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Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency.
J Allergy Clin Immunol. 2015 Sep;136(3):703-712.e10. doi: 10.1016/j.jaci.2015.02.022. Epub 2015 Apr 3.
J Allergy Clin Immunol. 2015.
PMID: 25843314
More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2.
Niehues T, Perez-Becker R, Schuetz C.
Niehues T, et al. Among authors: perez becker r.
Clin Immunol. 2010 May;135(2):183-92. doi: 10.1016/j.clim.2010.01.013. Epub 2010 Feb 20.
Clin Immunol. 2010.
PMID: 20172764
Review.
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A prospective study on the natural history of patients with profound combined immunodeficiency: An interim analysis.
Speckmann C, Doerken S, Aiuti A, Albert MH, Al-Herz W, Allende LM, Scarselli A, Avcin T, Perez-Becker R, Cancrini C, Cant A, Di Cesare S, Finocchi A, Fischer A, Gaspar HB, Ghosh S, Gennery A, Gilmour K, González-Granado LI, Martinez-Gallo M, Hambleton S, Hauck F, Hoenig M, Moshous D, Neven B, Niehues T, Notarangelo L, Picard C, Rieber N, Schulz A, Schwarz K, Seidel MG, Soler-Palacin P, Stepensky P, Strahm B, Vraetz T, Warnatz K, Winterhalter C, Worth A, Fuchs S, Uhlmann A, Ehl S; P-CID study of the Inborn Errors Working Party of the EBMT.
Speckmann C, et al. Among authors: perez becker r.
J Allergy Clin Immunol. 2017 Apr;139(4):1302-1310.e4. doi: 10.1016/j.jaci.2016.07.040. Epub 2016 Sep 19.
J Allergy Clin Immunol. 2017.
PMID: 27658761
Free PMC article.
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Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API*** Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) ** Arbeitsgemeinschaft Pädiatrische Immunologie.
Shai S, Perez-Becker R, Andres O, Bakhtiar S, Bauman U, von Bernuth H, Classen CF, Dückers G, El-Helou SM, Gangfuß A, Ghosh S, Grimbacher B, Hauck F, Hoenig M, Husain RA, Kindle G, Kipfmueller F, Klemann C, Krüger R, Lainka E, Lehmberg K, Lohrmann F, Morbach H, Naumann-Bartsch N, Oommen PT, Schulz A, Seidemann K, Speckmann C, Sykora KW, von Kries R, Niehues T.
Shai S, et al. Among authors: perez becker r.
J Clin Immunol. 2020 Jul;40(5):708-717. doi: 10.1007/s10875-020-00782-x. Epub 2020 May 26.
J Clin Immunol. 2020.
PMID: 32458183
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Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.
Felgentreff K, Perez-Becker R, Speckmann C, Schwarz K, Kalwak K, Markelj G, Avcin T, Qasim W, Davies EG, Niehues T, Ehl S.
Felgentreff K, et al. Among authors: perez becker r.
Clin Immunol. 2011 Oct;141(1):73-82. doi: 10.1016/j.clim.2011.05.007. Epub 2011 May 30.
Clin Immunol. 2011.
PMID: 21664875
Review.
Item in Clipboard
Rotavirus disease in Germany--a prospective survey of very severe cases.
Shai S, Perez-Becker R, von König CH, von Kries R, Heininger U, Forster J, Huppertz HI, Roos R, Göbel U, Niehues T.
Shai S, et al. Among authors: perez becker r.
Pediatr Infect Dis J. 2013 Feb;32(2):e62-7. doi: 10.1097/INF.0b013e31826f602b.
Pediatr Infect Dis J. 2013.
PMID: 22914558
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An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.
Perez-Becker R, Szczepanowski M, Leuschner I, Janka G, Gokel M, Imschweiler T, Völpel S, Niehues T, Klapper W.
Perez-Becker R, et al.
Pediatr Blood Cancer. 2011 May;56(5):859-62. doi: 10.1002/pbc.22756. Epub 2010 Sep 16.
Pediatr Blood Cancer. 2011.
PMID: 20848640
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Leishmania mexicana mexicana: genetic heterogeneity of mexican isolates revealed by restriction length polymorphism analysis of kinetoplast DNA.
Berzunza-Cruz M, Bricaire G, Romero SZ, Pérez-Becker R, Saavedra-Lira E, Pérez-Montfort R, Crippa-Rossi M, Velasco-Castrejón O, Becker I.
Berzunza-Cruz M, et al. Among authors: perez becker r.
Exp Parasitol. 2000 Aug;95(4):277-84. doi: 10.1006/expr.2000.4541.
Exp Parasitol. 2000.
PMID: 11038311
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