Chabchoub imen (86 résultats)

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Paperback. Etat : Brand New. 88 pages. French language. 8.66x5.91x0.20 inches. In Stock.

Paperback. Etat : Brand New. 52 pages. French language. 8.66x5.91x0.12 inches. In Stock.

Taschenbuch. Etat : Neu. Síndrome linfoproliferativo con autoinmunidad | Síndrome linfoproliferativo | Imen Chabchoub | Taschenbuch | Spanisch | 2021 | Ediciones Nuestro Conocimiento | EAN 9786203508734 | 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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Taschenbuch. Etat : Neu. Le syndrome lymphoprolifératif avec auto-immunité | Le syndrome lymphoprolifératif | Imen Chabchoub (u. a.) | Taschenbuch | 88 S. | Französisch | 2019 | Éditions universitaires européennes | EAN 9786139520091 | Verantwortliche Person für die EU: Editions universitaires europeennes, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu.…

Taschenbuch. Etat : Neu. Particularités de l'épilepsie associée au syndrome d'Aicardi | Epilepsie associée au syndrome d'Aicardi | Imen Chabchoub (u. a.) | Taschenbuch | 52 S. | Französisch | 2019 | Éditions universitaires européennes | EAN 9786139520084 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Taschenbuch. Etat : Neu. TOXICITE MUSCULAIRE DES STATINES CHEZ LE SUJET AGE | Imen Chabchoub (u. a.) | Taschenbuch | Französisch | 2021 | Éditions universitaires européennes | EAN 9786203413885 | Verantwortliche Person für die EU: Editions universitaires europeennes, Brivibas Gatve 197, 1039 RIGA, LETTLAND, customerservice[at]vdm-vsg[dot]de | Anbieter: preigu. …

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Taschenbuch. Etat : Neu. Besonderheiten der Epilepsie in Verbindung mit dem Aicardi-Syndrom | Epilepsie in Verbindung mit dem Aicardi-Syndrom | Imen Chabchoub | Taschenbuch | 52 S. | Deutsch | 2021 | Verlag Unser Wissen | EAN 9786204340319 | Verantwortliche Person für die EU: BoD - Books on Demand, In de Tarpen 42, 22848 Norderstedt, info[at]bod[dot]de | Anbieter: preigu. …

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Aicardi syndrome (AS), typically associated with severe epilepsy, severe psychomotor retardation, partial or total agenesis of the corpus callosum (CC), and chorioretinal abnormalities, is a very rare condition that affects all ethnic groups equally. Its incidence has been estimated to be between 1/105000 and 1/167000 in the United States and between 1/93000 and 1/99000 in some European countries. The exact prevalence of AS is unknown, but has been estimated to be at least 853 in the United States and over 4000 worldwide. Seizures, associated with AS, are often revelatory and appear early, usually in the first trimester of life. Spasms are usually in the foreground. They are most often asymmetrical. Other types of epileptic seizures may be associated. These are essentially focal seizures which also start early and often precede the appearance of spasms. The intercritical electroencephalogram shows the characteristic aspect of asymmetric and asynchronous hypsarythmia. This is also associated with the absence of a sleep spindle, and with the 'Supression-Burst' aspect. 52 pp. Englisch.…

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 64 pp. Englisch.

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Auto-immune lymphoproliferative syndrome (ALPS) is a rare inherited disorder that typically affects children and persists into adulthood. It is characterized by chronic benign lymphoproliferation, autoimmunity, elevated double-negative T cells, and an increased risk of progression to lymphoma, all as a consequence of a primary defect in apoptosis. The prevalence of this syndrome remains underestimated due to the non-specificity of its clinical signs. In fact, many patients with ALPS are diagnosed with other diseases with different treatment and prognosis. In the last few years, thanks to a better understanding of the pathophysiological mechanisms of apoptosis and the identification of its genetic determinants, considerable scientific progress has been made and has paved the way for the use of more targeted therapies. In this review, we outline the pathophysiological mechanisms and the epidemiological, clinical, biological, histological, genetic therapeutic and evolutionary aspects of ALPS. 80 pp. Englisch. …

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Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -El síndrome de Aicardi (AS), típicamente asociado a epilepsia grave, retraso psicomotor severo, agenesia parcial o total del cuerpo calloso (CC) y anomalías coriorretinianas, es una condición muy rara que afecta a todos los grupos étnicos por igual. Su incidencia se ha estimado entre 1/105000 y 1/167000 en Estados Unidos y entre 1/93000 y 1/99000 en algunos países europeos. Se desconoce la prevalencia exacta de la EA, pero se ha calculado que es de al menos 853 en EE.UU. y más de 4000 en todo el mundo. Las convulsiones, asociadas al SA, suelen ser reveladoras y aparecen pronto, normalmente en el primer trimestre de vida. Los espasmos suelen estar en primer plano. Suelen ser asimétricos. Pueden asociarse otros tipos de crisis epilépticas. Se trata principalmente de convulsiones focales, que también se inician tempranamente y suelen preceder a la aparición de espasmos. El electroencefalograma intercrítico muestra el aspecto característico de la hipsarritmia asimétrica y asincrónica. Esto también se asocia con la ausencia de un huso de sueño, y la apariencia de 'Supresión-estallido'. 52 pp. Spanisch.…

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -El síndrome linfoproliferativo autoinmune (ALPS) es una enfermedad hereditaria rara que suele afectar a los niños y persiste en la edad adulta. Se caracteriza por una linfoproliferación crónica benigna, autoinmunidad, elevados linfocitos T doblemente negativos y un mayor riesgo de progresión a linfoma, todo ello como consecuencia de un defecto primario en la apoptosis. La prevalencia de este síndrome sigue estando subestimada debido a la inespecificidad de sus signos clínicos. De hecho, a muchos pacientes con ALPS se les diagnostican, en cambio, otras enfermedades con diferente tratamiento y pronóstico. En los últimos años, gracias a una mejor comprensión de los mecanismos fisiopatológicos de la apoptosis y a la identificación de sus determinantes genéticos, se han realizado considerables avances científicos que han allanado el camino hacia terapias más específicas. En esta revisión, se exponen los mecanismos fisiopatológicos y los aspectos epidemiológicos, clínicos, biológicos, histológicos, genéticos, terapéuticos y evolutivos del ALPS. 80 pp. Spanisch. …

Taschenbuch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 64 pp. Spanisch.

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Taschenbuch. Etat : Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Auto-immune lymphoproliferative syndrome (ALPS) is a rare inherited disorder that typically affects children and persists into adulthood. It is characterized by chronic benign lymphoproliferation, autoimmunity, elevated double-negative T cells, and an increased risk of progression to lymphoma, all as a consequence of a primary defect in apoptosis. The prevalence of this syndrome remains underestimated due to the non-specificity of its clinical signs. In fact, many patients with ALPS are diagnosed with other diseases with different treatment and prognosis. In the last few years, thanks to a better understanding of the pathophysiological mechanisms of apoptosis and the identification of its genetic determinants, considerable scientific progress has been made and has paved the way for the use of more targeted therapies. In this review, we outline the pathophysiological mechanisms and the epidemiological, clinical, biological, histological, genetic therapeutic and evolutionary aspects of ALPS. …