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Retraso mental y psicomotor en la primera infancia: Revisión de la literatura y propuesta de un protocolo de valoración neuropsicológica

Author(s): Rosa Canovas | Lourdes Martinez | María del Mar Sánchez-Joya | Lola Roldán-Tapia
Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong Syndrome

Author(s): Andreea Liana Rachisan | Simona Cainap | Mariana Andreica | Nicolae Miu
Cerebrotendinous Xanthomatosis with Psychiatric Disorders: Report of Three Siblings and Literature Review

Author(s): Yu Lee | Pao-Yen Lin | Nien-Mu Chiu | Wen-Neng Chang | Jung-Kwang Wen
18p- syndrome: Presentation of two cases with alobar holoprosencenphaly

Author(s): Harry Pachajoa | Wilmar Saldarriaga | Carolina Isaza
Treating acid reflux disease in patients with Down syndrome: pharmacological and physiological approaches

Author(s): Francesco Macchini | Ernesto Leva | Maurizio Torricelli | et al
A Sri Lankan child with 49,XXXXY syndrome

Author(s): Dissanayake Vajira | Bandarage Palinda | Pedurupillay Christeen | Jayasekara Rohan
Methylphenidate-induced mania-like symptoms

Author(s): Chakraborty Kaustav | Grover Sandeep
Dyke-Davidoff-Masson syndrome: Classical imaging findings

Author(s): Singh Paramdeep | Saggar Kavita | Ahluwalia Archana
Bilateral progressive visual loss in an epileptic, mentally retarded boy

Author(s): Guerriero Silvana | Vetrugno Michele | Ciracì Lorenza | Artuso Lucia | Dell′Aglio Rosa | Petruzzella Vittoria
Rubinstein-Taybi Syndrome; A Case Report

Author(s): Mohammad Reza Salehi Omran | Hadi Sorkhi | Yasser Asghari Vostacolaee | Ali Ghabeli Juibari
RISK FACTORS AND PROGNOSIS OF EPILEPSY IN CHILDREN WITH HEMIPARETIC CEREBRAL PALSY

Author(s): Parvaneh KARIMZADEH | Mehran AGHA MOHAMMAD POUR | Susan AMIRSALARI | Seyyed Hassan TONEKABONI
Cerebral palsy and epilepsy

Author(s): Knežević-Pogančev Marija
This is about a complicated situation: mental illness from the perspective of military servers

Author(s): Sandra Leontina Graube, Leila Mariza Hildebrandt, Marinês Tambara Leite, Eniva Miladi Fernandes Stumm, Marli Maria Loro, Cleci Lourdes Piovesan Rosanelli
Identifying the ′mentally disabled′ in the community: How much more is to be imparted to the internees in training?

Author(s): Bindu Annigeri | Sathyanarayana Rao T | Ashok N | Prabhakar A | Manickam L. S. S
Cellular stress-induced up-regulation of FMRP promotes cell survival by modulating PI3K-Akt phosphorylation cascades

Author(s): Jeon Se | Seo Jung | Yang Sung-Il | Choi Ji | Wells David | Shin Chan | Ko Kwang
Dental and craniofacial characteristics in a patient with Dubowitz syndrome: a case report

Author(s): Ballini Andrea | Cantore Stefania | Tullo Domenica | Desiate Apollonia
Normal social seeking behavior, hypoactivity and reduced exploratory range in a mouse model of Angelman syndrome

Author(s): Allensworth Melody | Saha Anand | Reiter Lawrence | Heck Detlef
Case report of intrafamilial variability in autosomal recessive centronuclear myopathy associated to a novel BIN1 stop mutation

Author(s): Böhm Johann | Yiş Uluç | Ortaç Ragıp | Çakmakçı Handan | Kurul Semra | Dirik Eray | Laporte Jocelyn
Serum neutrophil gelatinase-B associated lipocalin (NGAL) levels in Down’s syndrome patients

