Suchergebnisse - "Mastrangelo, Mario"

PubPharm (142)

1

The burden of epilepsy on long-term outcome of genetic developmental and epileptic encephalopathies : A single tertiary center longitudinal retrospective cohort study

enthalten in: Epilepsy & behavior : E&B | 2024

von Mastrangelo, M. | Manti, F. | Ricciardi, G. | +4

2

L-serine treatment in patients with GRIN-related encephalopathy : A phase 2A, non-randomized study

enthalten in: Brain : a journal of neurology | 2024

von Juliá-Palacios, N. | Olivella, M. | Sigatullina Bondarenko, M. | +44

3

The impact of a newly established specialized pediatric epilepsy center in Tanzania : An observational study

enthalten in: Epilepsy & behavior : E&B | 2023

von Aricò, M. | Mastrangelo, M. | Di Noia, S. | +3

4

Sudden unexpected death in epilepsy : The need for age-specific evidence-based prevention

enthalten in: Developmental medicine and child neurology | 2023

von Mastrangelo, M. | Esposito, D. | Pisani, F.

CommentOn: Dev Med Child Neurol. 2023 Sep;65(9):1150-1156. - PMID 36802063

5

Natural Course of IQSEC2-Related Encephalopathy : An Italian National Structured Survey

enthalten in: Children (Basel, Switzerland) | 2023

von Leoncini, S. | Boasiako, L. | Lopergolo, D. | +10

6

Clinical profiles of acute arterial ischemic neonatal stroke

enthalten in: Minerva pediatrics | 2023

von Mastrangelo, M. | Bove, R. | Ricciardi, G. | +5

7

Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia : A Multicentric Cross-sectional Study

enthalten in: Pediatric neurology | 2023

von Toldo, I. | Brunello, F. | Cavasin, P. | +33

8

Epilepsy Phenotypes of Vitamin B6-Dependent Diseases : An Updated Systematic Review

enthalten in: Children (Basel, Switzerland) | 2023

von Mastrangelo, M. | Gasparri, V. | Bernardi, K. | +3

9

Generation of an induced pluripotent stem cell line CSSi015-A (9553), carrying a point mutation c.2915C > T in the human calcium sensing receptor (CasR) gene

enthalten in: Stem cell research | 2023

von Rotundo, G. | Turco, E. | Ruotolo, G. | +11

10

Biallelic variants in HECT E3 paralogs, HECTD4 and UBE3C, encoding ubiquitin ligases cause neurodevelopmental disorders that overlap with Angelman syndrome

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Faqeih, E. | Alghamdi, M. | Almahroos, M. | +34

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