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Genetic Counseling (Geneva, Switzerland)|February 12, 2002
An analysis of seven infants with Brachmann-de Lange syndrome, of whom two identical twin sistersH Caksen, S Kurtoğlu, Y Cesur, et al.The Turkish Journal of Pediatrics|October 1, 1992
Effects of anticonvulsant drugs on thyroid hormones in epileptic childrenG Deda, A Akinci, T Teziç, et al.Acta Psychiatrica Scandinavica|October 9, 2003
Psychotic disorder in a case with Hallervorden-Spatz diseaseO Oner, P Oner, G Deda, et al.Acta Neurologica Belgica|January 31, 2002
Neurophysiological changes in COPD patients with chronic respiratory insufficiencyO Kayacan, S Beder, G Deda, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|October 20, 1998
Collodion baby concomitant with congenital hypothyroidism: a patient report and review of the literatureS Kurtoğlu, H Caksen, R Erdoğan, et al.Journal of Child Neurology|May 3, 2001
Plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish children with cerebral infarct and effect on factor V 1691 A mutationN Akar, E Akar, E Yilmaz, et al.The Turkish Journal of Pediatrics|October 1, 1994
Brainstem auditory evoked potential, visual evoked potential and nerve conduction velocity and their relation with HbA1c and beta 2 microglobulin in children with insulin dependent diabetes mellitusA Akinci, G Deda, U Karagöl, et al.South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 14, 1998
Aarskog syndrome associated with hypermetropia and toe anomalyH Caksen, S Kurtoğlu, A Ciftçi, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2001
Asymmetric crying facies and congenital hypothyroidism: report of two patientsS Kurtoğlu, H Caksen, H Per, et al.Pageof 15