Apparent C trisomy in bone marrow cells. Report of two cases

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

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Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

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MicroRNA-related sequence variations in human cancers.

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Recurrent and founder mutations in the PMS2 gene.

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Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

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The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Gut·2010

Role of iron in the proliferation of the established human tumor cell lines U-937 and K-562: effects of suramin and a lipophilic iron chelator (PIH).

Scandinavian journal of haematology·1986

The efficacy and toxicity of VAD in the treatment of myeloma and related disorders.

Scandinavian journal of haematology·1986

RES phagocytosis in children with homozygous beta-thalassemia in relation to blood transfusion.

Scandinavian journal of haematology·1986

Two allotypes of factor IX present in haemophilia B.

Scandinavian journal of haematology·1986

Radioimmunoassay of erythropoietin in chronic uraemia or anephric patients.

Scandinavian journal of haematology·1986

Prognostic significance of a morphometric study of lymph node biopsies in chronic lymphocytic leukaemia.

Scandinavian journal of haematology·1986

Anterior Mediastinal Germ Cell Tumor Presenting With Superior Vena Cava Obstruction and Malignant Pericardial Effusion.

Cureus·2026

Obesity at antiretroviral therapy initiation and long-term risk of cardiovascular disease, cancer, or death in people with HIV in Italy: a prospective cohort study.

EClinicalMedicine·2026

Spontaneous Tumor Lysis Syndrome Revealing Advanced Ovarian Carcinoma: From Oncologic Emergency to Complete Pathologic Response.

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The solitary skull mass: An atypical presentation of anaplastic large cell lymphoma.

Radiology case reports·2026

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Apparent C trisomy in bone marrow cells. Report of two cases

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The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia.

Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia.

MicroRNA-related sequence variations in human cancers.

Recurrent and founder mutations in the PMS2 gene.

Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene.

The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease.

Role of iron in the proliferation of the established human tumor cell lines U-937 and K-562: effects of suramin and a lipophilic iron chelator (PIH).

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RES phagocytosis in children with homozygous beta-thalassemia in relation to blood transfusion.

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Prognostic significance of a morphometric study of lymph node biopsies in chronic lymphocytic leukaemia.

Anterior Mediastinal Germ Cell Tumor Presenting With Superior Vena Cava Obstruction and Malignant Pericardial Effusion.

Obesity at antiretroviral therapy initiation and long-term risk of cardiovascular disease, cancer, or death in people with HIV in Italy: a prospective cohort study.

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