Amit valbhani (9 risultati)
Lingua: Inglese
Editore: VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG 2014
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Da: Books Puddle, New York, NY, U.S.A.Books Puddle
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Condizione: New. pp. 140.
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Da: preigu, Osnabrück, Germaniapreigu
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Taschenbuch. Condizione: Neu. Painful crises in sickle cell anemia | Amit Valbhani (u. a.) | Taschenbuch | 152 S. | Englisch | 2015 | LAP LAMBERT Academic Publishing | EAN 9783659553196 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, , GermaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Sickle cell anemia is one of the major hereditary health problem in tropical Africa where the sickle cell gene frequency is particularly high. The disease occurs with high incidence in west,east and central Africa and this has been… related to the prevalence of malaria in these regions. The classic hallmark of sickle cell anemia are episodes of vaso-occlusive crisis often with multiorgan manifestation and chronic haemolytic anemia. vaso-occlusive crisis is the most common cause of hospitalization in sickle cell disease. It affects the growth and academic performance of individual. Thus it would be quite helpful to terminate such painful episodes at a very early stage. Serum CPK,LDH and 24 hour urinary creatinine can be used as potential markers of tissue ischemia in such painful episodes. 152 pp. Englisch.
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Da: moluna, Greven, , Germaniamoluna
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Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Valbhani AmitDr.Amit Valbhani(MBBS,MD)did his MBBS from Shri vasantrao naik government medical college,Yavatmal(Maharashtra,India)and MD Pediatrics from Pt.Jawaharlal nehru memorial medical college,Rai…pur(Chattisgarh,India).He Curren.
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Da: moluna, Greven, , Germaniamoluna
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Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Ahuja NehaDr. Neha Ahuja (M.D. PATHOLOGY), and am presently working as a Consultant Pathologist in DR LAL PATH LAB, Kanpur. Dr. Parul Ahuja (B.D.S), Dr. Amit Valbhani (M.D. PAEDIATRICS) is working as a… Senior Resident at Acharya Bhi.
Lingua: Inglese
Editore: VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG 2014
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Da: Majestic Books, Hounslow, , Regno UnitoMajestic Books
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Condizione: New. Print on Demand pp. 140 2:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on Creme w/Gloss Lam.
Lingua: Inglese
Editore: VDM Verlag Dr. Mueller Aktiengesellschaft & Co. KG 2014
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Da: Biblios, frankfurt am main, HESSE, GermaniaBiblios
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Condizione: New. PRINT ON DEMAND pp. 140.
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Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Sickle cell anemia is one of the major hereditary health problem in tropical Africa where the sickle cell gene frequency is particularly high. The disease occurs with high incidence in west,east and central Africa and this has been rel…ated to the prevalence of malaria in these regions. The classic hallmark of sickle cell anemia are episodes of vaso-occlusive crisis often with multiorgan manifestation and chronic haemolytic anemia. vaso-occlusive crisis is the most common cause of hospitalization in sickle cell disease. It affects the growth and academic performance of individual. Thus it would be quite helpful to terminate such painful episodes at a very early stage. Serum CPK,LDH and 24 hour urinary creatinine can be used as potential markers of tissue ischemia in such painful episodes.VDM Verlag, Dudweiler Landstraße 99, 66123 Saarbrücken 152 pp. Englisch.
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
Contatta il venditoreVenditore con 5 stelleCondizione: Nuovo
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Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Sickle cell anemia is one of the major hereditary health problem in tropical Africa where the sickle cell gene frequency is particularly high. The disease occurs with high incidence in west,east and central Africa and this has been rela…ted to the prevalence of malaria in these regions. The classic hallmark of sickle cell anemia are episodes of vaso-occlusive crisis often with multiorgan manifestation and chronic haemolytic anemia. vaso-occlusive crisis is the most common cause of hospitalization in sickle cell disease. It affects the growth and academic performance of individual. Thus it would be quite helpful to terminate such painful episodes at a very early stage. Serum CPK,LDH and 24 hour urinary creatinine can be used as potential markers of tissue ischemia in such painful episodes.
