Suchergebnisse - "Scorrano, Giovanna"

PubPharm (31)

1

Perinatal outcome in anti-NMDAr encephalitis during pregnancy-a systematic review with individual patients' data analysis

enthalten in: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2024

von Scorrano, G. | Dono, F. | Corniello, C. | +7

2

The latest advances in the pharmacological management of focal epilepsies in children : a narrative review

enthalten in: Expert review of neurotherapeutics | 2024

von Matricardi, S. | Scorrano, G. | Prezioso, G. | +5

3

Clinical and molecular heterogeneity of VPS13D-related neurodevelopmental and movement disorders

enthalten in: Gene | 2024

von Sultan, T. | Scorrano, G. | Panciroli, M. | +7

4

The Cognitive and Behavioural Effects of Perampanel in Children with Neurodevelopmental Disorders : A Systematic Review

enthalten in: Journal of clinical medicine | 2024

von Scorrano, G. | Lattanzi, S. | Salpietro, V. | +3

5

Corrigendum : Neuroimaging in PRUNE1 syndrome: a mini-review of the literature

enthalten in: Frontiers in neurology | 2024

von Scorrano, G. | Battaglia, L. | Spiaggia, R. | +10

ErratumFor: Front Neurol. 2023 Dec 21;14:1301147. - PMID 38178891

6

Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome

enthalten in: American journal of human genetics | 2024

von Salpietro, V. | Maroofian, R. | Zaki, M. | +164

7

Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disorders

enthalten in: Frontiers in molecular neuroscience | 2024

von Iacomino, M. | Houerbi, N. | Fortuna, S. | +30

8

A case of pediatric Guillain-Barré syndrome following hand-foot-and-mouth disease and the need for Brighton criteria revision in children

enthalten in: Acta neurologica Belgica | 2023

von Scorrano, G. | Russo, M. | Prezioso, G. | +2

9

Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections (PANDAS) Syndrome : A 10-Year Retrospective Cohort Study in an Italian Centre of Pediatric Rheumatology

enthalten in: Microorganisms | 2023

von La Bella, S. | Attanasi, M. | Di Ludovico, A. | +8

10

A PAK1 mutational hotspot within the regulatory CRIPaK domain is associated with severe neurodevelopmental disorders in children

enthalten in: Pediatric neurology | December 2023

von Scorrano, G. | D'Onofrio, G. | Accogli, A. | +23