Aetiology of the auto-immune haemolytic anaemias

Natural history of paroxysmal nocturnal hemoglobinuria.

The New England journal of medicine·1995

Non-tropical 'idiopathic splenomegaly': a follow-up study of ten patients described in 1969.

British journal of haematology·1978

Autoimmune hemolytic anemia.

Archives of internal medicine·1975

The use of granulocyte colony-stimulating factor in a neutropenic renal transplant recipient.

Haematologia·2003

Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.

Haematologia·2003

Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.

Haematologia·2003

Angiocentric lymphomatoid granulomatosis and severe hypogammaglobulinaemia.

Haematologia·2003

Vena cava superior syndrome due to sternal plasmacytoma in the course of systemic myeloma.

Haematologia·2003

Hepatosplenic gamma delta T-cell lymphoma with leukemic phase successfully treated with 2-chlorodeoxyadenosine.

Haematologia·2003

Role of Thrombectomy Technique in Alteplase Bridging Intravenous Thrombolysis for Basilar Artery Occlusion.

Journal of the American Heart Association·2026

Compound Heterozygous Mutations in FGA Cause Congenital Afibrinogenemia: A Case Report and Literature Review.

Birth defects research·2026

Anticoagulation Following Surgery for Glioblastoma: Case Report and Review of the Literature.

Journal of neurological surgery reports·2026

Jada System Versus Bakri Balloon for Postpartum Hemorrhage: A Retrospective Cohort Study.

Cureus·2026

Abnormally Low Hemoglobin A1c Due to a Heterozygous Alpha-Globin Variant (Hb I; HBA2 c.49A>G, p.Lys17Glu) in a Geriatric Patient.

Cureus·2026

Myeloablative Matched Sibling Donor Hematopoietic Stem Cell Transplantation as a Curative Treatment for Congenital Erythropoietic Porphyria: A Cohort Study from Low-Middle Income Country.

Missouri medicine·2026

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Aetiology of the auto-immune haemolytic anaemias

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Natural history of paroxysmal nocturnal hemoglobinuria.

Non-tropical 'idiopathic splenomegaly': a follow-up study of ten patients described in 1969.

Autoimmune hemolytic anemia.

The use of granulocyte colony-stimulating factor in a neutropenic renal transplant recipient.

Heterozygous methylene tetrahydrofolate reductase mutation with mild hyperhomocysteinemia associated with deep vein thrombosis.

Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.

Angiocentric lymphomatoid granulomatosis and severe hypogammaglobulinaemia.

Vena cava superior syndrome due to sternal plasmacytoma in the course of systemic myeloma.

Hepatosplenic gamma delta T-cell lymphoma with leukemic phase successfully treated with 2-chlorodeoxyadenosine.

Role of Thrombectomy Technique in Alteplase Bridging Intravenous Thrombolysis for Basilar Artery Occlusion.

Compound Heterozygous Mutations in FGA Cause Congenital Afibrinogenemia: A Case Report and Literature Review.

Anticoagulation Following Surgery for Glioblastoma: Case Report and Review of the Literature.

Jada System Versus Bakri Balloon for Postpartum Hemorrhage: A Retrospective Cohort Study.

Abnormally Low Hemoglobin A1c Due to a Heterozygous Alpha-Globin Variant (Hb I; HBA2 c.49A>G, p.Lys17Glu) in a Geriatric Patient.

Myeloablative Matched Sibling Donor Hematopoietic Stem Cell Transplantation as a Curative Treatment for Congenital Erythropoietic Porphyria: A Cohort Study from Low-Middle Income Country.

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