Catalogo dei prodotti della ricerca

CASALI, Carlo
 Distribuzione geografica
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Continente #
NA - Nord America 7.129
EU - Europa 1.637
AS - Asia 811
AF - Africa 49
SA - Sud America 41
OC - Oceania 14
Continente sconosciuto - Info sul continente non disponibili 2
Totale 9.683
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Nazione #
US - Stati Uniti d'America 7.089
IT - Italia 651
IN - India 294
CN - Cina 258
UA - Ucraina 212
SG - Singapore 197
SE - Svezia 184
FI - Finlandia 163
GB - Regno Unito 68
DE - Germania 67
FR - Francia 52
BE - Belgio 50
IE - Irlanda 43
BG - Bulgaria 38
CA - Canada 35
NL - Olanda 35
AR - Argentina 30
TG - Togo 29
KR - Corea 21
JP - Giappone 18
ES - Italia 14
RO - Romania 14
AU - Australia 12
ZA - Sudafrica 12
CH - Svizzera 10
HU - Ungheria 10
AT - Austria 8
TR - Turchia 8
IR - Iran 6
EC - Ecuador 4
EE - Estonia 4
BR - Brasile 3
CL - Cile 3
DK - Danimarca 3
GL - Groenlandia 3
IQ - Iraq 3
MA - Marocco 3
PL - Polonia 3
PT - Portogallo 3
SC - Seychelles 3
EU - Europa 2
HK - Hong Kong 2
MX - Messico 2
NZ - Nuova Zelanda 2
RU - Federazione Russa 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BT - Bhutan 1
CO - Colombia 1
EG - Egitto 1
GH - Ghana 1
ID - Indonesia 1
IL - Israele 1
JO - Giordania 1
RS - Serbia 1
Totale 9.683
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Città #
Fairfield 1.199
Dearborn 557
Ashburn 511
Chandler 511
Woodbridge 493
Houston 450
Seattle 439
Cambridge 395
Wilmington 296
Ann Arbor 254
Rome 215
Princeton 193
New York 175
Plano 155
Boston 135
Lawrence 122
San Paolo di Civitate 113
Beijing 100
Singapore 89
Jacksonville 84
San Diego 82
Millbury 59
Andover 47
Dublin 39
Sofia 38
Waanrode 35
Norwalk 34
Federal 29
Lomé 29
Toronto 28
Boardman 27
Jungnang-gu 21
Falls Church 20
Hefei 20
Los Angeles 19
Nanjing 19
Fuzhou 15
Kunming 15
Helsinki 14
Brussels 13
Bühl 13
Milan 13
Carol Stream 12
Florence 12
Mannheim 12
Bremen 11
Buffalo 11
Nanchang 11
Shanghai 11
Des Moines 10
Orte 10
Jinan 9
London 9
San Mateo 9
Redmond 8
Bolzano Vicentino 7
Chengdu 7
Plymouth 7
Shenyang 7
Sydney 7
Budapest 6
Chicago 6
Guangzhou 6
Muizenberg 6
Palermo 6
Tokyo 6
Torre del Greco 6
Birmingham 5
Edinburgh 5
Nagoya 5
Pisa 5
Quintanar de la Orden 5
Bern 4
Fremont 4
Indiana 4
Lumezzane 4
Paris 4
Phoenix 4
Pune 4
Quito 4
Sevilla 4
Taranto 4
Wuhan 4
Zurich 4
Asciano 3
Atlanta 3
Barcelona 3
Bologna 3
Castel San Giovanni 3
Cernobbio 3
Dallas 3
Dalmine 3
Galdo 3
Hebei 3
Istanbul 3
Izmir 3
Kirkuk 3
Messina 3
Monte Roberto 3
Naples 3
Totale 7.448
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Nome #
Use of dynamic movement orthoses to improve gait stability and trunk control in ataxic patients 156
Early-onset optic neuropathy as initial clinical presentation in SPG7 105
Harmony as a convergence attractor that minimizes the energy expenditure and variability in physiological gait and the loss of harmony in cerebellar ataxia 105
Riluzole in patients with hereditary cerebellar ataxia. a randomised, double-blind, placebo-controlled trial 103
Identification of gait unbalance and fallers among subjects with cerebellar ataxia by a set of trunk acceleration-derived indices of gait 99
Pathophysiology of hemimasticatory spasm. 98
Ataxia with oculomotor apraxia type 2: a clinical, pathologic and genetic study. 98
Identification of specific gait patterns in patients with cerebellar ataxia, spastic paraplegia, and Parkinson's disease. A non-hierarchical cluster analysis 93
The high prevalence of hereditary spastic paraplegia in Sardinia, insular Italy 92
Gait patterns in patients with hereditary spastic paraparesis 86
Increased lower limb muscle coactivation reduces gait performance and increases metabolic cost in patients with hereditary spastic paraparesis 85
Clinical and audiological follow up of a family with the 8363G > A mutation in the mitochondrial DNA 84
Cerebellum and neuropsychiatric disorders: Insights from ARSACS 84
Dataset on gait patterns in degenerative neurological diseases 84
Molecular and clinical examination of an italian DEFECT 11 family. 84
EARLY-ONSET PROGRESSIVE ATAXIA ASSOCIATED WITH THE FIRST CACNA1A MUTATION IDENTIFIED WITHIN THE I-II LOOP. 83
BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease. 83
GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients 82
Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum 81
Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia 81
Activity of protein phosphatase calcineurin is decreased in sporadic and familial amyotrophic lateral sclerosispatients 80
Oculomotor deficits affect neuropsychological performance in oculomotor apraxia type 2 80
Local stability of the trunk in patients with degenerative cerebellar ataxia during walking 80
Unilateral facial pain associated with recurrence of malignant thymoma: a case report 80
Respiratory chain defects in hereditary spastic paraplegias 79
Contrast Echocardiography and Migraine in Divers with Patent Foramen Ovale 79
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy 79
Spinocerebellar ataxia type 3 in Italy. time to change mind 79
Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease 78
Acute optic neuropathy associated with a novel MFN2 mutation 78
'When atlastin meets spastin' 78
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family 77
