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Allergy
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April 15, 2011
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities
L Maintz, C-F Yu, E Rodríguez, et al.
Vox Sanguinis
|
January 1, 1993
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature
I Yuasa, S Weidinger, K Umetsu, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
September 20, 2021
[Quality of care for patients with atopic dermatitis in Germany-no improvements in indicators after ten years]
A Langenbruch, N Mohr, F Abeck, et al.
The British Journal of Dermatology
|
February 1, 2006
The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girls
M Möhrenschlager, T Schäfer, J Huss-Marp, et al.
The Clinical Investigator
|
July 1, 1994
High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failure
M Pecherstorfer, I Zimmer-Roth, S Weidinger, et al.
Human Reproduction (Oxford, England)
|
December 4, 2004
Tryptase inhibits motility of human spermatozoa mainly by activation of the mitogen-activated protein kinase pathway
S Weidinger, A Mayerhofer, L Kunz, et al.
Allergy
|
April 19, 2016
Childhood atopic dermatitis-Brain-derived neurotrophic factor correlates with serum eosinophil cationic protein and disease severity
R Fölster-Holst, E Papakonstantinou, U Rüdrich, et al.
The British Journal of Dermatology
|
June 20, 2002
Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell death
M Mempel, C Schnopp, M Hojka, et al.
Genomics
|
September 1, 1993
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease
W Poller, J P Faber, S Weidinger, et al.
The British Journal of Dermatology
|
October 9, 2012
Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis
M J Visser, L Landeck, L E Campbell, et al.
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of 13
Search research articles
Search
Showing results (81-90 of 129) with videos related to
Sort By:
Page
of 13
Allergy
|
April 15, 2011
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities
L Maintz, C-F Yu, E Rodríguez, et al.
Vox Sanguinis
|
January 1, 1993
Orosomucoid system: 17 additional orosomucoid variants and proposal for a new nomenclature
I Yuasa, S Weidinger, K Umetsu, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
September 20, 2021
[Quality of care for patients with atopic dermatitis in Germany-no improvements in indicators after ten years]
A Langenbruch, N Mohr, F Abeck, et al.
The British Journal of Dermatology
|
February 1, 2006
The course of eczema in children aged 5-7 years and its relation to atopy: differences between boys and girls
M Möhrenschlager, T Schäfer, J Huss-Marp, et al.
The Clinical Investigator
|
July 1, 1994
High-dose intravenous melphalan in a patient with multiple myeloma and oliguric renal failure
M Pecherstorfer, I Zimmer-Roth, S Weidinger, et al.
Human Reproduction (Oxford, England)
|
December 4, 2004
Tryptase inhibits motility of human spermatozoa mainly by activation of the mitogen-activated protein kinase pathway
S Weidinger, A Mayerhofer, L Kunz, et al.
Allergy
|
April 19, 2016
Childhood atopic dermatitis-Brain-derived neurotrophic factor correlates with serum eosinophil cationic protein and disease severity
R Fölster-Holst, E Papakonstantinou, U Rüdrich, et al.
The British Journal of Dermatology
|
June 20, 2002
Invasion of human keratinocytes by Staphylococcus aureus and intracellular bacterial persistence represent haemolysin-independent virulence mechanisms that are followed by features of necrotic and apoptotic keratinocyte cell death
M Mempel, C Schnopp, M Hojka, et al.
Genomics
|
September 1, 1993
A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease
W Poller, J P Faber, S Weidinger, et al.
The British Journal of Dermatology
|
October 9, 2012
Impact of atopic dermatitis and loss-of-function mutations in the filaggrin gene on the development of occupational irritant contact dermatitis
M J Visser, L Landeck, L E Campbell, et al.
Page
of 13