Imene moalla (64 résultats)

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

Etat : New.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

Etat : New.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

Taschenbuch. Etat : Neu. Lympho-histiocytic hemophagocytosis in pediatrics | Imene Moalla (u. a.) | Taschenbuch | Englisch | 2026 | Sciencia Scripts | EAN 9786630071306 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

Etat : New.

Etat : New.

Etat : New.

Etat : New.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

PAP. Etat : New. New Book. Shipped from UK. Established seller since 2000.

Taschenbuch. Etat : Neu. Hémophagocytose lympho-histiocytaire en pédiatrie | Imene Moalla (u. a.) | Taschenbuch | Französisch | 2026 | Éditions universitaires européennes | EAN 9786209917608 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. Granulomatose septique chronique chez l'enfant | Granulomatose septique | Imene Moalla (u. a.) | Taschenbuch | Französisch | 2026 | Éditions universitaires européennes | EAN 9786630053791 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. Hemofagocytoza limfohistiocytarna w pediatrii | Imene Moalla (u. a.) | Taschenbuch | Polnisch | 2026 | Wydawnictwo Nasza Wiedza | EAN 9786630084108 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. Emofagocitosi linfo-istiocitica in pediatria | Imene Moalla (u. a.) | Taschenbuch | Italienisch | 2026 | Edizioni Sapienza | EAN 9786630086669 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. Hemofagocitose linfo-histiocítica em pediatria | Imene Moalla (u. a.) | Taschenbuch | Portugiesisch | 2026 | Edições Nosso Conhecimento | EAN 9786630081541 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. Lympho-histiozytäre Hämophagozytose in der Pädiatrie | Imene Moalla (u. a.) | Taschenbuch | 88 S. | Deutsch | 2026 | Verlag Unser Wissen | EAN 9786630076424 | Verantwortliche Person für die EU: SIA OmniScriptum Publishing, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

Paperback. Etat : new. Paperback. Chronic septic granulomatosis is a rare primary immunodeficiency caused by a dysfunction of the NADPH oxidase complex in phagocytes.The disease is genetic in origin, most commonly inherited in an X-linked recessive pattern, and less commonly in an autosomal recessive pattern. X-linked forms are generally more severe and manifest at an earlier age.The diagnosis is often made in the first few years of life due to severe and recurrent infections. Patients are particularly susceptible to bacterial and fungal infections, especially invasive aspergillosis.Chronic inflammatory granulomas can also affect multiple organs and impair the quality of life of affected children. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 80 pp. Englisch.

Paperback. Etat : new. Paperback. La Granulomatose septique chronique est un deficit immunitaire primaire rare du a un dysfonctionnement du complexe NADPH oxydase des phagocytes.La maladie est d'origine genetique, transmise le plus souvent selon un mode recessif lie a l'X, plus rarement autosomique recessif. Les formes liees a l'X sont generalement plus severes et plus precoces.Le diagnostic est souvent pose des les premieres annees de vie devant des infections severes et recidivantes. Les patients sont particulierement exposes aux infections bacteriennes et fongiques, notamment a Aspergillose invasive.Des granulomes inflammatoires chroniques peuvent egalement atteindre plusieurs organes et alterer la qualite de vie des enfants atteints. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.…

Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Hemophagocytic lymphohistiocytosis (HLH) in pediatrics is a rare and potentially fatal syndrome of severe hyperinflammation, linked to uncontrolled activation of the immune system. It is often difficult to diagnose due to its non-specific clinical manifestations, dominated by prolonged fever, cytopenias and hepatosplenomegaly, which may mimic many other pathologies. The distinction between primary and secondary forms of the disease determines its therapeutic management. Treatment is based on often severe immunosuppression, sometimes combined with hematopoietic stem cell transplantation. Early recognition is essential to improve prognosis and reduce mortality.…

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -La linfohistiocitosis hemofagocítica pediátrica (HLH) es un síndrome raro y potencialmente mortal de hiperinflamación grave relacionada con la activación incontrolada del sistema inmunitario. A menudo es difícil de diagnosticar debido a sus manifestaciones clínicas inespecíficas, dominadas por fiebre prolongada, citopenias y hepatoesplenomegalia, que pueden simular muchas otras patologías. La distinción entre formas primarias y secundarias determina el tratamiento. El tratamiento se basa en la inmunosupresión, que a menudo es severa, y a veces se combina con el trasplante de células madre hematopoyéticas. El reconocimiento precoz sigue siendo esencial para mejorar el pronóstico y reducir la mortalidad. 84 pp. Spanisch.…