Citescorey = Citationsy + Citationsy-1 + Citationsy-2 + Citations y-3 / Published articlesy + Published articlesy-1 + Published articlesy-2 + Published articles y-3
Lilljebjörn, Lisa Vikström, et al. "A role of the heme degradation pathway in shaping prostate inflammatory responses and lipid metabolism." The American journal of pathology 190.4 (2020): 830-843. View at Publisher|View at Google Scholar|View at Indexing
Johnston G, Dermatology Williams HC. Comparison of the two most commonly used treatments for pyoderma gangrenosum: results of the STOP Randomised Controlled Trial. View at Publisher|View at Google Scholar|View at Indexing
Vischer N, Pfeiffer C, Limacher M, Burri C. " You can save time if…"—A qualitative study on internal factors slowing down clinical trials in Sub-Saharan Africa. Plos one. 2017 Mar 16;12(3):e0173796. View at Publisher|View at Google Scholar|View at Indexing
Thompson, Rachel, Agata Robertson, and Hanns Lochmüller. "Natural history, trial readiness and gene discovery: advances in patient registries for neuromuscular disease." Rare Diseases Epidemiology: Update and Overview (2017): 97-124. View at Publisher|View at Google Scholar|View at Indexing
Vischer N, Pfeiffer C, Kealy J, Burri C. Increasing protocol suitability for clinical trials in sub-Saharan Africa: a mixed methods study. Global health research and policy. 2017 Dec;2(1):1-5. View at Publisher|View at Google Scholar|View at Indexing
Bishop, Courtney A., et al. "Semi-automated analysis of diaphragmatic motion with dynamic magnetic resonance imaging in healthy controls and non-ambulant subjects with Duchenne muscular dystrophy." Frontiers in neurology 9 (2018): 9. View at Publisher|View at Google Scholar|View at Indexing
Crispi, Vassili, and Antonios Matsakas. "Duchenne muscular dystrophy: genome editing gives new hope for treatment." Postgraduate medical journal 94.1111 (2018): 296-304. View at Publisher|View at Google Scholar|View at Indexing
Hamuro, Lora, et al. "Developing a Natural History Progression Model for Duchenne Muscular Dystrophy Using the Six?Minute Walk Test." CPT: pharmacometrics & systems pharmacology 6.9 (2017): 596-603. View at Publisher|View at Google Scholar|View at Indexing
Huguet F, Cayuela JM, Cambier N, Carpentier N, Tindel M, Violet I, Zunic P, Lascaux A, Etienne G, AdheRMC Investigators, Didier Innocent AD. Nilotinib efficacy, safety, adherence and impact on quality of life in newly diagnosed patients with chronic myeloid leukaemia in chronic phase: a prospective observational study in daily clinical practice. British journal of haematology. 2019 Dec;187(5):615-26. View at Publisher|View at Google Scholar|View at Indexing
Yin, Liang, et al. "T2 mapping and fat quantification of thigh muscles in children with Duchenne muscular dystrophy." Current medical science 39.1 (2019): 138-145. View at Publisher|View at Google Scholar|View at Indexing
Propp, Roni, et al. "Development and content validation of the Muscular Dystrophy Child Health Index of Life with Disabilities questionnaire for children with Duchenne muscular dystrophy." Developmental Medicine & Child Neurology 61.1 (2019): 75-81. View at Publisher|View at Google Scholar|View at Indexing
Pareyson D, Saveri P, Pisciotta C. New developments in CharcotâMarieâTooth neuropathy and related diseases. Current opinion in neurology. 2017 Oct 1;30(5):471-80. View at Publisher|View at Google Scholar|View at Indexing
Lucca, Silvana Aparecida de, and Eucia Beatriz Lopes Petean. "Paternidade: vivências de pais de meninos diagnosticados com distrofia muscular de Duchenne." Ciência & Saúde Coletiva 21 (2016): 3081-3089. View at Publisher|View at Google Scholar|View at Indexing
Weng, Wen-Chin, et al. "Instantaneous frequency as a new approach for evaluating the clinical severity of Duchenne muscular dystrophy through ultrasound imaging." Ultrasonics 94 (2019): 235-241. View at Publisher|View at Google Scholar|View at Indexing
Piscosquito G, Reilly MM, Schenone A, Fabrizi GM, Cavallaro T, Santoro L, Manganelli F, Vita G, Quattrone A, Padua L, Gemignani F. Responsiveness of clinical outcome measures in Charcot− Marie− Tooth disease. European journal of neurology. 2015 Dec;22(12):1556-63. View at Publisher|View at Google Scholar|View at Indexing
Hogrel, Jean-Yves, et al. "Normalized grip strength is a sensitive outcome measure through all stages of Duchenne muscular dystrophy." Journal of neurology 267.7 (2020): 2022-2028. View at Publisher|View at Google Scholar|View at Indexing
da Silva, Talita Dias, et al. "Evaluation of speed-accuracy trade-off in a computer task to identify motor difficulties in individuals with Duchenne Muscular Dystrophy-a cross-sectional study." Research in developmental disabilities 96 (2020): 103541. View at Publisher|View at Google Scholar|View at Indexing
