Cargando…

No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish Children

OBJECTIVE: Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impairment in social skills and communication with repetitive behaviors. Etiology is still unclear although it is thought to develop with interaction of genes and environmental factors. Oxytocin has extensive...

Descripción completa

Detalles Bibliográficos
Autores principales:	Bozdogan, Sevcan Tug, Kutuk, Meryem Ozlem, Tufan, Evren, Altıntaş, Zuhal, Temel, Gülhan Orekici, Toros, Fevziye
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean College of Neuropsychopharmacology 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245295/ https://www.ncbi.nlm.nih.gov/pubmed/30466214 http://dx.doi.org/10.9758/cpn.2018.16.4.415

Ejemplares similares

Persistent hiccups due to aripiprazole in an adolescent with obsessive compulsive disorder responding to dose reduction and rechallenge
por: Kutuk, Meryem Ozlem, et al.
Publicado: (2016)

Seasonal Variations in Obsessive-Compulsive Disorder: Analysis of Prospective-Clinical Data
por: ALTINTAŞ, Ebru, et al.
Publicado: (2021)

Evaluation of Preoperative Anxiety in Turkish Paediatric Patients and Validity and Reliability of the Turkish Modified Yale Preoperative Anxiety Scale
por: Topalel, Selen, et al.
Publicado: (2020)

E-mentoring program organized by the Turkish Association for Child and Adolescent Psychiatry during the COVID-19 pandemic
por: Ercan, Eyüp Sabri, et al.
Publicado: (2020)

Dystonia in an Adolescent on Risperidone Following the Discontinuation of Methylphenidate: A Case Report
por: Guler, Gulen, et al.
Publicado: (2015)

Achalasia as a complication of bulimia nervosa: A case report
por: Kutuk, Meryem O., et al.
Publicado: (2017)

Neuroleptic malignant syndrome due to risperidone misdiagnosed as status epilepticus
por: Arslankoylu, Ali Ertug, et al.
Publicado: (2011)

Early maladaptive schemas in episodic and chronic migraine in adolescents
por: Güler Aksu, Gülen, et al.
Publicado: (2023)

Developmental delays and psychiatric diagnoses are elevated in offspring staying in prisons with their mothers
por: Kutuk, Meryem Ozlem, et al.
Publicado: (2018)

Hiccup Due to Aripiprazole Plus Methylphenidate Treatment in an Adolescent with Attention Deficit and Hyperactivity Disorder and Conduct Disorder: A Case Report
por: Kutuk, Meryem Ozlem, et al.
Publicado: (2017)

Hereditary Spastic Paraplegia Type 35 with a Novel Mutation in Fatty Acid 2-Hydroxylase Gene and Literature Review of the Clinical Features
por: Incecik, Faruk, et al.
Publicado: (2018)

Alternative Confidence Interval Methods Used in the Diagnostic Accuracy Studies
por: Erdoğan, Semra, et al.
Publicado: (2016)

Cultural adaptation of the Michigan Hand Outcomes Questionnaire in patients with Carpal Tunnel Syndrome: A Turkish version study
por: Ilhanli, Ilker, et al.
Publicado: (2015)

GDF9 and BMP15 Expressions and Fine Structure Changes During Folliculogenesis in Polycystic Ovary Syndrome
por: Karagül, Meryem İlkay, et al.
Publicado: (2018)

Relationship Between Final Visual Acuity and Optical Coherence Tomography Findings in Patients with Diabetic Macular Edema Undergoing Anti-VEGF Therapy
por: Eraslan, Seher, et al.
Publicado: (2020)

Evaluation of the results of patients who applied to the Çukurova University, Medical Genetics Department for prenatal diagnosis and determination of genetic counseling principles
por: TUĞ BOZDOĞAN, Sevcan, et al.
Publicado: (2020)

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child
por: Ozcanyuz, Duygu G., et al.
Publicado: (2020)

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience
por: Bilge, Serap, et al.
Publicado: (2022)

Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey
por: Bozdogan, Sevcan Tug, et al.
Publicado: (2021)

Turkish nursing students’ compliance to standard precautions during the COVID-19 pandemic
por: Topçu, Sevcan, et al.
Publicado: (2023)

Knowledge, Beliefs, and Behaviors of Turkish Parents about Childhood Vaccination
por: Emlek Sert, Zuhal, et al.
Publicado: (2023)

IL-1RN VNTR, IL-2(-330), and IL-4 VNTR gene polymorphisms in patients with chronic rhinosinusitis with sinonasal polyposis
por: KURAN, Gökhan, et al.
Publicado: (2019)

Identification of a Novel Mutation in GRIN2A Gene with Global Developmental Delay and Refractory Epilepsy
por: Sarigecili, Esra, et al.
Publicado: (2020)

Association between acute kidney injury and mortality after successful cardiopulmonary resuscitation: a retrospective observational study
por: Para, Ender, et al.
Publicado: (2021)

Oxytocin-Trust Link in Oxytocin-Sensitive Participants and Those Without Autistic Traits
por: Kurokawa, Hirofumi, et al.
Publicado: (2021)

The first Turkish family with Rotor syndrome diagnosed at the molecular level
por: Gümüş, Evren, et al.
Publicado: (2020)

Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations
por: Demir Gündoğan, Begümhan, et al.
Publicado: (2021)

functional outcome in late adolescence/early adulthood of patients with autism spectrum disorder and its relationships with parental burnout and depression: A preliminary multi-center, cross-sectional study
por: Kutuk, Meryem Ozlem, et al.
Publicado: (2023)

Turkish perspective of Jervell and Lange-Nielsen syndrome
por: Temel, Sehime G, et al.
Publicado: (2013)

Salivary oxytocin in autistic patients and in patients with intellectual disability
por: Pichugina, Yulia A., et al.
Publicado: (2022)

Evaluation of Plasma miR-17-5p, miR-24-3p and miRNA-223-3p Profile of Hepatitis C Virus-Infected Patients after Treatment with Direct-Acting Antivirals
por: Öksüz, Zehra, et al.
Publicado: (2023)

Assessment of suicidality in children and adolescents with diagnosis of high functioning autism spectrum disorder in a Turkish clinical sample
por: Karakoç Demirkaya, Sevcan, et al.
Publicado: (2016)

β-Globin chain abnormalities with coexisting α-thalassemia mutations
por: Guvenc, Birol, et al.
Publicado: (2012)

β-Thalassemia mutations and hemoglobinopathies in Adana, Turkey: results from a single center study
por: Guvenc, Birol, et al.
Publicado: (2012)

Neonatal Hyperbilirubinemia in a Turkish Cohort: Association of Vitamin B(12)
por: Eroglu, Nilgun, et al.
Publicado: (2015)

Amenorrhea as a Side Effect of Low Dose Aripiprazole: An Adolescent Case
por: Guler, Gulen, et al.
Publicado: (2018)

Hair loss due to methylphenidate use: A case study
por: Bilaç, Öznur, et al.
Publicado: (2018)

Vitamin D deficiency is not related to eating habits in children with Autistic Spectrum Disorder
por: Riccio, Maria Pia, et al.
Publicado: (2020)

Neonatal Oxytocin Treatment Ameliorates Autistic-Like Behaviors and Oxytocin Deficiency in Valproic Acid-Induced Rat Model of Autism
por: Dai, Yu-Chuan, et al.
Publicado: (2018)

Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia
por: Incecik, Faruk, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_t40gtb54mceig9f98nl9borgj7