Citations with the tag: MENTAL retardation
Results 51 - 100
- A terrible thing to waste.
// Discover; Aug99, Vol. 20 Issue 8, p16
Reports on the finding by University of Virginia's physician Richard Guerrant that children who survive diarrhea may be handicapped by reduced intelligence.
- Reviews: Nonfiction.
Holmes, Mary // Book Report; Sep/Oct92, Vol. 11 Issue 2, p61
Reviews the book `Mental Retardation,' by Robert E. Dunbar.
- Book Notes.
Holmes, Mary // Exceptional Parent; Mar2000, Vol. 30 Issue 3, p63
Reviews the book `Mental Retardation in the 21st Century,' edited by Michael L. Wehmeyer and James R. Patton.
- Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations.
Rossi, Elena; Piccini, Flavia; Zollino, Marcella; Neri, Giovanni; Caselli, Desirée; Tenconi, Romano; Castellan, Claudio; Carrozzo, Romeo; Danesino, Cesare; Zuffardi, Orsetta; Ragusa, Angela; Castiglia, Lucia; Galesi, Ornella; Greco, Donatella; Romano, Corrado; Pierluigi, Mauro; Perfumo, Chiara; Rocco, Maia Di; Faravelli, Francesca; Dagna Bricarelli, Franca // Journal of Medical Genetics; Jun2001, Vol. 38 Issue 6, p417
Presents a letter to the editor about the association of cryptic telomeric rearrangements with mental retardation.
- Prevalence of Mutations in X-linked Mental Retardation Genes in Familial Mental Retardation.
Tarpey, Patrick; Fryer, A.; Gecz, J.; Goodship, J.; Partington, M.; Price, S.; Schwartz, C.; Stevenson, R.; Tolmie, J.; Turner, G.; Wooster, R.; Futreal, P. A.; Stratton, M. R.; Raymond, F. L. // Journal of Medical Genetics; Sep2005, Vol. 42, pS18
Presents an abstract of the article "Prevalence of Mutations in X-linked Mental Retardation Genes in Familial Mental Retardation," by Patrick Tarpey, A. Fryer, J. Gecz, J. Goodship, M. Partington, S. Price, C. Schwartz, R. Stevenson, J. Tolmie, G. Turner, R. Wooster, P.A. Futreal, M.R. Stratton,...
- Rubinstein-Taybi Syndrome: Dosage Analysis Using MLPA.
Cook, Ian; Bransfield, K. L.; Bennett, C. P.; Cockburn, D. J.; J. Williams; Taylor, G. R.; Delaney, C. A. // Journal of Medical Genetics; Sep2005, Vol. 42, pS26
Presents an abstract of the article "Rubinstein-Taybi Syndrome: Dosage Analysis Using MLPA," by Ian Cook, K.L. Bransfield, C.P. Bennett, D.J. Cockburn, J. Williams, G.R. Taylor, and C.A. Delaney.
- Kabuki Syndrome: Absence of 8p22-8p23.1 Duplication in Five Arab Children.
Marafie, Makia; Henedi, M. Abo; Bastaki, L.; Abulhasan, S. // Journal of Medical Genetics; Sep2005, Vol. 42, pS44
Presents an abstract of the article "Kabuki Syndrome: Absence of 8p22-8p23.1 Duplication in Five Arab Children," by Makia Marafie, M. Abo Henedi, L. Bastaki, and S. Abulhasan.
- Kabuki Syndrome and Hyperinsulinism - A Report of Two Cases.
Robert, M. L. P.; Turnpenny, P.; Whitehead, M. // Journal of Medical Genetics; Sep2005, Vol. 42, pS51
Presents an abstract of the article "Kabuki Syndrome and Hyperinsulinism - A Report of Two Cases," by M.L.P. Robert, P. Turnpenny, and M. Whiteford.
- Cryptic Subtelomeric Rearrangements in Children With Mental Retardation and Dysmorphism.
Sousa, Ana Berta; Medeira, A.; Cordeiro, I.; Lemos, R.; Rendeiro, P.; Santos, H. G. // Journal of Medical Genetics; Sep2005, Vol. 42, pS56
Presents an abstract of the article "Cryptic Subtelomeric Rearrangements in Children With Mental Retardation and Dysmorphism," by Ana Berta Sousa, A. Medeira, I. Cordeiro, R. Lemos, P. Rendeiro, and H. G. Santos.
