Semmola-Meryon-Duchenne syndrome

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There is no satisfactory therapy for many of the disabling genetic disorders such as Semmola-Meryon-Duchenne syndrome. However, it is hoped that advances arising from the accumulating research evidence can contribute to improving treatment of such conditions. Therefore, reviewing the literature for the recent research evidence is recommended to improve the therapeutic services for patients with such disorders. The occurrence of Semmola-Meryon-Duchenne syndrome in Iraq has not been documented. In addition to providing the historical documentation of this syndrome, particularly the early history of its documentation, this book describes the occurrence of Semmola-Meryon-Duchenne syndrome in two Iraqi brothers. This book also reviews the available research evidence which may contribute to improving its treatment.

Autorentext

Professor Aamir Jalal Al Mosawi, is senior advisor doctor at Baghdad Medical City. He is the Head of Iraq Headquarter of Copernicus Scientists International Panel. He is member of the American Academy of Pediatrics. He served as a member of the advisory council the International Association of Medical Colleges (IAMC).

Weitere Informationen

  • Allgemeine Informationen
    • Sprache Englisch
    • Autor Aamir Al Mosawi
    • Titel Semmola-Meryon-Duchenne syndrome
    • Veröffentlichung 20.07.2018
    • ISBN 6139883156
    • Format Kartonierter Einband
    • EAN 9786139883158
    • Jahr 2018
    • Größe H220mm x B150mm x T4mm
    • Untertitel Pediatric neurology
    • Gewicht 113g
    • Genre Medizin
    • Anzahl Seiten 64
    • Herausgeber LAP LAMBERT Academic Publishing
    • GTIN 09786139883158

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