Author(s): Dogliotti Giada | Galliera Emanuela | Licastro Federico | Porcellini Elisa | Corsi Massimiliano
Prenatal exposure of ethanol induces increased glutamatergic neuronal differentiation of neural progenitor cells

Author(s): Kim Ki | Go Hyo | Bak Hae | Choi Chang | Choi Inha | Kim Pitna | Han Seol-Heui | Han So | Shin Chan | Ko Kwang
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32

Author(s): Hattersley Kathryn | Laurie Kate | Liebelt Jan | Gecz Jozef | Durkin Shane | Craig Jamie | Burdon Kathryn
Spontaneous massive hemoperitoneum: A potentially life threatening presentation of the wandering spleen

Author(s): Iswanto Sucandy | Yasir Mohammad Akmal | Jon D. Gabrielsen
Autistic spectrum in West syndrome - Original Article

Author(s): Selda Hançerli | Mine Çalışkan | Nahit Motavallı Mukaddes | Burak Tatlı | Nur Aydınlı | Meral Özmen
Clinical and Cytogenetic Effects in Habitants under Large Duration Exposure of Endosulfan

Author(s): R. Saraswathy | G. Alex, B.M. Basil, A.R.S. Badarinath, R. Girish, G. Ribu, V.G. Abilash, G.D.J. Cruz and K.M. Marimuthu
Johanson-Blizzard syndrome with mild phenotypic features confirmed by UBR1 gene testing

Author(s): Naim Alkhouri, Barbara Kaplan, Marsha Kay, Amy Shealy, Carol Crowe, Susanne Bauhuber, Martin Zenker
Maternally Inherited Diabetes and Deafness (MIDD) Syndrome: A Clinical and Molecular Genetic Study of a Taiwanese Family.

Author(s): Yung-Nien Chen | Chia-Wei Liou | Chin-Chang Huang | Tsu-Kung Lin | Yau-Huei Wei
Dental status of institutionalized persons with special needs who live in Special institution “Srce u jabuci” in Pancevo

Author(s): Savić-Stanković Tatjana | Jovanović-Medojević Milica | Živković Slavoljub
Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

Author(s): Al-Zahrani Jawaher | Al-Dosari Naji | AbuDheim Nada | Alshidi Tarfa | Colak Dilek | Al-Habit Ola | Al-Odaib Ali | Sakati Nadia | Meyer Brian | Ozand Pinar | Kaya Namik
The impact of ADHD and conduct disorder in childhood on adult delinquency: A 30 years follow-up study using official crime records

Author(s): Mordre Marianne | Groholt Berit | Kjelsberg Ellen | Sandstad Berit | Myhre Anne
Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

Author(s): Tucker Tracy | Montpetit Alexandre | Chai David | Chan Susanna | Chénier Sébastien | Coe Bradley | Delaney Allen | Eydoux Patrice | Lam Wan | Langlois Sylvie | Lemyre Emmanuelle | Marra Marco | Qian Hong | Rouleau Guy | Vincent David | Michaud Jacques | Friedman Jan
Nutritional status of iodine in pregnant women in Catalonia (Spain): study on hygiene-dietetic habits and iodine in urine

Author(s): Prieto Gemma | Torres Maria | Francés Lidia | Falguera Gemma | Vila Lluis | Manresa Josep | Casamitjana Roser | Barrada Juan | Acera Amèlia | Guix Dolors | Torrent Anna | Grau Josep | Torán Pere
Evidence for population variation in TSC1 and TSC2 gene expression

Author(s): Jentarra Garilyn | Rice Stephen | Olfers Shannon | Saffen David | Narayanan Vinodh
Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

Author(s): Salih Mustafa | Abu-Amero Khaled | Alrasheed Saleh | Alorainy Ibrahim | Liu Lu | McGrath John | Van Maldergem Lionel | Al-Faky Yasser | AlSuhaibani Adel | Oystreck Darren | Bosley Thomas
Mental Retardation and Parenting Stress

