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Tim Niehues

Showing results (71-80 of 141) with videos related to

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Clinical Immunology (Orlando, Fla.)|December 10, 2008
Saving the red baby: successful allogeneic cord blood transplantation in Omenn syndromeStefan Schönberger, Hagen Ott, Sonja Gudowius, et al.
Antiviral Therapy|May 12, 2004
Safety and efficacy of a NRTI-sparing HAART regimen of efavirenz and lopinavir/ritonavir in HIV-1-infected childrenPieter L A Fraaij, Jennifer Neubert, Alina S Bergshoeff, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2013
Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be testedCatharina Schuetz, Ulrich Pannicke, Eva-Maria Jacobsen, et al.
Rheumatology (Oxford, England)|September 2, 2017
Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increaseAnne-Marie Knieper, Jens Klotsche, Elke Lainka, et al.
Blood|August 30, 2008
Clinical and immunologic consequences of a somatic reversion in a patient with X-linked severe combined immunodeficiencyCarsten Speckmann, Ulrich Pannicke, Elisabeth Wiech, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|February 8, 2021
Analysis of chromosomal aberrations and γH2A.X foci to identify radiation-sensitive ataxia-telangiectasia patientsMartin Bucher, David Endesfelder, Ute Roessler, et al.
Journal of Clinical Immunology|June 8, 2006
Rapid subcutaneous IgG replacement therapy is effective and safe in children and adults with primary immunodeficiencies--a prospective, multi-national studyAnn Gardulf, Uwe Nicolay, Oscar Asensio, et al.
The Pediatric Infectious Disease Journal|October 31, 2013
Prevalence of hepatitis E virus antibodies in children in GermanyAndi Krumbholz, Anne Neubert, Sebastian Joel, et al.
The New England Journal of Medicine|May 9, 2008
An immunodeficiency disease with RAG mutations and granulomasCatharina Schuetz, Kirsten Huck, Sonja Gudowius, et al.
European Journal of Immunology|March 18, 2020
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndromeTim Niehues, Tuba Turul Özgür, Marie Bickes, et al.
Pageof 15

Showing results (71-80 of 141) with videos related to

Sort By:
Pageof 15
Clinical Immunology (Orlando, Fla.)|December 10, 2008
Saving the red baby: successful allogeneic cord blood transplantation in Omenn syndromeStefan Schönberger, Hagen Ott, Sonja Gudowius, et al.
Antiviral Therapy|May 12, 2004
Safety and efficacy of a NRTI-sparing HAART regimen of efavirenz and lopinavir/ritonavir in HIV-1-infected childrenPieter L A Fraaij, Jennifer Neubert, Alina S Bergshoeff, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2013
Lesson from hypomorphic recombination-activating gene (RAG) mutations: Why asymptomatic siblings should also be testedCatharina Schuetz, Ulrich Pannicke, Eva-Maria Jacobsen, et al.
Rheumatology (Oxford, England)|September 2, 2017
Familial Mediterranean fever in children and adolescents: factors for colchicine dosage and predicting parameters for dose increaseAnne-Marie Knieper, Jens Klotsche, Elke Lainka, et al.
Blood|August 30, 2008
Clinical and immunologic consequences of a somatic reversion in a patient with X-linked severe combined immunodeficiencyCarsten Speckmann, Ulrich Pannicke, Elisabeth Wiech, et al.
Mutation Research. Genetic Toxicology and Environmental Mutagenesis|February 8, 2021
Analysis of chromosomal aberrations and γH2A.X foci to identify radiation-sensitive ataxia-telangiectasia patientsMartin Bucher, David Endesfelder, Ute Roessler, et al.
Journal of Clinical Immunology|June 8, 2006
Rapid subcutaneous IgG replacement therapy is effective and safe in children and adults with primary immunodeficiencies--a prospective, multi-national studyAnn Gardulf, Uwe Nicolay, Oscar Asensio, et al.
The Pediatric Infectious Disease Journal|October 31, 2013
Prevalence of hepatitis E virus antibodies in children in GermanyAndi Krumbholz, Anne Neubert, Sebastian Joel, et al.
The New England Journal of Medicine|May 9, 2008
An immunodeficiency disease with RAG mutations and granulomasCatharina Schuetz, Kirsten Huck, Sonja Gudowius, et al.
European Journal of Immunology|March 18, 2020
Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndromeTim Niehues, Tuba Turul Özgür, Marie Bickes, et al.
Pageof 15