Bibliografie tematiche / Genetic disorders in children

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Letteratura scientifica selezionata sul tema "Genetic disorders in children"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 29 luglio 2024

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Articoli di riviste sul tema "Genetic disorders in children"

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Ćirić, Sanela. "DIFFERENCES IN PARENTS' ATTITUDES TOWARDS THE CAUSES OF NEURODEVELOPMENTAL DISORDERS." Multidisciplinarni Pristupi u Edukaciji i Rehabilitaciji 6, no. 7 (August 15, 2024): 161–70. http://dx.doi.org/10.59519/mper6115.

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Abstract (sommario):
Neurodevelopmental disorders are a heterogeneous group of clinical conditions characterized by deficits in one or more aspects of development, with the most prevalent subgroups being autism spectrum disorders and intellectual developmental disorders. Longitudinal studies have shown a significant increase in the number of children with autism spectrum disorders over the past few decades compared to the stable prevalence of intellectual developmental disorders. The aim of this study was to examine and compare the attitudes of parents of children with autism spectrum disorders and parents of chil
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Fisch, Gene S., Nancy Carpenter, Patricia N. Howard-Peebles, Jeanette J. A. Holden, Jack Tarleton, Richard Simensen, and Agatino Battaglia. "Developmental Trajectories in Syndromes With Intellectual Disability, With a Focus on Wolf-Hirschhorn and Its Cognitive–Behavioral Profile." American Journal on Intellectual and Developmental Disabilities 117, no. 2 (February 1, 2012): 167–79. http://dx.doi.org/10.1352/1944-7558-117.2.167.

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Abstract Few studies exist of developmental trajectories in children with intellectual disability, and none for those with subtelomeric deletions. We compared developmental trajectories of children with Wolf-Hirschhorn syndrome to other genetic disorders. We recruited 106 children diagnosed with fragile X, Williams-Beuren syndrome, or Wolf-Hirschhorn syndrome, assessing their intellectual and adaptive behavior abilities. We retested 61 children 2 years later. We compared Time 1 and Time 2 difference scores related to genetic disorder, age, initial IQ, or adaptive behavior composite. Results sh
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Lashwood, Alison. "Preimplantation genetic diagnosis to prevent genetic disorders in children." British Journal of Nursing 14, no. 2 (January 2005): 64–70. http://dx.doi.org/10.12968/bjon.2005.14.2.17433.

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Barrie, Alpha-Umaru. "Youth perspectives on genetic inheritance, carrier status and disclosure." Journal of Haemophilia Practice 3, no. 2 (July 1, 2016): 21–28. http://dx.doi.org/10.17225/jhp00077.

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Abstract Knowledge about genetic inheritance as a concept in children and young people with bleeding disorders is synonymous, in many ways, with other inherited genetic conditions. Children and young people have a more physiological understanding of inheritance, but may hold mistaken and inaccurate beliefs in understanding basic genetics. There are complex ethical and social problems in the genetic testing of youngsters with bleeding disorders to establish carrier status. Current guideline recommendations indicate circumstances where clear psychosocial and medical benefits can be demonstrated.
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Rudin, I. V. "SPEECH DISORDERS OF GENETIC ORIGIN IN TEACHING PRACTICE." Education & Pedagogy Journal, no. 1(1) (July 6, 2021): 56–63. http://dx.doi.org/10.23951/2782-2575-2021-1-56-63.

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Abstract (sommario):
In recent years, there has been a significant increase in children with various speech disorders. Also, identifying the factors causing these disorders early and providing proper support is increasingly important. If the steps to correct such speech disorders are not taken quickly, secondary issues, such as communication, socialization, and educational problems, are observed. Training and corrective measures should be carried out while considering both the individual’s psychological and physiological characteristics. Identifying the cause and symptoms of a speech disorder plays an important ro
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Mueller, Sven C., Pamela Ng, Ninet Sinaii, Ellen W. Leschek, Liza Green-Golan, Carol VanRyzin, Monique Ernst, and Deborah P. Merke. "Psychiatric characterization of children with genetic causes of hyperandrogenism." European Journal of Endocrinology 163, no. 5 (November 2010): 801–10. http://dx.doi.org/10.1530/eje-10-0693.

