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Safe Administration of Electroconvulsive Therapy in a Patient With Catatonia and Neuropsychiatric Lupus Comorbid With Fragile X Syndrome.

Subjects: Catatonia*/Catatonia*/Catatonia*/complications ; Catatonia*/Catatonia*/Catatonia*/therapy ; Electroconvulsive Therapy*

  • Source: The journal of ECT [J ECT] 2022 Dec 01; Vol. 38 (4), pp. 258-260. Date of Electronic Publication: 2022 May 05.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 9808943 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Mechanisms Driving the Emergence of Neuronal Hyperexcitability in Fragile X Syndrome.

  • Authors : Bülow P; Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.; Segal M

Subjects: Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics ; Nervous System Physiological Phenomena*; Animals

  • Source: International journal of molecular sciences [Int J Mol Sci] 2022 Jun 05; Vol. 23 (11). Date of Electronic Publication: 2022 Jun 05.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

[The cellular functions of G-quadruplex in neurological diseases].

  • Authors : Shioda N; Department of Genomic Neurology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University.

Subjects: Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/drug therapy ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics ; G-Quadruplexes*

  • Source: Nihon yakurigaku zasshi. Folia pharmacologica Japonica [Nihon Yakurigaku Zasshi] 2022; Vol. 157 (3), pp. 182-186.Publisher: Nippon Yakuri Gakkai Country of Publication: Japan NLM ID: 0420550 Publication Model: Print Cited Medium: Print ISSN: 0015-5691

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Academic Journal

Central Nervous System Trial Failures: Using the Fragile X Syndrome-mGluR5 Drug Target to Highlight the Complexities of Translating Preclinical Discoveries Into Human Trials.

  • Authors : Grabb MC; From the National Institute of Mental Health, NIH Rockville, MD.; Potter WZ

Subjects: Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/drug therapy; Brain ; Central Nervous System

  • Source: Journal of clinical psychopharmacology [J Clin Psychopharmacol] 2022 May-Jun 01; Vol. 42 (3), pp. 234-237.Publisher: Williams And Wilkins Country of Publication: United States NLM ID: 8109496 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Rescued from the fate of neurological disorder.

  • Authors : Li Y; Department of Biomedical Engineering, Tufts University, Medford, MA, USA.; Glass Z

Subjects: Fragile X Syndrome* ; Nanoparticles* ; Nervous System Diseases*

  • Source: Nature biomedical engineering [Nat Biomed Eng] 2018 Jul; Vol. 2 (7), pp. 469-470.Publisher: Springer Nature Country of Publication: England NLM ID: 101696896 Publication Model: Print Cited Medium: Internet ISSN: 2157-846X

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Academic Journal

Wnd/DLK Is a Critical Target of FMRP Responsible for Neurodevelopmental and Behavior Defects in the Drosophila Model of Fragile X Syndrome.

  • Authors : Russo A; Department of Developmental Biology, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.; DiAntonio A

Subjects: Behavior, Animal*; Drosophila Proteins/Drosophila Proteins/Drosophila Proteins/*metabolism ; Drosophila melanogaster/Drosophila melanogaster/Drosophila melanogaster/*physiology

  • Source: Cell reports [Cell Rep] 2019 Sep 03; Vol. 28 (10), pp. 2581-2593.e5.Publisher: Cell Press Country of Publication: United States NLM ID: 101573691 Publication Model: Print Cited Medium: Internet ISSN: 2211-1247

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Academic Journal

Metformin for Treatment of Fragile X Syndrome and Other Neurological Disorders.

  • Authors : Gantois I; Department of Biochemistry, McGill University, Montréal H3A 2T5, Québec, Canada; email: , , .

Subjects: Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*drug therapy ; Metformin/Metformin/Metformin/*therapeutic use

  • Source: Annual review of medicine [Annu Rev Med] 2019 Jan 27; Vol. 70, pp. 167-181. Date of Electronic Publication: 2018 Oct 26.Publisher: Annual Reviews Country of Publication: United States NLM ID: 2985151R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndrome.

