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International Urology and Nephrology|July 8, 2015
Nocturnal enuresis with spina bifida occulta: Does it interfere behavioral management success?Omer Kurt, Cenk Murat Yazici, Cem PaketciPaediatrics & Child Health|January 15, 2014
Paediatricians' awareness of children's oral health: Knowledge, training, attitudes and practices among Turkish paediatriciansRabia Gonul Sezer, Cem Paketci, Abdulkadir BozaykutJournal of Clinical Medicine Research|August 27, 2013
Evaluation of risk factors for recurrent wheezing episodesAbdulkadir Bozaykut, Ahu Paketci, Rabia Gonul Sezer, et al.Renal Failure|October 21, 2011
VACTERL association: a new case with biotinidase deficiency and annular pancreasRabia Gonul Sezer, Gökhan Aydemir, Abdulkadir Bozaykut, et al.American Journal of Medical Genetics. Part A|May 19, 2019
Biallelic variant in AGTPBP1 causes infantile lower motor neuron degeneration and cerebellar atrophyMert Karakaya, Cem Paketci, Janine Altmueller, et al.European Journal of Medical Genetics|January 2, 2021
De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathyNatalie Keller, Cem Paketci, Pinar Edem, et al.Journal of Neurovirology|September 14, 2019
Herpes simplex virus-1 as a rare etiology of isolated acute cerebellitis: case report and literature reviewCem Paketci, Pinar Edem, Canan Okumus, et al.Journal of Clinical Medicine Research|February 8, 2013
Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosisRabia Gonul Sezer, Gokhan Aydemir, Abdullah Baris Akcan, et al.Pituitary|August 23, 2014
Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal functionTulay Guran, Omer Guran, Cem Paketci, et al.Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.Pageof 1