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H Erdem

Showing results (31-40 of 98) with videos related to

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The Turkish Journal of Pediatrics|January 20, 1998
Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy familiesH Erdem, S Pehlivan, H Topaloğlu, et al.
Rheumatology International|January 10, 2001
Sulfasalazine-induced angioimmunoblastic lymphadenopathy developing in a patient with juvenile chronic arthritisS Pay, A Dinc, I Simsek, et al.
Journal of Medical Genetics|February 1, 1993
Mutation analysis in Turkish phenylketonuria patientsM 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 patientsM Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics|January 1, 1993
Deletion analysis of Duchenne muscular dystrophyH 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 erythematosusI Simsek, M Cinar, H Erdem, et al.
Clinical Rheumatology|August 15, 2000
A case of Churg-Strauss syndrome presenting with cortical blindnessA 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 esophagitisM 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 patientsM Ozgüç, E Yilmaz, H Erdem, et al.
Pageof 10

Showing results (31-40 of 98) with videos related to

Sort By:
Pageof 10
The Turkish Journal of Pediatrics|January 20, 1998
Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy familiesH Erdem, S Pehlivan, H Topaloğlu, et al.
Rheumatology International|January 10, 2001
Sulfasalazine-induced angioimmunoblastic lymphadenopathy developing in a patient with juvenile chronic arthritisS Pay, A Dinc, I Simsek, et al.
Journal of Medical Genetics|February 1, 1993
Mutation analysis in Turkish phenylketonuria patientsM 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 patientsM Ozgüç, I Ozalp, T Coşkun, et al.
The Turkish Journal of Pediatrics|January 1, 1993
Deletion analysis of Duchenne muscular dystrophyH 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 erythematosusI Simsek, M Cinar, H Erdem, et al.
Clinical Rheumatology|August 15, 2000
A case of Churg-Strauss syndrome presenting with cortical blindnessA 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 esophagitisM 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 patientsM Ozgüç, E Yilmaz, H Erdem, et al.
Pageof 10