  • Authors : Ram S; Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis Medical Center, 2825 50th Street, Sacramento, California, 95817, USA.; Devapriya IA

Subjects: Heterozygote*; Ataxia/Ataxia/Ataxia/*diagnosis ; Ataxia/Ataxia/Ataxia/*genetics Fragile X Tremor Ataxia Syndrome

  • Source: Muscle & nerve [Muscle Nerve] 2015 Aug; Vol. 52 (2), pp. 234-9.Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 7803146 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

The Repeat Expansion Diseases: The dark side of DNA repair.

  • Authors : Zhao XN; Section on Genomic Structure and Function Laboratory of Cell and Molecular Biology National Institute of Diabetes, Digestive and Kidney Diseases National Institutes of Health, Bethesda, MD 20892-0830, USA.; Usdin K

Subjects: DNA Repair* ; Genome* ; Trinucleotide Repeat Expansion*

  • Source: DNA repair [DNA Repair (Amst)] 2015 Aug; Vol. 32, pp. 96-105. Date of Electronic Publication: 2015 Apr 30.Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101139138 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

FXTAS: new insights and the need for revised diagnostic criteria.

Subjects: Ataxia/Ataxia/Ataxia/*diagnosis ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*diagnosis ; Parkinsonian Disorders/Parkinsonian Disorders/Parkinsonian Disorders/*diagnosis

  • Source: Neurology [Neurology] 2012 Oct 30; Vol. 79 (18), pp. 1898-907. Date of Electronic Publication: 2012 Oct 17.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Dysregulation of mRNA Localization and Translation in Genetic Disease.

  • Authors : Wang ET; Center for NeuroGenetics, University of Florida, Gainesville, Florida 32610, .; Taliaferro JM

Subjects: Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics ; Nervous System Diseases/Nervous System Diseases/Nervous System Diseases/*genetics ; RNA, Messenger/RNA, Messenger/RNA, Messenger/*genetics

  • Source: The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2016 Nov 09; Vol. 36 (45), pp. 11418-11426.Publisher: Society for Neuroscience Country of Publication: United States NLM ID: 8102140 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Fragile X syndrome: an update on developing treatment modalities.

  • Authors : Healy A; Seaside Therapeutics, 840 Memorial Drive, Cambridge, Masssachusetts 02139, USA.; Rush R

Subjects: Central Nervous System Agents/Central Nervous System Agents/Central Nervous System Agents/*chemistry ; Central Nervous System Agents/Central Nervous System Agents/Central Nervous System Agents/*therapeutic use ; Drug Discovery/Drug Discovery/Drug Discovery/*trends

  • Source: ACS chemical neuroscience [ACS Chem Neurosci] 2011 Aug 17; Vol. 2 (8), pp. 402-10. Date of Electronic Publication: 2011 Mar 22.Publisher: American Chemical Society Country of Publication: United States NLM ID: 101525337 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome.

  • Authors : Sheridan SD; Center for Human Genetic Research, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.; Theriault KM

Subjects: Epigenesis, Genetic* ; Models, Biological*; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics

  • Source: PloS one [PLoS One] 2011; Vol. 6 (10), pp. e26203. Date of Electronic Publication: 2011 Oct 12.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Modest alterations in patterns of motor neuron dendrite morphology in the Fmr1 knockout mouse model for fragile X.

  • Authors : Thomas CC; Undergraduate Neuroscience Program, Tulane University, New Orleans, LA 70118, USA.; Combe CL

Subjects: Dendrites/Dendrites/Dendrites/*pathology ; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*pathology

  • Source: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience [Int J Dev Neurosci] 2008 Nov; Vol. 26 (7), pp. Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 8401784 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Editorial & Opinion

MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome.

Subjects: Basal Ganglia Diseases/Basal Ganglia Diseases/Basal Ganglia Diseases/*diagnostic imaging ; Basal Ganglia Diseases/Basal Ganglia Diseases/Basal Ganglia Diseases/*pathology ; Brain/Brain/Brain/*diagnostic imaging

  • Source: Journal of neurology [J Neurol] 2008 Jan; Vol. 255 (1), pp. 144-6. Date of Electronic Publication: 2007 Dec 19.Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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Academic Journal

Peripheral nervous system pathology in fragile X tremor/ataxia syndrome (FXTAS).

