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Cells|September 19, 2019
Expression of FGFR1-4 in Malignant Pleural Mesothelioma Tissue and Corresponding Cell Lines and its Relationship to Patient Survival and FGFR Inhibitor SensitivityGregor Vlacic, Mir A Hoda, Thomas Klikovits, et al.
Neurogenetics|March 19, 2024
Whole exome sequencing in Serbian patients with hereditary spastic paraplegiaMarija Brankovic, Vukan Ivanovic, Ivana Basta, et al.
Oxidative Medicine and Cellular Longevity|May 10, 2021
Predictors of Mortality in Critically Ill COVID-19 Patients Demanding High Oxygen Flow: A Thin Line between Inflammation, Cytokine Storm, and CoagulopathyViseslav Popadic, Slobodan Klasnja, Natasa Milic, et al.
Clinical Chemistry and Laboratory Medicine|May 9, 2020
Stabilization patterns and variability of hs-CRP, NT-proBNP and ST2 during 1 year after acute coronary syndrome admission: results of the BIOMArCS studyVictor J van den Berg, Victor A W M Umans, Milos Brankovic, et al.
Journal of Medical Genetics|August 2, 2020
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disordersFrancesco Nicita, Monia Ginevrino, Lorena Travaglini, et al.
Oxidative Medicine and Cellular Longevity|July 14, 2021
Development and Validation of a Multivariable Predictive Model for Mortality of COVID-19 Patients Demanding High Oxygen Flow at Admission to ICU: AIDA ScoreMarija Zdravkovic, Viseslav Popadic, Slobodan Klasnja, et al.
Human Mutation|February 19, 2013
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseMiriam Schmidts, Valeska Frank, Tobias Eisenberger, et al.
Journal of Medical Genetics|June 4, 2021
Refining the mutational spectrum and gene-phenotype correlates in pontocerebellar hypoplasia: results of a multicentric studySara Nuovo, Alessia Micalizzi, Romina Romaniello, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 5, 2019
A clinical diagnostic algorithm for early onset cerebellar ataxiaR Brandsma, C C Verschuuren-Bemelmans, D Amrom, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 12, 2022
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar AtaxiaLiedewei Van de Vondel, Jonathan De Winter, Danique Beijer, et al.
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