statistiche ricercatore

Continente	#
NA - Nord America	1.448
EU - Europa	1.108
AS - Asia	435
SA - Sud America	55
Continente sconosciuto - Info sul continente non disponibili	39
AF - Africa	24
OC - Oceania	4
Totale	3.113

Nazione	#
US - Stati Uniti d'America	1.430
GB - Regno Unito	248
RU - Federazione Russa	216
IT - Italia	213
CN - Cina	158
IE - Irlanda	141
SG - Singapore	136
DE - Germania	62
SE - Svezia	58
UA - Ucraina	53
FR - Francia	45
VN - Vietnam	43
BR - Brasile	38
HK - Hong Kong	34
FI - Finlandia	19
ES - Italia	15
ZA - Sudafrica	14
KR - Corea	13
IN - India	12
AT - Austria	8
CA - Canada	8
TR - Turchia	8
MX - Messico	7
BD - Bangladesh	6
BE - Belgio	6
AR - Argentina	5
JP - Giappone	5
NL - Olanda	5
AU - Australia	4
CO - Colombia	4
IQ - Iraq	4
LT - Lituania	4
PK - Pakistan	4
MA - Marocco	3
PL - Polonia	3
AE - Emirati Arabi Uniti	2
AZ - Azerbaigian	2
CH - Svizzera	2
CZ - Repubblica Ceca	2
HU - Ungheria	2
LV - Lettonia	2
NG - Nigeria	2
PE - Perù	2
SK - Slovacchia (Repubblica Slovacca)	2
UY - Uruguay	2
VE - Venezuela	2
AL - Albania	1
CI - Costa d'Avorio	1
CL - Cile	1
CR - Costa Rica	1
CW - ???statistics.table.value.countryCode.CW???	1
DO - Repubblica Dominicana	1
EC - Ecuador	1
EG - Egitto	1
ET - Etiopia	1
GR - Grecia	1
IR - Iran	1
JM - Giamaica	1
KG - Kirghizistan	1
KH - Cambogia	1
LB - Libano	1
LK - Sri Lanka	1
MN - Mongolia	1
NP - Nepal	1
PH - Filippine	1
SN - Senegal	1
TN - Tunisia	1
Totale	3.075

Nome	#
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia	383
Negative chronotropism, positive inotropism and lusitropism of 3,5-di-t-butyl-4-hydroxyanisole (DTBHA) on rat heart preparations occur through reduction of RyR2 Ca2+ leak	346
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q)	337
Molecular determinants of homo- and heteromeric interactions of Junctophilin-1 at triads in adult skeletal muscle fibers	312
Diagnosis of calcium pyrophosphate dihydrate crystal deposition disease: ultrasonographic criteria proposed.	299
A truncation in the RYR1 gene associated with central core lesions in skeletal muscle fibres	298
Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity	278
Distinct regions of triadin are required for targeting and retention at the junctional domain of the sarcoplasmic reticulum	274
Expression of macrophage migration inhibitory factor in diffuse systemic sclerosis	240
The dissolution of mono-sodium urate monohydrate crystals: formulation of a biocompatible buffer solution with potential use in the treatment of gouty arthropaties	176
Multiple regions within junctin drive its interaction with calsequestrin-1 and its localization to triads in skeletal muscle	170
Totale	3.113

	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2021/2022	199	0	28	10	13	15	12	17	11	21	12	20	40
2022/2023	255	11	26	31	35	28	50	4	19	20	15	9	7
2023/2024	220	2	6	24	9	3	77	77	2	1	2	3	14
2024/2025	354	7	19	46	16	52	15	5	25	44	12	40	73
2025/2026	988	55	121	183	131	189	54	104	20	29	35	15	52
2026/2027	50	23	27	0	0	0	0	0	0	0	0	0	0
Totale													3.113