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psychiatric manifestations of neuro disease

https://read.qxmd.com/read/35706352/new-onset-and-persistent-neurological-and-psychiatric-sequelae-of-covid-19-compared-to-influenza-a-retrospective-cohort-study-in-a-large-new-york-city-healthcare-network
#21
JOURNAL ARTICLE
Andrei L Iosifescu, Wouter S Hoogenboom, Alexandra J Buczek, Roman Fleysher, Tim Q Duong
OBJECTIVES: Neurological and neuropsychiatric manifestations of post-acute SARS-CoV-2 infection (neuro-PASC) are common among COVID-19 survivors, but it is unknown how neuro-PASC differs from influenza-related neuro-sequelae. This study investigated the clinical characteristics of COVID-19 patients with and without new-onset neuro-PASC, and of flu patients with similar symptoms. METHODS: We retrospectively screened 18,811 COVID-19 patients and 5772 flu patients between January 2020 and June 2021 for the presence of new-onset neuro-sequelae that persisted at least 2 weeks past the date of COVID-19 or flu diagnosis...
June 15, 2022: International Journal of Methods in Psychiatric Research
https://read.qxmd.com/read/35638048/late-onset-wilson-disease-with-normal-neuro-psychiatric-status-a-case-report
#22
Bishal Dhakal, K C Prabhat, Abinash Karki, Ayush Mohan Bhattarai, Sachin Sapkota, Binaya Subedi, Abhinav Dahal
Introduction: Late onset Wilson disease (WD) is a rare form of WD. WD has variability of clinical presentations from acute liver failure to chronic liver disease (CLD). The hepatic and neurological variants of WD have wider variations. Case presentation: A 55-year-old female, known case of CLD, presenting with generalized body swelling and abdominal pain, was diagnosed with late onset WD with normal neuro-psychiatric status. She was treated with zinc and considered for liver transplantation...
May 2022: Annals of Medicine and Surgery
https://read.qxmd.com/read/35472603/neuro-ophthalmological-manifestations-of-wolfram-syndrome-case-series-and-review-of-the-literature
#23
REVIEW
Anna Kabanovski, Laura Donaldson, Edward Margolin
Wolfram Syndrome (WS) is a rare progressive hereditary neurodegenerative disease with hallmark features of diabetes mellitus, optic atrophy, and hearing loss. Its other clinical manifestations may include diabetes insipidus, urological, neurological, and psychiatric abnormalities. We review systemic and ocular manifestations of WS as well as its pathophysiology, diagnostic approach, and treatment options. We then describe a case series of 5 patients (ages 15-38, 60% male) with WS. All had significant progressive visual loss...
June 15, 2022: Journal of the Neurological Sciences
https://read.qxmd.com/read/35121209/mid-and-long-term-neurological-and-neuropsychiatric-manifestations-of-post-covid-19-syndrome-a-meta-analysis
#24
REVIEW
Lavienraj Premraj, Nivedha V Kannapadi, Jack Briggs, Stella M Seal, Denise Battaglini, Jonathon Fanning, Jacky Suen, Chiara Robba, John Fraser, Sung-Min Cho
IMPORTANCE: Neurological and neuropsychiatric symptoms that persist or develop three months after the onset of COVID-19 pose a significant threat to the global healthcare system. These symptoms are yet to be synthesized and quantified via meta-analysis. OBJECTIVE: To determine the prevalence of neurological and neuropsychiatric symptoms reported 12 weeks (3 months) or more after acute COVID-19 onset in adults. DATA SOURCES: A systematic search of PubMed, EMBASE, Web of Science, Google Scholar and Scopus was conducted for studies published between January 1st, 2020 and August 1st, 2021...
March 15, 2022: Journal of the Neurological Sciences
https://read.qxmd.com/read/35092831/contemporary-advances-in-anti-nmdar-antibody-ab-mediated-encephalitis
#25
REVIEW
Nabil Seery, Helmut Butzkueven, Terence J O'Brien, Mastura Monif
The study of antibody (Ab)-mediated encephalitis has advanced dramatically since the discovery of antibodies directed against the N-methyl-D-aspartate receptor (NMDAR) in association with a unique neuro-psychiatric syndrome, over a decade-and-a-half ago. Anti-NMDAR Ab-mediated encephalitis now represents the most well characterised form of autoimmune encephalitis. The disease most commonly manifests in young women, but all ages and both sexes can be affected. Autoantibodies may arise in the context of two well-recognised disease triggers in a proportion of patients, and ultimately facilitate NMDAR displacement from synapses...
