statistiche per VALENTINO, MARIA LUCIA

Distribuzione geografica

Continente	#
NA - Nord America	607
EU - Europa	125
AS - Asia	51
SA - Sud America	4
AF - Africa	3
Totale	790

Salva come PNG Salva come JPEG

Nazione	#
US - Stati Uniti d'America	597
IT - Italia	44
GB - Regno Unito	27
DE - Germania	21
IN - India	21
VN - Vietnam	18
FR - Francia	13
CA - Canada	10
CN - Cina	6
CL - Cile	4
RU - Federazione Russa	4
UA - Ucraina	4
JP - Giappone	3
NL - Olanda	3
ZA - Sudafrica	3
CH - Svizzera	2
RS - Serbia	2
TW - Taiwan	2
ES - Italia	1
FI - Finlandia	1
GR - Grecia	1
HU - Ungheria	1
LB - Libano	1
LT - Lituania	1
Totale	790

Salva come PNG Salva come JPEG

Città	#
Fairfield	107
Santa Cruz	62
Seattle	54
Woodbridge	46
Houston	43
Buffalo	39
Cambridge	35
Ashburn	29
Wilmington	24
Southend	22
Ann Arbor	17
Bologna	16
Chicago	12
Dong Ket	10
Grafing	10
San Diego	10
Las Vegas	9
Lake Forest	7
Ottawa	7
Phoenix	7
Andover	6
Castel Bolognese	6
Clearwater	6
Falls Church	6
Henderson	4
Jacksonville	4
Milpitas	4
Comano	3
Encino	3
Milan	3
Mountain View	3
Russi	3
Chengdu	2
Fujita	2
Los Angeles	2
Munich	2
Provo	2
Riva	2
Silverton	2
Taipei	2
Toronto	2
Abbasanta	1
Ancona	1
Auburn	1
Baotou	1
Basking Ridge	1
Beirut	1
Budapest	1
Büdelsdorf	1
Chandler	1
Cheyenne	1
Dallas	1
Dearborn	1
Fano	1
Garbagnate Milanese	1
Hamilton	1
Kansas City	1
Klaipeda	1
Kunming	1
Lugo	1
Muizenberg	1
Mumbai	1
Norwalk	1
Parsippany	1
Pittsburgh	1
Redwood City	1
Saint Petersburg	1
San Jose	1
San Mateo	1
Santiago	1
Sunnyvale	1
Tianjin	1
Trumbull	1
University Park	1
Waltham	1
Wuhan	1
Yellow Springs	1
Totale	671

Salva come PNG Salva come JPEG

Nome	#
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber's hereditary optic neuropathy, file 467392	96
Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells., file 407483	83
Secondary post-geniculate involvement in Leber's hereditary optic neuropathy., file 462530	71
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454792	70
A novel null homozygous mutation confirms CACNA2D2 as a gene mutated in epileptic encephalopathy., file 464100	69
A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck., file 46815	64
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways, file 631487	43
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome, file 656676	42
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy, file 767619	42
Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy?, file 635530	41
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file 636084	40
Novel mutations in DNA2 associated with myopathy and mtDNA instability, file 617100	38
Hearing dysfunction in a large family affected by dominant optic atrophy (OPA8-related DOA): A human model of hidden auditory neuropathy, file 636888	37
Syndromic parkinsonism and dementia associated with OPA1 missense mutations, file 808468	24
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome, file 656677	17
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation., file 822796	13
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454802	8
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454796	7
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454803	7
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454793	6
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454794	6
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., file 454795	6
Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways, file 631488	5
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network, file 937841	4
Novel mutations in DNA2 associated with myopathy and mtDNA instability, file 617321	3
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network, file 937842	2
Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation, file 312029	1
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy, file 636088	1
Totale	846

Salva come PNG Salva come JPEG

Categoria	#
all - tutte	846
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	846

Salva come PNG Salva come JPEG

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2017/2018	1	0	0	0	0	0	0	1	0	0	0	0	0
2018/2019	13	0	0	0	0	0	0	3	0	0	0	0	10
2019/2020	241	3	1	0	14	27	28	28	32	38	22	29	19
2020/2021	260	22	28	9	21	10	19	25	22	22	22	30	30
2021/2022	330	14	22	21	18	40	12	17	44	17	31	94	0
Totale													846

CRIS Current Research Information System

statistiche per VALENTINO, MARIA LUCIA