GALLUS, GIAN NICOLA
 Distribuzione geografica
Continente #
NA - Nord America 126
EU - Europa 98
AS - Asia 52
OC - Oceania 5
AF - Africa 1
SA - Sud America 1
Totale 283
Nazione #
US - Stati Uniti d'America 118
IT - Italia 38
JP - Giappone 28
DE - Germania 18
IE - Irlanda 11
FR - Francia 10
CA - Canada 8
CN - Cina 7
HK - Hong Kong 5
AU - Australia 4
ES - Italia 4
IN - India 4
DK - Danimarca 3
GB - Regno Unito 3
NL - Olanda 3
VN - Vietnam 3
JO - Giordania 2
PT - Portogallo 2
TR - Turchia 2
BE - Belgio 1
BR - Brasile 1
CZ - Repubblica Ceca 1
FI - Finlandia 1
HU - Ungheria 1
IR - Iran 1
NZ - Nuova Zelanda 1
RO - Romania 1
RU - Federazione Russa 1
ZA - Sudafrica 1
Totale 283
Città #
Siena 21
Nishijin 18
Essen 12
Dublin 10
Chicago 8
New Brunswick 8
Ashburn 7
San Diego 7
Columbus 6
Madison 6
Ottawa 6
Santa Cruz 6
Boardman 5
Central 5
Fairfield 5
Denver 4
Seattle 4
Taku 4
Amsterdam 3
Baldwin 3
Dong Ket 3
Houston 3
Rome 3
Sydney 3
Vigo 3
Beijing 2
Bengaluru 2
Cernusco sul Naviglio 2
Elâzığ 2
Freiburg im Breisgau 2
Las Vegas 2
Lisbon 2
Milan 2
Nottinghamshire 2
Paris 2
Pavia 2
Sassari 2
Singen 2
Toronto 2
Vicopisano 2
Adirampattinam 1
Amman 1
Ann Arbor 1
Auckland 1
Barcelona 1
Cambridge 1
Columbia 1
Council Bluffs 1
Crugers 1
Durban 1
Genoa 1
Hangzhou 1
Helsinki 1
Henrico 1
Karasawa 1
Kobe 1
La Jolla 1
Lake Forest 1
Manchester 1
Menlo Park 1
Momoyamadai 1
Muncie 1
Mérignac 1
Namur 1
Naples 1
New Orleans 1
New York 1
Nuremberg 1
Perth 1
Ponta Grossa 1
Prague 1
Providence 1
Rockville 1
Salt Lake City 1
San Francisco 1
Shanghai 1
South Bend 1
Tokyo 1
Toulouse 1
University Park 1
Totale 233
Nome #
Cerebrotendinous xanthomatosis with progressive cerebellar vacuolation. Six-year MRI follow-up, file e0feeaa6-5a07-44d2-e053-6605fe0a8db0 117
Evaluation of cholesterol metabolism in cerebrotendinous xanthomatosis, file e0feeaa6-71e7-44d2-e053-6605fe0a8db0 46
Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene, file e0feeaa6-6d23-44d2-e053-6605fe0a8db0 36
Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease, file e0feeaab-c246-44d2-e053-6605fe0a8db0 27
Sporadic PEO caused by a novel POLG variation and a Twinkle mutation: digenic inheritance?, file e0feeaa6-6d62-44d2-e053-6605fe0a8db0 25
Leber's hereditary optic neuropathy associated with cocaine, ecstasy and telithromycin consumption, file e0feeaa6-037a-44d2-e053-6605fe0a8db0 11
Cerebellar hypometabolism with normal structural findings in Cerebrotendinous xanthomatosis. A case report, file e0feeaa5-7d0c-44d2-e053-6605fe0a8db0 8
Parkinsonism as neurological presentation of late-onset cerebrotendinous xanthomatosis, file e0feeaa5-fbd4-44d2-e053-6605fe0a8db0 5
Polyneuropathy in cerebrotendinous xanthomatosis and response to treatment with chenodeoxycholic acid., file e0feeaa4-eb81-44d2-e053-6605fe0a8db0 3
High frequency of OPA1 mutations causing high ADOA prevalence in south-eastern Sicily, Italy., file e0feeaa4-c207-44d2-e053-6605fe0a8db0 1
Alu-element insertion in an OPA1 intron sequence associated with autosomal dominant optic atrophy, file e0feeaa4-ea59-44d2-e053-6605fe0a8db0 1
Mitochondria, oxidative stress and neurodegeneration., file e0feeaa5-a306-44d2-e053-6605fe0a8db0 1
Clinical relevance and neurophysiological correlates of spasticity in cerebrotendinous xanthomatosis, file e0feeaa5-e0b5-44d2-e053-6605fe0a8db0 1
Novel POLG mutations and variable clinical phenotypes in 13 Italian patients, file e0feeaaa-6321-44d2-e053-6605fe0a8db0 1
Totale 283
Categoria #
all - tutte 1.477
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 1.477


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20217 0 1 0 1 0 0 0 1 0 0 1 3
2021/202247 0 2 1 6 6 2 4 0 1 6 15 4
2022/2023155 5 12 11 7 17 11 10 35 9 32 6 0
2023/202457 1 2 5 6 3 5 5 6 0 7 12 5
Totale 283