Search Results - "Bozatli, Leyla"

Author Correction: Using urine FTIR spectra to screen autism spectrum disorder.

Authors: Sarigul, Neslihan Bozatli, Leyla Kurultak, Ilhan et al.

Source: Scientific Reports. 3/21/2024, Vol. 14 Issue 1, p1-2. 2p.

Çocuk ve Ergenlerde Obsesif Kompulsif Bozukluk Fenomenolojisi: Bir Üniversite Hastanesi Örneklemi.

Alternate Title: Phenomenology of Obsessive Compulsive Disorder in Children and Adolescents: A University Hospital Sample.

Authors: GÜNEYDAŞ YILDIRIM, Burcu BOZATLI, Leyla AYKUTLU, Hasan Cem et al.

Source: Journal of Harran University Medical Faculty / Harran Üniversitesi Tıp Fakültesi Dergisi. 2025, Vol. 22 Issue 3, p484-492. 9p.

Using urine FTIR spectra to screen autism spectrum disorder.

Authors: Sarigul, Neslihan Bozatli, Leyla Kurultak, Ilhan et al.

Source: Scientific Reports. 11/9/2023, Vol. 13 Issue 1, p1-12. 12p.

Clinical exome sequencing reveals an important role for clinical diagnosis of intellectual disability with definition of seven novel variants.

Authors: Yalcintepe, Sinem Gorker, Isik Bozatli, Leyla et al.

Source: Neurology Asia. 2023, Vol. 28 Issue 4, p1041-1052. 18p.

The Probable Prevalence and Sociodemographic Characteristics of Specific Learning Disorder in Primary School Children in Edirne.

Authors: GÖRKER, Işık BOZATLI, Leyla KORKMAZLAR, Ümran et al.

Source: Archives of Neuropsychiatry / Nöropsikiyatri Arşivi. Dec2017, Vol. 54 Issue 4, p343-349. 7p.

Improvement of stuttering with use of methylphenidate in a child who was diagnosed with concomitant stuttering and ADHD.

Alternate Title: DEHB ile birlikte kekemeliği olan bir çocukta metilfenidatla kekemeliğin düzelmesi.

Authors: BOZATLI, Leyla BERBEROĞLU, Kıvanç Kudret CEYLAN, Cansın et al.

Source: Anatolian Journal of Psychiatry / Anadolu Psikiyatri Dergisi. 2016 Supplement 3, Vol. 17, p71-73. 3p.

Investigation the etiology of syndromic autism with targeted gene analysis.

Authors: Yalcintepe, Sinem Gurkan, Hakan Demir, Selma et al.

Source: Annals of Medical Research. Dec2021, Vol. 28 Issue 12, p2174-2178. 5p.

Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders.

Authors: GÜRKAN, Hakan ATLI, Emine İkbal ATLI, Engin et al.

Source: Archives of Neuropsychiatry / Nöropsikiyatri Arşivi. Sep2020, Vol. 57 Issue 3, p177-191. 15p.

Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders.

Authors: Görker, Işık Gürkan, Hakan Ulusal, Selma et al.

Source: Archives of Neuropsychiatry / Nöropsikiyatri Arşivi. sep2018, Vol. 55 Issue 3, p215-219. 5p.