Статті в журналах з теми "Neurogenetic syndrome"
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Harrop, Clare, Aaron R. Dallman, Luc Lecavalier, James W. Bodfish, and Brian A. Boyd. "Behavioral Inflexibility Across Two Neurogenetic Conditions: Down Syndrome and Fragile X Syndrome." American Journal on Intellectual and Developmental Disabilities 126, no. 5 (August 24, 2021): 409–20. http://dx.doi.org/10.1352/1944-7558-126.5.409.
Повний текст джерелаDuis, Jessica. "The Road to Personalized Therapies: Lessons Learned From Angelman Syndrome." American Journal on Intellectual and Developmental Disabilities 127, no. 2 (February 18, 2022): 95–98. http://dx.doi.org/10.1352/1944-7558-127.2.95.
Повний текст джерелаCoppus, Antonia M. W. "Neurogenetic Syndrome: Behavioral Issues and Their Treatment." Journal of Policy and Practice in Intellectual Disabilities 8, no. 2 (June 2011): 139–40. http://dx.doi.org/10.1111/j.1741-1130.2011.00299.x.
Повний текст джерелаBuiting, Karin, Charles Williams, and Bernhard Horsthemke. "Angelman syndrome — insights into a rare neurogenetic disorder." Nature Reviews Neurology 12, no. 10 (September 12, 2016): 584–93. http://dx.doi.org/10.1038/nrneurol.2016.133.
Повний текст джерелаWalter, E., P. K. Mazaika, and A. L. Reiss. "Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome." Neuroscience 164, no. 1 (November 2009): 257–71. http://dx.doi.org/10.1016/j.neuroscience.2009.04.033.
Повний текст джерелаFussiger, Helena, José Luiz Pedroso, and Jonas Alex Morales Saute. "Diagnostic reasoning in neurogenetics: a general approach." Arquivos de Neuro-Psiquiatria 80, no. 09 (September 2022): 944–52. http://dx.doi.org/10.1055/s-0042-1755275.
Повний текст джерелаAndelman‐Gur, Michal M., Richard J. Leventer, Mohammad Hujirat, Christos Ganos, Keren Yosovich, Nirit Carmi, Dorit Lev, et al. "Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?" American Journal of Medical Genetics Part A 182, no. 10 (August 17, 2020): 2207–13. http://dx.doi.org/10.1002/ajmg.a.61795.
Повний текст джерелаGorchkhanova, Z. K., E. A. Nikolaeva, A. M. Pivovarova, S. V. Bochenkov, and E. D. Belousova. "Difficulties in the differential diagnosis of Angelman’s syndrome." Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 67, no. 6 (January 8, 2023): 113–22. http://dx.doi.org/10.21508/1027-4065-2022-67-6-113-122.
Повний текст джерелаKomissarova, O. A., O. A. Milovanova, G. G. Avakyan, and S. V. Bugriy. "Childhood autism associated with neurological manifestations and corpus callosum hypoplasia: literature review and clinical cases." Epilepsy and paroxysmal conditions 12, no. 1 (April 16, 2020): 51–58. http://dx.doi.org/10.17749/2077-8333.2020.12.1.51-58.
Повний текст джерелаGipson, Tanjala T., and Michael V. Johnston. "Plasticity and mTOR: Towards Restoration of Impaired Synaptic Plasticity in mTOR-Related Neurogenetic Disorders." Neural Plasticity 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/486402.
Повний текст джерелаShatalin, A. V., E. V. Mukhina, A. S. Kotov, and M. G. Amirkhanyan. "Modern neurogenetic representations of MELAS syndrome. Clinical cases (the lecture)." Russian Journal of Child Neurology 14, no. 4 (May 16, 2020): 26–31. http://dx.doi.org/10.17650/2073-8803-2019-14-4-26-31.
Повний текст джерелаDennen, Catherine A., Kenneth Blum, Abdalla Bowirrat, Jag Khalsa, Panayotis K. Thanos, David Baron, Rajendra D. Badgaiyan, Ashim Gupta, Eric R. Braverman, and Mark S. Gold. "Neurogenetic and Epigenetic Aspects of Cannabinoids." Epigenomes 6, no. 3 (August 26, 2022): 27. http://dx.doi.org/10.3390/epigenomes6030027.
Повний текст джерелаMattie, Laura J., and Pamela A. Hadley. "Characterizing the Richness of Maternal Input for Word Learning in Neurogenetic Disorders." Seminars in Speech and Language 42, no. 04 (July 26, 2021): 301–17. http://dx.doi.org/10.1055/s-0041-1730914.
Повний текст джерелаMusin, M. F., and A. F. Yusupova. "Algesic syndrome in the epigastric region in extraabdominal pathology, its place in intensive diagnosis." Kazan medical journal 78, no. 5 (October 15, 1997): 332–35. http://dx.doi.org/10.17816/kazmj83563.