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ObjectiveVery little is known about the mental health status in children with genetic causes of hyperandrogenism. This study sought to characterize psychiatric morbidity in this group.Design/methodsChildren (8–18 years) with the diagnosis of classic congenital adrenal hyperplasia (CAH) or familial male precocious puberty (FMPP) underwent a semi-structured psychiatric interview, the Kiddie Schedule for Affective Disorders and Schizophrenia-Present and Lifetime Version. According to sex and the literature, incidence of identified psychopathology was compared between the two endocrinological grou
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Zhestkova, M. A., and D. Yu Ovsyannikov. "GENETIC DISORDERS OF SURFACTANT PROTEINS." Pediatria. Journal named after G.N. Speransky 100, no. 5 (October 11, 2021): 82–89. http://dx.doi.org/10.24110/0031-403x-2021-100-5-82-89.

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The literature review provides up-to-date information on rare interstitial lung diseases, manifesting both in children, starting from the neonatal period, and in adults, – genetic disorders of surfactant proteins B, C, ATP-binding cassette protein A3 (ABCA3), manifested by such histopathological patterns, as chronic pneumonitis of infants, pulmonary alveolar proteinosis, desquamative interstitial pneumonia , nonspecific interstitial pneumonia. Information on epidemiology, genetics, pathogenesis, clinical picture, diagnosis and differential diagnosis, treatment of these diseases is given.
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You, Haizhen, Junyao Shi, Fangfang Huang, Zhiyun Wei, Gary Jones, Wenchong Du, and Jing Hua. "Advances in Genetics and Epigenetics of Developmental Coordination Disorder in Children." Brain Sciences 13, no. 6 (June 11, 2023): 940. http://dx.doi.org/10.3390/brainsci13060940.

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Developmental coordination disorder (DCD) is a developmental disorder characterized by impaired motor coordination, often co-occurring with attention deficit disorder, autism spectrum disorders, and other psychological and behavioural conditions. The aetiology of DCD is believed to involve brain changes and environmental factors, with genetics also playing a role in its pathogenesis. Recent research has identified several candidate genes and genetic factors associated with motor impairment, including deletions, copy number variations, single nucleotide polymorphisms, and epigenetic modificatio
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Pletcher, Beth A., and Nelson L. Turcios. "Pulmonary Manifestations of Genetic Disorders in Children." Pediatric Clinics of North America 68, no. 1 (February 2021): 1–24. http://dx.doi.org/10.1016/j.pcl.2020.09.010.

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Clauss, Sarah B., and Peter O. Kwiterovich. "Genetic disorders of lipoprotein transport in children." Progress in Pediatric Cardiology 17, no. 2 (September 2003): 123–33. http://dx.doi.org/10.1016/s1058-9813(03)00049-3.

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Tesi sul tema "Genetic disorders in children"

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Robinson, Sally Jane. "Semantic knowledge representation and access in children with genetic disorders." Thesis, University of Essex, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.435580.

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Bava, Sunita. "Reduced microstructural white matter integrity in a genetic metabolic disorder a diffusion tensor MRI study /." Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 2007. http://wwwlib.umi.com/cr/ucsd/fullcit?p3274808.

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Abstract (sommario):
Thesis (Ph. D.)--University of California, San Diego and San Diego State University, 2007.<br>Title from first page of PDF file (viewed January 8, 2008). Available via ProQuest Digital Dissertations. Vita. Includes bibliographical references (p. 75-84).
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Glass, Jennifer Elaine. "CURRENT PRACTICES OF PEDIATRICIANS REGARDING SCREENING FOR METABOLIC DISORDERS AMONG INTERNATIONALLY ADOPTED CHILDREN." Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1244084138.

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Ichikawa, Shoji. "The molecular genetic analysis of three human neurological disorders." free online free to MU campus, others may purchase, 2002. http://wwwlib.umi.com/cr/mo/preview?3074409.

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Winslow, Hayley R. "Pre- and Post-Test Parent Perceptions of Genetic Testing for Children with Autism Spectrum Disorder (ASD)." The Ohio State University, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492505122437373.

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Komulainen-Ebrahim, J. (Jonna). "Genetic aetiologies and phenotypic variations of childhood-onset epileptic encephalopathies and movement disorders." Doctoral thesis, Oulun yliopisto, 2019. http://urn.fi/urn:isbn:9789526222356.