- Evaluating MLPA for Use in Diagnostic Telomere Screening: A Comparison With Commercially Available FISH Kits.
Massie, Doreen; Clark, C.; Grant, F.; Goldie, B.; Gallagher, L.; Couzin, D.; Dean, J. C. S. // Journal of Medical Genetics; Sep2005, Vol. 42, pS75
Presents an abstract of the article "Evaluating MLPA for Use in Diagnostic Telomere Screening: A Comparison With Commercially Available FISH Kits," by Doreen Massie, C. CLark, F. Grant, B. Goldie, L. Gallagher, D. Couzin, and J. C. S. Dean.
- High-Throughput Screening Service for Submicroscopic Genomic Imbalance.
Joo Wook Ahn; Hallam, A.; Ogilvie, C. Mackie; Mann, K. // Journal of Medical Genetics; Sep2005, Vol. 42, pS76
Presents an abstract of the article "High-Throughput Screening Service for Submicroscopic Genomic Imbalance," by Joo Wook Ahn, A. Hallam, C. Mackie Ogilvie, and K. Mann.
- Analysis of Subtelomeric Rearrangements Using MLPA in Patients With Mental Retardation, a Comparison With FISH.
Delaney, Carol A.; Mavrogiannis, L.; Morris, S. P.; Roberts, P.; Cockburn, D. J.; Williams, J.; Taylor, G. R. // Journal of Medical Genetics; Sep2005, Vol. 42, pS86
Presents an abstract of the article "Analysis of Subtelomeric Rearrangements Using MLPA in Patients With Mental Retardation, a Comparison With FISH," by Carol A. Delaney, L. Mavrogiannis, S. P. Morris, P. Roberts, D. J. Cockburn, J. Williams, and G. R. Taylor.
- The Emerging 22q11 Duplication Syndrome: Two Familial Cases.
Carolina, Irene; Geddes, N.; Sibbald, J.; Larkins, S. A.; Davison, E. V. // Journal of Medical Genetics; Sep2005, Vol. 42, pS87
Presents an abstract of the article "The Emerging 22q11 Duplication Syndrome: Two Familial Cases," by Irene Carolina, N. Geddes, J. Sibbald, S. A. Larkins, and E. V. Davison.
- First in vivo evidence of microRNA-induced fragile X mental retardation syndrome.
Lin, S-L.; S-Je Chang; Ying, S-Y. // Molecular Psychiatry; Jul2006, Vol. 11 Issue 7, p616
A letter to the editor is presented in response to the article on micro-RNA-induced fragile X mental retardation syndrome published in a previous issue of the periodical.
- Breaking the silence in Rett syndrome.
Willard, Huntington F; Hendrich, Brian D // Nature Genetics; Oct99, Vol. 23 Issue 2, p127
Comments on an article on the genetics of Rett syndrome (RTT), published in the October 1999 issue of 'Nature Genetics.' Presence of several mutations in MECP2 in a proportion of RTT patients; Identification of RTT as one of growing number of human diseases involving abnormal chromatin assembly.
- The optimal time to clamp the umbilical cord.
Morley, G. M. // Archives of Disease in Childhood -- Fetal & Neonatal Edition; Jan2008, Vol. 93 Issue 1, pF77
A letter to the editor is presented in response to the article on the connection between immediate cord clamping (ICC) to childhood mental retardation (MR) that was published in the previous issue.
- Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
Sismani, Carolina; Armour, John AL; Flint, Jonathan; Girgalli, Christina; Regan, Regina; Patsalis, Philippos C // European Journal of Human Genetics; Jul2001, Vol. 9 Issue 7, p527
Subtelomeric chromosomal abnormalities are emerging as an important cause of human genetic disorders. The scope of this investigation was to screen a selected group of children with idiopathic mental retardation for subtelomeric anomalies using the multiprobe telomeric FISH method and also to...
- The Changing Prevalence of Autism in California.
Croen, Lisa A.; Grether, Judith K.; Hoogstrate, Jenny; Selvin, Steve // Journal of Autism & Developmental Disorders; Jun2002, Vol. 32 Issue 3, p207
We conducted a population-based study of eight successive California births cohorts to examine the degree to which improvements in detection and changes in diagnosis contribute to the observed increase in autism prevalence. Children born in 1987-1994 who had autism were identified from the...
- INTERNATIONAL SCHOOL OF NEUROLOGICAL SCIENCES.
