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Life Sciences
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January 1, 1992
Studies of the role of the N-methyl-D-aspartate (NMDA) receptor in the hypothalamic control of prolactin secretion
M Arslan, C R Pohl, M S Smith, et al.
Life Sciences
|
January 1, 1991
Possible modulation of N-methyl-D,L-aspartic acid induced prolactin release by testicular steroids in the adult male rhesus monkey
M Arslan, S S Rizvi, S Jahan, et al.
Nigerian Journal of Clinical Practice
|
March 30, 2016
Biomechanical analysis of titanium fixation plates and screws in mandibular angle fractures
F Atik, M S Atac, A Özkan, et al.
Bratislavske Lekarske Listy
|
November 24, 2012
Effect of dexmedetomidine on erythrocyte deformability during ischemia-reperfusion injury of liver in diabetic rats
M Arslan, F M Comu, B Isik, et al.
International Urology and Nephrology
|
March 25, 2005
A case report: adrenal ganglioneuroblastoma in a 59-year old man
B Gunlusoy, M Arslan, E Selek, et al.
International Journal of Legal Medicine
|
October 18, 2008
Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture
M Klintschar, U Bilkenroth, M Arslan-Kirchner, et al.
Nigerian Journal of Clinical Practice
|
January 13, 2016
Biomechanical analysis of titanium fixation plates and screws in sagittal split ramus osteotomies
F Atik, M S Atac, A Özkan, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12→q21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature review
D Torun, M Arslan, H Akar, et al.
Bratislavske Lekarske Listy
|
March 1, 2016
Effects of iron overload and exenatide on erythrocyte deformability in a rat model
S M Kuskonmaz, H Kara, F M Comu, et al.
European Journal of Pediatrics
|
December 11, 1999
A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients
S Borgmann, I Luhmer, M Arslan-Kirchner, et al.
Page
of 25
Search research articles
Search
Showing results (91-100 of 247) with videos related to
Sort By:
Page
of 25
Life Sciences
|
January 1, 1992
Studies of the role of the N-methyl-D-aspartate (NMDA) receptor in the hypothalamic control of prolactin secretion
M Arslan, C R Pohl, M S Smith, et al.
Life Sciences
|
January 1, 1991
Possible modulation of N-methyl-D,L-aspartic acid induced prolactin release by testicular steroids in the adult male rhesus monkey
M Arslan, S S Rizvi, S Jahan, et al.
Nigerian Journal of Clinical Practice
|
March 30, 2016
Biomechanical analysis of titanium fixation plates and screws in mandibular angle fractures
F Atik, M S Atac, A Özkan, et al.
Bratislavske Lekarske Listy
|
November 24, 2012
Effect of dexmedetomidine on erythrocyte deformability during ischemia-reperfusion injury of liver in diabetic rats
M Arslan, F M Comu, B Isik, et al.
International Urology and Nephrology
|
March 25, 2005
A case report: adrenal ganglioneuroblastoma in a 59-year old man
B Gunlusoy, M Arslan, E Selek, et al.
International Journal of Legal Medicine
|
October 18, 2008
Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture
M Klintschar, U Bilkenroth, M Arslan-Kirchner, et al.
Nigerian Journal of Clinical Practice
|
January 13, 2016
Biomechanical analysis of titanium fixation plates and screws in sagittal split ramus osteotomies
F Atik, M S Atac, A Özkan, et al.
Genetic Counseling (Geneva, Switzerland)
|
February 28, 2018
Central nervous system abnormalities and psychomotor retardation in a girl with a 15.4-MB deletion of 14q12→q21.2 and a 550-KB deletion of 18p11.23: microarray delineation of an unbalanced chromosome rearrangement and a literature review
D Torun, M Arslan, H Akar, et al.
Bratislavske Lekarske Listy
|
March 1, 2016
Effects of iron overload and exenatide on erythrocyte deformability in a rat model
S M Kuskonmaz, H Kara, F M Comu, et al.
European Journal of Pediatrics
|
December 11, 1999
A search for chromosome 22q11.2 deletions in a series of 176 consecutively catheterized patients with congenital heart disease: no evidence for deletions in non-syndromic patients
S Borgmann, I Luhmer, M Arslan-Kirchner, et al.
Page
of 25