April 2022: Autoimmunity Reviews
https://read.qxmd.com/read/34999654/multidomain-cognitive-impairment-in-children-with-pseudotumor-cerebri-syndrome
#26
JOURNAL ARTICLE
Muhammad Mahajnah, Ariel T Suchi, Hazar Zahakah, Rajech Sharkia, Shaden R Shuhaiber, Isaac Srugo, Jacob Genizi
BACKGROUND: Although prompt and suitable treatment of pseudotumor cerebri syndrome (PTCS) leads to an excellent prognosis and can prevent optic nerve atrophy, adults show long-lasting neurocognitive deficits even with prompt treatment. The purpose of our study was to evaluate cognitive outcomes in pediatric patients with PTCS. METHODS: We performed a prospective study on children diagnosed with PTCS and a healthy control group. Children with pre-existing neurological conditions or psychiatric drug use were excluded...
March 1, 2022: Journal of Neuro-ophthalmology: the Official Journal of the North American Neuro-Ophthalmology Society
https://read.qxmd.com/read/34993563/genetic-and-phenotypic-variability-in-adult-patients-with-niemann-pick-type-c-from-serbia-single-center-experience
#27
JOURNAL ARTICLE
Nikola Kresojević, Valerija Dobričić, Milica Ječmenica Lukić, Aleksandra Tomić, Igor Petrović, Nataša Dragašević, Ivana Perović, Ana Marjanović, Marija Branković, Milena Janković, Ivana Novaković, Marina Svetel, Vladimir S Kostić
BACKGROUND: Niemann Pick type C is an autosomal recessive lysosomal storage disorder caused by mutations in NPC1 and NPC2 genes. It is a neuro-visceral disease with a heterogeneous phenotype. Clinical features depend on the age at onset. Visceral manifestations are more prominent in the early onset (infantile) form, while neuro-psychiatric symptoms are more prominent in the late disease onset (juvenile and adult forms). METHODS: A total number of 150 patients have been screened for changes in NPC1 and NPC2 gene at the Neurology Clinic, University Clinical Centre of Serbia in the period 2012-2020...
June 2022: Journal of Neurology
https://read.qxmd.com/read/34816972/cognitive-consequences-of-covid-19-results-of-a-cohort-study-from-south-america
#28
JOURNAL ARTICLE
Lucía Crivelli, Ismael Calandri, Nicolás Corvalán, María Agostina Carello, Greta Keller, Carlos Martínez, Micaela Arruabarrena, Ricardo Allegri
BACKGROUND: Neurological and psychiatric manifestations associated with SARS-CoV-2 infection have been reported throughout the scientific literature. However, studies on post-COVID cognitive impairment in people with no previous cognitive complaint are scarce. OBJECTIVE: We aim to investigate the impact of COVID-19 on cognitive functions in adults without cognitive complaints before infection and to study cognitive dysfunction according to disease severity and cognitive risk factors...
March 2022: Arquivos de Neuro-psiquiatria
https://read.qxmd.com/read/34706364/tit-for-tat-costly-punishment-in-manifest-huntington-s-disease
#29
JOURNAL ARTICLE
Beatrice Heim, Marina Peball, Carsten Saft, Sarah Maria von Hein, Johanna Maria Piater, Philipp Ellmerer, Klaus Seppi, Atbin Djamshidian-Tehrani
OBJECTIVE: We aimed to investigate costly punishment in patients with HD. BACKGROUND: Huntington's disease (HD) is an autosomal dominant neurodegenerative disease with motor, cognitive, and psychiatric symptoms. As neuropsychiatric abnormalities often precede motor symptoms, we wanted to assess whether costly punishment is part of the neuropsychological profile of patients with HD. METHODS: A total of 40 non demented subjects were prospectively enrolled in this study with a between-subject design comparing manifest HD patients (n=18) to healthy controls (HC; n=22)...
October 27, 2021: Neuro-degenerative Diseases
https://read.qxmd.com/read/34512404/a-review-of-the-potential-use-of-pinene-and-linalool-as-terpene-based-medicines-for-brain-health-discovering-novel-therapeutics-in-the-flavours-and-fragrances-of-cannabis
#30
REVIEW
Katrina Weston-Green, Helen Clunas, Carlos Jimenez Naranjo
"Medicinal cannabis" is defined as the use of cannabis-based products for the treatment of an illness. Investigations of cannabis compounds in psychiatric and neurological illnesses primarily focus on the major cannabinoids, cannabidiol (CBD) and Δ9 -tetrahydrocannabinol (Δ9 -THC), which are hypothesised to benefit multiple illnesses manifesting cognitive impairment, neurodegeneration and neuro-inflammation, as well as chronic pain, epilepsy and post-traumatic stress disorder, respectively. The cannabis plant contains >500 compounds, including terpenes responsible for the flavour and fragrance profiles of plants...
