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A Helbling

Showing results (91-100 of 112) with videos related to

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Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|July 1, 1996
Immunopathogenesis of fish allergy: identification of fish-allergic adults by skin test and radioallergosorbent testA Helbling, M L McCants, J J Musmand, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 16, 1999
T-cell reaction to local anaesthetics: relationship to angioedema and urticaria after subcutaneous application--patch testing and LTT in patients with adverse reaction to local anaestheticsC E Orasch, A Helbling, M P Zanni, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCRB P Chadwick, L A Helbling, M Angrist, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|January 5, 2000
Fish allergy: is cross-reactivity among fish species relevant? Double-blind placebo-controlled food challenge studies of fish allergic adultsA Helbling, R Haydel, M L McCants, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 19, 2011
An increase in serum tryptase even below 11.4 ng/mL may indicate a mast cell-mediated hypersensitivity reaction: a prospective study in Hymenoptera venom allergic patientsM Borer-Reinhold, G Haeberli, M Bitzenhofer, et al.
Journal of Investigational Allergology & Clinical Immunology|December 5, 2017
Dysregulated Innate Lymphocytes in Patients With Primary Antibody Deficiency Treated With Intravenous ImmunoglobulinS Vigano, S Trabanelli, F Indulsi, et al.
American Journal of Human Genetics|August 12, 1999
Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypesS A Slaugenhaupt, J S Acierno, L A Helbling, et al.
Allergy|November 1, 1990
Mastocytosis and atopy: a study of 33 patients with urticaria pigmentosaU Müller, A Helbling, T Hunziker, et al.
Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|July 1, 1996
Immunopathogenesis of fish allergy: identification of fish-allergic adults by skin test and radioallergosorbent testA Helbling, M L McCants, J J Musmand, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|October 16, 1999
T-cell reaction to local anaesthetics: relationship to angioedema and urticaria after subcutaneous application--patch testing and LTT in patients with adverse reaction to local anaestheticsC E Orasch, A Helbling, M P Zanni, et al.
Cytogenetics and Cell Genetics|March 11, 1999
Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCRB P Chadwick, L A Helbling, M Angrist, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|January 5, 2000
Fish allergy: is cross-reactivity among fish species relevant? Double-blind placebo-controlled food challenge studies of fish allergic adultsA Helbling, R Haydel, M L McCants, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|November 19, 2011
An increase in serum tryptase even below 11.4 ng/mL may indicate a mast cell-mediated hypersensitivity reaction: a prospective study in Hymenoptera venom allergic patientsM Borer-Reinhold, G Haeberli, M Bitzenhofer, et al.
Journal of Investigational Allergology & Clinical Immunology|December 5, 2017
Dysregulated Innate Lymphocytes in Patients With Primary Antibody Deficiency Treated With Intravenous ImmunoglobulinS Vigano, S Trabanelli, F Indulsi, et al.
American Journal of Human Genetics|August 12, 1999
Mapping of the mucolipidosis type IV gene to chromosome 19p and definition of founder haplotypesS A Slaugenhaupt, J S Acierno, L A Helbling, et al.
Allergy|November 1, 1990
Mastocytosis and atopy: a study of 33 patients with urticaria pigmentosaU Müller, A Helbling, T Hunziker, et al.
Nature Genetics|October 1, 1995
Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophyA Helbling-Leclerc, X Zhang, H Topaloglu, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.
Pageof 12