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Molecular & General Genetics : MGG|March 10, 1998
Screening of larval/pupal P-element induced lethals on the second chromosome in Drosophila melanogaster: clonal analysis and morphology of imaginal discsF Roch, F Serras, F J Cifuentes, et al.
Acta Ophthalmologica|May 9, 2017
Optical coherence tomography morphology and evolution in cblC disease-related maculopathy in a case series of very young patientsGiacomo M Bacci, Maria A Donati, Elisabetta Pasquini, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 25, 2018
Functional and pharmacological evaluation of novel GLA variants in Fabry disease identifies six (two de novo) causative mutations and two amenable variants to the chaperone DGJLorenzo Ferri, Duccio Malesci, Antonella Fioravanti, et al.
American Journal of Otolaryngology|May 14, 2020
Early experience in tracheostomy and tracheostomy tube management in Covid-19 patientsOttavio Piccin, Riccardo Albertini, Umberto Caliceti, et al.
BMC Cancer|October 6, 2009
Anti-HER2 IgY antibody-functionalized single-walled carbon nanotubes for detection and selective destruction of breast cancer cellsYan Xiao, Xiugong Gao, Oleh Taratula, et al.
Biochimica Et Biophysica Acta|November 28, 2009
Functional studies of new GLA gene mutations leading to conformational Fabry diseaseC Filoni, A Caciotti, L Carraresi, et al.
International Journal of Molecular Sciences|January 25, 2018
Late-Onset N-Acetylglutamate Synthase Deficiency: Report of a Paradigmatic Adult Case Presenting with Headaches and Review of the LiteratureCatia Cavicchi, Chiara Chilleri, Antonella Fioravanti, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
Intra-individual plasticity of the TAZ gene leading to different heritable mutations in siblings with Barth syndromeLorenzo Ferri, Maria A Donati, Silvia Funghini, et al.
Scandinavian Journal of Gastroenterology|May 9, 2019
Comparison of 20-gauge Procore® and 22-gauge Acquire® needles for EUS-FNB of solid pancreatic masses: an observational studyDavid Karsenti, Gaëlle Tharsis, Jean-David Zeitoun, et al.
Orphanet Journal of Rare Diseases|July 17, 2014
Sudden unexpected fatal encephalopathy in adults with OTC gene mutations-Clues for early diagnosis and timely treatmentCatia Cavicchi, Maria Donati, Rossella Parini, et al.
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