Author(s): Savvas Karasavvidis | Chrisanthi Avgerinou | Eirini Lianou | Dimitrios Priftis | Anastasia Lianou | Eleni Siamaga
Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report

Author(s): Beata Wikiera | Ewa Głąb | Ryszard Ślęzak | Elżbieta Wójcik | Anna Noczyńska
DIAGNOSIS AND TREATMENT OF DEPRESSION IN PERSONS WITH INTELLECTUAL DISABILITY

Author(s): Katarina Tomić1, | Goran Mihajlović2, | Natalija Jovanović Mihajlović3 | Slavica Đukić Dejanović2, and | Katarina Mihajlović4 | Goran Petrović2
Comparison of Cerebral Lateralization in Mentally Retarded Children vs. Normal Children

Author(s): S. B. Jaamei | M. Kiani | M. T. Jaghataei | Sh. Sirous | M. Hadadian
Teachers’ Attitudes Towards inclusive Education in Austria

Author(s): Markus Gebhardt | Susanne Schwab | Hannelore Reicher | Barbara Ellmeier | Sonja Gmeiner | Peter Rossmann | Barbara Gasteiger Klicpera
Microarray-based comparative genomic hybridization (aCGH) between basic research and clinical diagnostic

Author(s): Andreea Cristina Tutulan-Cunita | Magdalena Budisteanu | Sorina Mihaela Chirieac | Aurora Arghir | Georgeta Cardos | Agripina Lungeanu
Hydroelectrolytic imbalance in mental retardation and autism spectrum disorders

Author(s): Dobre Michaela | Gurau Gabriela | Nechita Aurel | Lucian Puiu Georgescu
Effect of Enzyme Type, Enzyme Substrate Ratio and Temperature on Phenylalanine Removal from Milk

Author(s): Marialice P.C. Silvestre | Mariana W.S. de Souza | Carlos O. Lopes Junior | Viviane D.M. Silva | Marcos J.B. Aguiar | Wendel O. Afonso | Mauro R. Silva
Cytogenetic diseases

Author(s): Khavari Khorassani H
X-linked mental retardation (Fragile X-syndrome)

Author(s): Khavari Khorasani H
Seckel syndrome

Author(s): Ashrafi MR
Menkes Kinky Hair; a case report

Author(s): M Seifhashemi
The outcome of renal transplantation in Bardet-Biedl syndrome

Author(s): M Sharifian | M Dadkhah | B Einollahi | M Nafar | N Simfroosh | A Basiri | H Otukesh
Fraser syndrome and cryptophthalmos; a case report

Author(s): N Khalesi | F Salehi | A Mohamadi poor
Lowe Syndrome: Report of a Case and Brief Literature Review

Author(s): Gholamhossein Amirhakimi | Mohamad-Hosein Fallahzadeh | Hedyeh Saneifard
Giant Asterional Dermoid Cyst with Dermal Sinus; a Case Report

Author(s): Amit Agrawal | Sudhakar Ratanlal Joharapurkar | Vinay Vasudev Shahapurkar
Incidence of Neonatal Hyperphenylalaninemia in Fars Province, South Iran

Author(s): Hamdollah Karamifar | Mahtab Ordoei | Zohreh Karamizadeh | Gholamhossein Amirhakimi
Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong Syndrome

Author(s): Andreea Liana Rachisan | Simona Cainap | Mariana Andreica | Nicolae Miu
Family Social Status and Dietary Adherence of Patients with Phenylketonuria

Author(s): Mohammadreza Alaei | Gelareh Asadzadeh-Totonchi | Latif Gachkar | Shirin Farivar
 Profile Difference Between Male and Female Psychiatric Patients Seeking Certificate of Disability

