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Ceren Yılmaz

Showing results (1-10 of 16) with videos related to

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Geriatric Nursing (New York, N.Y.)|April 13, 2025
Psychometric properties of the Turkish version of the nursing home adjustment scaleNilay Ercan-Şahin, Ceren Yılmaz
Geriatric Nursing (New York, N.Y.)|June 18, 2026
"I feel bad… weak, miserable, left behind, defeated, useless…": A phenomenological qualitative study of frailty in nursing home residentsCeren Yılmaz, Nilay Ercan Şahin
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndromeCeren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan
Plos One|April 24, 2026
Psychometric properties of the Probability Bias MeasureRobert W Booth, Gubse N Aydın, Beril Başara, et al.
Bioresource Technology|September 10, 2022
Modeling and optimization of process parameters in co-composting of tea waste and food waste: Radial basis function neural networks and genetic algorithmElif Ceren Yılmaz, Fulya Aydın Temel, Ozge Cagcag Yolcu, et al.
Skeletal Radiology|July 1, 2022
Spondyloepimetaphyseal dysplasia-Maroteaux type due to dominant TRPV4 mutation: expanding the phenotype with a case reportCeren Yılmaz Uzman, Tufan Çankaya, Handan Güleryüz, et al.
Molecular Syndromology|June 16, 2022
Blended Phenotype of Pelger-Huet Anomaly with Osteochondroma and Autosomal Recessive Deafness with Enlarged Vestibular AqueductTayfun Cinleti, Ceren Yılmaz Uzman, Şefika Akyol, et al.
Hormones (Athens, Greece)|February 20, 2019
A toddler with a novel LEPR mutationCoşkun Armağan, Ceren Yılmaz, Altuğ Koç, et al.
Molecular Syndromology|February 15, 2024
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing PanelsGamze Sarıkaya Uzan, Ceren Yılmaz Uzman, Tayfun Çinleti, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 7, 2023
Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single centerMehmet Kocabey, Hande Özkalaycı, Tufan Çankaya, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Geriatric Nursing (New York, N.Y.)|April 13, 2025
Psychometric properties of the Turkish version of the nursing home adjustment scaleNilay Ercan-Şahin, Ceren Yılmaz
Geriatric Nursing (New York, N.Y.)|June 18, 2026
"I feel bad… weak, miserable, left behind, defeated, useless…": A phenomenological qualitative study of frailty in nursing home residentsCeren Yılmaz, Nilay Ercan Şahin
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 19, 2023
A rare cause of intellectual disability: Novel mutations of NFIX gene in two patients with clinical features of Marshall-Smith syndrome and Malan syndromeCeren Yılmaz Uzman, Semra Gürsoy, Filiz Hazan
Plos One|April 24, 2026
Psychometric properties of the Probability Bias MeasureRobert W Booth, Gubse N Aydın, Beril Başara, et al.
Bioresource Technology|September 10, 2022
Modeling and optimization of process parameters in co-composting of tea waste and food waste: Radial basis function neural networks and genetic algorithmElif Ceren Yılmaz, Fulya Aydın Temel, Ozge Cagcag Yolcu, et al.
Skeletal Radiology|July 1, 2022
Spondyloepimetaphyseal dysplasia-Maroteaux type due to dominant TRPV4 mutation: expanding the phenotype with a case reportCeren Yılmaz Uzman, Tufan Çankaya, Handan Güleryüz, et al.
Molecular Syndromology|June 16, 2022
Blended Phenotype of Pelger-Huet Anomaly with Osteochondroma and Autosomal Recessive Deafness with Enlarged Vestibular AqueductTayfun Cinleti, Ceren Yılmaz Uzman, Şefika Akyol, et al.
Hormones (Athens, Greece)|February 20, 2019
A toddler with a novel LEPR mutationCoşkun Armağan, Ceren Yılmaz, Altuğ Koç, et al.
Molecular Syndromology|February 15, 2024
Molecular Diagnosis of Limb-Girdle Muscular Dystrophy Using Next-Generation Sequencing PanelsGamze Sarıkaya Uzan, Ceren Yılmaz Uzman, Tayfun Çinleti, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|June 7, 2023
Genetic evaluation of 50 Turkish patients with neurofibromatosis type 1: 2 years experience of a single centerMehmet Kocabey, Hande Özkalaycı, Tufan Çankaya, et al.
Pageof 2