?????, ?. ?., et al. "?????????? ?????????? ????????? ? ????????????????? (???????? ????????? ???????/???????): ?????????? ????????????????? ???? ? ?????????????? ??????? ????????????." ??????-???????? ??????? 3 (2014). View at Publisher|View at Google Scholar|View at Indexing
Mulyadi HA, Sianturi OR. The Occurrence of Harmful Jellyfish Outbreaks and Human Stung Reported at Recreational Beaches in Special Region of Yogyakarta, Indonesia. InIOP Conference Series: Earth and Environmental Science 2021 Jun 1 (Vol. 789, No. 1, p. 012005). IOP Publishing. View at Publisher|View at Google Scholar|View at Indexing
Schofield, C., et al. "The development of a consensus statement for the prescription of powered wheelchair standing devices in Duchenne muscular dystrophy." Disability and Rehabilitation (2020): 1-9. View at Publisher|View at Google Scholar|View at Indexing
Chrzanowski, Stephen M., Basil T. Darras, and Seward B. Rutkove. "The value of imaging and composition-based biomarkers in Duchenne muscular dystrophy clinical trials." Neurotherapeutics 17.1 (2020): 142-152. View at Publisher|View at Google Scholar|View at Indexing
Biswas S, Dey SK. A Comparative study for Diagnostic Evaluation of Polycystic Ovarian Syndrome (PCOS) by Estimation of High Sensitivity C-reactive protein (hsCRP) and Insulin Resistance. JMSCR. 2018;6(5):69-74. View at Publisher|View at Google Scholar|View at Indexing
Propp, Roni. Development and psychometric evaluation of the muscular dystrophy child health index of life with disabilities (MDCHILD) questionnaire in children with Duchenne muscular dystrophy. Diss. University of Toronto (Canada), 2017. View at Publisher|View at Google Scholar|View at Indexing
Finkel, Richard S., et al. "Disease-modifying effects of edasalonexent, an NF-κB inhibitor, in young boys with Duchenne muscular dystrophy: Results of the MoveDMD phase 2 and open label extension trial." Neuromuscular Disorders 31.5 (2021): 385-396. View at Publisher|View at Google Scholar|View at Indexing
Lavezzi, S. M., et al. "Assessing drug effect from distributional data: A population approach with application to Duchenne muscular dystrophy treatment." Computer methods and programs in biomedicine 178 (2019): 329-342. View at Publisher|View at Google Scholar|View at Indexing
Obisike, U. A., et al. "Assessment of Antioxidant Effects of Aqueous and Ethanolic Extracts of Zingiber officinale Rhizome in Testosterone Induced Benign Prostatic Hyperplasia Rat Model." Journal of Complementary and Alternative Medical Research (2019): 1-12. View at Publisher|View at Google Scholar|View at Indexing
Gowran, Aoife, et al. "Multiomic approaches to uncover the complexities of dystrophin-associated cardiomyopathy." International Journal of Molecular Sciences 22.16 (2021): 8954. View at Publisher|View at Google Scholar|View at Indexing
Goemans, Nathalie, et al. "Prognostic factors for changes in the timed 4-stair climb in patients with Duchenne muscular dystrophy, and implications for measuring drug efficacy: A multi-institutional collaboration." PloS one 15.6 (2020): e0232870. View at Publisher|View at Google Scholar|View at Indexing
Liu, Wenjing, et al. "Chemical characterization and 5α-reductase inhibitory activity of phenolic compounds in goji berries." Journal of Pharmaceutical and Biomedical Analysis 201 (2021): 114119. View at Publisher|View at Google Scholar|View at Indexing
Arteaga, David, et al. "Assessing physical activity using accelerometers in youth with duchenne muscular dystrophy." Journal of neuromuscular diseases 7.3 (2020): 331-342. View at Publisher|View at Google Scholar|View at Indexing
Malkovskiy AV, Yacob AA, Dunn CE, Zirbes JM, Ryan SP, Bollyky PL, Rajadas J, Milla CE. Salivary Thiocyanate as a Biomarker of Cystic Fibrosis Transmembrane Regulator Function. Analytical chemistry. 2019 May 22;91(12):7929-34. View at Publisher|View at Google Scholar|View at Indexing
Arora, Harneet. Examination of Disease Progression in Upper and Lower Limb Muscles in Boys with DMD Using Functional Clinical Endpoints and Magnetic Resonance Imaging. Diss. University of Florida, 2017. View at Publisher|View at Google Scholar|View at Indexing
Finkel, Richard S., et al. "A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD Trial." Journal of Neuromuscular Diseases Preprint (2021): 1-16. View at Publisher|View at Google Scholar|View at Indexing
Gonzales, Gustavo F., Cinthya Vasquez-Velasquez, and Dulce Esperanza Alarcón-Yaquetto. "Science Behind Maca: A Traditional Crop from the Central Andes." Nutraceuticals and Dietary Supplements. Apple Academic Press, 2020. 241-263. View at Publisher|View at Google Scholar|View at Indexing