Search Results - "Lefter, Antonia"
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Small Intestinal Bacterial Overgrowth as Potential Therapeutic Target in Parkinson's Disease
Published in International journal of molecular sciences (28-10-2021)“…Increasing evidence suggests that the gut microbiota and the brain are closely connected via the so-called gut-brain axis. Small intestinal bacterial…”
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Serum and Fecal Markers of Intestinal Inflammation and Intestinal Barrier Permeability Are Elevated in Parkinson’s Disease
Published in Frontiers in neuroscience (18-06-2021)“…Parkinson’s disease (PD) is characterized by alpha-synuclein misfolding with subsequent intraneuronal amyloid formation and accumulation, low grade…”
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Serum Uric Acid Levels in Parkinson's Disease: A Cross-Sectional Electronic Medical Record Database Study from a Tertiary Referral Centre in Romania
Published in Medicina (Kaunas, Lithuania) (06-02-2022)“…: Parkinson's disease (PD) is a prevalent neurodegenerative condition responsible for progressive motor and non-motor symptoms. Currently, no prophylactic or…”
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Tuberous Sclerosis Complex – a Multidisciplinary Conundrum: Case Reports
Published in Medicina modernă (Bucharest, Romania) (26-06-2020)“…Introduction: Tuberous sclerosis complex (TSC) is a genetic disorder with a heterogenous clinical phenotype, with possible involvement of virtually any organ…”
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Primary versus Secondary Central Nervous System Melanoma: a Diagnostic Dilemma and Report of a Case
Published in Medicina modernă (Bucharest, Romania) (27-03-2019)“…Malignant melanoma is a cancer of melanocytic origin, typically cutaneous. Despite recent advances, the prognosis is poor. Brain metastases occur in…”
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ANTI AQUAPORIN 4 POSITIVE NEUROMYELITIS OPTICA SPECTRUM DISORDER AND PRIMARY SJÖGREN SYNDROME FOLLOWING SUCCESSFUL THERAPY FOR CHRONIC HEPATITIS C – REPORT OF A CLINICAL CASE
Published in Romanian journal of neurology (30-06-2017)“…Neuromyelitis optica spectrum disorders (NMOSD) are a heterogeneous group of potentially disabling central nervous system inflammatory disorders. Association…”
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Novel C19orf12 loss-of-function variant leading to neurodegeneration with brain iron accumulation
Published in Neurocase (01-12-2021)“…Neurodegeneration with brain iron accumulation (NBIA) is a group of inherited disorders characterised by cerebral iron overload mainly in the basal ganglia…”
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