2021: Frontiers in Psychiatry
https://read.qxmd.com/read/34336508/neuropsychiatric-lupus-a-challenging-journey-of-a-patient-with-pulmonary-tuberculosis
#31
Ammar Farook Chapra, Fadi Khir, Ans Alamami, Khaled M Salem, Alhady Yusof
Systemic lupus erythematosus (SLE) is a disease that affects multiple systems in the body. Due to its variable manifestations, it can at times pose challenges for physicians to hold SLE as the culprit behind an affected system. This is most true when encountering patients with neuropsychiatric manifestations of SLE. We present a case of a 38-year-old female with known SLE limited to skin involvement and on treatment for active pulmonary tuberculosis (TB), yet otherwise healthy, who presented with acute fever associated with generalized tonic-clonic seizures...
June 2021: Curēus
https://read.qxmd.com/read/34152246/neuro-psychiatric-manifestations-in-patients-with-systemic-lupus-erythematosus-a-systematic-review-and-results-from-the-swiss-lupus-cohort-study
#32
JOURNAL ARTICLE
Aline L Meier, Nicolas S Bodmer, Carla Wirth, Lucas M Bachmann, Camillo Ribi, Anne-Katrin Pröbstel, David Waeber, Ilijas Jelcic, Urs C Steiner
OBJECTIVES: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease associated with neuro-psychiatric (NP) manifestations. Frequency and patterns of neuro-psychiatric systemic lupus erythematosus (NPSLE) vary substantially between patients. We conducted a systematic review (SR) of the literature and examined prevalence and characteristics of NPSLE in the Swiss SLE cohort study (SSCS). METHODS: The SR search was performed between January 1999 and January 2020...
September 2021: Lupus
https://read.qxmd.com/read/34080449/enteric-fever-presenting-as-catatonia-syndrome-case-report
#33
JOURNAL ARTICLE
S Jagadeesan, Aniket B Jagtap, Ramesh Chand Meena
Enteric or typhoid fever is an emerging tropical infectious disease and a global public health problem with a documented spectrum of neuro-psychiatric manifestations especially from endemic countries. Although neuro-psychiatric manifestations are reported in nearly 50-75% of patients at any phase of enteric fever, the chance of their misdiagnosis and deferred diagnosis of the prime illness is quite common. Atypical symptoms are commonly attributed to be a part of 'typhoid toxaemia', the acute febrile phase of the illness...
October 2021: Tropical Doctor
https://read.qxmd.com/read/33942164/neurosyphilis-a-series-of-178-cases-at-the-3rd-level-hospital-of-marrakesh-morocco
#34
JOURNAL ARTICLE
Najib Kissani, Sanaa Nafia, Safaa Zahlane, Nisserine Louhab
Neurosyphilis (NS) is an infection of the central nervous system (CNS), caused by Treponema pallidum. Up to 4-10% of patients with untreated syphilis may develop NS which still constitutes a health challenge. The aim of this study is to analyze epidemiological, clinical, paraclinical, therapeutic, and progression profiles of NS in the south of Morocco. Authors analyzed retrospectively 178 files of patients with neurosyphilis, collected in the Neurology Department of Marrakesh over 25 years from January 1994 to March 2019...
October 2021: European Journal of Clinical Microbiology & Infectious Diseases
https://read.qxmd.com/read/33768607/analyses-of-peripheral-blood-dendritic-cells-and-magnetic-resonance-spectroscopy-support-dysfunctional-neuro-immune-crosstalk-in-tourette-syndrome
#35
JOURNAL ARTICLE
Marianna Sarchioto, Franklyn Howe, Ingrid E Dumitriu, Francesca Morgante, Jeremy Stern, Mark J Edwards, Davide Martino
BACKGROUND: Evidence supports that neurodevelopmental diseases, such as Tourette syndrome (TS), may involve dysfunctional neural-immune crosstalk. This could lead to altered brain maturation and differences in immune and stress responses. Dendritic cells (DCs) play a major role in immunity as professional antigen-presenting cells; changes in their frequency have been observed in several autoimmune conditions. METHODS: In 18 TS patients (15 on stable pharmacological treatment, three unmedicated) and 18 age-matched healthy volunteers (HVs), we explored circulating blood-derived DCs and their relationship with clinical variables and brain metabolites, measured via proton magnetic resonance spectroscopy (1H-MRS)...
