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1. Clinical dissection of early onset absence epilepsy in children and prognostic implications. Issue 10 (27th August 2013)

2. Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients. (September 2020)

3. Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1. Issue 1 (26th October 2019)

4. Coexistence of childhood absence epilepsy and benign epilepsy with centrotemporal spikes: A case series. (May 2017)

8. Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications. (14th August 2018)

9. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022)

10. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022)