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Eva Rákóczi

Showing results (1-10 of 10) with videos related to

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The Journal of Urology|February 25, 2009
Association of renal ectopia with Fabry's disease in 3 patientsEva Rákóczi, Beáta Tóth, Sándor Görögh, et al.
Experimental Hematology|October 19, 2006
Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS geneMelinda Erdos, Krisztina Alapi, István Balogh, et al.
Human Mutation|April 21, 2005
Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative diseaseMelinda Erdõs, Eva Uzvölgyi, Zoltán Nemes, et al.
Autoimmunity|March 27, 2012
Association of ANCA-associated vasculitis-rheumatoid arthritis overlap syndrome in four patients: rituximab may be the right choice?Mária Szilasi, János Mátyus, Ibolya File, et al.
Clinical Immunology (Orlando, Fla.)|September 23, 2008
Neuroendocrine carcinoma associated with X-linked hyper-immunoglobulin M syndrome: report of four cases and review of the literatureMelinda Erdos, Miklós Garami, Eva Rákóczi, et al.
Orvosi Hetilap|June 5, 2007
[Molecular pathology and clinical manifestations of Fabry disease]Eva Rákóczi, Sándor Görögh, János Grubits, et al.
Molecular Genetics and Metabolism|October 14, 2008
Novel sequence variants of the alpha-galactosidase A gene in patients with Fabry diseaseMelinda Erdos, Krisztina Németh, Beáta Tóth, et al.
Molecular Immunology|August 19, 2008
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groupsHong Jiao, Beáta Tóth, Melinda Erdos, et al.
Orvosi Hetilap|February 6, 2010
[Fabry disease--diagnostic guideline]Tamás Constantin, Eva Rákóczi, Andrea Ponyi, et al.
Orvosi Hetilap|July 27, 2010
[Management of Fabry disease]Tamás Constantin, Annamária Székely, Andrea Ponyi, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of Urology|February 25, 2009
Association of renal ectopia with Fabry's disease in 3 patientsEva Rákóczi, Beáta Tóth, Sándor Görögh, et al.
Experimental Hematology|October 19, 2006
Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS geneMelinda Erdos, Krisztina Alapi, István Balogh, et al.
Human Mutation|April 21, 2005
Characterization of a new disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative diseaseMelinda Erdõs, Eva Uzvölgyi, Zoltán Nemes, et al.
Autoimmunity|March 27, 2012
Association of ANCA-associated vasculitis-rheumatoid arthritis overlap syndrome in four patients: rituximab may be the right choice?Mária Szilasi, János Mátyus, Ibolya File, et al.
Clinical Immunology (Orlando, Fla.)|September 23, 2008
Neuroendocrine carcinoma associated with X-linked hyper-immunoglobulin M syndrome: report of four cases and review of the literatureMelinda Erdos, Miklós Garami, Eva Rákóczi, et al.
Orvosi Hetilap|June 5, 2007
[Molecular pathology and clinical manifestations of Fabry disease]Eva Rákóczi, Sándor Görögh, János Grubits, et al.
Molecular Genetics and Metabolism|October 14, 2008
Novel sequence variants of the alpha-galactosidase A gene in patients with Fabry diseaseMelinda Erdos, Krisztina Németh, Beáta Tóth, et al.
Molecular Immunology|August 19, 2008
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groupsHong Jiao, Beáta Tóth, Melinda Erdos, et al.
Orvosi Hetilap|February 6, 2010
[Fabry disease--diagnostic guideline]Tamás Constantin, Eva Rákóczi, Andrea Ponyi, et al.
Orvosi Hetilap|July 27, 2010
[Management of Fabry disease]Tamás Constantin, Annamária Székely, Andrea Ponyi, et al.
Pageof 1