Повний текст джерелаLEVITIN, D. J. "Musical Behavior in a Neurogenetic Developmental Disorder: Evidence from Williams Syndrome." Annals of the New York Academy of Sciences 1060, no. 1 (December 1, 2005): 325–34. http://dx.doi.org/10.1196/annals.1360.027.
Повний текст джерелаDe Molfetta, Greice Andreotti, Temis Maria Felix, Mariluce Riegel, Victor Evangelista de Faria Ferraz, and João Monteiro de Pina Neto. "A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect." Arquivos de Neuro-Psiquiatria 60, no. 4 (December 2002): 1011–14. http://dx.doi.org/10.1590/s0004-282x2002000600024.
Повний текст джерелаWalter, E., P. K. Mazaika, and A. L. Reiss. "Corrigendum to “Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and Velocardiofacial syndrome” [Neuroscience 164 (2009) 257–271]." Neuroscience 165, no. 3 (February 2010): 1011. http://dx.doi.org/10.1016/j.neuroscience.2009.11.014.
Повний текст джерелаJiang, Chun, Ningren Cui, Weiwei Zhong, Christopher M. Johnson, and Yang Wu. "Breathing abnormalities in animal models of Rett syndrome a female neurogenetic disorder." Respiratory Physiology & Neurobiology 245 (November 2017): 45–52. http://dx.doi.org/10.1016/j.resp.2016.11.011.
Повний текст джерелаZarchi, O., A. Diamond, R. Weinberger, D. Abbott, M. Carmel, A. Frisch, E. Michaelovsky, et al. "A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: Velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes." European Psychiatry 29, no. 4 (May 2014): 203–10. http://dx.doi.org/10.1016/j.eurpsy.2013.07.001.
Повний текст джерелаSánchez, Javier, Ana Peciña, Olga Alonso-Luengo, Antonio González-Meneses, Rocío Vázquez, Guillermo Antiñolo, and Salud Borrego. "Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13." Case Reports in Genetics 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/517091.
Повний текст джерелаBattaglia, Agatino. "The inv dup(15) or idic(15) syndrome: A clinically recognisable neurogenetic disorder." Brain and Development 27, no. 5 (August 2005): 365–69. http://dx.doi.org/10.1016/j.braindev.2004.08.006.
Повний текст джерелаAguilera, Cinthia, Elisabeth Gabau, Ariadna Ramirez-Mallafré, Carme Brun-Gasca, Jana Dominguez-Carral, Veronica Delgadillo, Steve Laurie, et al. "New genes involved in Angelman syndrome-like: Expanding the genetic spectrum." PLOS ONE 16, no. 10 (October 15, 2021): e0258766. http://dx.doi.org/10.1371/journal.pone.0258766.
Повний текст джерелаPina-Neto, João M. de, Victor Evangelista F. Ferraz, Greice Andreotti de Molfetta, Jess Buxton, Sarah Richards, and Sue Malcolm. "Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman Syndromes." Arquivos de Neuro-Psiquiatria 55, no. 2 (June 1997): 199–208. http://dx.doi.org/10.1590/s0004-282x1997000200006.
Повний текст джерелаGood, Jean-Marc, Isis Atallah, Mayte Castro Jimenez, David Benninger, Thierry Kuntzer, Andrea Superti-Furga, and Christel Tran. "NGS-Based Diagnosis of Treatable Neurogenetic Disorders in Adults: Opportunities and Challenges." Genes 12, no. 5 (May 6, 2021): 695. http://dx.doi.org/10.3390/genes12050695.
Повний текст джерелаSiegert, Sandy, Gabriel T. Mindler, Christof Brücke, Andreas Kranzl, Janina Patsch, Markus Ritter, Andreas R. Janecke, and Julia Vodopiutz. "Expanding the Phenotype of the FAM149B1-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single Family." Genes 12, no. 11 (October 20, 2021): 1648. http://dx.doi.org/10.3390/genes12111648.
Повний текст джерелаBlum, Kenneth, Marlene Oscar-Berman, Zsolt Demetrovics, Debmalya Barh, and Mark S. Gold. "Genetic Addiction Risk Score (GARS): Molecular Neurogenetic Evidence for Predisposition to Reward Deficiency Syndrome (RDS)." Molecular Neurobiology 50, no. 3 (May 31, 2014): 765–96. http://dx.doi.org/10.1007/s12035-014-8726-5.
Повний текст джерелаRondal, Jean A. "Language in mental retardation: Individual and syndromic differences, and neurogenetic variation 1Based on a keynote presentation at the Third European Conference on Psychological Theory and Research in Mental Retardation, Geneva, September 1st, 2000." Swiss Journal of Psychology 60, no. 3 (September 2001): 161–78. http://dx.doi.org/10.1024//1421-0185.60.3.161.