  • Authors : Gokden M; Department of Pathology, University of Arkansas for Medical Sciences, 4301 West Markham Street # 517, Little Rock, AR 72205, USA. ; Al-Hinti JT

Subjects: Ataxia/Ataxia/Ataxia/*pathology ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*pathology ; Peripheral Nervous System/Peripheral Nervous System/Peripheral Nervous System/*pathology

  • Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2009 Jun; Vol. 29 (3), pp. 280-4. Date of Electronic Publication: 2008 Jun 30.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Lessons from fragile X regarding neurobiology, autism, and neurodegeneration.

  • Authors : Hagerman RJ; Department of Pediatrics, M.I.N.D. Institute, University of California Davis Health System, Sacramento, California 95817, USA.

Subjects: Autistic Disorder/Autistic Disorder/Autistic Disorder/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics ; Heredodegenerative Disorders, Nervous System/Heredodegenerative Disorders, Nervous System/Heredodegenerative Disorders, Nervous System/*genetics

  • Source: Journal of developmental and behavioral pediatrics : JDBP [J Dev Behav Pediatr] 2006 Feb; Vol. 27 (1), pp. 63-74.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8006933 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Testing for fragile X gene mutations throughout the life span.

  • Authors : Hagerman RJ; M.I.N.D. Institute, and Department of Pediatrics, School of Medicine, University of California, Davis, USA. ; Hagerman PJ

Subjects: Genetic Testing* ; Neonatal Screening*; Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/Fragile X Mental Retardation Protein/*genetics

  • Source: JAMA [JAMA] 2008 Nov 26; Vol. 300 (20), pp. 2419-21.Publisher: American Medical Association Country of Publication: United States NLM ID: 7501160 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Olfactory bulb mitral cell dendritic pruning abnormalities in a mouse model of the Fragile-X mental retardation syndrome: further support for FMRP's involvement in dendritic development.

  • Authors : Galvez R; Neuroscience Program, University of Illinois, Urbana, IL 61801, USA.; Smith RL

Subjects: Dendrites/Dendrites/Dendrites/*pathology ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*pathology ; Nerve Tissue Proteins/Nerve Tissue Proteins/Nerve Tissue Proteins/*deficiency

  • Source: Brain research. Developmental brain research [Brain Res Dev Brain Res] 2005 Jun 30; Vol. 157 (2), pp. 214-6.Publisher: Elsevier Science Publishers Country of Publication: Netherlands NLM ID: 8908639 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

The cyclic AMP cascade is altered in the fragile X nervous system.

  • Authors : Kelley DJ; Waisman Laboratory for Brain Imaging and Behavior, Waisman Center, University of Wisconsin, Madison, Wisconsin, USA.; Davidson RJ

Subjects: Cyclic AMP/Cyclic AMP/Cyclic AMP/*metabolism ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*metabolism ; Nervous System/Nervous System/Nervous System/*metabolism

  • Source: PloS one [PLoS One] 2007 Sep 26; Vol. 2 (9), pp. e931. Date of Electronic Publication: 2007 Sep 26.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Electronic Cited Medium: Internet

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Academic Journal

Neuropathic features in fragile X premutation carriers.

  • Authors : Berry-Kravis E; Department of Neurological Sciences, RUSH University Medical Center, Chicago, Illinois, USA. ; Goetz CG

Subjects: Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*diagnosis ; Peripheral Nervous System Diseases/Peripheral Nervous System Diseases/Peripheral Nervous System Diseases/*diagnosis; Female

  • Source: American journal of medical genetics. Part A [Am J Med Genet A] 2007 Jan 01; Vol. 143A (1), pp. 19-26.Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Print ISSN: 1552-4825

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Academic Journal

Come FLY with us: toward understanding fragile X syndrome.

  • Authors : Zarnescu DC; Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322, USA.; Shan G

Subjects: Drosophila Proteins/Drosophila Proteins/Drosophila Proteins/*genetics ; Drosophila melanogaster/Drosophila melanogaster/Drosophila melanogaster/*genetics ; Fragile X Syndrome/Fragile X Syndrome/Fragile X Syndrome/*genetics

  • Source: Genes, brain, and behavior [Genes Brain Behav] 2005 Aug; Vol. 4 (6), pp. 385-92.Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print Cited Medium: Print ISSN: 1601-1848 (Print)

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