Author(s): Yatan Pal Singh Balhara | Deepak Gauba | Smita N. Deshpande
CRANIOFACIAL MORPHOLOGY AND DENTAL FINDINGS OF SECKEL SYNDROME: CASE REPORTS OF TWO SIBLINGS

Author(s): Zuhal Kirzioglu | M. Semra Ozay Erturk | Yildirim Erdogan
Women Reproductive Rights in India: Prospective Future

Author(s): Srinivas Kosgi | Vaishali Hegde N | Satheesh Rao | Shrinivasa Bhat Undaru | Nagesh Pai
A REVIEW ON SYNTHESIS OF SOME N-(p-METHOXY BENZENE SULPHONYL) GLUTAMAMIDE

Author(s): Banerjee Bhaskar | Banerjee Tanushree | Kumar Rajesh | Garg Atul Kumar | Kumar Avanish
MENTAL RETARDATION

Author(s): NAUREEN ASLAM KHATTAK | ABIDA RAZA | MUZAMMIL AHMAD KHAN
Síndrome biopercular: presentación de dos casos y revisión de la literatura Biopercular syndrome: report of two cases and literature review

Author(s): Carlos Santiago Uribe | Paula Andrea Millán | María Isabel Montes | Dagoberto Cabrera | Alejandra Arboleda
ORAL FEATURES IN CORNELIA DE LANGE SYNDROME

Author(s): Ambika L | Raghavendra B. Nayak
Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report

Author(s): Krgovic Danijela | Marcun Varda Natasa | Zagorac Andreja | Kokalj-Vokac Nadja
Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations

Author(s): Ravn Kirstine | Roende Gitte | Duno Morten | Fuglsang Kathrine | Eiklid Kristin | Tümer Zeynep | Nielsen Jytte | Skjeldal Ola
Identification and characterization of a set of conserved and new regulators of cytoskeletal organization, cell morphology and migration

Author(s): Bai Siau | Herrera-Abreu Maria | Rohn Jennifer | Racine Victor | Tajadura Virginia | Suryavanshi Narendra | Bechtel Stephanie | Wiemann Stefan | Baum Buzz | Ridley Anne
De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation

Author(s): S Aswini | Padmalatha Venkata | G Saranya | T Durgadatta | T Raseswari | Kulashekaran Kanakavalli | J Meena | N Chandra | S Lalji | Kandukuri Lakshmi
Prolonged-release melatonin versus placebo for benzodiazepine discontinuation in patients with schizophrenia: a randomized clinical trial - the SMART trial protocol

Author(s): Baandrup Lone | Fagerlund Birgitte | Jennum Poul | Lublin Henrik | Hansen Jane | Winkel Per | Gluud Christian | Oranje Bob | Glenthoj Birte
New Dystrophin/Dystroglycan interactors control neuron behavior in Drosophila eye

Author(s): Marrone April | Kucherenko Mariya | Rishko Valentyna | Shcherbata Halyna
Johanson-Blizzard syndrome

Author(s): Nabeel Almashraki | Mukarram Zainuddin Abdulnabee | Maja Sukalo | Abdullah Alrajoudi | Iman Sharafadeen | Martin Zenker
The effect of eye - hand coordination activities on hand skills of educable mental retarded students (7-10 years)

Author(s): Hadian M.R | Mortazavi S | Abdolvahab | M | Bagheri H Jalili; M.
Cornelia De Lange Syndrome: A Case Report

Author(s): Mohammad Yousef Aarabi Moghaddam | Hojatollah Mortezaian | Seyed Reza Miri
SEROEPIDEMIOLOGIC STUDY OF HUMAN TOXOPLASMA INFECTION IN RESIDENTS OF MESHKIN - SHAHR

Author(s): Soltan Mohammad Zadeh M. | Keshavarz H. | Mohebali M. | Holakouie Naieni K. |  Arshi SH.
Tuberous Sclerosis: Multiple Presentations

Author(s): M. Sanei Taheri | M. Noori
Trisomy 13 (Patau Syndrome)

Author(s): Masoud Poureisa
Intracranial Manifestations of Tuberous Sclerosis: A Pictorial Essay

Author(s): M.H Kharrazi | H.R Haghighatkhah | M Noori | M Sanei Taheri
IS THERE ANY ASSOCIATION BETWEEN MATERNAL DEPRESSION AND BIOPHYSICAL PROFILE?