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Abstract Novel genetic aetiologies for epileptic encephalopathies and movement disorders have been discovered by using next-generation sequencing methods. The phenotypic and genotypic variability in these conditions is very wide. The aim of this study was to discover novel genetic causes and phenotypes of childhood-onset drug-resistant epilepsy and epileptic or developmental encephalopathies that occur separately or together with movement disorders, and familial movement disorders. Furthermore, the use of whole-exome sequencing (WES) as a diagnostic tool in clinical practice was evaluated. Alt
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Gaonkar, Shraddha. "Challenges in counseling for rare chromosome conditions genetic counselors' perspective /." Waltham, Mass. : Brandeis University, 2009. http://dcoll.brandeis.edu/handle/10192/23239.

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Carlisle, Kathleen Walker. "School Factors Related to the Social and Behavioral Success of Children and Adolescents with Tuberous Sclerosis: Special Education Placement, Services, and Parental Involvement." [Tampa, Fla.] : University of South Florida, 2003. http://purl.fcla.edu/fcla/etd/SFE0000154.

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Kovac, Ilija. "Genetic epidemiology and phenotypic resolution of complex traits : studies in specific language impairment and alcoholism." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=36974.

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Rationale. Definition of complex behavioral disorders is generally phenomenological in nature and guided by pragmatic, rather than genetic, concerns. Consequently, important aspect of genetic analysis is the search for novel phenotypic definitions from the familial/genetic perspective. SLI study 1. SLI denotes an inability to acquire normal language in the absence of peripheral hearing impairment, neurological disorder, and mental retardation. Sibling resemblance for several theoretically derived specific components of the SLI phenotype was examined in families of SLI children. In 38 sib-pairs
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Holt, Erika Tyne. "Perceptions of Severity of Children's Bleeding Disorders: Impact on Parental Quality of Life and Reproductive Decisions." Case Western Reserve University School of Graduate Studies / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=case1383060340.

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Libri sul tema "Genetic disorders in children"

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Manes, Singer Sandra, and Pauls David L, eds. The heredity of behavior disorders in adults and children. New York: Plenum Medical Book Co., 1986.

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Baker-Gomez, Sherry. Missing genetic pieces: Strategies for living with VCFS, the chromosome 22q11 deletion. Phoenix, Ariz: Desert Pearl Pub., 2004.

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J, Epstein Charles, Erickson Robert P. 1939-, and Wynshaw-Boris Anthony Joseph, eds. Inborn errors of development: The molecular basis of clinical disorders of morphogenesis. Oxford: Oxford University Press, 2004.

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Lipsanen-Nyman, Marita. Mulibrey-nanismi. Helsinki: Helsingin yliopistollisen keskussairaalan ja Helsingin yliopiston I lastentautien klinikka, 1986.

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J, Epstein Charles, Erickson Robert P. 1939-, and Wynshaw-Boris Anthony Joseph, eds. Inborn errors of development: The molecular basis of clinical disorders of morphogenesis. 2nd ed. Oxford: Oxford University Press, 2008.

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Gilbert, Patricia. The A-Z reference book of syndromes and inherited disorders. 2nd ed. San Disgo, Calif: Singular Pub. Group, 1996.

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Blum, Laurie. Laurie Blum's Free money for childhood behavioral and genetic disorders. New York: Simon & Schuster, 1992.

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K, Lloyd June, and Scriver Charles R, eds. Genetic and metabolic disease in pediatrics. London: Butterworths, 1985.

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C, McCabe Paul, Shaw Steven R, and National Association of School Psychologists., eds. Genetic and acquired disorders: Current topics and interventions for educators. Thousand Oaks, Calif: Corwin Press, 2010.

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Oliver, Quarrell, ed. Juvenile Huntington's disease: (and other trinucleotide repeat disorders). Oxford: Oxford University Press, 2009.

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Capitoli di libri sul tema "Genetic disorders in children"

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Nicoll, Neil. "Genetic and chromosomal disorders." In Assessment and Diagnosis of Neurodevelopmental Disorders in Young Children, 32–39. London: Routledge, 2021. http://dx.doi.org/10.4324/9781003169925-3.

