Search | Global Index Medicus

Atypical presentation of infectious mononucleosis.

Fernandopule, Maxi; Fernandopulle, Nilesh; Kurukulasuriya, A P.

Article in English | IMSEAR | ID: sea-150131

Direct oxidant damage to red cells associated with propanil ingestion.

Kurukulasuriya, A P; Asokan, P; Dissanayake, H W.

Ceylon Med J ; 2003 Sep; 48(3): 88-9

Article in English | IMSEAR | ID: sea-48943

Subject(s)

Anemia, Hemolytic/chemically induced , Blood Transfusion , Erythrocytes/drug effects , Follow-Up Studies , Humans , Male , Middle Aged , Oxidative Stress , Propanil/adverse effects , Risk Assessment , Treatment Outcome

Fragmented red cells, thrombocytopaenia and elevated D-dimers do not always indicate the presence of disseminated intravascular coagulation, even in the presence of a bleeding tendency.

Kurukulasuriya, A P.

Ceylon Med J ; 2003 Jun; 48(2): 61

Article in English | IMSEAR | ID: sea-48586

Subject(s)

Aged , Aged, 80 and over , Disseminated Intravascular Coagulation/diagnosis , Erythrocytes , Fibrin Fibrinogen Degradation Products/analysis , Humans , Male , Middle Aged , Thrombocytopenia/etiology

Juvenile pernicious anaemia in a Sri Lankan child.

Senanayake, M P; Kurukulasuriya, A P.

Ceylon Med J ; 2000 Jun; 45(2): 80-1

Article in English | IMSEAR | ID: sea-48342

Subject(s)

Anemia, Pernicious/diagnosis , Child , Humans , Male , Sri Lanka , Vitamin B 12/therapeutic use

Pure red cell aplasia associated with a thymoma.

Kurukulasuriya, A P; de Silva, M V.

Ceylon Med J ; 1999 Jun; 44(2): 94-5

Article in English | IMSEAR | ID: sea-48431

Subject(s)

Biopsy, Needle , Bone Marrow/pathology , Female , Humans , Middle Aged , Red-Cell Aplasia, Pure/diagnosis , Thymectomy , Thymoma/complications , Thymus Neoplasms/complications , Tomography, X-Ray Computed , Treatment Outcome

Immunophenotyping in leukaemias is not a luxury.

Kurukulasuriya, A P; Wijesiriwardene, B; Perera, T K.

Ceylon Med J ; 1998 Jun; 43(2): 117-8

Article in English | IMSEAR | ID: sea-48496

Subject(s)

Antigens, Surface/analysis , Diagnosis, Differential , Humans , Immunophenotyping , Leukemia, Lymphocytic, Chronic, B-Cell/diagnosis , Leukemia, Lymphoid/diagnosis , Leukemia, Myeloid/diagnosis , Male , Middle Aged , Sensitivity and Specificity

Does beta thalassaemia major manifest clinically at three months of age?

Kurukulasuriya, A P; Kumarasinghe, U; Perera, K T.

Article in English | IMSEAR | ID: sea-47976

ABSTRACT

Does beta thalassaemia major manifest clinically at three months of age? Yes, it does, contrary to traditional teaching. Traditionally, it is taught that this disease manifests clinically around six months to one year of age and that a haemoglobinopathy which manifests at three months of age cannot be beta thalassaemia major.

Subject(s)

Age Factors , Female , Humans , Infant , Sri Lanka , beta-Thalassemia/diagnosis

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