A non-invasive solution for monitoring of the activity and dehydration of organisms is proposed in the work. For this purpose, a wireless standalone chemical sensor platform using two separate measurement techniques has been developed. The first approach for activity monitoring is based on humidity measurement.
View Article and Find Full Text PDFGematol Transfuziol
August 1989
The bone marrow histological picture was studied in 13 patients with hairy-cell leukemia (HCL) who were followed up at the Hematological Centre in the Latvian SSR. The diagnosis was made or proved in all the cases, among them in 9 patients - on the basis of the proliferation type of leukemia cells in the bone marrow trephine biopsy that is characteristic of HCL. The analysis of the clinical and morphological features of the disease has permitted the authors to distinguish specific types of HCL: 1) splenic and bone-marrow variants predominantly were diagnosed clinically, 2) typical and atypical variants resembling malignant lymphoma or chronic lymphoid leukemia were diagnosed histomorphologically.
View Article and Find Full Text PDFAnalysis of the disease course in 17 patients afflicted with hairy-cell leukemia enabled the authors to specify 3 clinico-hematologic variants of the disease: a typical or a splenic one (with a predominant injury to the spleen), an atypical or bone marrow one (with a predominant injury to bone marrow), and a hypoplastic one. The bone marrow variant was characterized by the most pronounced leukemic injuries to bone marrow, severe bacterial complications, and the most unfavourable prognosis. The remaining variants were marked by their own individual features and ran a more favourable course.
View Article and Find Full Text PDFWe report on 12 patients who fulfilled the FAB diagnosis criteria of chronic myelomonocytic leukemia (CMML). Some clinical findings (splenomegaly) as well as biological parameters (WBC count, cellularity of bone marrow sections, presence of dyserythropoiesis in bone marrow smears) were subjected to particular analysis. This allowed the assignment of each patient onto one of three separate hematological syndromes: (1) RA or RAEB with monocytosis, (2) myelomonocytic dysplasia (a novel syndrome) and (3) true CMML.
View Article and Find Full Text PDFProbl Gematol Pereliv Krovi
August 1981
Probl Gematol Pereliv Krovi
January 1977
Probl Gematol Pereliv Krovi
October 1975
Vestn Otorinolaringol
February 1968