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526 results on '"Bisulli, F."'

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51. Erratum to: Survival prediction in high-grade gliomas using CT perfusion imaging [J Neurooncol (2015) 123, 93-102, DOI 10.1007/s11060-015-1766-5]

52. Insight into epileptic and physiological déjà vu : from a multicentric cohort study

53. The Prognostic Roles of Gender and O6-Methylguanine-DNA Methyltransferase Methylation Status in Glioblastoma Patients: The Female Power

54. Exon-disrupting deletions ofNRXN1in idiopathic generalized epilepsy

55. Myoclonus Epilepsy and Ataxia due to KCNC1 Mutation: Analysis of 20 Cases and K plus Channel Properties

56. Erratum: Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy (Epilepsia (2013) 54 (256-264) DOI:10.1111/epi.12517)

57. Insight into epileptic and physiological déjà vu: from a multicentric cohort study.

59. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

60. Definition and diagnostic criteria of sleep-related hypermotor epilepsy

61. Family study of epilepsy in first degree relatives: data from the Italian Episcreen Study

62. Expression of 19 microRNAs in glioblastoma and comparison with other brain neoplasia of grades I-III

64. PRIMA1 mutation: A new cause of nocturnal frontal lobe epilepsy

65. PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

66. Epilepsy with auditory features: A heterogeneous clinico-molecular disease.

67. Erratum to: Survival prediction in high-grade gliomas using CT perfusion imaging

68. Definition of miRNAs Expression Profile in Glioblastoma Samples: The Relevance of Non-Neoplastic Brain Reference

69. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1,2q22.3 and 17q21.32

70. Assenze ad esordio precoce: una sindrome isolata? Studio collaborativo LICE su 33 casi

72. Mutations in Mammalian Target of Rapamycin Regulator DEPDC5 Cause Focal Epilepsy with Brain Malformations

73. Nocturnal Frontal Lobe Epilepsy

74. Health-related quality of life in epilepsy: findings obtained with a new Italian instrument

75. Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy

80. Pattern of care and effectiveness of treatment for glioblastoma patients in the real world: Results from a prospective population-based registry. Could survival differ in a high-volume center?

81. Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families

82. Right mesial temporal sclerosis and left temporal seizures? Description of a case | [Sclerosi temporale mesiale (STM) destra e crisi temporali sinistre: Epilessia sintomatica a destra e criptogenetica a sinistra? Discussione di un caso]

86. Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy

87. Neurophysiological study of paroxysmal EEG activity during 'electrical status epilepticus during sleep' in a patient with Landau-Kleffner syndrome | [Studio neurofisiologico delle attivita parossistiche durante 'stato di male elettrico durante il sonno' in un paziente con sindrome di Landau- Kleffner]

89. STRUCTURAL ANOMALY OF LEFT LATERAL TEMPORAL LOBE IN EPILEPSY DUE TO MUTATED LGI1

92. Clinical features and long term outcome of epilepsy in periventricular nodular heterotopia. Simple compared with plus forms.

93. Cerebral areas involved in music perception: Studying musicogenic epilepsy

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