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1-85 out of 85 article(s)
Title Author Type Date Words
Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family. Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Mohammed Mohammed Jan, Adeel G. Chaudhary and Oct 31, 2020 1806
Detection and Characterization of New Coronavirus in Bottlenose Dolphin, United States, 2019. Wang, Leyi; Maddox, Carol; Terio, Karen; Lanka, Saraswathi; Fredrickson, Richard; Novick, Brittany; Letter to the editor Jul 1, 2020 1284
Cyclin-Dependent Kinase-Like 5 (CDKL5): Possible Cellular Signalling Targets and Involvement in CDKL5 Deficiency Disorder. Katayama, Syouichi; Sueyoshi, Noriyuki; Inazu, Tetsuya; Kameshita, Isamu Jun 30, 2020 10057
Regulation of Iron Homeostasis and Related Diseases. Li, Yikun; Huang, Xiali; Wang, Jingjing; Huang, Ruiling; Wan, Dan May 31, 2020 8903
Genome-Wide Characterization and Analysis of bHLH Transcription Factors Related to Crocin Biosynthesis in Gardenia jasminoides Ellis (Rubiaceae). Tian, Ya; Pu, Xiangdong; Yu, Haoying; Ji, Aijia; Gao, Ranran; Hu, Yating; Xu, Zhichao; Wang, Hualei Apr 30, 2020 5487
Candidate Genes Associated with Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20. Correa, Thiago; Venancio, Amanda Cristina; Galera, Marcial Francis; Riegel, Mariluce Mar 1, 2020 4248
Efficient One-Step Induction of Human Umbilical Cord-Derived Mesenchymal Stem Cells (UC-MSCs) Produces MSC-Derived Neurospheres (MSC-NS) with Unique Transcriptional Profile and Enhanced Neurogenic and Angiogenic Secretomes. Peng, Chunyang; Li, Yajiao; Lu, Li; Zhu, Jianwen; Li, Huiyu; Hu, Jingqiong Dec 31, 2019 8144
Scientists halt ALS using virus-delivered gene silencing therapy. ANI Dec 28, 2019 886
Two Cases of Menkes Disease Diagnosed with Hair Findings and Novel Mutation. Isikay, Sedat; Kirik, Serkan Clinical report Dec 1, 2019 1676
PKAN Overview and Disease Awareness. Monduy, Migvis Disease/Disorder overview Nov 1, 2019 1731
CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76. Garcia-Berlanga, Jesus Eduardo; Moscovich, Mariana; Palacios, Isaac Jair; Banegas-Lagos, Alejandro; Jul 31, 2019 2065
Tissue Inhibitor of Metalloproteinase-2 Polymorphisms and Risk for HIV-Associated Neurocognitive Disorder. Singh, HariOm; Jadhav, Sushma; Samani, Dharmesh; Nain, Sumitra Jun 30, 2019 8245
Predicting the molecular phenotype of familial amyotrophic lateral sclerosis: Computational studies of the rare SOD1 A4T mutant protein. Terali, Kerem; Diker, Sevda; Arsal, Pinar Gelener Jun 1, 2019 273
Mannose-Binding Lectin 2 Gene Polymorphism in PANDAS Patients. Celik, Gonca Gul; Tas, Didem Arslan; Tahiroglu, Aysegul Yolga; Erken, Eren; Seydaoglu, Gulsah; Ray, Jun 1, 2019 5952
Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey. Sayan, Saadet; Kotan, Dilcan; Gundogdu-Eken, Asli; Sahbaz, Irmak; Kocoglu, Cemile; Basak, A. Nazli Clinical report Jun 1, 2019 2982
RAD51B (rs8017304 and rs2588809), TRIB1 (rs6987702, rs4351379, and rs4351376), COL8A1 (rs13095226), and COL10A1 (rs1064583) Gene Variants with Predisposition to Age-Related Macular Degeneration. Vilkeviciute, Alvita; Kriauciuniene, Loresa; Chaleckis, Romanas; Deltuva, Vytenis Pranas; Liutkevici May 31, 2019 5821
Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report. Moghanloo, Ehsan; Morovvati, Ziba; Seifi, Maghsoud; Minoochehr, Fatemeh; Morovvati, Saeid; Teimouria Report May 1, 2019 1446
