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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|April 18, 2016
The structure of the lipooligosaccharide from Xanthomonas oryzae pv. Oryzae: the causal agent of the bacterial leaf blight in riceFlaviana Di Lorenzo, Angelo Palmigiano, Alba Silipo, 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.
Autism Research : Official Journal of the International Society for Autism Research|August 20, 2015
CSF N-glycan profile reveals sialylation deficiency in a patient with GM2 gangliosidosis presenting as childhood disintegrative disorderRita Barone, Luisella Sturiale, Agata Fiumara, 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.
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.
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.
European Journal of Medical Genetics|July 7, 2009
A new mutation in COG7 extends the spectrum of COG subunit deficienciesRenate Zeevaert, François Foulquier, David Cheillan, 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.
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