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The New England Journal of Medicine
|
October 27, 2006
The genotype of the original Wiskott phenotype
Vera Binder, Michael H Albert, Maria Kabus, et al.
Pediatric Blood & Cancer
|
August 27, 2014
X-linked thrombocytopenia in three males with normal sized platelets due to novel WAS gene mutations
Elpis Mantadakis, Julie Sawalle-Belohradsky, Marianna Tzanoudaki, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 7, 2005
Parenteral nutrition is not superior to replacement fluid therapy for the supportive treatment of chemotherapy induced oral mucositis in children
Irene Schmid, Melanie Schmitt, Monika Streiter, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 19, 2023
[Newborn screening for severe combined immunodeficiencies (SCID) in Germany]
Sujal Ghosh, Michael H Albert, Fabian Hauck, et al.
Journal of Clinical Immunology
|
June 3, 2021
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency
Johannes Raedler, Thomas Magg, Meino Rohlfs, et al.
European Journal of Haematology
|
January 16, 2021
Treating secondary antibody deficiency in patients with haematological malignancy: European expert consensus
Stephen Jolles, Mauricette Michallet, Carlo Agostini, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 29, 2012
Diagnostic value of combined ¹⁸F-FDG PET/MRI for staging and restaging in paediatric oncology
Thomas Pfluger, Henriette I Melzer, Wolfgang P Mueller, et al.
Journal of Clinical Immunology
|
February 28, 2021
Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency
Anna Eichinger, Horst von Bernuth, Cinzia Dedieu, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
May 28, 2011
¹²³I-MIBG scintigraphy/SPECT versus ¹⁸F-FDG PET in paediatric neuroblastoma
Henriette Ingrid Melzer, Eva Coppenrath, Irene Schmid, et al.
Clinical Immunology (Orlando, Fla.)
|
March 24, 2018
IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T<sub>Reg</sub> cell engraftment
Thomas Magg, Volker Wiebking, Raffaele Conca, et al.
Page
of 16
Search research articles
Search
Showing results (21-30 of 151) with videos related to
Sort By:
Page
of 16
The New England Journal of Medicine
|
October 27, 2006
The genotype of the original Wiskott phenotype
Vera Binder, Michael H Albert, Maria Kabus, et al.
Pediatric Blood & Cancer
|
August 27, 2014
X-linked thrombocytopenia in three males with normal sized platelets due to novel WAS gene mutations
Elpis Mantadakis, Julie Sawalle-Belohradsky, Marianna Tzanoudaki, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 7, 2005
Parenteral nutrition is not superior to replacement fluid therapy for the supportive treatment of chemotherapy induced oral mucositis in children
Irene Schmid, Melanie Schmitt, Monika Streiter, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 19, 2023
[Newborn screening for severe combined immunodeficiencies (SCID) in Germany]
Sujal Ghosh, Michael H Albert, Fabian Hauck, et al.
Journal of Clinical Immunology
|
June 3, 2021
Lineage-Specific Chimerism and Outcome After Hematopoietic Stem Cell Transplantation for DOCK8 Deficiency
Johannes Raedler, Thomas Magg, Meino Rohlfs, et al.
European Journal of Haematology
|
January 16, 2021
Treating secondary antibody deficiency in patients with haematological malignancy: European expert consensus
Stephen Jolles, Mauricette Michallet, Carlo Agostini, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
August 29, 2012
Diagnostic value of combined ¹⁸F-FDG PET/MRI for staging and restaging in paediatric oncology
Thomas Pfluger, Henriette I Melzer, Wolfgang P Mueller, et al.
Journal of Clinical Immunology
|
February 28, 2021
Upfront Enzyme Replacement via Erythrocyte Transfusions for PNP Deficiency
Anna Eichinger, Horst von Bernuth, Cinzia Dedieu, et al.
European Journal of Nuclear Medicine and Molecular Imaging
|
May 28, 2011
¹²³I-MIBG scintigraphy/SPECT versus ¹⁸F-FDG PET in paediatric neuroblastoma
Henriette Ingrid Melzer, Eva Coppenrath, Irene Schmid, et al.
Clinical Immunology (Orlando, Fla.)
|
March 24, 2018
IPEX due to an exon 7 skipping FOXP3 mutation with autoimmune diabetes mellitus cured by selective T<sub>Reg</sub> cell engraftment
Thomas Magg, Volker Wiebking, Raffaele Conca, et al.
Page
of 16