Повний текст джерелаJesse, Sarah, Jan Philipp Delling, Michael Schön, Tobias M. Boeckers, Albert Ludolph, and Makbule Senel. "Phelan McDermid Syndrome: Multiple Sclerosis as a Rare but Treatable Cause for Regression—A Case Report." International Journal of Molecular Sciences 22, no. 5 (February 25, 2021): 2311. http://dx.doi.org/10.3390/ijms22052311.
Повний текст джерелаWilson, Kathleen, Ethan Whitman, Allysa Warling, Ajay Nadig, Cassidy McDermott, Liv Clasen, Srishti Rau, et al. "A Framework for Modeling Familial Predictors of Proband Outcomes in Neurogenetic Disorders: Initial Findings in XYY Syndrome." Biological Psychiatry 87, no. 9 (May 2020): S355. http://dx.doi.org/10.1016/j.biopsych.2020.02.910.
Повний текст джерелаKummerfeld, Delf-Magnus, Carsten A. Raabe, Juergen Brosius, Dingding Mo, Boris V. Skryabin, and Timofey S. Rozhdestvensky. "A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research." International Journal of Molecular Sciences 22, no. 7 (March 31, 2021): 3613. http://dx.doi.org/10.3390/ijms22073613.
Повний текст джерелаNikitina, Е. А., A. V. Medvedeva, G. А. Zakharov, and Е. V. Savvateeva-Popova. "Williams Syndrome As a Model for Elucidation of the Pathway Genes - the Brain - Cognitive Functions: Genetics and Epigenetics." Acta Naturae 6, no. 1 (March 15, 2014): 9–22. http://dx.doi.org/10.32607/20758251-2014-6-1-9-22.
Повний текст джерелаDebbané, M., M. Van der Linden, B. Glaser, and S. Eliez. "Source monitoring for actions in adolescents with 22q11.2 deletion syndrome (22q11DS)." Psychological Medicine 38, no. 6 (November 16, 2007): 811–20. http://dx.doi.org/10.1017/s003329170700222x.
Повний текст джерелаGur, R. E., A. S. Bassett, D. M. McDonald-McGinn, C. E. Bearden, E. Chow, B. S. Emanuel, M. Owen, et al. "A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium." Molecular Psychiatry 22, no. 12 (August 1, 2017): 1664–72. http://dx.doi.org/10.1038/mp.2017.161.
Повний текст джерелаKoriath, C., J. Kenny, G. Adamson, R. Druyeh, W. Taylor, J. Beck, L. Quinn, et al. "Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series." Molecular Psychiatry 25, no. 12 (October 2, 2018): 3399–412. http://dx.doi.org/10.1038/s41380-018-0224-0.
Повний текст джерелаCrespi, Bernard, Silven Read, Iiro Salminen, and Peter Hurd. "A genetic locus for paranoia." Biology Letters 14, no. 1 (January 2018): 20170694. http://dx.doi.org/10.1098/rsbl.2017.0694.
Повний текст джерелаBlum, Kenneth, Thomas McLaughlin, Abdalla Bowirrat, Edward J. Modestino, David Baron, Luis Llanos Gomez, Mauro Ceccanti, et al. "Reward Deficiency Syndrome (RDS) Surprisingly Is Evolutionary and Found Everywhere: Is It “Blowin’ in the Wind”?" Journal of Personalized Medicine 12, no. 2 (February 21, 2022): 321. http://dx.doi.org/10.3390/jpm12020321.
Повний текст джерелаBlum, Kenneth, Marcelo Febo, Rajendra Badgaiyan, Zsolt Demetrovics, Thomas Simpatico, Claudia Fahlke, Oscar-Berman M., Mona Li, Kristina Dushaj, and Mark Gold. "Common Neurogenetic Diagnosis and Meso-Limbic Manipulation of Hypodopaminergic Function in Reward Deficiency Syndrome (RDS): Changing the Recovery Landscape." Current Neuropharmacology 15, no. 1 (December 14, 2016): 184–94. http://dx.doi.org/10.2174/1570159x13666160512150918.
Повний текст джерелаLiu, Shu, Kaihui Zhang, Fengling Song, Yali Yang, Yuqiang Lv, Min Gao, Yi Liu, and Zhongtao Gai. "Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking." Cytogenetic and Genome Research 152, no. 1 (2017): 1–8. http://dx.doi.org/10.1159/000477520.
Повний текст джерелаAlmomen, MM, KA Martens, A. Hanson, L. Korngut, and G. pfeffer. "P.071 Novel mutations in SPG7 identified from patients with late-onset spasticity." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 45, s2 (June 2018): S35. http://dx.doi.org/10.1017/cjn.2018.173.