Croen, Lisa A.; Grether, Judith K.; Hoogstrate, Jenny; Selvin, Steve // Journal of Child Neurology; Jul2002, Vol. 17 Issue 7, p528
Presents information on several topics related to advances in the field of behavioral neurogenetics discussed in the 12th annual meeting of the Child Neurology Section of International School of Neurological Sciences held in Rome, Italy from September 27-28, 2002. Techniques for the genetic...
- Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.
Basel-Vanagaite, L.; Alkelai, A.; Straussberg, R.; Magal, N.; Inbar, D.; Mahajna, M.; Shohat, M. // Journal of Medical Genetics; Oct2003, Vol. 40 Issue 10, p729
Objective: To identify and clinically evaluate four consanguineous families of Israeli Arab origin with nonsyndromic mental retardation (NSMR), comprising a total of 10 affected and 24 unaffected individuals. Participants and methods: All the families originated from the same small village and...
- An interaction of instructions and training design on stimulus class formation: Extending the...
Saunders, Kathryn J.; Saunders, Richard R. // Psychological Record; Fall93, Vol. 43 Issue 4, p725
Describes the results of studies designed to investigate variables that might influence the greater effectiveness of the comparison-as-node (CaN) procedure on subjects with mild mental retardation. Discrimination analysis of sample-as-node and CaN procedures; Role of instructions.
- New developments in the fragile X syndrome.
Moore, D.W. York // BMJ: British Medical Journal (International Edition); 7/25/92, Vol. 305 Issue 6847, p208
Focuses on the characteristics of fragile X syndrome. Form of familial mental retardation; Expression of the fragile X mutation; Diagnosis of the disease.
- Behavior in early treated phenylketonuria: a systemic review.
Smith, Isabel; Knowles, Julie // European Journal of Pediatrics. Supplement; 2000, Vol. 159, pS89
Presents a study which reviewed the published information on phenylketonuria in terms of behavior, psychiatric status and individual's perceptions of self, thoughts and feelings. Methods used to assess behavior in selected studies; Results of the study; Conclusions.
- Comments on the international collaborative study of maternal phenylketonuria status report 1998.
Lee, Philip J. // European Journal of Pediatrics. Supplement; 2000, Vol. 159, pS161
Comments on the international collaborative study of maternal phenylketonuria status report in 1998. Diet restriction of study participants.
- Summary of the roundtable discussion.
Burgard, Peter; Link, Reinhild; Schweitzer-Krantz, susanne // European Journal of Pediatrics. Supplement; 2000, Vol. 159, pA163
Presents a summary of reports on phenylketonuria patients during a roundtable and a general discussion. Cognition and intelligence of the patients; Behavior and academic achievements of patients; Neuropathology of mental retardation; Compliance of the patients in diet therapy.
- Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation.
Schlotawa, Lars; Hotz, Alrun; Zeschnigk, Christine; Hartmann, Britta; Gärtner, Jutta; Morris-Rosendahl, Deborah // Journal of Neurology; Jun2013, Vol. 260 Issue 6, p1678
A letter to the editor is presented in which the authors discuss a case study of a male patient born to German parents who was diagnosed with cerebellar ataxia, mental retardation and dysequillibrium syndrome 1.
- Ability of institutionalized and community-based adults with retardation to respond to questions...
Brinton, Bonnie; Fujiki, Martin // Journal of Speech & Hearing Research; Apr94, Vol. 37 Issue 2, p369
Examines the ability of adults with mild and moderate levels of retardation to respond to simple and complex questions. Background history on residential placement for individuals with mental retardation; Use of a conversational language sample; Scoring procedures; Analysis of variance with...
- Facial and digital clues.
Brinton, Bonnie; Fujiki, Martin // Patient Care; 1/30/1999, Vol. 32 Issue 2, p125
Presents a case report of a six-year-old white girl with mental and growth deficiencies and physical abnormalities. Lack of recognizable language; History of urinary tract infections in the mother and grandmother; Consistency of the physical findings with the description for Coffin-Siris syndrome.
- The Behavioral Profile of Severe Mental Retardation in a Genetic Mouse Model of Phenylketonuria.
Cabib, Simona; Pascucci, Tiziana; Ventura, Rossella; Romano, Valentino; Puglisi-Allegra, Stefano // Behavior Genetics; May2003, Vol. 33 Issue 3, p301
Pah[sup enu2] mice, created by chemically induced genetic mutation, are characterized by biochemical phenotypes closely resembling untreated human phenylketonuria (PKU). However, studies conducted in adult Pah[sup enu2] mice have shown no indices of the severe mental retardation that...
