Search Results - "Calandra, Cristian R"
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Gastrointestinal manifestations in Parkinson’s disease: prevalence and occurrence before motor symptoms
Published in Journal of neurology (01-05-2013)“…To assess the prevalence of gastrointestinal symptoms (GIS) in Parkinson’s disease (PD) compared to control subjects and their timing of appearance in…”
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Weight Loss in Parkinson’s Disease: The Relationship with Motor Symptoms and Disease Progression
Published in BioMed research international (01-01-2018)“…Objectives. To determine the prevalence of weight loss (WL) in PD patients, its relationship to the severity of motor manifestations and appetite changes…”
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Spastic ataxia with eye-of-the-tiger-like sign in 4 siblings due to novel compound heterozygous AFG3L2 mutation
Published in Parkinsonism & related disorders (01-04-2020)Get full text
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Practice guideline for the treatment of familial amyloid polyneuropathy
Published in Medicina (01-05-2022)“…This clinical practice guideline for the treatment of familial amyloid polyneuropathy is based on the best available evidence of clinical effectiveness. A list…”
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Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings
Published in Movement disorders clinical practice (Hoboken, N.J.) (01-03-2019)“…View Supplementary Video 1…”
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Sensory neuronopathy. Its recognition and early treatment
Published in Medicina (Buenos Aires) (2015)“…Sensory neuronopathies or ganglionopathies, or dorsal root ganglion disorders, represent a subgroup of peripheral nervous system diseases, frequently…”
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Dry mouth: an overlooked autonomic symptom of Parkinson's disease
Published in Journal of Parkinson's disease (2011)“…There is involvement of salivary glands by α-synuclein pathology in PD. However, the prevalence of dry mouth has not been systematically assessed in these…”
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Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy
Published in JAMA : the journal of the American Medical Association (17-10-2023)“…Transthyretin gene silencing is an emerging treatment strategy for hereditary transthyretin (ATTRv) amyloidosis. To evaluate eplontersen, an investigational…”
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Gordon Holmes Syndrome Caused by RNF216 Novel Mutation in 2 Argentinean Siblings
Published in Movement disorders clinical practice (01-03-2019)Get full text
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