Browsing by Department "Çocuk ve Ergen Ruh Sağlığı ve Hastalıkları"

Now showing items 1-20 of 22

    • 4-10 Yaş Grubu Çocuklarda Fonksiyonel Bağırsak Hastalıkları Belirtilerinin Psikiyatrik Belirtiler İle İlişkisi 

      Yaprakcı, Rahime Kadir (Tıp Fakültesi, 2020)
      Yaprakcı, R. The relationship between functional gastrointestinal symptoms and psychiatric symptoms among children ages 4 to 10 years, Hacettepe University Faculty of Medicine, Child and Adolescent Psychiatry, Ankara, 2020. ...

    • A Qualitative Study on Corporal Punishment And Emotionally Abusive Disciplinary Practices Among Mothers of Children With Adhd 

      Evinc, S. Gulin; Ozdemir, Dilsad Foto; Karadag, Ferda; Akdemir, Devrim; Gencoz, Tulin; Surucu, Ozlem; Unal, Fatih (Taylor & Francis Ltd, 2018)
      OBJECTIVES: The present study aimed to investigate actual disciplinary behaviours of Turkish mothers' in the context of relational environment and to investigate ADHD as a risk factor on abusive disciplinary practices. ...

    • Ankara ve İstanbul’daki Hıv/Aıds Merkezlerinde Takipli Hıv (+) Olan Çocuk ve Ergenlerin Ruh Sağlığı ve Bilişsel Fonksiyonları Açısından İncelenmesi ve Orta-Ağır Şiddetli Astımlı Çocuklarla Karşılaştırılması 

      Karakök, Burak (Tıp Fakültesi, 2018)
      Karakok, B., An investigation of psychopathology and cognitive functioning of HIV infected children and adolescents in Ankara and Istanbul and comparison with children with moderate and severe asthma, Hacettepe University ...

    • Cognitive And Behavioral Impairment In Mild Hyperphenylalaninemia 

      Evinc, S. Gulin; Pektas, Emine; Foto-Ozdemir, Dilsad; Yildiz, Yilmaz; Karaboncuk, Yamac; Bilginer-Gurbuz, Berrak; Dursun, Ali; Tokatli, Aysegul; Coskun, Turgay; Oktem, Ferhunde; Sivri, H. Serap (Turkish J Pediatrics, 2018)
      As elevated phenylalanine (Phe) is detrimental to brain functions, determining a safe upper limit of blood Phe is important for initiation of treatment plans and setting Phe targets in hyperphenlalaninemic patients. It is ...

    • Dikkat Eksikliği Hiperaktivite Bozukluğu Olan Çocuklarda Motor Taşma Hareketi: Bir Elektroensefalografi Çalışması 

      Karaokur, Remzi (Tıp Fakültesi, 2017)
      The aim of this study was to compare children with Attention Deficit Hyperactivity Disorder (ADHD) and age matched healthy controls in terms of motor skills and amplitude changes in active cortical regions during a voluntary ...

    • Dysregulation in Children: Origins and Implications From Age 5 to Age 28 

      McQuillan, Maureen E.; Kultur, Ebru C.; Bates, John E.; O'Reilly, Lauren M.; Dodge, Kenneth A.; Lansford, Jennifer E.; Pettit, Gregory S. (Cambridge Univ Press, 2018)
      Research shows that childhood dysregulation is associated with later psychiatric disorders. It does not yet resolve discrepancies in the operationalization of dysregulation. It is also far from settled on the origins and ...

    • Ergen Bağlanma Biçimlerinin Tematik Uyaranlara Verilen Öyküsel Tepkiler Aracılığıyla Değerlendirilmesi 

      Tuzun, Zeynep; Soygut, Gonca (Turkiye Sinir Ve Ruh Sagligi Dernegi, 2017)
      Objective: The aim of this research is to develop a new protocol with a projective test and qualitative assessment approach for investigating mental representations effective for the formation of attachment styles and to ...

    • Human Intracellular Isg15 Prevents Interferon-Alpha/Beta Over-Amplification And Auto-Inflammation 

