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Melinda Erdos

Showing results (1-10 of 30) with videos related to

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Orvosi Hetilap|June 19, 2007
[WHIM syndrome]Melinda Erdos, László Maródi
Orvosi Hetilap|March 14, 2007
[Shwachman-Diamond syndrome: clinical manifestations and molecular genetics]Melinda Erdos, László Maródi
Orvosi Hetilap|June 20, 2006
[Invasive pneumococcal infections in patients with primary immunodeficiency disorders]Melinda Erdos, László Maródi
European Journal of Haematology|February 13, 2003
Rebound hepatosplenomegaly in type 1 Gaucher diseaseJudit Tóth, Melinda Erdos, László Maródi
Haematologica|February 14, 2007
Retrospective diagnosis of X-linked hyper-IgM syndrome in a family with multiple deaths of affected malesMelinda Erdos, Krisztina Alapi, László Maródi
Immunology Letters|January 1, 2005
Genetically acquired class-switch recombination defects: the multi-faced hyper-IgM syndromeMelinda Erdos, Anne Durandy, László Maródi
Orvosi Hetilap|April 23, 2008
[Gaucher disease: importance of early diagnosis and therapy]Gábor Simon, Melinda Erdos, László Maródi, et al.
European Journal of Haematology|November 8, 2006
Recurrent CXCR4 sequence variation in a girl with WHIM syndromeKrisztina Alapi, Melinda Erdos, Gabriella Kovács, et al.
Orvosi Hetilap|February 10, 2012
[Enzyme replacement therapy for Gaucher disease introduced in late adulthood]Pálma Juhász, Beáta Tóth, László Maródi, et al.
Clinical Chemistry|April 28, 2006
Prenatal diagnosis of the WAS R86H sequence variation in heterozygous twinsKrisztina Alapi, Melinda Erdos, Olga Török, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Orvosi Hetilap|June 19, 2007
[WHIM syndrome]Melinda Erdos, László Maródi
Orvosi Hetilap|March 14, 2007
[Shwachman-Diamond syndrome: clinical manifestations and molecular genetics]Melinda Erdos, László Maródi
Orvosi Hetilap|June 20, 2006
[Invasive pneumococcal infections in patients with primary immunodeficiency disorders]Melinda Erdos, László Maródi
European Journal of Haematology|February 13, 2003
Rebound hepatosplenomegaly in type 1 Gaucher diseaseJudit Tóth, Melinda Erdos, László Maródi
Haematologica|February 14, 2007
Retrospective diagnosis of X-linked hyper-IgM syndrome in a family with multiple deaths of affected malesMelinda Erdos, Krisztina Alapi, László Maródi
Immunology Letters|January 1, 2005
Genetically acquired class-switch recombination defects: the multi-faced hyper-IgM syndromeMelinda Erdos, Anne Durandy, László Maródi
Orvosi Hetilap|April 23, 2008
[Gaucher disease: importance of early diagnosis and therapy]Gábor Simon, Melinda Erdos, László Maródi, et al.
European Journal of Haematology|November 8, 2006
Recurrent CXCR4 sequence variation in a girl with WHIM syndromeKrisztina Alapi, Melinda Erdos, Gabriella Kovács, et al.
Orvosi Hetilap|February 10, 2012
[Enzyme replacement therapy for Gaucher disease introduced in late adulthood]Pálma Juhász, Beáta Tóth, László Maródi, et al.
Clinical Chemistry|April 28, 2006
Prenatal diagnosis of the WAS R86H sequence variation in heterozygous twinsKrisztina Alapi, Melinda Erdos, Olga Török, et al.
Pageof 3