Author(s): M Z Pezeshki | M H Daghighi | M Pourisa | S H Shahin | S Pezeshki | M H Abdkarimi
Phenotypic and Cytogenetic Variety of Pure Partial Trisomy

Author(s): Noruzinia Mehrdad | Lefort Genevieve | Chaze Anne Marie | Puechberty Jacques | Pellestor Franck | Blanchet Patricia | Cacheux Valerie | Sarda Pierre
Appropriate Iodine Nutrition in Iran: 20 Years of Success

Author(s): Hossein Delshad | Ladan Mehran | Fereidoun Azizi
Case finding in integration of Mental Health Services into Primary Health Care System: systematic review of the studies conducted in Iran in recent two decades

Author(s): Banafsheh Gharraee | Seyed Vahid Shariat | Naghmeh Mansouri | Seyed Jafar Bolhari | Reza Yusefi Nouraee | Afarin Rahimi Movaghar
Prevalence of Intestinal Parasitic Infections among Mentally Disabled Children and Adults of Urmia, Iran

Author(s): Kh Hazrati Tappeh | H Mohammadzadeh | R Nejad Rahim | A Barazesh | Sh Khashaveh | H Taherkhani
A Fanconi Anemias Pationt with Bilateral Totall Hearing Loss

Author(s): Dr. Seyed Moosa Sadr Hoseyni | Shahnaz Alamdari | Dr. Azam Alamdari | Dr. Leila Mashali
Stress in Mothers of Hearing Impaired Children Compared to Mothers of Normal and Other Disabled Children

Author(s): Mahnaz Aliakbari Dehkordi | Ali Asghar Kakojoibari | Tayebeh Mohtashami | Soroor Yektakhah
Anesthetic Management of a Pediatric Patient with Arginase Deficiency

Author(s): Abdulkadir Atım | Hüseyin Oğuz Yılmaz | Tuncer Çaycı | Mehmet Emin Orhan
Evaluation of Patients with Tuberculous Meningitis

Author(s): Şefika Elmas Bozdemir | Solmaz Çelebi | Mustafa Hacımustafaoğlu | Deniz Çakır | F. Deniz Aygün | Uğur Çelik | Şahin Sincar | Melek Özdener
Mechanical colonic obstruction secondary to core of the pomegranate

Author(s): Çiğdem Aliosmanoğlu | İbrahim Aliosmanoğlu | Hüseyin Timuçin | Mesut Gül | Akın Önder | Murat Kapan
Mechanical colonic obstruction secondary to core of the pomegranate

Author(s): Çiğdem Aliosmanoğlu | İbrahim Aliosmanoğlu | Hüseyin Timuçin | Mesut Gül | Akın Önder | Murat Kapan
Family Social Status and Dietary Adherence of Patients with Phenylketonuria

Author(s): Mohammadreza Alaei | Gelareh Asadzadeh-Totonchi | Latif Gachkar | Shirin Farivar
Valproic acid inhibits neural progenitor cell death by activation of NF-κB signaling pathway and up-regulation of Bcl-XL

Author(s): Go Hyo | Seo Jung | Kim Ki | Han So | Kim Pitna | Kang Young | Han Seol | Shin Chan | Ko Kwang
Three Supernumerary Marker Chromosomes in a Patient with Developmental Delay, Mental Retardation, and Dysmorphic Features

Author(s): Jie Hu | Suneeta Madan-Khetarpal | Alvaro H. Serrano Russi | Sally Kochmar | Stephanie J. DeWard | Malini Sathanoori | Urvashi Surti
The relation between consanguineous marriage and mental retardation of the offspring

