Bouatay amina (69 resultados)

Condición: New.

Condición: New.

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. Congenital neutropenia | Amina Bouatay (u. a.) | Taschenbuch | Englisch | 2022 | Our Knowledge Publishing | EAN 9786205279243 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condición: Neu. Polyglobulia Vaquez | Diagnostic criteria and therapeutic news | Amina Bouatay (u. a.) | Taschenbuch | Englisch | 2022 | Our Knowledge Publishing | EAN 9786205294697 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Condición: New.

paperback. Condición: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

paperback. Condición: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condición: New.

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. Polyglobulie de Vaquez | Critères Diagnostiques et actualités thérapeutiques | Amina Bouatay (u. a.) | Taschenbuch | Französisch | 2022 | Éditions universitaires européennes | EAN 9786203440683 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Condición: New.

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. Poliglobuliniq Vakez | Diagnosticheskie kriterii i aktual'nye woprosy lecheniq | Amina Bouatay (u. a.) | Taschenbuch | Russisch | 2022 | Sciencia Scripts | EAN 9786205294765 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Condición: New.

Condición: New.

Taschenbuch. Condición: Neu. Neutropenia congenita | Amina Bouatay (u. a.) | Taschenbuch | Italienisch | 2022 | Edizioni Sapienza | EAN 9786205279267 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condición: Neu. Poliglobulinia Vaquez | Criteri diagnostici e problemi di trattamento attuali | Amina Bouatay (u. a.) | Taschenbuch | Italienisch | 2022 | Edizioni Sapienza | EAN 9786205294727 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Condición: New.

Taschenbuch. Condición: Neu. Polyglobulinia Vaquez | Critérios de diagnóstico e questões de tratamento actuais | Amina Bouatay (u. a.) | Taschenbuch | Portugiesisch | 2022 | Edições Nosso Conhecimento | EAN 9786205294758 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condición: Neu. Vaquez-Polyglobulie | Diagnostische Kriterien und aktuelle therapeutische Entwicklungen | Amina Bouatay (u. a.) | Taschenbuch | 64 S. | Deutsch | 2022 | Verlag Unser Wissen | EAN 9786205294598 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Condición: Neu. Die ätiologische Diagnose von Zytopenien bei älteren Menschen | Welche Bedeutung hat das Myelogramm? | Amina Bouatay (u. a.) | Taschenbuch | 100 S. | Deutsch | 2022 | Verlag Unser Wissen | EAN 9786205383049 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu.…

Condición: New. Print on Demand.

Condición: New. Print on Demand.

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Policitemiq Vakesa (PV) - äto mieloproliferatiwnoe nowoobrazowanie, woznikaüschee w rezul'tate klonal'noj äxpansii plüripotentnoj gemopoäticheskoj stwolowoj kletki, chto priwodit k proliferacii mieloidnoj tkani preimuschestwenno äritrocitarnogo rqda. On harakterizuetsq uwelicheniem obschej massy äritrocitow i gemoglobina bez chrezmernoj stimulqcii äritropoätinom. Ego rasprostranennost' nizka (2-3 sluchaq na 100 000 zhitelej w god). Nachal'naq stadiq zabolewaniq chasto protekaet bessimptomno. U nekotoryh pacientow wozniknowenie tromboticheskogo sobytiq ili simptomow, swqzannyh s sindromom giperwqzkosti, priwodit k diagnozu PV.Otkrytie mutacii JAK2 V617F polnost'ü izmenilo diagnostiku PV i pozwolilo ne tol'ko luchshe ponqt' patofiziologicheskie mehanizmy, no i razrabotat' celewuü molekulqrnuü terapiü, swqzannuü s äffektiwnym molekulqrnym monitoringom. 64 pp. Russisch.…

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Vaquez polycythemia (PV) is a myeloproliferative neoplasm resulting from clonal expansion of a pluripotent hematopoietic stem cell, causing proliferation of myeloid tissue predominantly in the erythrocyte lineage. It is characterized by an increase in total erythrocyte mass and hemoglobin without excessive stimulation by erythropoietin. Its incidence is low (2 to 3 cases per 100,000 inhabitants/year). The initial presentation is often pauci symptomatic. In some patients the occurrence of a thrombotic event or symptoms related to hyperviscosity syndrome leads to the diagnosis of PV.The discovery of the JAK2 V617F mutation has completely changed the diagnosis of PV and has allowed not only a better understanding of the pathophysiological mechanisms, but also the development of a targeted molecular therapy associated with an efficient molecular monitoring. 60 pp. Englisch.…

Taschenbuch. Condición: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Congenital neutropenia is a group of rare diseases. They correspond to quantitative neutrophil deficiencies of genetic origin and constitute a very heterogeneous group on the phenotypic and genotypic level. There are two forms: primary constitutional neutropenia and neutropenia associated with a genetic disease. The diagnosis is based on clinical and biologic arguments: family and personal history, recurrent bacterial or fungal infections, persistence of neutropenia and specific appearance on the myelogram. Recent advances in genetics and molecular biology have made it possible to describe about twenty genes as responsible for these pathologies. The severity of infections during congenital neutropenia is related to the depth of neutropenia and its duration on the one hand, and to the genetic origin on the other hand, which requires an adequate management based on antibiotic therapy and the administration of G-CSF. Hematopoietic stem cell transplantation remains the only curative therapy. 72 pp. Englisch.…