Mitotic activity of circulating atypical lymphocytes

Congenital heart defects in the recurrent 2q13 deletion syndrome.

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Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Clinical genetics·2018

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Clinical genetics·2018

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Clinical genetics·2017

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Clinical genetics·2017

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

Molecular syndromology·2013

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

Dabrafenib-Induced Cutaneous Eruptions in a Patient With Langerhans Cell Histiocytosis.

Case reports in dermatological medicine·2026

Type 1 diabetes mellitus induced by sintilimab: a case report and related case literature analysis.

Frontiers in endocrinology·2026

Lipocalin-2 Emerges as a Core Pathogenic Mediator and Biomarker in Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD via Transcriptomic Profiling.

Kidney diseases (Basel, Switzerland)·2026

Diffuse Large B-cell Lymphoma Initially Managed As Secondary Immune Thrombocytopenia: A Case Report.

Cureus·2026

Adverse pregnancy outcome associations among women prior to a diagnosis of systemic lupus erythematosus.

Frontiers in lupus·2026

Targeting TKT-associated immunometabolic remodeling attenuates experimental lupus nephritis and NET-related inflammation.

Frontiers in cell and developmental biology·2026

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Mitotic activity of circulating atypical lymphocytes

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Congenital heart defects in the recurrent 2q13 deletion syndrome.

Atrioventricular canal defect and genetic syndromes: The unifying role of sonic hedgehog.

Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene.

Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review.

Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.

Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations.

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).

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

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

Two allotypes of factor IX present in haemophilia B.

Radioimmunoassay of erythropoietin in chronic uraemia or anephric patients.

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

Dabrafenib-Induced Cutaneous Eruptions in a Patient With Langerhans Cell Histiocytosis.

Type 1 diabetes mellitus induced by sintilimab: a case report and related case literature analysis.

Lipocalin-2 Emerges as a Core Pathogenic Mediator and Biomarker in Autosomal Dominant Tubulointerstitial Kidney Disease-UMOD via Transcriptomic Profiling.

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Mitotic activity of circulating atypical lymphocytes

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