نتائج البحث - "Rosa Lomastro"

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دورية أكاديمية

Evaluation of SMN protein, transcript, and copy number in the biomarkers for spinal muscular atrophy (BforSMA) clinical study.

المؤلفون: Thomas O Crawford, Sergey V Paushkin, Dione T Kobayashi, Suzanne J Forrest, Cynthia L Joyce, Richard S Finkel, Petra Kaufmann, Kathryn J Swoboda, Danilo Tiziano, Rosa Lomastro, Rebecca H Li, Felicia L Trachtenberg, Thomas Plasterer, Karen S Chen, Pilot Study of Biomarkers for Spinal Muscular Atrophy Trial Group

المصدر: PLoS ONE, Vol 7, Iss 4, p e33572 (2012)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3338744?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/f65b26b6b1164e5db7f0b7bdb0277c5d

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Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol

المساهمون: Tiziano, Francesco Danilo, Lomastro, Rosa, Abiusi, Emanuela, Pasanisi, Maria Barbara, Di Pietro, Lorena, Fiori, Stefania, Baranello, Giovanni, Angelini, Corrado, Sorarù, Gianni, Gaiani, Alessandra, Mongini, Tiziana, Vercelli, Liliana, Mercuri, Eugenio, Vasco, Gessica, Pane, Marika, Vita, Giuseppe, Vita, Gianluca, Messina, Sonia, Petillo, Roberta, Passamano, Luigia, Politano, Luisa, Campanella, Angela, Mantegazza, Renato, Morandi, Lucia

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, double-blind clinical trial, real-time PCR, salbutamol, spinal muscular atrophy, Adolescent, Adrenergic beta-2 Receptor Agonists, Aged, Aged, 80 and over, Albuterol, Female, Gene Expression, Gene Expression Regulation, Humans, Middle Aged, Muscular Atrophy, Spinal, Survival of Motor Neuron 1 Protein, Survival of Motor Neuron 2 Protein, Treatment Outcome, Young Adult, Biomarkers, Spinal, SMN1, 030105 genetics & heredity, Pharmacology, Placebo, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Genetics, medicine, 80 and over, Genetics (clinical), business.industry, Spinal muscular atrophy, medicine.disease, SMA, Clinical trial, Muscular Atrophy, 030104 developmental biology, Pharmacodynamics, Salbutamol, Biomarker (medicine), business, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e15f3bb56205f6b79b005fa60f764b
http://hdl.handle.net/11591/402603

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Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study

المساهمون: Tiziano, Fd, Lomastro, R, Di Pietro, L, Pasanisi, Mb, Fiori, S, Angelozzi, C, Abiusi, E, Angelini, C, Sorarù, G, Gaiani, A, Mongini, T, Vercelli, L, Vasco, G, Vita, G, Vita, G. L., Messina, S, Politano, Luisa, Passamano, L, Di Gregorio, Mg, Montomoli, C, Orsi, C, Campanella, A, Mantegazza, R, Morandi, L.

المصدر: European Journal of Human Genetics. 21:630-636

مصطلحات موضوعية: Male, Oncology, Messenger, Vital Capacity, SMN1, Spinal Muscular Atrophies of Childhood, Settore MED/03 - GENETICA MEDICA, Cohort Studies, Exon, Range of Motion, Articular, Genetics (clinical), spinal muscular atrophy, biomarker, outcome measure, real-time PCR, SMN, Adolescent, Adult, Biomarkers, Biomechanical Phenomena, Body Weight, Cross-Sectional Studies, Female, Genetic Loci, Genotype, Humans, Middle Aged, Motor Activity, RNA, Messenger, Survival of Motor Neuron 2 Protein, Young Adult, Genetics, SMA, medicine.anatomical_structure, Biomarker (medicine), Range of Motion, medicine.medical_specialty, Biology, Article, Internal medicine, medicine, Proximal spinal muscular atrophy, Spinal muscular atrophy, Motor neuron, medicine.disease, nervous system diseases, Lean body mass, RNA, Articular