatory leiomyosarcoma/rhabdomyoblastic tumor : A report of two cases with novel genetic findings

enthalten in: Genes, chromosomes & cancer | 2022

von Sukhanova, M. | Obeidin, F. | Streich, L. | +1

3

SLFN11 negatively regulates non-canonical NFkB signaling to promote glioblastoma progression

enthalten in: Cancer research communications | 2022

von Fischietti, M. | Eckerdt, F. | Perez, R. | +11

4

Diagnosis of giant cell-rich bone tumors on core needle biopsy : A practical approach

enthalten in: Pathology, research and practice | 2022

von Jager, L. | Johnson, D. | Sukhanova, M. | +3

5

Inflammatory leiomyosarcoma/rhabdomyoblastic tumor : A report of two cases with novel genetic findings

enthalten in: Genes, Chromosomes and Cancer | 2022

von Sukhanova, M. | Obeidin, F. | Streich, L. | +1

6

Solitary fibrous tumor of thoracic cavity, extra-thoracic sites and central nervous system : Clinicopathologic features and association with local recurrence and metastasis

enthalten in: Pathology, research and practice | 2021

von Alexiev, B. | Finkelman, B. | Streich, L. | +4

7

Synovial sarcoma with overwhelming glandular (adenocarcinoma-like) component : A case report and review of the literature

enthalten in: Pathology, research and practice | 2021

von Streich, L. | Johnson, D. | Alexiev, B.

8

Aggressive morphologic variants of mantle cell lymphoma characterized with high genomic instability showing frequent chromothripsis, CDKN2A/B loss, and TP53 mutations : A multi-institutional study

enthalten in: Genes, chromosomes & cancer | 2020

von Streich, L. | Sukhanova, M. | Lu, X. | +10

9

Aggressive morphologic variants of mantle cell lymphoma characterized with high genomic instability showing frequent chromothripsis, CDKN2A/B loss, and TP53 mutations : A multi‐institutional study

enthalten in: Genes, Chromosomes and Cancer | 2020

von Streich, L. | Sukhanova, M. | Lu, X. | +10

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