يعرض 1 - 10 نتائج من 136 نتيجة بحث عن '"Pfliegler, György"', وقت الاستعلام: 1.28s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Rare disease education in Europe and beyond: time to act

    المؤلفون: Tumiene, Birute, Peters, HarmAff2, Aff3, Melegh, Bela, Peterlin, Borut, Utkus, AlgirdasAff1, Aff3, Fatkulina, Natalja, Pfliegler, György, Graessner, HolmAff8, Aff9, Hermanns, SanjaAff8, Aff9, Scarpa, Maurizio, Blay, Jean-Yves, Ashton, Sharon, McKay, Lucy, Baynam, GarethAff14, Aff15, Aff16, IDs1302302202527y_cor14

    المصدر: Orphanet Journal of Rare Diseases. 17(1)

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  2. 2
    دورية أكاديمية
    A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions.

    المؤلفون: Obajed Al-Ali, Omar, Pfliegler, György, Magyari, Ferenc, Borics, Fanni, Pinczés, László Imre, Illés, Árpád, Brúgós, Boglárka

    المصدر: Thalassemia Reports; Mar2024, Vol. 14 Issue 1, p18-25, 8p

    مصطلحات موضوعية: SICKLE cell anemia, FETOFETAL transfusion, SYNDROMES, BLOOD transfusion, HOSPITAL admission & discharge

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  3. 3
    دورية أكاديمية
    FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies

    المؤلفون: Madar, László, Szakszon, Katalin, Pfliegler, György, Szabó, Gabriella P., Brúgós, Boglárka, Ronen, Natali, Papp, Judit, Zahuczky, Katalin, Szakos, Erzsébet, Fekete, György, Oláh, Éva, Koczok, Katalin, Balogh, István

    المصدر: In Journal of Biotechnology 10 August 2019 301:105-111

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  4. 4
    دورية أكاديمية
    Intravascular Occlusion by Leukemic Blast Cells Causing Multiplex Hand Necrosis in a Patient with Acute Myeloid Leukemia

    المؤلفون: Pinczés, LászlóAff1, Magyari, Ferenc, Reményi, Gyula, Pfliegler, György, Barna, Sándor, Bedekovics, Judit, Illés, Árpád

    المصدر: Pathology & Oncology Research: Official Journal of the Arányi Lajos Foundation. 26(2):1349-1351

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  5. 5
    كتاب إلكتروني
    Vascular Diseases of the Optic Nerve: Internal Medicine Aspects

    المؤلفون: Pfliegler, GyörgyAff3

    المساهمون: Somlai, Judit, editorAff1, Kovács, Tibor, editorAff2

    المصدر: Neuro-Ophthalmology. :369-375

    Degree: M.D., med. habil.

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  6. 6
    كتاب إلكتروني
    Visual and Oculomotor Disorders in Internal Diseases

    المؤلفون: Pfliegler, GyörgyAff3

    المساهمون: Somlai, Judit, editorAff1, Kovács, Tibor, editorAff2

    المصدر: Neuro-Ophthalmology. :19-25

    Degree: M.D., med. habil.

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  7. 7
    دورية أكاديمية
    Clinical Investigation of Hereditary and Acquired Thrombophilic Factors in Patients with Venous and Arterial Thromboembolism.

    المؤلفون: Kovács, Erzsebet, Bereczky, Zsuzsanna, Kerényi, Adrienne, Laczik, Renáta, Nagy, Valéria, Kovács, Dávid Ágoston, Kovács, Sándor, Pfliegler, György

    المصدر: International Journal of General Medicine; Nov2023, Vol. 16, p5425-5437, 13p

    مصطلحات موضوعية: THROMBOEMBOLISM, POSTTHROMBOTIC syndrome, BLOOD coagulation factor VIII, MEDICAL screening, THROMBOSIS, VARICOSE veins, CEREBRAL embolism & thrombosis

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  8. 8
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  9. 9
    Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing

    المؤلفون: Gindele, Réka, Kerényi, Adrienne, Kállai, Judit, Pfliegler, György, Schlammadinger, Ágota, Szegedi, István, Major, Tamás, Szabó, Zsuzsanna, Bagoly, Zsuzsa, Kiss, Csongor, Kappelmayer, János, Bereczky, Zsuzsanna

    المصدر: Life
    Life, Vol 11, Iss 202, p 202 (2021)
    Volume 11
    Issue 3

    مصطلحات موضوعية: next generation sequencing, rare bleeding disorders, hemic and lymphatic diseases, differential diagnosis, APTT prolongation, prekallikrein deficiency, hereditary hemorrhagic telangiectasia, lcsh:Q, hemophilia A, lcsh:Science, von Willebrand disease, Article

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c5e844d16051feddc164c13a417efeab
    http://europepmc.org/articles/PMC7999415

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  10. 10
    دورية أكاديمية
    Three novel germ-line VHL mutations in Hungarian von Hippel-Lindau patients, including a nonsense mutation in a fifteen-year-old boy with renal cell carcinoma

    المؤلفون: Losonczy Gergely, Fazakas Ferenc, Pfliegler György, Komáromi István, Balázs Erzsébet, Pénzes Krisztina, Berta András

    المصدر: BMC Medical Genetics, Vol 14, Iss 1, p 3 (2013)

    مصطلحات موضوعية: Genotype-phenotype correlation, Germline mutation, Renal cell carcinoma, Von Hippel-Lindau disease, Internal medicine, RC31-1245, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: http://www.biomedcentral.com/1471-2350/14/3; https://doaj.org/toc/1471-2350

    URL الوصول: https://doaj.org/article/e724d65c71324be88240f5db4299bc53

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