Effect of monoamine oxidase B A644G variant on nicotine dependence and/or schizophrenia risk. Pehlivan, Sacide; Aydin, Pinar Cetinay; Uysal, Mehmet Atilla; Ciftci, Hayriye Senturk; Sever, Ulgen; Report Jan 1, 2019 3506
Emergent Sand Fly--Borne Phleboviruses in the Balkan Region. Ayhan, Nazli; Charrel, Remi N. Report Dec 1, 2018 4581
Over 200 genes linked to autism identified. Nov 3, 2018 340
Role of non-coding RNAs in non-aging-related neurological disorders. Vieira, A.S.; Dogini, D.B.; Lopes-Cendes, I. Report Aug 1, 2018 6583
Two Families with SOD1 (L144F) and C9orf72 Gene Mutations and an Overview of Amyotrophic Lateral Sclerosis/SOD1 (L144F) ve C9orf72 Gen Mutasyonlari Saptanan Iki Aile ve Amiyotrofik Lateral Skleroza Genel Bakis. Bulbul, Nazli Gamze; Secil, Yaprak; Basak, Nazli; Beckmann, Yesim; Ture, Hatice Sabiha; Tunca, Ceren Report Jun 1, 2018 3457
De Novo Mutation in ATP7A Gene with Severe Menkes Disease. Ustkoyuncu, Pembe Soylu; Guven, Ahmet Sami; Kiraz, Aslihan; Yilmaz, Aysegul; Bozdemir, Sefika Elmas; Jun 1, 2018 1728
Genetic Characterization of Enterovirus A71 Circulating in Africa. Fernandez-Garcia, Maria Dolores; Volle, Romain; Joffret, Marie-Line; Sadeuh-Mba, Serge Alain; Gouand Apr 1, 2018 2708
An Evalution of the Demographic and Clinical Characterictics of Patients with GM2 Gangliosidosis. Er, Esra; Canda, Ebru; Yazici, Havva; Eraslan, Cenk; Sozmen, Eser; Ucar, Sema Kalkan; Coker, Mahmut Report Mar 1, 2018 2756
Evaluating the current state of the art of Huntington disease research: a scientometric analysis. Barboza, L.A.; Ghisi, N.C. Report Mar 1, 2018 5354
Cochlear Implantation in Charcot-Marie-Tooth Disease: Case Report and Review of the Literature. Anzalone, C. Lane; Nuhanovic, Sarah; Olund, Amy P.; Carlson, Matthew L. Case study Jan 1, 2018 1351
Maximizing the Survival of Amyotrophic Lateral Sclerosis Patients: Current Perspectives. Khairoalsindi, Osama A.; Abuzinadah, Ahmad R. Jan 1, 2018 10089
Molecular Mechanisms of Transdifferentiation of Adipose-Derived Stem Cells into Neural Cells: Current Status and Perspectives. Luo, Liang; Hu, Da-Hai; Yin, James Q.; Xu, Ru-Xiang Jan 1, 2018 10459
Friedreich's Ataxia: Clinical Presentation of a Compound Heterozygote Child with a Rare Nonsense Mutation and Comparison with Previously Published Cases. Rao, Vamshi K.; DiDonato, Christine J.; Larsen, Paul D. Jan 1, 2018 2428
Huntington's Disease in a Patient Misdiagnosed as Conversion Disorder. Nogueira, Joao Machado; Franco, Ana Margarida; Mendes, Susana; Valadas, Anabela; Semedo, Cristina; J Jan 1, 2018 2771
Activation of Phosphotyrosine-Mediated Signaling Pathways in the Cortex and Spinal Cord of [SOD1.sup.G93A], a Mouse Model of Familial Amyotrophic Lateral Sclerosis. Mallozzi, Cinzia; Spalloni, Alida; Longone, Patrizia; Domenici, Maria Rosaria Jan 1, 2018 6541
Omega Class Glutathione S-Transferase: Antioxidant Enzyme in Pathogenesis of Neurodegenerative Diseases. Kim, Youngjo; Cha, Sun Joo; Choi, Hyun-Jun; Kim, Kiyoung Jan 1, 2018 4610
A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C. Colak, Ruya; Ozdemir, Senem Alkan; Ergon, Ezgi Yangin; Kagnici, Mehtap; Calkavur, Sebnem Nov 1, 2017 1937
Scientists Create Pnenogenetic Map For Stem Cell Models Of Neurological Diseases. Oct 23, 2017 548