- Questionable pathogenicity of FOXG1 duplication.
Amor, David J; Burgess, Trent; Tan, Tiong Y; Pertile, Mark D // European Journal of Human Genetics; Jun2012, Vol. 20 Issue 6, p595
A letter commenting on researcher N. Brunetti-Pierri and colleagues report "Duplications of FOXG1 in 14q12 Are Associated With Developmental Epilepsy, Mental Retardation, and Severe Speech Impairment," published in the "Europen Journal of Human Genetics" is presented.
- Rattled with PTSD: Post Traumatic Snake Disorder.
Monroe, Irene // Bay Windows; 7/4/2013, Vol. 31 Issue 30, p6
The article presents the author's views on post traumatic snake disorder.
- Let's get rid of the 'R' word.
Clark, Karen Fox // St. Charles Journal; 8/21/2011, Vol. 46 Issue 67, pA7
In this article, the author discusses about the life of people with learning difficulties.
- Leg Strength Is Related to Endurance Run Performance in Children and Adolescents With Mental Retardation.
Fernhall, Bo; Pitetti, Kenneth H. // Pediatric Exercise Science; Aug2000, Vol. 12 Issue 3, p324
Evaluates the interrelation between leg strength and endurance run performance in children and adolescents with mental retardation. Influence of gender on leg strength and endurance; Dependence of endurance run performance on maximal oxygen consumption; Improvement in endurance through strength...
- Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males.
Poirier, Karine; Francis, Fiona; Hamel, Ben; Moraine, Claude; Fryns, Jean Pierre; Ropers, Hans H.; Chelly, Jamel; Bienvenu, Thierry // European Journal of Human Genetics; May2005, Vol. 13 Issue 5, p523
Presents a letter to the editor about the association of mutations in exon 1 of MECP2B gene with X-linked mental retardation in males.
- Inborn Errors in Folate Metabolism--A Cause of Mental Retardation?
Herbert, Victor // Annals of Internal Medicine; Apr68, Vol. 68 Issue 4, p956
Editorial. Speculates on the association of inborn errors in folate metabolism with mental retardation. Overview of three cases of congenital cyclohydrolase deficiency, manifested by mental retardation with microcephaly, hyperfolatemia without formiminoglutamate in the urine; Suggestion of...
- Deciphering mental retardation.
Herbert, Victor // U.S. News & World Report; 6/10/91, Vol. 110 Issue 22, p15
Details some recent research into the gene that causes `fragile X syndrome,' the most common inherited form of mental retardation. Developing a fail-safe test for the syndrome, that would help prevent misdiagnosis of mental defects.
- INCIDENCE OF SAVANT SYNDROME IN FINLAND.
Saloviita, Timo; Ruusila, Liisa // Perceptual & Motor Skills; Aug2000, Vol. 91 Issue 1, p120
Explores the incidence of Savant Syndrome in Finland. Survey of facilities in Finland which served people with mental retardation; Relative frequency of types of exceptional skills, the most common form of which was calendar calculation and feats of memory.
- New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation.
Tsukahara, M.; Sugio, Yoshitsugu // Journal of Human Genetics; 1998, Vol. 43 Issue 4, p224
Abstract We report on three brothers, aged 6, 3, and 2 years, with a hitherto undescribed combination of microcephaly, facial abnormalities, micromelia, and mild mental retardation. Their facial abnormalities included a forehead with bitemporal constriction, upslanting palpebral fissures,...
- MULTIPLE DISORDERS IN PEOPLE WITH MILD AND HARD MENTAL RETARDATION AND THEIR INFLUENCE ON PSYCHOMOTOR ORGANIZATION.
Mishovska-Stojkovska, Tanja // Journal of Special Education & Rehabilitation; 2007, Issue 3/4, p131
The issue of the multiple disabilities is as old as the existence of the man. But the awareness of the problem about existence of the people with multiple disabilities and also finding the methods, means and ways of tuition, education and rehabilitation is relatively new and appears in the...
- The Clinical Significance of DG Heterozygosity: Literature Review and Meta-Analysis.
Creswick, H.; Barnes, M.; Lawson, L.; Proud, V. // Journal of Genetic Counseling; Dec2002, Vol. 11 Issue 6, p494
Discusses the abstract of the study 'The Clinical Significance of DG Heterozygosity: Literature Review and Meta-Analysis,' presented at the 21st Annual Education Conference of the National Society of Genetic Counselors held in Phoenix, Arizona in November 2002.
