Search research articles
Contact Us
Filters
Showing results (31-40 of 98) with videos related to
Page
of 10
Sort By:
The Turkish Journal of Pediatrics
|
January 20, 1998
Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families
H Erdem, S Pehlivan, H Topaloğlu, et al.
Rheumatology International
|
January 10, 2001
Sulfasalazine-induced angioimmunoblastic lymphadenopathy developing in a patient with juvenile chronic arthritis
S Pay, A Dinc, I Simsek, et al.
Journal of Medical Genetics
|
February 1, 1993
Mutation analysis in Turkish phenylketonuria patients
M Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics
|
January 1, 1993
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients
M Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics
|
January 1, 1993
Deletion analysis of Duchenne muscular dystrophy
H Erdem, S Ayter, M Ozgüç, et al.
Clinical Rheumatology
|
November 26, 2002
Comparison of synovial MMP-1 and TIMP-1 levels in patients with various inflammatory arthritides: is there any difference between rheumatoid arthritis, Behçet's disease and familial Mediterranean fever?
S Pay, H Erdem, M Serdar, et al.
Lupus
|
June 10, 2008
Efficacy of plasmapheresis in the treatment of refractory toxic epidermal necrolysis-like acute cutaneous lupus erythematosus
I Simsek, M Cinar, H Erdem, et al.
Clinical Rheumatology
|
August 15, 2000
A case of Churg-Strauss syndrome presenting with cortical blindness
A Dinç, M Soy, S Pay, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus
|
March 20, 2014
Protective effect of glucagon-like peptide-2 in experimental corrosive esophagitis
M Tekin, N Topaloğlu, A Küçük, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients
M Ozgüç, E Yilmaz, H Erdem, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 98) with videos related to
Sort By:
Page
of 10
The Turkish Journal of Pediatrics
|
January 20, 1998
Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families
H Erdem, S Pehlivan, H Topaloğlu, et al.
Rheumatology International
|
January 10, 2001
Sulfasalazine-induced angioimmunoblastic lymphadenopathy developing in a patient with juvenile chronic arthritis
S Pay, A Dinc, I Simsek, et al.
Journal of Medical Genetics
|
February 1, 1993
Mutation analysis in Turkish phenylketonuria patients
M Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics
|
January 1, 1993
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients
M Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics
|
January 1, 1993
Deletion analysis of Duchenne muscular dystrophy
H Erdem, S Ayter, M Ozgüç, et al.
Clinical Rheumatology
|
November 26, 2002
Comparison of synovial MMP-1 and TIMP-1 levels in patients with various inflammatory arthritides: is there any difference between rheumatoid arthritis, Behçet's disease and familial Mediterranean fever?
S Pay, H Erdem, M Serdar, et al.
Lupus
|
June 10, 2008
Efficacy of plasmapheresis in the treatment of refractory toxic epidermal necrolysis-like acute cutaneous lupus erythematosus
I Simsek, M Cinar, H Erdem, et al.
Clinical Rheumatology
|
August 15, 2000
A case of Churg-Strauss syndrome presenting with cortical blindness
A Dinç, M Soy, S Pay, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus
|
March 20, 2014
Protective effect of glucagon-like peptide-2 in experimental corrosive esophagitis
M Tekin, N Topaloğlu, A Küçük, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients
M Ozgüç, E Yilmaz, H Erdem, et al.
Page
of 10