Amyotrophic Lateral Sclerosis: Precise Diagnosis and Individualized Treatment. Tao, Qing-Qing; Wu, Zhi-Ying Editorial Oct 5, 2017 2530
Unique Gene Therapy Reverses MS in Animals. Sep 23, 2017 564
Apolipoprotein E: Remarkable Protein Sheds Light on Cardiovascular and Neurological Diseases. Mahley, Robert W. Report Jan 1, 2017 4511
Neuroinflammation and ALS: Transcriptomic Insights into Molecular Disease Mechanisms and Therapeutic Targets. Morello, Giovanna; Spampinato, Antonio Gianmaria; Cavallaro, Sebastiano Report Jan 1, 2017 6164
Insights into the Mechanisms Involved in Protective Effects of VEGF-B in Dopaminergic Neurons. Caballero, Beatrice; Sherman, Scott J.; Falk, Torsten Report Jan 1, 2017 11176
The Neuroprotective Effects of SIRT1 on NMDA-Induced Excitotoxicity. Yang, Xiaorong; Si, Peipei; Qin, Huaping; Yin, Litian; Yan, Liang-Jun; Zhang, Ce Report Jan 1, 2017 5598
Neurodevelopmental Disorders and Environmental Toxicants: Epigenetics as an Underlying Mechanism. Tran, Nguyen Quoc Vuong; Miyake, Kunio Report Jan 1, 2017 17368
Epigenetics and Signaling Pathways in Glaucoma. Gauthier, Angela C.; Liu, Ji Report Jan 1, 2017 9216
Breakthroughs on rare neurologic disease. Brief article Feb 1, 2016 297
Is Modulation of Oxidative Stress an Answer? The State of the Art of Redox Therapeutic Actions in Neurodegenerative Diseases. Chiurchiu, Valerio; Orlacchio, Antonio; Maccarrone, Mauro Jan 1, 2016 10029
Single-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese Cohort. Ju, Xiao-Dong; Liu, Tao; Chen, Jing; Li, Xiao-Gang; Liu, Xin-Xiu; Liu, Wen-Chao; Wang, Kai; Deng, Mi Report Dec 20, 2015 3319
Sindbis and middelburg old world alphaviruses associated with neurologic disease in horses, South Africa. van Niekerk, Stephanie; Human, Stacey; Williams, June; van Wilpe, Erna; Pretorius, Marthi; Swanepoel Report Dec 1, 2015 2811
Changes in Rat Brain MicroRNA Expression Profiles Following Sevoflurane and Propofol Anesthesia. Lu, Yu; Jian, Min-Yu; Ouyang, Yi-Bing; Han, Ru-Quan Report Nov 1, 2015 3732
Activate your brain's anti-aging gene and heal your neurological conditions. Jul 1, 2014 1233
Amyotrophic lateral sclerosis caused by misregulation of protein formation. Apr 15, 2014 843
PDGF suppresses oxidative stress induced [Ca.sup.2+] overload and calpain activation in neurons. Zheng, Lian-Shun; Ishii, Yoko; Zhao, Qing-Li; Kondo, Takashi; Sasahara, Masakiyo Report Jan 1, 2014 4710
Adrenal disorders and the paediatric brain: pathophysiological considerations and clinical implications. Salpietro, Vincenzo; Polizzi, Agata; Rosa, Gabriella Di; Romeo, Anna Claudia; Dipasquale, Valeria; M Report Jan 1, 2014 10807
The impact of restless legs syndrome: a familial case study. Snider, Scott Clinical report Dec 1, 2013 2473
On a bad day you feel 95; Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition. Sep 13, 2013 1293
Onabadday Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition but life is tough Kymica's a fighter. Sep 11, 2013 1508
On a bad day you feel 95; Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition. Sep 11, 2013 1293
On a bad day you feel 95; Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition. Sep 10, 2013 1252
On a bad dayyou feel 95; Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition. Sep 10, 2013 1272
On a bad day you feel 95; Charcot-Marie-Tooth is one of the most common inherited neurological disorders, yet few have heard of it. LAUREN TAYLOR talks to those living with the nerve condition. Sep 10, 2013 1293
