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Neuromuscular Disorders : NMD|July 23, 2014
Milder course in Duchenne patients with nonsense mutations and no muscle dystrophinM Zatz, R C M Pavanello, M Lazar, et al.Minerva Chirurgica|November 27, 1999
[Palliative treatment of esophageal and cardial carcinoma]L Norberto, R Ranzato, F Erroi, et al.Minerva Pediatrica|November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomyA Consales, P Striano, P Nozza, et al.Journal of Neuromuscular Diseases|November 19, 2016
Reviewing Large LAMA2 Deletions and Duplications in Congenital Muscular Dystrophy PatientsJorge Oliveira, Ana Gonçalves, Márcia E Oliveira, et al.Muscle & Nerve|January 18, 2007
Central core disease due to recessive mutations in RYR1 gene: is it more common than described?Patrícia M Kossugue, Júlia F Paim, Monica M Navarro, et al.American Journal of Medical Genetics. Part A|December 7, 2013
Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1V Capra, M Severino, A Rossi, et al.Minerva Gastroenterology|October 5, 2023
Diagnostic accuracy of antiendomysial antibodies biopsy test for celiac disease in clinical practiceElisa Benelli, Giulia Zavarise, Paolo M Pavanello, et al.Neuromuscular Disorders : NMD|April 22, 2004
A novel stop codon mutation in the PMP22 gene associated with a variable phenotypeK T Abe, A M M Lino, M T A Hirata, et al.Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 24, 2006
Genetic abnormalities and CNS tumors: report of two cases of ependymoma associated with Klinefelter's Syndrome (KS)M L Garrè, V Capra, E Di Battista, et al.European Journal of Human Genetics : EJHG|December 4, 2002
Clinical variability in calpainopathy: what makes the difference?Flávia de Paula, Mariz Vainzof, Maria Rita Passos-Bueno, et al.Pageof 12