IRIS
GAGLIARDI, MONICA
 Distribuzione geografica
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Continente #
NA - Nord America 34
EU - Europa 9
AS - Asia 2
AF - Africa 1
Totale 46
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Nazione #
US - Stati Uniti d'America 34
IT - Italia 5
IN - India 2
BF - Burkina Faso 1
CZ - Repubblica Ceca 1
DE - Germania 1
FR - Francia 1
GB - Regno Unito 1
Totale 46
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Città #
Fleming Island 11
Milan 3
Ashburn 2
Hyderabad 2
Tappahannock 2
Boardman 1
Catanzaro 1
Chicago 1
Council Bluffs 1
Naples 1
Ouagadougou 1
Paris 1
Shoreline 1
Slough 1
Totale 29
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Nome #
DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB, file 0968c49a-2520-4db2-a40c-94a9044297d4 10
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease, file 3737324e-7878-42ca-9109-f5500ee78230 5
A novel phenotype in an Italian family with a rare progranulin mutation, file b6dadfce-1565-4246-92bb-df6274b6fdf9 4
Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy, file bdf8222d-e66c-445a-b50a-16aa2f950316 4
Analysis of the LRP10 gene in patients with Parkinson’s disease and dementia with Lewy bodies from Southern Italy, file 94418c11-32c3-4905-b0dd-6f90c9cc24e1 2
Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease, file 9e29b938-d1e8-4621-b931-2e6d659f347b 2
Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria, file ab42b7d3-c627-419e-bc22-603f0579d134 2
Corrigendum to “A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy” [J. Neurol. Sci. 381C (2017) 209–212] (S0022510X17337528) (10.1016/j.jns.2017.08.3260)), file bdc22658-59ce-4233-98ed-8e4d4797abba 2
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences, file c406f666-5226-4d8f-910d-cf7d3a20fe63 2
A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies, file de164cb4-4a82-6b31-e053-1705fe0a395c 2
PCDH19 mutations in female patients from southern Italy, file 0b1b2e88-ff52-4481-8c98-cae66911a1a6 1
Mutational analysis of TARDBP gene in patients affected by Parkinson's disease from Calabria, file 0be92a74-d308-4c4a-98ff-2123449f010a 1
Sacsin-related spastic ataxia caused by a novel missense mutation p.arg272his in a patient from sicily, Southern Italy, file 1553c483-3cfa-4e30-8a95-4084093b07a4 1
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP, file 1d624c9a-62b6-427c-b618-9456916b9eb4 1
Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy, file 31aa6e04-840f-48ad-889b-3664b5aeaebc 1
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy, file 613f0f8c-c7d7-454d-ab02-394ec825dfb8 1
Aceruloplasminemia: a multimodal imaging study in an Italian family with a novel mutation, file 715a2ef4-d0ed-428d-8a36-65cf2840f64a 1
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited, file 86240bc8-9497-448d-a688-441ed5179ba6 1
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium, file 8c97f36e-26b8-4629-91e0-1e6fe6c9d61f 1
Predicting functional effects of missense variants in voltage-gated sodium and calcium channels, file d3e09e84-a4ef-4501-90ce-2a0be5824b65 1
Analysis of the TMEM230 gene in familial Parkinson's disease from south Italy, file e632bd84-7110-4706-845a-60fe5a540a19 1
Totale 46
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Categoria #
all - tutte 135
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 135
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2022/202346 0 0 0 0 1 10 15 13 4 1 2 0
Totale 46