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Listar Neurología por título

Listar Neurología por título

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  • Can we stop the stuttering in stroke? Interventions in 40 patients with acute lacunes 
    Hawkes, Maximiliano Alberto; Braksick, Sherri A.; Zhang, Wei; Wijdicks, Eelco F.M.; Rabinstein, Alejandro A. (Elsevier, 2019-06-15)
    Background Whether any treatment can stop fluctuations of stuttering lacunar syndromes (SLS) is unclear. Case reports have variably suggested effectiveness of intravenous thrombolysis, dual antiplatelet treatment, blood ...
  • Carcinoma pituitario: ¿es demasiado tarde? 
    Caffaratti, Guido; Villalonga, Juan Francisco; Katz, Débora Adela; Cervio, Andrés Eduardo (Viguera, 2019-09-16)
    Resumen no disponible
  • Cardiac Involvement in Movement Disorders 
    Rossi, Malco Damián; Wainsztein, Néstor Adrián; Merello, Marcelo (Wiley, 2021-03-11)
    Background Several conditions represented mainly by movement disorders are associated with cardiac disease, which can be overlooked in clinical practice in the context of a prominent primary neurological disorder. Ob ...
  • CC102. Paroxysmal facial pain in a patient with Parry Romberg Syndrome 
    Bravo, Yasmín; Esliman, Celeste; Arena, Julieta E.; Goicochea, María Teresa (International Headache Society, 2022)
  • CC105. Abnormal CT perfusion in a patient during a migraine with aura episode: Case report 
    Wainberg, Florencia N.; Ricciardi, Mario Emiliano; Chaves, Hernán; Goicochea, María Teresa (International Headache Society, 2022)
  • Cerebellar Ataxia With Extreme Photophobia Associated With Anti-SOX1 Antibodies 
    Alessandro, Lucas; Schachter, Daniel; Farez, Mauricio Franco; Varela, Francisco José (Sage, 2019-07)
    Anti-SOX1 antibodies are associated with diverse neurological syndromes, targeting both the central (paraneoplastic cerebellar degeneration) and peripheral nervous systems (Lambert Eaton myasthenic syndrome, paraneoplastic ...
  • Cerebral venous thrombosis in Argentina: clinical presentation, predisposing factors, outcomes and literature review 
    Alet, Matías Javier; Ciardi, Celina; Alemán, Alberto; Bandeo, Lucrecia; Bonardo, Pablo; Cea, Clarisa; Cirio, Juan; Cossio, Jerónimo; Cuculic, María; Esnaola, María Martha; García-Pérez, Fernando; Giner, Federico; Gómez Schneider, Maia Macarena; Isaac, Cristian Flavo; Lepera, Sandra; Martínez, Carlos; Martínez-Lorenzín, Román; Montes, Mariana; Orzuza, Gabriela; Persi, Gabriel; Povedano, Guillermo Pablo; Pujol Lereis, Virginia Andrea; Quiroga Narváez, Julieta; Romano, Marina; Sabio, Rodrigo; Viglione, Juan; Zurrú, María Cristina; Saposnik, Gustavo; Argentinian Stroke and Cerebrovascular Diseases Study Group - Argentine Neurological Society (Demos Publications, 2020-10)
    Background: Cerebral venous thrombosis (CVT) is a rare medical condition that primarily affects young adults. The clinical spectrum is broad and its recognition remains a challenge for clinicians. Limited information is ...
  • Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer's disease 
    Johnson, Erik C. B.; Bian, Shijia; Haque, Rafi U.; Carter, E. Kathleen; Watson, Caroline M.; Gordon, Brian A.; Ping, Lingyan; Duong, Duc M.; Epstein, Michael P.; McDade, Eric; Barthélemy, Nicolas R.; Karch, Celeste M.; Xiong, Chengjie; Cruchaga, Carlos; Perrin, Richard J.; Wingo, Aliza P.; Dominantly Inherited Alzheimer Network (Nature Publishing Company, 2023-08-07)
    Alzheimer's disease (AD) pathology develops many years before the onset of cognitive symptoms. Two pathological processes-aggregation of the amyloid-β (Aβ) peptide into plaques and the microtubule protein tau into ...
