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Experimental and Clinical Immunogenetics
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March 2, 2002
Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction
A Császár, J Duba, B Melegh, et al.
Clinical and Experimental Rheumatology
|
March 11, 2008
No influence of SLC22A4 C6607T and RUNX1 G24658C genotypic variants on the circulating carnitine ester profile in patients with rheumatoid arthritis
K Komlósi, G C Talián, B Faragó, et al.
Clinical and Experimental Rheumatology
|
September 25, 2007
Prevalence of functional haplotypes of the peptidylarginine deiminase citrullinating enzyme gene in patients with rheumatoid arthritis: no influence of the presence of anti-citrullinated peptide antibodies
B Faragó, G C Talián, A Maász, et al.
Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
Acta Neurologica Scandinavica
|
December 15, 2004
Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke
Z Szolnoki, V Havasi, J Bene, et al.
Annals of the Rheumatic Diseases
|
July 4, 2007
Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis
B Faragó, L Magyari, E Sáfrány, et al.
Orvosi Hetilap
|
November 17, 1996
[Molecular biologic study and the factor VIII gene in hemophilia A]
I Bock, B Melegh, A Nagy, et al.
Clinical and Experimental Dermatology
|
June 10, 2017
Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome
K Tripolszki, K Farkas, A Sulák, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 21, 2009
Haplotype analysis of the apolipoprotein A5 gene in patients with the metabolic syndrome
P Kisfali, M Mohás, A Maász, et al.
Neuropathology and Applied Neurobiology
|
February 1, 2013
Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)
U Rüb, K Farrag, K Seidel, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 99) with videos related to
Sort By:
Page
of 10
Experimental and Clinical Immunogenetics
|
March 2, 2002
Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction
A Császár, J Duba, B Melegh, et al.
Clinical and Experimental Rheumatology
|
March 11, 2008
No influence of SLC22A4 C6607T and RUNX1 G24658C genotypic variants on the circulating carnitine ester profile in patients with rheumatoid arthritis
K Komlósi, G C Talián, B Faragó, et al.
Clinical and Experimental Rheumatology
|
September 25, 2007
Prevalence of functional haplotypes of the peptidylarginine deiminase citrullinating enzyme gene in patients with rheumatoid arthritis: no influence of the presence of anti-citrullinated peptide antibodies
B Faragó, G C Talián, A Maász, et al.
Molecular Genetics and Metabolism
|
February 9, 2020
The Undiagnosed Diseases Network International: Five years and more!
D Taruscio, G Baynam, H Cederroth, et al.
Acta Neurologica Scandinavica
|
December 15, 2004
Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke
Z Szolnoki, V Havasi, J Bene, et al.
Annals of the Rheumatic Diseases
|
July 4, 2007
Functional variants of interleukin-23 receptor gene confer risk for rheumatoid arthritis but not for systemic sclerosis
B Faragó, L Magyari, E Sáfrány, et al.
Orvosi Hetilap
|
November 17, 1996
[Molecular biologic study and the factor VIII gene in hemophilia A]
I Bock, B Melegh, A Nagy, et al.
Clinical and Experimental Dermatology
|
June 10, 2017
Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome
K Tripolszki, K Farkas, A Sulák, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD
|
August 21, 2009
Haplotype analysis of the apolipoprotein A5 gene in patients with the metabolic syndrome
P Kisfali, M Mohás, A Maász, et al.
Neuropathology and Applied Neurobiology
|
February 1, 2013
Involvement of the cholinergic basal forebrain nuclei in spinocerebellar ataxia type 2 (SCA2)
U Rüb, K Farrag, K Seidel, et al.
Page
of 10