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Journal of Clinical Microbiology|August 17, 1999
Onychomycosis caused by Blastoschizomyces capitatusD D'Antonio, F Romano, A Iacone, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Familial Ohtahara syndrome due to a novel ARX gene mutationL Giordano, S Sartori, S Russo, et al.
American Journal of Medical Genetics. Part A|June 18, 2009
Joubert syndrome with bilateral polymicrogyria: clinical and neuropathological findings in two brothersL Giordano, A Vignoli, L Pinelli, et al.
Seizure|April 18, 2024
Early onset absence epilepsy of childhood: Epidemiologic data, treatment and outcome in a sample of 56 patients born between 2000 and 2018C Filippi, S Damioli, P Accorsi, et al.
Clinical Genetics|June 21, 2008
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disordersF Brancati, L Travaglini, D Zablocka, et al.
Bone Marrow Transplantation|October 10, 2017
Secondary solid cancer following hematopoietic cell transplantation in patients with thalassemia majorS Santarone, A Pepe, A Meloni, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|September 20, 2018
Apheresis treatment of cryoglobulinemic vasculitis: A multicentre cohort study of 159 patientsP Marson, G Monti, F Montani, et al.
Acta Neurologica Scandinavica|January 25, 2018
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15)S Matricardi, F Darra, A Spalice, et al.
European Journal of Neurology|October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolutionS Agostinelli, M Traverso, P Accorsi, et al.
Neurology|May 28, 2010
Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiencyL Brun, L H Ngu, W T Keng, et al.
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