Search Results - "ZOUMBOS, Nikolaos"

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    A case of severe ADAMTS13 deficiency presenting as thrombotic thrombocytopenic purpura in pregnancy by Nikolaou, Marinos, Karakantza, Marina, Adonakis, George, Theodorou, George, Zoumbos, Nikolaos, Decavalas, George

    Published in Medicinski pregled (01-09-2012)
    “…Thrombotic thrombocytopenic purpura is a rare life-threatening disorder characterized by thrombocytopenia and microangiopathic hemolytic anemia. It is caused…”
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    Journal Article
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    A case of severe ADAMTS 13 deficiency presenting as thrombotic thrombocytopenic purpura in pregnancy by Nikolaou, Marinos, Karakantza, Marina, Adonakis, George, Theodorou, George, Zoumbos, Nikolaos, Decavalas, George

    Published in Medicinski pregled (2012)
    “…Introduction. Thrombotic thrombocytopenic purpura is a rare lifethreatening disorder characterized by thrombocytopenia and microangiopathic hemolytic anemia…”
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    Journal Article
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    Lung function measurements in traditional bakers by Patouchas, Dimitrios, Efremidis, Georgios, Karkoulias, Kiriakos, Zoumbos, Nikolaos, Goumas, Panos, Spiropoulos, Kostas

    Published in Acta bio-medica de l'Ateneo Parmense (01-12-2008)
    “…Respiratory disease is common and amenable to early detection and management in the primary care setting. Spirometric and phlethysmographic evaluation of…”
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    Journal Article
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    Comparison of DXA, QCT and trabecular structure in β-thalassaemia by Mylona, Maria, Leotsinides, Michalis, Alexandrides, Theodoros, Zoumbos, Nikolaos, Dimopoulos, Panagiotis A.

    Published in European journal of haematology (01-05-2005)
    “…:  Osteopathy, as a major feature of homozygous β‐thalassaemia, is a multifactorial disorder, not fully understood. We studied the lumbar vertebrae of 48…”
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    Contrast sensitivity function in patients with beta‐thalassemia major by Gartaganis, Sotirios P., Zoumbos, Nikolaos, Koliopoulos, John X., Mela, Ephigenia K.

    Published in Acta ophthalmologica Scandinavica (01-10-2000)
    “…Purpose: To investigate contrast sensitivity function in patients with beta‐thalassemia major, after regular transfusion and chelation therapy. Methods: We…”
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    Journal Article