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Mitchell, Jonathan A., and Christopher M. Cielo. "Genetic Studies of Sleep in Children." In Genetics of Sleep and Sleep Disorders, 437–57. Cham: Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-62723-1_17.

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Nicoll, Neil. "Selected genetic and chromosomal disorders." In Assessment and Diagnosis of Neurodevelopmental Disorders in Young Children, 40–55. London: Routledge, 2021. http://dx.doi.org/10.4324/9781003169925-4.

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Witt, H. "Gene Mutations in Children with Chronic Pancreatitis." In Genetic Disorders of the Exocrine Pancreas, 23–29. Basel: KARGER, 2002. http://dx.doi.org/10.1159/000070339.

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Lai-Cheong, Joey E., and Amy S. Paller. "Current and Novel Approaches for Genetic Skin Disorders." In Severe Skin Diseases in Children, 189–202. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39532-1_11.

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Depositario-Cabacar, Dewi Frances T., William McClintock, and Tom Reehal. "Common Genetic and Neurocutaneous Disorders in Childhood Epilepsy." In Epilepsy in Children and Adolescents, 59–72. Chichester, UK: John Wiley & Sons, Ltd, 2012. http://dx.doi.org/10.1002/9781119998600.ch4.

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Bonduelle, Maryse, Ayse Aytoz, Ann Wilikens, Andrea Buysse, Elvire Van Assche, Paul Devroey, Andre Van Steirteghem, and Inge Liebaers. "Genetic Problems and Congenital Malformations in 1987 ICSI Children." In Male Sterility and Motility Disorders, 282–97. New York, NY: Springer New York, 1999. http://dx.doi.org/10.1007/978-1-4612-1522-6_26.

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Pf�ffle, R. "Diagnosis of Endocrine Disorders with Molecular Genetic Methods." In Diagnostics of Endocrine Function in Children and Adolescents, 30–50. Basel: KARGER, 2003. http://dx.doi.org/10.1159/000073543.

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McDuffie, Andrea, Angela John Thurman, Marie Moore Channell, and Leonard Abbeduto. "Language Disorders in Children with Intellectual Disability of Genetic Origin." In Handbook of Child Language Disorders, 52–81. New York, NY : Routledge, 2017.: Psychology Press, 2017. http://dx.doi.org/10.4324/9781315283531-2.

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Russell, Jo. "Genesis of a dissociative child." In Treating Children with Dissociative Disorders, 139–54. London: Routledge, 2021. http://dx.doi.org/10.4324/9781003246541-10.

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Atti di convegni sul tema "Genetic disorders in children"

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Nayır Büyükşahin, H., N. Emiralioglu, P. O. Simsek Kiper, B. Sunman, I. Güzelkaş, D. Alboğa, M. Akgül Erdal, et al. "Evaluation of polysomnography findings in children with genetic skeletal disorders." In ERS International Congress 2022 abstracts. European Respiratory Society, 2022. http://dx.doi.org/10.1183/13993003.congress-2022.526.

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PONOMARI, Dorina. "Speech therapy assistance in the context of genetic disorders." In Ştiință și educație: noi abordări și perspective. "Ion Creanga" State Pedagogical University, 2023. http://dx.doi.org/10.46727/c.v1.24-25-03-2023.p179-184.

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Abstract (sommario):
Language presents a complex psychic process and many negative factors can affect it in its evolutionary path. These factors can be external psychosocial but also internal. Genetic disorders can mark to a greater or lesser extent the phenotype of the child with impact on the central nervous system and the speech apparatus. Children with some genetic conditions have difficulties in language development and often need speech therapy assistance, however early speech therapy intervention given at an early age will improve language development.
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Voinova, V. Y., M. A. M.A., O. S. Grosnova, and S. V. Bochenkov. "Syndromic Forms of Children’s Mental Development Disorders." In Proceedings of III Research-to-Practice Conference with International Participation “The Value of Everyone. The Life of a Person with Mental Disorder: Support, Life Arrangements, Social Integration”. Terevinf, 2023. http://dx.doi.org/10.61157/978-5-4212-0676-7-2023-68-72.

