Suchergebnisse - "Procopio, Radha"

1

Analysis of the

von: Procopio, Radha

2019, in: Journal of the neurological sciences

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2

Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy

von: Procopio, Radha

2019, in: 26957 A study of dermoscopic features in relation to vitiligo activity

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3

Analysis of the TMEM230 gene in patients with multiple system atrophy

von: Procopio, Radha

2018, in: A new global analytical potential energy surface of NaH

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4

DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB

von: Procopio, Radha

2020transfer abstract, in: Corrigendum to “Electrical and thermal transport properties of Fe–Ni based ternary alloys in the earth's inner core: An ab initio study” [Physics of the Earth and Planetary Interiors

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5

Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy

von: Gagliardi, Monica

2020, in: Neurological sciences

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6

Mild case of Unverricht-Lundborg disease presenting as Juvenile myoclonic epilepsy

von: Giugno, Alessia

2021, in: Journal of the neurological sciences

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7

Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients

von: Bonapace, Giuseppe

2022, in: Corrigendum to “Electrical and thermal transport properties of Fe–Ni based ternary alloys in the earth's inner core: An ab initio study” [Physics of the Earth and Planetary Interiors

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8

Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria

von: Gagliardi, Monica

2018, in: A new global analytical potential energy surface of NaH

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9

Headache and sleep-related breathing disorders among patients with sclerosteosis and disease carriers

von: Rapisarda, Laura

2021, in: Journal of the neurological sciences

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10

DNAJC13 mutation screening in patients with Parkinson's disease from South Italy

von: Gagliardi, Monica

2018, in: Parkinsonism & related disorders

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11

Mutation analysis of the ATP13A2 gene in patients with PD and MSA from Italy

von: Gagliardi, Monica

2021, in: A new global analytical potential energy surface of NaH

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12

Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis

von: Bono, Francesco

2022, in: Neurological sciences

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13

A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy

von: Iannello, Grazia

2017, in: A new global analytical potential energy surface of NaH

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14

Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy” [J. Neurol. Sci. 381C (2017) 209–212]

von: Iannello, Grazia

2018, in: A new global analytical potential energy surface of NaH

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15

A novel phenotype in an Italian family with a rare progranulin mutation

von: Russillo, Maria Claudia

2022, in: Journal of neurology

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