Search research articles
Contact Us
Filters
Showing results (31-40 of 43) with videos related to
Page
of 5
Sort By:
International Journal of Pancreatology : Official Journal of the International Association of Pancreatology
|
April 1, 1989
Cytokines and pancreatic cancer. Sensitivity of xenotransplants of predominantly pancreatic carcinomas to rIFN-gamma and rTFN-alpha in nude mice
J S Kühl, R Klapdor, M Bahlo, et al.
Internal Medicine Journal
|
November 5, 2014
Maturity-onset diabetes of the young type 5 in a family with diabetes and mild kidney disease diagnosed by whole exome sequencing
J M Wentworth, V Lukic, M Bahlo, et al.
Annals of the Rheumatic Diseases
|
November 14, 2002
Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population
J Stankovich, M M Sale, H M Cooley, et al.
Deutsche Medizinische Wochenschrift (1946)
|
December 21, 1984
[CA 12-5 in cancer of the digestive tract. A comparison with CA 19-9 and CEA in cancer of the pancreas and colon]
R Klapdor, U Klapdor, M Bahlo, et al.
American Journal of Human Genetics
|
August 5, 2000
Identification and analysis of error types in high-throughput genotyping
K R Ewen, M Bahlo, S A Treloar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 15, 2010
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition
Anneke Van der Walt, J Stankovich, M Bahlo, et al.
Neurology
|
September 30, 2009
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
A van der Walt, J Stankovich, M Bahlo, et al.
The Journal of Allergy and Clinical Immunology
|
August 10, 2001
The -590C/T and -34C/T interleukin-4 promoter polymorphisms are not associated with atopic eczema in childhood
K Elliott, E Fitzpatrick, D Hill, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 10, 2013
GFI1B mutation causes a bleeding disorder with abnormal platelet function
W S Stevenson, M-C Morel-Kopp, Q Chen, et al.
Clinical Genetics
|
February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
M S Hildebrand, N P Thorne, C J Bromhead, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
International Journal of Pancreatology : Official Journal of the International Association of Pancreatology
|
April 1, 1989
Cytokines and pancreatic cancer. Sensitivity of xenotransplants of predominantly pancreatic carcinomas to rIFN-gamma and rTFN-alpha in nude mice
J S Kühl, R Klapdor, M Bahlo, et al.
Internal Medicine Journal
|
November 5, 2014
Maturity-onset diabetes of the young type 5 in a family with diabetes and mild kidney disease diagnosed by whole exome sequencing
J M Wentworth, V Lukic, M Bahlo, et al.
Annals of the Rheumatic Diseases
|
November 14, 2002
Investigation of chromosome 2q in osteoarthritis of the hand: no significant linkage in a Tasmanian population
J Stankovich, M M Sale, H M Cooley, et al.
Deutsche Medizinische Wochenschrift (1946)
|
December 21, 1984
[CA 12-5 in cancer of the digestive tract. A comparison with CA 19-9 and CEA in cancer of the pancreas and colon]
R Klapdor, U Klapdor, M Bahlo, et al.
American Journal of Human Genetics
|
August 5, 2000
Identification and analysis of error types in high-throughput genotyping
K R Ewen, M Bahlo, S A Treloar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
December 15, 2010
Heterogeneity at the HLA-DRB1 allelic variation locus does not influence multiple sclerosis disease severity, brain atrophy or cognition
Anneke Van der Walt, J Stankovich, M Bahlo, et al.
Neurology
|
September 30, 2009
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
A van der Walt, J Stankovich, M Bahlo, et al.
The Journal of Allergy and Clinical Immunology
|
August 10, 2001
The -590C/T and -34C/T interleukin-4 promoter polymorphisms are not associated with atopic eczema in childhood
K Elliott, E Fitzpatrick, D Hill, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 10, 2013
GFI1B mutation causes a bleeding disorder with abnormal platelet function
W S Stevenson, M-C Morel-Kopp, Q Chen, et al.
Clinical Genetics
|
February 6, 2010
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
M S Hildebrand, N P Thorne, C J Bromhead, et al.
Page
of 5