  • Change in Cerebrospinal Fluid Tau Microtubule Binding Region Detects Symptom Onset, Cognitive Decline, Tangles, and Atrophy in Dominantly Inherited Alzheimer's Disease 
    Horie, Kanta; Li, Yan; Barthélemy, Nicolas R.; Gordon, Brian A.; Hassenstab, Jason; Benzinger, Tammie L.S.; Fagan, Anne M.; Morris, John C.; Karch, Celeste M.; Xiong, Chengjie; Allegri, Ricardo Francisco; Chrem Méndez, Patricio Alexis; Ikeuchi, Takeshi; Kasuga, Kensaku; Noble, James M.; Farlow, Martin R.; Chhatwal, Jasmeer P.; Day, Gregory S.; Schofield, Peter R.; Dominantly Inherited Alzheimer Network (Wiley, 2023-03-16)
    Objective: Identifying cerebrospinal fluid measures of the microtubule binding region of tau (MTBR-tau) species that reflect tau aggregation could provide fluid biomarkers that track Alzheimer's disease related neurofibrillary ...
  • Changes in cognitive functioning after COVID-19: A systematic review and meta-analysis 
    Crivelli, Lucía; Palmer, Katie; Calandri, Ismael Luis; Guekht, Alla; Beghi, Ettore; Carroll, William; Frontera, Jennifer; García-Azorín, David; Westenberg, Erica; Winkler, Andrea Sylvia; Mangialasche, Francesca; Allegri, Ricardo Francisco; Kivipelto, Miia (2022-05)
    Introduction: We conducted a systematic review and meta-analysis of the cognitive effects of coronavirus disease 2019 (COVID-19) in adults with no prior history of cognitive impairment. Methods: Searches in Medline/Web ...
  • Changes in the Care of Neurological Diseases During the First Wave of the COVID-19 Pandemic: A Single Private Center Study in Argentina 
    Calandri, Ismael Luis; Hawkes, Maximiliano Alberto; Marrodán, Mariano; Ameriso, Sebastián Francisco; Correale, Jorge; Allegri, Ricardo Francisco (Frontiers Research Foundation, 2021-09-03)
    Introduction: Healthcare systems are struggling to cope with the rapid evolution of the COVID-19 pandemic. In Argentina, the pandemic is advancing despite prolonged lockdown measures. We aim to analyze the impact of the ...
  • Characteristics of children ≤36 months of age with DIPG: A report from the international DIPG registry 
    Bartlett, Allison L.; Lane, Adam; Chaney, Brooklyn; Yanez Escorza, Nancy; Black, Katie; Cochrane, Anne; Minturn, Jane; Bartels, Ute; Warren, Kathy; Hansford, Jordan; Ziegler, David; Diez, Blanca; Goldman, Stewart; Packer, Roger; Kieran, Mark; DeWire-Schottmiller, Mariko; Erker, Craig; Monje-Deisseroth, Michelle; Wagner, Lars; Koschmann, Carl (Oxford University Press, 2022-12-01)
    Background: Children ≤36 months with diffuse intrinsic pontine glioma (DIPG) have increased long-term survival (LTS, overall survival (OS) ≥24 months). Understanding distinguishing characteristics in this population is ...
  • Characteristics of patients with autonomic dysfunction in the Transthyretin Amyloidosis Outcomes Survey (THAOS) 
    Barroso, Fabio Adrián; Coelho, Teresa; Dispenzieri, Angela; Conceição, Isabel; Waddington Cruz, Marcia; Wixner, Jonas; Maurer, Mathew S.; Rapezzi, Claudio; Planté-Bordeneuve, Violaine; Kristen, Arnt V.; González-Duarte, Alejandra; Chapman, Doug; Stewart, Michelle; Amass, Leslie; THAOS investigators (Taylor & Francis, 2022-09)
    Background: Autonomic dysfunction is common in transthyretin amyloidosis (ATTR amyloidosis), but its frequency, characteristics, and quality-of-life (QoL) impact are not well understood. Methods: The Transthyretin ...
  • Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen 
    Coelho, Teresa; Waddington Cruz, Marcia; Chao, Chi-Chao; Parman, Yeşim; Wixner, Jonas; Weiler, Markus; Barroso, Fabio Adrián; Dasgupta, Noel R.; Jung, Shiangtung W.; Schneider, Eugene; Viney, Nicholas J.; Dyck, P. James B.; Ando, Yukio; Gillmore, Julian D.; Khella, Sami; Gertz, Morie; Obici, Laura; Berk, John L. (Springer, 2022-12-16)
    Introduction: Hereditary transthyretin (ATTRv) amyloidosis is a rare, severe, progressive, debilitating, and ultimately fatal disease caused by systemic deposition of transthyretin (TTR) amyloid fibrils. ATTRv amyloidosis ...