      Zhang, Xianqin; Bogunovic, Dusan; Payelle-Brogard, Beatrice; Francois-Newton, Veronique; Speer, Scott D.; Yuan, Chao; Volpi, Stefano; Li, Zhi; Sanal, Ozden; Mansouri, Davood; Tezcan, Ilhan; Rice, Gillian I.; Chen, Chunyuan; Mansouri, Nahal; Mahdaviani, Seyed Alireza; Itan, Yuval; Boisson, Bertrand; Okada, Satoshi; Zeng, Lu; Wang, Xing; Jiang, Hui; Liu, Wenqiang; Han, Tiantian; Liu, Delin; Ma, Tao; Wang, Bo; Liu, Mugen; Liu, Jing-Yu; Wang, Qing K.; Yalnizoglu, Dilek; Radoshevich, Lilliana; Uze, Gilles; Gros, Philippe; Rozenberg, Flore; Zhang, Shen-Ying; Jouanguy, Emmanuelle; Bustamante, Jacinta; Garcia-Sastre, Adolfo; Abel, Laurent; Lebon, Pierre; Notarangelo, Luigi D.; Crow, Yanick J.; Boisson-Dupuis, Stephanie; Casanova, Jean-Laurent; Pellegrini, Sandra (Nature Publishing Group, 2015)
      Intracellular ISG15 is an interferon (IFN)-alpha/beta-inducible ubiquitin-like modifier which can covalently bind other proteins in a process called ISGylation; it is an effector of IFN-alpha/beta-dependent antiviral ...

    • Identification Of A New Locus For A Peculiar Form Of Congenital Muscular Dystrophy With Early Rigidity Of The Spine, On Chromosome 1P35-36 

      Moghadaszadeh, B; Desguerre, I; Topaloglu, H; Muntoni, FN; Pavek, S; Sewry, C; Mayer, M; Fardeau, M; Tome, FMS; Guicheney, P (Univ Chicago Press, 1998)
      Classical congenital muscular dystrophies (CMDs) are autosomal recessive neuromuscular disorders characterized by early onset of hypotonia and weakness, atrophy of limbs and trunk muscles, contractures, and dystrophic ...

    • Impaired Amino Acid Transport At The Blood Brain Barrier Is A Cause Of Autism Spectrum Disorder 

      Tarlungeanu, Dora C.; Deliu, Elena; Dotter, Christoph P.; Kara, Majdi; Janiesch, Philipp Christoph; Scalise, Mariafrancesca; Galluccio, Michele; Tesulov, Mateja; Morelli, Emanuela; Sonmez, Fatma Mujgan; Bilguvar, Kaya; Ohgaki, Ryuichi; Kanai, Yoshikatsu; Johansen, Anide; Esharif, Seham; Ben-Omran, Tawfeg; Topcu, Meral; Schlessinger, Avner; Indiveri, Cesare; Duncan, Kent E.; Caglayan, Ahmet Okay; Gunel, Murat; Gleeson, Joseph G.; Novarino, Gaia (Cell Press, 2016)
      Autism spectrum disorders (ASD) are a group of genetic disorders often overlapping with other neurological conditions. We previously described abnormalities in the branched-chain amino acid (BCAA) catabolic pathway as a ...

    • International Comparisons of Behavioral and Emotional Problems in Preschool Children: Parents' Reports from 24 Societies 

      Rescorla, Leslie A.; Achenbach, Thomas M.; Ivanova, Masha Y.; Harder, Valerie S.; Otten, Laura; Bilenberg, Niels; Bjarnadottir, Gudrun; Capron, Christiane; De Pauw, Sarah S. W.; Dias, Pedro; Dobrean, Anca; Doepfner, Manfred; Duyme, Michel; Eapen, Valsamma; Erol, Nese; Esmaeili, Elaheh Mohammad; Ezpeleta, Lourdes; Frigerio, Alessandra; Fung, Daniel S. S.; Goncalves, Miguel; Guomundsson, Halldor; Jeng, Suh-Fang; Jusiene, Roma; Kim, Young Ah; Kristensen, Solvejg; Liu, Jianghong; Lecannelier, Felipe; Leung, Patrick W. L.; Machado, Barbara Cesar; Montirosso, Rosario; Oh, Kyung Ja; Ooi, Yoon Phaik; Plueck, Julia; Pomalima, Rolando; Pranvera, Jetishi; Schmeck, Klaus; Shahini, Mimoza; Silva, Jaime R.; Simsek, Zeynep; Sourander, Andre; Valverde, Jose; van der Ende, Jan; Van Leeuwen, Karla G.; Wu, Yen-Tzu; Yurdusen, Sema; Zubrick, Stephen R.; Verhulst, Frank C. (Routledge Journals, Taylor & Francis Ltd, 2011)
      International comparisons were conducted of preschool children's behavioral and emotional problems as reported on the Child Behavior Checklist for Ages 11/2-5 by parents in 24 societies (N=19,850). Item ratings were ...

    • Intraspinal Lipomas without Associated Spinal Dysraphism 

      Arslan, Erhan; Kuzeyli, Kayhan; Acar Arslan, Elif (2014)
      Introduction: The aim of this study was to report surgical strategies and clinical outcomes for thoraco-lumbar intradural lipomas. Intraspinal lipomas are rare congenital histologically benign neoplasms, which account for ...