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The molecular genetic basis of autism spectrum disorders (ASD) was analyzed in a cohort of more than 4,000 Russian patients with hereditary diseases. 88 children in the examined cohort had genetic variants, probably pathogenic or pathogenic, in genes associated with the development of ASD. Whole genome sequencing revealed 114 different molecular events that could be the cause of their disease. 60% of molecular events are annotated as variants of unclear clinical significance. The greatest number of variants was found in the CHD8 gene. Pathogenic variants in this gene are considered one of the
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Brew, Bronwyn, Tong Gong, Cecilia Lundholm, Henrik Larsson, and Catarina Almqvist. "Is there a genetic association between atopic disease and internalizing disorders in children?" In ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.oa503.

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García-Vélez, Roberto, Luis Serpa-Andrade, and Graciela Serpa-Andrade. "Information and Communication Technologies Learning Methodologies for Children with ADHD." In 13th International Conference on Applied Human Factors and Ergonomics (AHFE 2022). AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1001889.

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ADHD is a disorder due to attention deficit, impulsiveness and hyperactivity due to various functional disputes, these anatomical brain inconsistencies can be genetic and/or environmental that hinders the child's lifestyle and their environment. Within the educational field, teachers cannot distinguish the attitude of a child with ADHD from one without disorders, especially in the preschool stage, which motivates the search for teaching alternatives, among them we have information and communication technologies - ICT, which allow evaluating, diagnosing, enriching and strengthening the learning
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Guerrero Granda, Steven, Luis Serpa-Andrade, and Luis Guerrero. "Playful strategies to enhance teaching-learning and the inclusion of children with Down syndrome." In 8th International Conference on Human Interaction and Emerging Technologies. AHFE International, 2022. http://dx.doi.org/10.54941/ahfe1002804.

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Abstract (sommario):
Down Syndrome is a genetic disorder characterized by the appearance of an extra chromosome in the human genome, discovered in 1866. This is one of the few genetic disorders where there are other chromosomes that are compatible with life. In Ecuador, Down syndrome occurs in 1 in 550 live births, an average much higher than the world rate of 1 in 700. The phenotypic characteristics that can occur in DS, there are 12 to 14 characteristics, but in each individual, it is presented between 6 to 8 the common ones are epicanthus, rounded head, short stature, coated and protruding tongue, wide and shor
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Nakano, Bruno Eiji, Gabriel Flamarin Cavasana, Paula Carolina Grande Nakazato, Alana Strucker Barbosa, Isabela Badan Fernandes, Eduardo Silveira Marques Branco, Sarah de Souza Chinelato, et al. "Huntington Disease-Like 2: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.494.

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Case presentation: Male, 56-year-old, previously epileptic started with involuntary movements in the right hand at 47 years old evolving to torso, incoordination, behavioral and cognition disturbs. Paternal grandmother, father and cousin with similar symptoms, in addition to four asymptomatic children. From the onset of symptoms, it progressively worsened presenting involuntary movements, hallucinations, aggressiveness and neck drop. During the neurological examination had frequent cervical falls, tremors at rest in the limbs, and mood swings. Cranial magnetic resonance imaging (MRI) was with
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Constantin, Iuliana Luminița, and Marin Chirazi. "Manifestări comportamentale deviante ale elevilor din ciclul primar – în special ale celor cu tulburări din spectrul autist." In Congresul Ştiinţific Internaţional "Sport. Olimpism. Sănătate". State University of Physical Education and Sport, Republic of Moldova, 2022. http://dx.doi.org/10.52449/soh22.11.

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Abstract (sommario):
According to research in the field of ASD, among the triggers of this disorder have been detected so far "those genetic, environmental or neurobiological; these factors play a key role in the manifestation of behavioral symptoms, the latter being the main element by which TSA is diagnosed in many cases” [12]. The bibliographic resources allowed us to know what are the specific behavioral manifestations of children diagnosed with ASD (and with elements from the ADHD sphere), in order to be able to identify concretely among the primary school students where the experiment was performed all those
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Bhaskaran, Smitha, and Pramod Nair. "430 X-linked ichthyosis, an under diagnosed genetic skin disorder in children-case report." In RCPCH Conference Singapore. BMJ Publishing Group Ltd, 2021. http://dx.doi.org/10.1136/bmjpo-2021-rcpch.241.