Divergent astrovirus associated with neurologic disease in cattle. Li, Linlin; Diab, Santiago; McGraw, Sabrina; Barr, Bradd; Traslavina, Ryan; Higgins, Robert; Talbot, Report Sep 1, 2013 4344
Therapy could help prevent inherited neurological disease. Aug 5, 2013 497
Neurons and support cells change each other for the worse in Lou Gehrig's disease. Feb 18, 2013 475
Immature dentate gyrus: an endophenotype of neuropsychiatric disorders. Hagihara, Hideo; Takao, Keizo; Walton, Noah M.; Matsumoto, Mitsuyuki; Miyakawa, Tsuyoshi Report Jan 1, 2013 16379
Possible involvement of TLRs and hemichannels in stress-induced CNS dysfunction via mastocytes, and glia activation. Aguirre, Adam; Maturana, Carola J.; Harcha, Paloma A.; Saez, Juan C. Report Jan 1, 2013 15303
New gene mutations 'may be behind fatal neurological disease'. Jul 16, 2012 445
Huntington's disease mutation corrected in iPSCs. Jul 9, 2012 504
Huntington's disease mutation corrected in iPSCs. Jul 2, 2012 504
Stem cell product could be used in treatment of orphan neurological disorders. Clinical report Apr 23, 2012 319
Brain ferritin iron as a risk factor for age at onset in neurodegenerative diseases. Report Mar 1, 2012 256
Difficulties with diagnosis and differential diagnosis in childhood cerebral phenotype of adrenoleukodystrophy: a case report/Cocukluk cagi serebral tip adrenolokodistrofi'de tani ve ayirici tani zorluklari: bir olgu sunumu. Yildiz, Ozlem; Memik, Nursu Cakin; Kara, Bulent; Ardic, Hasan; Agaoglu, Belma Case study Dec 1, 2011 2511
Mitochondrial biogenesis. Abstract Nov 1, 2011 2373
Genes behind rare neurodegenerative disorder identified. Jun 20, 2011 244
Lead-induced changes in gene expression. Report May 1, 2011 151
Global gene expression analysis reveals dynamic and developmental stage-dependent enrichment of Lead-induced neurological gene alterations. Peterson, Samuel M.; Zhang, Jun; Weber, Gregory; Freeman, Jennifer L. Report May 1, 2011 6470
Understanding the serum vitamin B12 level and its implications for treating neuropsychiatric conditions: an Orthomolecular perspective. Prousky, Jonathan E. Report Feb 1, 2011 6920
Growing knowledge: using stem cells to study developmental neurotoxicity. Betts, Kellyn S. Report Oct 1, 2010 4973
Vegetative nervous system disturbance in congenital heart diseases. Nurmukhamedova, Mukhlisakhon Report Apr 1, 2010 3640
Acute amnesia in MS revisited. Larner, A.J.; Young, C.A. Report Nov 1, 2009 1369
Pediatric neuroradiology, part 1: Embryologic basis for brain malformation. Bardo, Dianna M.E. Report Jul 1, 2009 4089
How a gene mutation causes devastation of Huntington's disease. Jun 15, 2009 574
Biochemical switch needed for nerve cells to respond to DNA damage identified. Jan 19, 2009 393
"Much Madness is Divinest Sense". Potter, Polyxeni Essay Jul 1, 2008 1171
Verbal memory decline seen after ecstasy use. Jancin, Bruce Clinical report May 1, 2008 558
Immunoassay to measure ataxia-telangiectasia mutated protein in cellular lysates. Butch, Anthony W.; Chun, Helen H.; Nahas, Shereef A.; Gatti, Richard A. Dec 1, 2004 4461
Mitochondrial DNA-related mitochondrial dysfunction in neurodegenerative disease. (Advances in the Science of Pathology). Swerdlow, Russell H. Mar 1, 2002 9532

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