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significant burden on families, most of the previous studies on tonsillitis evaluated only the role of upper respiratory tract infections and not enough attention has been given to improve children’s quality of life (QOL) [ 4 ]. Because of the

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Hematológia–Transzfuziológia
Authors: Béla Ifj. Nagy, Ambrus Gángó, László Rejtő, Szilvia Krizsán, Anikó Ujfalusi, and Péter Antal-Szalmás

. Blood 2011; 117: 221–233. 7 Pabst T, Eyholzer M, Haefliger S, et al. Somatic CEBPA mutations are a frequent second event in families with germline CEBPA mutations and

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Hematológia–Transzfuziológia
Authors: Richárd Kiss, Gergő Papp, Szilvia Krizsán, Lili Kotmayer, Ambrus Gángó, Noémi Nagy, Bence Bátai, Zoltán Mátrai, Csaba Bödör, and Donát Alpár

immunophenotyping. Leukemia 2007; 21: 2442−2451. 16 Guipaud O, Deriano L, Salin H, et al. B-cell chronic lymphocytic leukaemia: a polymorphic family unified by genomic features. Lancet

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Hematológia–Transzfuziológia
Authors: Szilvia Krizsán, Zsófia Dénes, Ambrus Gángó, Bence Gerecs, Judit Demeter, Zsolt Nagy, Ilona Tárkányi, Tamás Masszi, Péter Farkas, András Masszi, Gergely Szombath, Szabolcs Benedek, Judit Várkonyi, Laura Horváth, Zsolt Nagy, Gáspár Radványi, István Takács, Aryan Hamed, Zsolt Lázár, Erzsébet Süveges, Ágnes Kárpáti, Márk Plander, Tamás Szendrei, Katalin Pál, Mihály Gurzó, János Jakucs, Miklós Egyed, and Csaba Bödör

myeloid leukemia. N Engl J Med. 2004; 351: 2403–2407. 36 Pabst T, Eyholzer M, Haefliger S, et al. Somatic CEBPA mutations are a frequent second event in families with germline

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Orvosi Hetilap
Authors: Balázs Sarkadi, Vince Kornél Grolmusz, Henriett Butz, Annamária Kövesdi, István Likó, Gábor Nyirő, Péter Igaz, and Attila Patócs

: 567–610. 10 Igaz P, Rácz K, Tóth M, et al. Ret-protooncogene mutation, verified by molecular genetic methods, in a Hungarian MEN Type 2a family. [Molekuláris genetikai

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Imaging
Authors: Sabrina Oebel, Alexander Gotschy, Ingo Paetsch, Cosima Jahnke, Sven Plein, Rolf Gebker, Sandra Hamada, Michael Frick, Jochen von Spiczak, Malgorzata Polacin, Frank Enseleit, Nikolaus Marx, Thomas F. Lüscher, Frank Ruschitzka, Sebastian Kozerke, Hatem Alkadhi, and Robert Manka

patients with an EF>50% matched for age, gender and major cardiovascular risk factors (arterial hypertension, diabetes, smoking, positive family history, obesity and hyperlipidemia) was selected from the same cohort. All patients had given written informed

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; 160: 153–159. 2 Taupenot L, Harper KL, O’Connor DT. The chromogranin–secretogranin family. NEJM 2003; 348: 1134–1149. 3 Bartolomucci A, Possenti R, Mahata

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Orvosi Hetilap
Authors: András Mohos, Albert Varga, Csenge Hargittay, Dalma Csatlós, László Kalabay, and Péter Torzsa

cross-sectional study. BMC Public Health 2019; 19: 179. 16 Soler JK, Yaman H, Esteva M, et al. Burnout in European family doctors: the EGPRN study. Fam Pract. 2008; 25

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-Alföldön.] Népegészségügy 2004; 83: 12–17. [Hungarian] 20 Balogh S. Family medicine in the mirror of social security data I. First months of departure. [A háziorvoslás a társadalombiztosítási adatok

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Imaging
Authors: György Jermendy, Márton Kolossváry, Ibolya Dudás, Ádám L. Jermendy, Alexisz Panajotu, Imre F. Suhai, Zsófia D. Drobni, Júlia Karády, Ádám D. Tárnoki, Dávid L. Tárnoki, Szilard Voros, Béla Merkely, and Pál Maurovich-Horvat

siblings, and unique factors (E), which cause differences within families. Both MZ and DZ twins shared 100% of their C factors and none of their E factors. Since measurement error in the phenotype is also uncorrelated across measurements, it appears as part

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