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Reis, Drielly Tífany Ferreira, Rafaela Rodrigues Pereira, and Rogerio Alves da Silva. "Influence of physiotherapy in the treatment of children with autism spectrum disorder." In II INTERNATIONAL SEVEN MULTIDISCIPLINARY CONGRESS. Seven Congress, 2023. http://dx.doi.org/10.56238/homeinternationalanais-034.

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Abstract (sommario):
Abstract Introduction: The etiology of the disorder is not yet well defined, what is known is that several factors can predispose the child to have autism, which may be genetic and environmental factors, according to scientific evidence. The TEA has three measurement degrees, classified as mild, moderate and severe. It is important that the autistic child and his family have the support of a multidisciplinary team that instructs them to overcome the diagnosis and the current situation in which they find themselves. Based on the characteristics presented by the autistic individual, there is a n
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Rapporti di organizzazioni sul tema "Genetic disorders in children"

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Riley, Catherine, and Kate Wilson. Anaesthesia for Children with Skin Disorders. World Federation of Societies of Anaesthesiologists, August 2024. http://dx.doi.org/10.28923/atotw.530.

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This tutorial explores the provision of anaesthesia for children with skin disorders, which range from mild to life-threatening. The anaesthetist must balance prevention of skin trauma or infection with the provision of safe anaesthesia, including airway and temperature management.
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Andrews, Lori, B. Complex Genetic Disorders and Intellectual Property Rights Final Report. Office of Scientific and Technical Information (OSTI), November 2006. http://dx.doi.org/10.2172/895052.

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Jacobsen, George. Group experience with parents of preschool children with seizure disorders. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2892.

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PELIKHOVA, ANNA. Methodology of health-improving work with preschool children with speech disorders. Science and Innovation Center Publishing House, December 2020. http://dx.doi.org/10.12731/metodika-ozdorovitelnoy-raboty.

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Пособие нацелено на формирование педагогов ДОУ готовности к педагогической деятельности в области здоровьесбережения детей с нарушениями речи, на реализации государственного образовательного стандарта, обогащению профессионального опыта педагогов. Учебно-методическое пособие предназначено для организации учебных занятий в рамках курсовой подготовки и переподготовки педагогов ДОУ по программам: «Педагогическая деятельность в условиях реализации ФГОС ДО» и «Теория и методика воспитания и обучения детей с ОВЗ».
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Wallace, Ina F. Universal Screening of Young Children for Developmental Disorders: Unpacking the Controversies. RTI Press, February 2018. http://dx.doi.org/10.3768/rtipress.2018.op.0048.1802.

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In the past decade, American and Canadian pediatric societies have recommended that pediatric care clinicians follow a schedule of routine surveillance and screening for young children to detect conditions such as developmental delay, speech and language delays and disorders, and autism spectrum disorder. The goal of these recommendations is to ensure that children with these developmental issues receive appropriate referrals for evaluation and intervention. However, in 2015 and 2016, the US Preventive Services Task Force (USPSTF) and the Canadian Task Force on Preventive Health Care issued re
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Shin, Su-Jeong Hwang, Brianna Smith, and Kristi Gaines. Investigation of Therapy Clothing Products for Children with Autism Spectrum Disorders. Ames: Iowa State University, Digital Repository, November 2015. http://dx.doi.org/10.31274/itaa_proceedings-180814-1151.

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Mitcham, Sara. Location of Dyspraxic Characteristics in Children with Severe "Functional" Articulation Disorders. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.2277.

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Andrews, Lori. Ethical and legal issues arising from complex genetic disorders. DOE final report. Office of Scientific and Technical Information (OSTI), October 2002. http://dx.doi.org/10.2172/805433.

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Saini, Ravinder, Syed Altafuddin, Sunil Vaddamanu, Vishwanath Gurumurthy, and Masroor Kanji. The Association Between Genetic Factors and Temporomandibular Disorders: A Systematic Literature Review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2024. http://dx.doi.org/10.37766/inplasy2024.4.0063.

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Ylvisaker, Mark. Rehabilitation of Children and Adults With Cognitive-Communication Disorders After Brain Injury. Rockville, MD: American Speech-Language-Hearing Association, 2003. http://dx.doi.org/10.1044/policy.tr2003-00146.

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