June 2021: European Journal of Neurology
https://read.qxmd.com/read/33767623/the-anti-inflammatory-effect-of-the-tricyclic-antidepressant-clomipramine-and-its-high-penetration-in-the-brain-might-be-useful-to-prevent-the-psychiatric-consequences-of-sars-cov-2-infection
#36
JOURNAL ARTICLE
B Nobile, M Durand, E Olié, S Guillaume, J P Molès, E Haffen, P Courtet
At the time of writing (December 2020), coronavirus disease 2019 (COVID-19) has already caused more than one million deaths worldwide, and therefore, it is imperative to find effective treatments. The "cytokine storm" induced by Severe Acute Respiratory Syndrome-Coronavirus type 2 (SARS-CoV-2) is a good target to prevent disease worsening, as indicated by the results obtained with tocilizumab and dexamethasone. SARS-CoV-2 can also invade the brain and cause neuro-inflammation with dramatic neurological manifestations, such as viral encephalitis...
2021: Frontiers in Pharmacology
https://read.qxmd.com/read/33657940/a-case-of-spastic-quadriparesis-secondary-to-enteric-fever
#37
JOURNAL ARTICLE
Ajay Bhatta, Prabhat Kumar
Enteric fever is a systemic disease characterised predominantly by fever and abdominal pain, caused by dissemination of Salmonella Typhi or Salmonella Paratyphi . Enteric fever can affect many organ systems including liver, gastrointestinal tract, kidney and brain. Neurological manifestations occur in 2%-40% of patients and include meningitis, Gullian-Barré syndrome, neuritis and neuro-psychiatric symptoms. Spastic quadriparesis is a rare complication.
July 2021: Tropical Doctor
https://read.qxmd.com/read/33548496/the-three-frontlines-against-covid-19-brain-behavior-and-immunity
#38
REVIEW
Shao-Cheng Wang, Kuan-Pin Su, Carmine M Pariante
The pandemic outbreak of coronavirus disease 2019 (COVID-19) is raising global anxiety and fear of both real and perceived health threat from the virus. Overwhelming evidence shows infected patients experiencing neuropsychiatric complications, suggesting that the "psychoneuroimmunity" model might be beneficial in understanding the impact of the virus. Therefore, this Special Issue on "Immunopsychiatry of COVID-19 Pandemic" was launched immediately after the pandemic was declared, with the first paper accepted on the March 25th, 2020...
March 2021: Brain, Behavior, and Immunity
https://read.qxmd.com/read/33421734/the-neuropsychiatric-manifestations-of-covid-19-interactions-with-psychiatric-illness-and-pharmacological-treatment
#39
REVIEW
Esmé Jansen van Vuren, Stephan F Steyn, Christiaan B Brink, Marisa Möller, Francois P Viljoen, Brian H Harvey
The recent outbreak of the corona virus disease (COVID-19) has had major global impact. The relationship between severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection and psychiatric diseases is of great concern, with an evident link between corona virus infections and various central and peripheral nervous system manifestations. Unmitigated neuro-inflammation has been noted to underlie not only the severe respiratory complications of the disease but is also present in a range of neuro-psychiatric illnesses...
March 2021: Biomedicine & Pharmacotherapy
https://read.qxmd.com/read/33326973/the-expanding-phenotypic-spectrums-associated-with-atp1a3-mutation-in-a-family-with-rapid-onset-dystonia-parkinsonism
#40
JOURNAL ARTICLE
Yi Yuan, Longfeng Ran, Lifang Lei, Haixia Zhu, Xiying Zhu, Han Chen
INTRODUCTION: Rapid-onset dystonia parkinsonism (RDP), also referred to as Dystonia 12, is a rare autosomal dominant genetic disease characterized by abrupt onset of a rostrocaudal gradient of dystonia with prominent bulbar symptoms, and parkinsonian features, primarily bradykinesia and postural instability without tremor. The purpose of this study was to identify the genetic defect in a Chinese pedigree with familial RDP and to explore genotype-phenotype correlation. METHODS: A 3-generation Chinese Han pedigree consisting of 9 members and 3 patients with RDP, and 200 unrelated ethnically matched normal subjects were recruited in this study...
2020: Neuro-degenerative Diseases
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