Повний текст джерелаJärvinen-Pasley, Anna, Ursula Bellugi, Judy Reilly, Debra L. MILLS, Albert Galaburda, Allan L. Reiss, and Julie R. Korenberg. "Defining the social phenotype in Williams syndrome: A model for linking gene, the brain, and behavior." Development and Psychopathology 20, no. 1 (2008): 1–35. http://dx.doi.org/10.1017/s0954579408000011.
Повний текст джерелаKengne Kamga, Karen, Séraphin Nguefack, Khuthala Minka, Edmond Wonkam Tingang, Alina Esterhuizen, Syntia Nchangwi Munung, Jantina De Vries, and Ambroise Wonkam. "Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa)." Genes 11, no. 2 (January 28, 2020): 136. http://dx.doi.org/10.3390/genes11020136.
Повний текст джерелаSerur, Yaffa, Dafin Sofrin Frumber, Keren Daon, Dolly Sobal-Havia, Ronnie Weinberger, Cory Shulman, and Doron Gothelf. "Psychiatric disorders and autism in young children with 22q11.2 deletion syndrome compared to children with idiopathic autism." European Psychiatry 55 (January 2019): 116–21. http://dx.doi.org/10.1016/j.eurpsy.2018.10.007.
Повний текст джерелаHeaney, Alice, Jeanette Wilburn, Shannon Langmead, Jaishri Blakeley, Susan Huson, Carly Jim, and Stephen P. McKenna. "A qualitative study of the impact of plexiform neurofibromas on need fulfilment in adults with neurofibromatosis type 1." SAGE Open Medicine 7 (January 2019): 205031211982968. http://dx.doi.org/10.1177/2050312119829680.
Повний текст джерелаSemenzin, Chiara, Lisa Hamrick, Amanda Seidl, Bridgette L. Kelleher, and Alejandrina Cristia. "Describing Vocalizations in Young Children: A Big Data Approach Through Citizen Science Annotation." Journal of Speech, Language, and Hearing Research 64, no. 7 (July 16, 2021): 2401–16. http://dx.doi.org/10.1044/2021_jslhr-20-00661.
Повний текст джерелаBlum, Kenneth, Shan Kazmi, Edward J. Modestino, Bill William Downs, Debasis Bagchi, David Baron, Thomas McLaughlin, et al. "A Novel Precision Approach to Overcome the “Addiction Pandemic” by Incorporating Genetic Addiction Risk Severity (GARS) and Dopamine Homeostasis Restoration." Journal of Personalized Medicine 11, no. 3 (March 16, 2021): 212. http://dx.doi.org/10.3390/jpm11030212.
Повний текст джерелаAbijo, Tomilowo, Kenneth Blum, and Marjorie C. Gondré-Lewis. "Neuropharmacological and Neurogenetic Correlates of Opioid Use Disorder (OUD) As a Function of Ethnicity: Relevance to Precision Addiction Medicine." Current Neuropharmacology 18, no. 7 (July 28, 2020): 578–95. http://dx.doi.org/10.2174/1570159x17666191118125702.
Повний текст джерелаGuo, Miao, Yucai Chen, Longlong Lin, Yilin Wang, Anqi Wang, Fang Yuan, Chunmei Wang, Simei Wang, and Yuanfeng Zhang. "The Study on the Clinical Phenotype and Function of HPRT1 Gene." Child Neurology Open 9 (January 2022): 2329048X2211088. http://dx.doi.org/10.1177/2329048x221108821.
Повний текст джерелаPinto, Irene Plaza, Lysa Bernardes Minasi, Cláudio Carlos da Silva, and Aparecido Divino da Cruz. "Identification of 1q21.1 microduplication by microarray analysis in a boy with intellectual disability." Semina: Ciências Biológicas e da Saúde 38, no. 1supl (February 16, 2018): 186. http://dx.doi.org/10.5433/1679-0367.2017v38n1suplp186.
Повний текст джерелаGoldson, Edward. "Neurogenetic Syndromes." Journal of Developmental & Behavioral Pediatrics 33, no. 3 (April 2012): 260. http://dx.doi.org/10.1097/dbp.0b013e31825577b3.
Повний текст джерелаKim, Min-Jee, Mi-Sun Yum, Go Hun Seo, Yena Lee, Han Na Jang, Tae-Sung Ko, and Beom Hee Lee. "Clinical Application of Whole Exome Sequencing to Identify Rare but Remediable Neurologic Disorders." Journal of Clinical Medicine 9, no. 11 (November 20, 2020): 3724. http://dx.doi.org/10.3390/jcm9113724.
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