    • Joubert Syndrome: A Model for Untangling Recessive Disorders with Extreme Genetic Heterogeneity 

      Bachmann-Gagescu, R.; Dempsey, J. C.; Phelps, I. G.; O'Roak, B. J.; Knutzen, D. M.; Rue, T. C.; Ishak, G. E.; Isabella, C. R.; Gorden, N.; Adkins, J.; Boyle, E. A.; de Lacy, N.; O'Day, D.; Alswaid, A.; Ramadevi, Radha A.; Lingappa, L.; Lourenco, C.; Martorell, L.; Garcia-Cazorla, A.; Ozyurek, H.; Haliloglu, G.; Tuysuz, B.; Topcu, M.; Chance, P.; Parisi, M. A.; Glass, I. A.; Shendure, J.; Doherty, D. (Bmj Publishing Group, 2015)
      Background Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterised by hypotonia, ataxia, cognitive impairment, abnormal eye movements, respiratory control disturbances and a distinctive mid-hindbrain ...

    • Kendine Zarar Verme Davranışı Olan ve Olmayan Ergenlerin Kimlik Gelişimi ve Bilinçli Farkındalık Düzeylerinin Karşılaştırılması 

      Yazgılı Kahveci, Neslihan Gökçe (Tıp Fakültesi, 2020)
      Yazgılı Kahveci, Neslihan Gökçe. Evaluation of Identity Development and Mindfulness in Adolescents with and without Nonsuicidal Self-Injurious Behavior Hacettepe University Faculty of Medicine Department of Child and ...

    • L-2-Hydroxyglutaric Aciduria: Identification of a Mutant Gene C14Orf160, Localized on Chromosome 14Q22.1 

      Topcu, M; Jobard, F; Halliez, S; Coskun, T; Yalcinkayal, C; Gerceker, FO; Wanders, RJA; Prud'homme, JF; Lathrop, M; Ozguc, M; Fischer, J (Oxford Univ Press, 2004)
      l-2-Hydroxyglutaric aciduria (l-2-HGA) is characterized by progressive deterioration of central nervous system function including epilepsy and macrocephaly in 50% of cases, and elevated levels of l-2-hydroxyglutaric acid ...

    • Maternal Brain Response to Own Baby-Cry Is Affected by Cesarean Section Delivery 

      Swain, James E.; Tasgin, Esra; Mayes, Linda C.; Feldman, Ruth; Constable, R. Todd; Leckman, James F. (Wiley-Blackwell, 2008)
      A range of early circumstances surrounding the birth of a child affects peripartum hormones, parental behavior and infant wellbeing. One of these factors, which may lead to postpartum depression, is the mode of delivery: ...

    • Molecular Cytogenetic Analysis And Resequencing Of Contactin Associated Protein-Like 2 In Autism Spectrum Disorders 

      Bakkaloglu, Betul; O'Roak, Brian J.; Louvi, Angeliki; Gupta, Abha R.; Abelson, Jesse E.; Morgan, Thomas M.; Chawarska, Katarzyna; Klin, Ami; Ercan-Sencicek, A. Gulhan; Stillman, Althea A.; Tanriover, Gamze; Abrahams, Brett S.; Duvall, Jackie A.; Robbins, Elissa M.; Geschwind, Daniel H.; Biederer, Thomas; Gunel, Murat; Lifton, Richard P.; State, Matthew W. (Cell Press, 2008)
      Autism spectrum disorders (ASD) are a group of related neurodevelopmental syndromes with complex genetic etiology.(1) We identified a de novo chromosome 7q inversion disrupting Autism susceptibility candidate 2 (AUTS2) and ...

    • Neurobiology Of Tourette Syndrome 

      Unal, Dilek; Akdemir, Devrim (Turkiye Sinir Ve Ruh Sagligi Dernegi, 2016)
      Tourette Syndrome (TS) is a neurodevelopmental disorder characterized by chronic motor and vocal tics. Although it is a common disorder in childhood, the etiology of Tourette Syndrome has not been fully elucidated yet. ...

    • Otizm Spektrum Bozukluğunda Regresyon ile İlişkili Klinik ve Otoimmün Değişkenler 

      Aslan, Cihan (Tıp Fakültesi, 2016)
      In this cross-sectional case-control study it is aimed to investigatethe differences between ASD(Autism Spectrum Disorders) cases with regression and without regression in terms of autoimmune markers and clinical manifestations ...

    • Otzim Spektrum Bozukluğu Tanısı Konulan Çocuklarda Uyku ve Beslenme Sorunları 

      Taşyürek, Emine (Tıp Fakültesi, 2017)
      In this study autistic children’s sleep and nutrition problems and associated gastrointestinal system symptoms, autistic symptom severity, body mass index, mothers’ anxiety, depression levels and quality of life has been ...