Search research articles
Contact Us
Filters
Showing results (51-60 of 63) with videos related to
Page
of 7
Sort By:
Bratislavske Lekarske Listy
|
September 10, 2015
Association between the neutrophil to lymphocyte ratio and prehypertension
M Aydin, M Yuksel, A Yildiz, et al.
Clinical and Experimental Immunology
|
July 15, 2016
The induction of autoimmune hepatitis in the human leucocyte antigen-DR4 non-obese diabetic mice autoimmune hepatitis mouse model
M Yuksel, X Xiao, N Tai, et al.
The Senior Care Pharmacist
|
April 29, 2025
Impact of a Geriatric Medication Safety Initiative (GEMSI) Pharmacist-Driven Procedure on Opioid Use in a Transitional Care Unit
Jaylan M Yuksel, Kyle R Eilert, John Noviasky, et al.
Yearbook of Medical Informatics
|
May 24, 2014
Healthcare information technology infrastructures in Turkey
A Dogac, M Yuksel, G L Ertürkmen, et al.
Prenatal Diagnosis
|
September 5, 2002
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families
S Savas, S Eraslan, S Kantarci, et al.
Fetal Diagnosis and Therapy
|
June 12, 2004
The results of cytogenetic analysis with regard to intracytoplasmic sperm injection in males, females and fetuses
S Basaran, A Engur, M Aytan, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations
O Uyguner, E Goicoechea de Jorge, A Cefle, et al.
Journal of Medical Genetics
|
May 3, 2005
A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qter
T Tukel, A Uzumcu, A Gezer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2003
A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency
T Tukel, O Uyguner, J Q Wei, et al.
Neurology
|
August 22, 2008
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type
L Van Maldergem, M Yuksel-Apak, H Kayserili, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 63) with videos related to
Sort By:
Page
of 7
Bratislavske Lekarske Listy
|
September 10, 2015
Association between the neutrophil to lymphocyte ratio and prehypertension
M Aydin, M Yuksel, A Yildiz, et al.
Clinical and Experimental Immunology
|
July 15, 2016
The induction of autoimmune hepatitis in the human leucocyte antigen-DR4 non-obese diabetic mice autoimmune hepatitis mouse model
M Yuksel, X Xiao, N Tai, et al.
The Senior Care Pharmacist
|
April 29, 2025
Impact of a Geriatric Medication Safety Initiative (GEMSI) Pharmacist-Driven Procedure on Opioid Use in a Transitional Care Unit
Jaylan M Yuksel, Kyle R Eilert, John Noviasky, et al.
Yearbook of Medical Informatics
|
May 24, 2014
Healthcare information technology infrastructures in Turkey
A Dogac, M Yuksel, G L Ertürkmen, et al.
Prenatal Diagnosis
|
September 5, 2002
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families
S Savas, S Eraslan, S Kantarci, et al.
Fetal Diagnosis and Therapy
|
June 12, 2004
The results of cytogenetic analysis with regard to intracytoplasmic sperm injection in males, females and fetuses
S Basaran, A Engur, M Aytan, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations
O Uyguner, E Goicoechea de Jorge, A Cefle, et al.
Journal of Medical Genetics
|
May 3, 2005
A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qter
T Tukel, A Uzumcu, A Gezer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 13, 2003
A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency
T Tukel, O Uyguner, J Q Wei, et al.
Neurology
|
August 22, 2008
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type
L Van Maldergem, M Yuksel-Apak, H Kayserili, et al.
Page
of 7