- Corrigendum: Lamin B1 duplications cause autosomal dominant leukodystrophy.
Padiath, Quasar S; Saigoh, Kazumasa; Schiffmann, Raphael; Asahara, Hideaki; Yamada, Takeshi; Koeppen, Anulf; Hogan, Kirk; Ptáček, Louis J; Fu, Ying-Hui // Nature Genetics; Feb2007, Vol. 39 Issue 2, p276
A correction to the article on Lamin B1 duplications as the cause of autosomal dominant leukodystrophy is presented.
- MENTAL RETARDATION.
Spencer, D. A. // British Journal of Psychiatry; Jan70, Vol. 116 Issue 530, p127
A letter to the editor is presented in response to the adoption of the term mental retardation.
- Corrigendum: Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome).
Zenker, Martin; Mayerle, Julia; Lerch, Markus M; Tagariello, Andreas; Zerres, Klaus; Durie, Peter R; Beier, Matthias; Hülskamp, Georg; Guzman, Celina; Rehder, Helga; Beemer, Frits A; Hamel, Ben; Vanlieferinghen, Philippe; Gershoni-Baruch, Ruth; Vieira, Marta W; Dumic, Miroslav; Auslender, Ron; Gil-da-Silva-Lopes, Vera L; Steinlicht, Simone; Rauh, Manfred // Nature Genetics; Feb2006, Vol. 38 Issue 2, p265
A correction to the article "Deficiency of UBR1: A Ubiquitin Ligase of the N-End Rule Pathway, Causes Pancreatic Dysfunction, Malformations and Mental Retardation," previously published in the article is presented.
- Identification and Evaluation of Mental Retardation.
Daily, Donna K.; Ardinger, Holly H.; Holmes, Grace E. // American Family Physician; 2/15/2000, Vol. 61 Issue 4, p1059
Provides information on mental retardation in young children. Prevalence; Etiology; Developmental characteristics related to level of mental retardation.
- MENTAL RETARDATION RESEARCH, ECOLOGICAL VALIDITY, AND THE DELIVERY OF LONGITUDINAL EDUCATION PROGRAMS.
Gaylord-Ross, Robert J. // Journal of Special Education; Spring79, Vol. 13 Issue 1
Discusses the schism that has developed between mental retardation research and the programmatic reform activities taking place in the educational and residential sectors. Principles for conducting ecologically valid research; Scientific status of mental retardation research; Examples of...
- AN INTERNATIONAL PERSPECTIVE ON TERMINOLOGY, PREVALENCE, AND CLASSIFICATION OF COGNITIVE DISABILITIES.
Holowinsky, Ivan Z. // Journal of Special Education; Fall86, Vol. 20 Issue 3
Provides some international perspective on the terminology, prevalence and classification of cognitive disabilities. Inclusion of intellectual abnormality, mental retardation, mental deficiency and oligophrenia in the term 'cognitive disabilities'; Factors influencing terminology development in...
- Nutrition and the brain.
Holowinsky, Ivan Z. // British Medical Journal; 6/17/1978, Vol. 1 Issue 6127, p1569
Examines the correlation between nutrition and brain functions. Reduction of human achievement following nutritional growth restriction; Association of mental retardation with malnutrition; Physical basis of mental function.
- Cerebral hemi atrophy as a consequence of cerebral insult in infancy: Is it difficult to diagnose?
Saldanha, Daniel; Chaudhari, Bushan; Mehta, Suresh Kumar; Javadekar, Archana Narender; Kharat, Amit // Industrial Psychiatry Journal; Jan-Jun2014, Vol. 23 Issue 1, p71
A letter to the editor is presented in response to the article related to case studies of hemi paresis, seizures and mental retardation in the previous issue.
- From the Editor.
Hessels, Marco G. P. // Journal of Cognitive Education & Psychology; 2012, Vol. 11 Issue 1, p1
An introduction is presented in which the editor discusses various reports within the issue on topics including intellectual and developmental disabilities, mental retardation, and genetic syndromes.
- BECOMING WHOLE.
McGraw, Caroline // Ability; Apr/May2013, p58
A personal narrative is presented which explores the author's experience of a would-be childhood paleontologists who digs for treasure in people with autism and intellectual disabilities.