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WHIM Syndrome Cured by Chromothripsis

Cancer genetics, 2015-06, Vol.208 (6), p.358-359

2015

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Adult T-cell leukemia/lymphoma with EBV-positive Hodgkin-like cells

Human pathology, 2011-02, Vol.42 (7), p.1042-1046

2011

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The importance of accounting method and sampling depth to estimate changes in soil carbon stocks

Carbon balance and management, 2024-01, Vol.19 (1), p.2-2, Article 2

2024

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High level MYCN amplification and distinct methylation signature define an aggressive subtype of spinal cord ependymoma

Acta neuropathologica communications, 2020-07, Vol.8 (1), p.1-101, Article 101

2020

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MGMT Status as a Clinical Biomarker in Glioblastoma

Trends in cancer, 2020-05, Vol.6 (5), p.380-391

2020

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The clinical spectrum of Erdheim-Chester disease: an observational cohort study

Blood advances, 2017-02, Vol.1 (6), p.357-366

2017

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Case report: Oligodendroglioma, IDH-mutant and 1p/19q-codeleted, associated with a germline mutation in PMS2

Frontiers in oncology, 2022-08, Vol.12

2022

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P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report

Genetics in Medicine Open, 2024, Vol.2, p.100996, Article 100996

2024

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Clonal expansion of CAR T cells harboring lentivector integration in the CBL gene following anti-CD22 CAR T-cell therapy

Blood advances, 2019-08, Vol.3 (15), p.2317-2322

2019

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Longitudinal Circulating Tumor DNA Analysis in Blood and Saliva for Prediction of Response to Osimertinib and Disease Progression in EGFR-Mutant Lung Adenocarcinoma

Cancers, 2021-07, Vol.13 (13), p.3342

2021

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Human Herpes Virus 6 (HHV-6)–associated Lymphadenitis: Pitfalls in Diagnosis in Benign and Malignant Settings

The American journal of surgical pathology, 2018-10, Vol.42 (10), p.1402-1408

2018

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Abstract 1518: Benign oncocytic tumors in the setting of HLRCC syndrome

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.1518-1518

2023

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CCND1 Genomic Rearrangement as a Secondary Event in High Grade B‐Cell Lymphoma

HemaSphere, 2021-01, Vol.5 (1), p.e505-n/a

2021

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SAT556 An Unusual Case of Papillary Thyroid Carcinoma With Biallelic MEN1 Variants In a Patient With MEN1

Journal of the Endocrine Society, 2023-10, Vol.7 (Supplement_1)

2023

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P670: A collaborative model integrating clinical genetics and molecular pathology for tumor/normal paired whole exome sequencing testing

Genetics in Medicine Open, 2024, Vol.2, p.101574, Article 101574

2024

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Phase 1 trial of anti-CD22 recombinant immunotoxin moxetumomab pasudotox combined with rituximab for relapsed/refractory hairy cell leukemia

Journal of clinical oncology, 2021-05, Vol.39 (15_suppl), p.7036-7036

2021

Volltextzugriff (PDF)

Abstract 3387: Mutational analysis in metastatic melanoma to the breast and ovary: correlation with clinic-pathological and immunohistochemical findings

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.3387-3387

2017

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Inherited predisposition to malignant mesothelioma (MM) due to mutations in DNA repair genes

Journal of clinical oncology, 2018-05, Vol.36 (15_suppl), p.8504-8504

2018

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Case report of adrenocortical carcinoma associated with double germline mutations in MSH2 and RET

American journal of medical genetics. Part A, 2021-04, Vol.185 (4), p.1282-1287

2021

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Whole Exome Sequencing Reveals Multiple Driver Events in Chronic Lymphocytic Leukemia Patients with Acquired Ibrutinib Resistance

Blood, 2019-11, Vol.134 (Supplement_1), p.1287-1287

2019

Volltextzugriff (PDF)

PATH-28. THE NATURAL HISTORY OF BRAF V600E-MUTATED GLIOBLASTOMAS IN ADULTS

Neuro-oncology (Charlottesville, Va.), 2018-11, Vol.20 (suppl_6), p.vi164-vi164

2018

Volltextzugriff (PDF)

KSHV- and EBV-associated Germinotropic Lymphoproliferative Disorder: New Findings and Review of the Literature

The American journal of surgical pathology, 2017-06, Vol.41 (6), p.795-800

2017

Volltextzugriff (PDF)

Expanding the Spectrum of EBV-positive Marginal Zone Lymphomas: A Lesion Associated With Diverse Immunodeficiency Settings

The American journal of surgical pathology, 2018-10, Vol.42 (10), p.1306-1316

2018

Volltextzugriff (PDF)

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WHIM Syndrome Cured by Chromothripsis

Adult T-cell leukemia/lymphoma with EBV-positive Hodgkin-like cells

The importance of accounting method and sampling depth to estimate changes in soil carbon stocks

High level MYCN amplification and distinct methylation signature define an aggressive subtype of spinal cord ependymoma

MGMT Status as a Clinical Biomarker in Glioblastoma

The clinical spectrum of Erdheim-Chester disease: an observational cohort study

The lymph node microenvironment promotes B-cell receptor signaling, NF-κB activation, and tumor proliferation in chronic lymphocytic leukemia

Case report: Oligodendroglioma, IDH-mutant and 1p/19q-codeleted, associated with a germline mutation in PMS2

P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report

Greenhouse gas mitigation on croplands: clarifying the debate on knowns, unknowns and risks to move forward with effective management interventions

Clonal expansion of CAR T cells harboring lentivector integration in the CBL gene following anti-CD22 CAR T-cell therapy

Longitudinal Circulating Tumor DNA Analysis in Blood and Saliva for Prediction of Response to Osimertinib and Disease Progression in EGFR-Mutant Lung Adenocarcinoma

Human Herpes Virus 6 (HHV-6)–associated Lymphadenitis: Pitfalls in Diagnosis in Benign and Malignant Settings

Abstract 1518: Benign oncocytic tumors in the setting of HLRCC syndrome

CCND1 Genomic Rearrangement as a Secondary Event in High Grade B‐Cell Lymphoma

SAT556 An Unusual Case of Papillary Thyroid Carcinoma With Biallelic MEN1 Variants In a Patient With MEN1

P670: A collaborative model integrating clinical genetics and molecular pathology for tumor/normal paired whole exome sequencing testing

Phase 1 trial of anti-CD22 recombinant immunotoxin moxetumomab pasudotox combined with rituximab for relapsed/refractory hairy cell leukemia

Abstract 3387: Mutational analysis in metastatic melanoma to the breast and ovary: correlation with clinic-pathological and immunohistochemical findings

Inherited predisposition to malignant mesothelioma (MM) due to mutations in DNA repair genes

Case report of adrenocortical carcinoma associated with double germline mutations in MSH2 and RET

Whole Exome Sequencing Reveals Multiple Driver Events in Chronic Lymphocytic Leukemia Patients with Acquired Ibrutinib Resistance

PATH-28. THE NATURAL HISTORY OF BRAF V600E-MUTATED GLIOBLASTOMAS IN ADULTS

KSHV- and EBV-associated Germinotropic Lymphoproliferative Disorder: New Findings and Review of the Literature

Expanding the Spectrum of EBV-positive Marginal Zone Lymphomas: A Lesion Associated With Diverse Immunodeficiency Settings

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