Author(s): Mohhammad H. Nazarabadi | Arman Arghami | Mohsen Ghanbari
Microarray based analysis of an inherited terminal 3p26.3 deletion, containing only the CHL1 gene, from a normal father to his two affected children

Author(s): Cuoco Cristina | Ronchetto Patrizia | Gimelli Stefania | Béna Frédérique | Divizia Maria | Lerone Margherita | Mirabelli-Badenier Marisol | Mascaretti Monica | Gimelli Giorgio
Advanced paternal age is a risk factor for schizophrenia in Iranians

Author(s): Naserbakht Morteza | Ahmadkhaniha Hamid-Reza | Mokri Bahareh | Smith Cassandra
Meta-analysis of heterogeneous Down Syndrome data reveals consistent genome-wide dosage effects related to neurological processes

Author(s): Vilardell Mireia | Rasche Axel | Thormann Anja | Maschke-Dutz Elisabeth | Pérez-Jurado Luis | Lehrach Hans | Herwig Ralf
A canine model of Cohen syndrome: Trapped Neutrophil Syndrome

Author(s): Shearman Jeremy | Wilton Alan
ATRX has a critical and conserved role in mammalian sexual differentiation

Author(s): Huyhn Kim | Renfree Marilyn | Graves Jennifer | Pask Andrew
Opitz trigonocephaly syndrome presenting with sudden unexplained death in the operating room: a case report

Author(s): Travan Laura | Pecile Vanna | Fertz Mariacristina | Fabretto Antonella | Brovedani Pierpaolo | Demarini Sergio | Opitz John
Mutation spectrum of MLL2 in a cohort of kabuki syndrome patients

Author(s): Micale Lucia | Augello Bartolomeo | Fusco Carmela | Selicorni Angelo | Loviglio Maria | Silengo Margherita | Reymond Alexandre | Gumiero Barbara | Zucchetti Federica | D'Addetta Ester | Belligni Elga | Calcagnì Alessia | Digilio Maria | Dallapiccola Bruno | Faravelli Francesca | Forzano Francesca | Accadia Maria | Bonfante Aldo | Clementi Maurizio | Daolio Cecilia | Douzgou Sofia | Ferrari Paola | Fischetto Rita | Garavelli Livia | Lapi Elisabetta | Mattina Teresa | Melis Daniela | Patricelli Maria | Priolo Manuela | Prontera Paolo | Renieri Alessandra | Mencarelli Maria | Scarano Gioacchino | Monica Matteo | Toschi Benedetta | Turolla Licia | Vancini Alessandra | Zatterale Adriana | Gabrielli Orazio | Zelante Leopoldo | Merla Giuseppe
Evaluation of the Patients with Congenital Hypothyroidism: Effect of the National Screening Program Original Article¬

Author(s): Erdal Eren | Halil Sağlam | Aysel Zengin | Yahya Gül | Esra Deniz P. Çakır | Taner Özgür | Ömer Tarım
Dental treatment of twin monozygotic brothers with Fragile X syndrome

Author(s): Flavia Melo Meira | Luis Candido Pinto Silva | Regina Haddad Rezek Ferreira | Roberval Almeida Cruz
Symptom predictors of response to electroconvulsive therapy in older patients with treatment-resistant depression

Author(s): Tominaga K | Okazaki M | Higuchi H | Utagawa I | Nakamura E | Yamaguchi N
Acquisition of Avoidance Responding in the Fmr1 Knockout Mouse

Author(s): Maria G. Valdovinos | Kelly Ippolito | Lauren Nawrocki | Greg Woods
Diagnoses of patients referring to a child and adolescent psychiatry outpatient clinic

Author(s): İbrahim Durukan | Dursun Karaman | Koray Kara | Türker Türker | Ali Evren Tufan | Özhan Yalçın | Koray Karabekiroğlu
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