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Genes|May 4, 2026
NLRP12 as a Regulator of Inflammation: Insights into the Correlation with Autoinflammatory DisordersBeatrice Rosa, Elisabetta Tabolacci, Roberta Pietrobono, et al.
Psychopharmacology|November 16, 2013
Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug developmentAndreea S Pop, Baltazar Gomez-Mancilla, Giovanni Neri, et al.
Nanomaterials (Basel, Switzerland)|March 29, 2017
CO and NO₂ Selective Monitoring by ZnO-Based SensorsMokhtar Hjiri, Lassaad El Mir, Salvatore Gianluca Leonardi, et al.
Nanomaterials (Basel, Switzerland)|November 27, 2021
Electrochemical and Fluorescent Properties of Crown Ether Functionalized Graphene Quantum Dots for Potassium and Sodium Ions DetectionDaniela Iannazzo, Claudia Espro, Angelo Ferlazzo, et al.
Sensors (Basel, Switzerland)|March 6, 2021
Fabrication of a Novel Electrochemical Sensor Based on Carbon Cloth Matrix Functionalized with MoO3 and 2D-MoS2 Layers for Riboflavin DeterminationRayhane Zribi, Antonino Foti, Maria Grazia Donato, et al.
European Journal of Human Genetics : EJHG|October 31, 2002
A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutationMarie A Shaw, Pietro Chiurazzi, Dennis R Romain, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 12, 2012
Real-time monitoring of breath ammonia during haemodialysis: use of ion mobility spectrometry (IMS) and cavity ring-down spectroscopy (CRDS) techniquesGiovanni Neri, Antonio Lacquaniti, Giuseppe Rizzo, et al.
European Journal of Human Genetics : EJHG|December 2, 2010
Integrated analysis of clinical signs and literature data for the diagnosis and therapy of a previously undescribed 6p21.3 deletion syndromeMarcella Zollino, Fiorella Gurrieri, Daniela Orteschi, et al.
American Journal of Medical Genetics. Part A|October 30, 2013
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies. 1984Giovanni Neri, Maria Enrica Martini-Neri, Ben E Katz, et al.
European Journal of Human Genetics : EJHG|September 26, 2024
New Insight into the genotype-phenotype correlation of PTH1R variants and primary failure of tooth eruption on an Italian CohortClarissa Modafferi, Elisabetta Tabolacci, Filomena Lo Vecchio, et al.
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