  • Characteristics of Patients with Late- vs. Early-Onset Val30Met Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey (THAOS) 
    Waddington Cruz, Marcia; Wixner, Jonas; Amass, Leslie; Kiszko, Jan; Chapman, Doug; Ando, Yukio; THAOS investigators (Springer, 2021-05-22)
    Introduction: Hereditary transthyretin amyloidosis (ATTRv amyloidosis) is a clinically heterogeneous disease caused by mutations in the transthyretin (TTR) gene. The most common mutation, Val30Met, can manifest as an early- ...
  • Characteristics of Recurrent Ischemic Stroke After Embolic Stroke of Undetermined Source: Secondary Analysis of a Randomized Clinical Trial 
    Veltkamp, Roland C.; Pearce, Lesly A.; Korompoki, Eleni; Sharma, Mukul; Kasner, Scott E.; Toni, Danilo; Ameriso, Sebastián Francisco; Mundl, Hardi; Tatlisumak, Turgut; Hankey, Graeme J.; Lindgren, Arne; Berkowitz, Scott D.; Arauz-Gongora, Antonio; Ozturk, Serefnur; Muir, Keith W.; Chamorro, Ángel; Perera, Kanjana S.; Shuaib, Ashfaq; Rudilosso, Salvatore; Shoamanesh, Ashkan; Connolly, Stuart J.; Hart, Robert G. (American Medical Association, 2020-09-01)
    Importance: The concept of embolic stroke of undetermined source (ESUS) unifies a subgroup of cryptogenic strokes based on neuroimaging, a defined minimum set of diagnostic tests, and exclusion of certain causes. Despite ...
  • Childhood focal compressive mononeuropathies during the COVID-19 pandemic in Buenos Aires, Argentina 
    Brand, Patricio; Cejas, Claudia Patricia; Rivero, Alberto Daniel (John Wiley & Sons, 2022-05)
    Introduction/aims: Focal peripheral neuropathies are infrequently seen in pediatric patients. The COVID-19 pandemic has disrupted normal life for many people, including complete lockdowns and school closing for long periods ...
  • CL28. ¿Es útil la evaluación ósea estándar en pacientes con acromegalia? 
    González Pernas, Mariana Soledad; Danilowicz, Karina; Katz, Débora Adela; Sosa, Soledad; Slavinsky, Patricia; Longobardi, Vanesa; Zanchetta, María Belén (Asociación Argentina de Osteología y Metabolismo Mineral, 2022)
  • Clinical and demographic characteristics of male MS patients included in the national registry-RelevarEM. Does sex or phenotype make the difference in the association with poor prognosis? 
    Luetic, Geraldine G.; Menichini, María Laura; Vrech, Carlos; Pappolla, Agustín; Patrucco, Liliana; Cristiano, Edgardo; Marrodán, Mariano; Ysrraelit, María Célica; Fiol, Marcela Paula; Correale, Jorge; Cohen, Leila; Alonso, Ricardo; Silva, Berenice Anabel; Casas, Magdalena; Garcea, Orlando; Deri, Norma; Burgos, Marcos; Liwacki, Susana; Tkachuk, Verónica A.; Barboza, Andrés G. (Elsevier, 2021-11-17)
    Background In multiple sclerosis demographics there is a well-known female prevalence and male patients have been less specifically evaluated in clinical studies, though some clinical differences have been reported between ...
  • Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update 
    Dispenzieri, Angela; Coelho, Teresa; Conceição, Isabel; Waddington Cruz, Marcia; Wixner, Jonas; Kristen, Arnt V.; Rapezzi, Claudio; Planté-Bordeneuve, Violaine; Gonzalez-Moreno, Juan; Maurer, Mathew S.; Grogan, Martha; Chapman, Doug; Amass, Leslie; Barroso, Fabio Adrián; THAOS investigators (BioMed Central, 2022-06-18)
    Background: Transthyretin amyloidosis (ATTR amyloidosis) is a rare, life-threatening disease caused by the accumulation of variant or wild-type (ATTRwt amyloidosis) transthyretin amyloid fibrils in the heart, peripheral ...

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