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American Journal of Medical Genetics. Part A|July 17, 2008
Clinical phenotype correlates to glycoprotein phenotype in a sib pair with CDG-IaRita Barone, Luisa Sturiale, Vito Sofia, et al.
Carbohydrate Research|November 3, 2004
Structure of minor oligosaccharides from the lipopolysaccharide fraction from Pseudomonas stutzeri OX1Serena Leone, Viviana Izzo, Luisa Sturiale, et al.
Proteomics|August 21, 2008
Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI-TOF MSLuisa Sturiale, Rita Barone, Angelo Palmigiano, et al.
Carbohydrate Research|February 1, 2006
Structural elucidation of the core-lipid A backbone from the lipopolysaccharide of Acinetobacter radioresistens S13, an organic solvent tolerant Gram-negative bacteriumSerena Leone, Antonio Molinaro, Enrica Pessione, et al.
Advances in Experimental Medicine and Biology|November 29, 2018
Biophysical Approaches to Solve the Structures of the Complex Glycan Shield of ChlorovirusesCristina De Castro, Garry A Duncan, Domenico Garozzo, et al.
Glycoconjugate Journal|March 1, 2021
Mass spectrometry glycophenotype characterization of ALG2-CDG in Argentinean patients with a new genetic variant in homozygosisGabriela Magali Papazoglu, Marisa Cubilla, Marcela Pereyra, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 22, 2019
CSF N-Glycoproteomics Using MALDI MS Techniques in Neurodegenerative DiseasesAngela Messina, Angelo Palmigiano, Rosaria Ornella Bua, et al.
The Journal of Biological Chemistry|July 29, 2005
The elicitation of plant innate immunity by lipooligosaccharide of Xanthomonas campestrisAlba Silipo, Antonio Molinaro, Luisa Sturiale, et al.
European Journal of Medical Genetics|January 27, 2023
Higher frequency of TMEM199-CDG in the southern mediterranean area is associated with c.92G>C (p.Arg31Pro) mutationAgata Fiumara, Annamaria Sapuppo, Lorenzo Ferri, et al.
Glycoconjugate Journal|September 11, 2020
HILIC-UPLC-MS for high throughput and isomeric N-glycan separation and characterization in Congenital Disorders Glycosylation and human diseasesAngela Messina, Angelo Palmigiano, Francesca Esposito, et al.
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