Liver as a source for thymidine phosphorylase replacement in mitochondrial neurogastrointestinal encephalomyopathy. 77
Neuromuscular adjustments of gait associated with unstable conditions 76
A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias. A pilot open-labeled study 75
An age standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 75
Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism 75
Consensus paper. Revisiting the symptoms and signs of cerebellar syndrome 74
ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy 74
SPG3A: An additional family carrying a new atlastin mutation. 74
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy 73
A novel mtDNA point mutation in maternally inherited cardiomyopathy. 72
Trunk-lower limb coordination pattern during gait in patients with ataxia 72
Progression of gait ataxia in patients with degenerative cerebellar disorders. A 4-year follow-up study 72
mtDNA A3243G MELAS mutation is not associated with multigenerational female migraine. 71
Stability of erythropoietin repackaging in polypropylene syringes for clinical use 71
Antioxidant enzymes in blood of patients with Friedreich's ataxia 71
Variable phenotype in a P102L Gerstmann-Straussler-Scheinker Italian family 70
Atassia cerebellare di Friedreich. Uno studio di voxel-based morphometry (VBM). 70
De novo FTL mutation: A clinical, neuroimaging, and molecular study 70
Detection of deleted mitochondrial DNA in Kearns-Sayre syndrome using laser capture microdissection 70
The emerging concept of mitochondrial cardiomyopathies. 69
Inflammatory myopathies 69
Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance 69
Neonatal myasthenia gravis: clinical and immunological study of seven mothers and their newborn infants. 68
MtDNA-related idiopathic dilated cardiomyopathy 68
Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy 68
Familial frontotemporal dementia with parkinsonism associated with the progranulin c.C1021T (p.Q341X) mutation 68
Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy 68
Combination of mtDNA mutations in a patient with a mitochondrial multisystem syndrome. 67
Cerebral mitochondrial microangiopathy leads to leukoencephalopathy in mitochondrial neurogastrointestinal encephalopathy 67
Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions 67
Quetiapine: an alternative treatment in painless legs and moving toes 66
Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE. 66
Glutathione in blood of patients with Friedreich's ataxia 65
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss. 63
Epilepsy and polymicrogyria in Kabuki make-up (Niikawa-Kuroki) syndrome 62
Advances in the genetics of spinocerebellar ataxias 62
Parkinson disease in farm workers. 62
Planned Gait Termination in Cerebellar Ataxias 62
Chronic diarrhea associated with the A3243G mtDNA mutation. 62
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 62
Lower Limb Antagonist Muscle Co-Activation and its Relationship with Gait Parameters in Cerebellar Ataxia 61
Distal muscular dystrophy with autosomal recessive inheritance. 61
Olfactory hallucinations as a manifestation of hidden rhinosinusitis 61
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population 61
Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type 60
Hydroxyzine hydrochloride in familial restless legs syndrome 60
Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs 60
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1 60
Mutation analysis of the ATP7B gene in a new group of Wilson's disease patients: Contribution to diagnosis 60
INTRAFAMILIAL VARIABILITY IN HEREDITARY SPASTIC PARAPLEGIA ASSOCIATED WITH AN SPG4 GENE MUTATION 60
Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family. 59
Aumento della coattivazione muscolare nei muscoli antagonisti degli arti inferiori nei pazienti affetti da atassia cerebellare: razionale per l'utilizzo di ortesi elastiche per migliorare l'equilibrio 59
Attrv in lazio-italy: A high-prevalence region in a non-endemic country 58
Early onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop - Reply 57
Missense and splice site mutations in SPG4 suggest loss-of-function in dominant spastic paraplegia. 57
Clinical and genetic characterization of Chanarin-Dorfman syndrome 57
Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association. 56
Charcot-Marie-Tooth disease in Molise, a central-southern region of Italy: An epidemiological study 55
Paraneoplastic neuromuscular disease in lung large cell neuroendocrine carcinoma 54
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations. 54
Uncoupling protein-1 mRNA expression in lipomas from patients bearing pathogenic mitochondrial DNA mutations. 54
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Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family. 52
Dermatomyositis spares extraocular muscles. 52
Infantile autosomal dominant distal myopathy. 52
Cerebellar Atrophy in Congenital Fibrosis of the Extraocular Muscles Type 1 52
Mitochondrial tRNA(Cys) gene mutation (A5814G): A second family with mitochondrial encephalopathy 52
Totale 7.166
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Categoria #
all - tutte 25.739
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 25.739
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019367 0 0 0 0 0 0 0 0 0 0 0 367
2019/20202.728 351 72 27 171 263 582 433 268 248 159 89 65
2020/2021795 76 118 33 62 18 38 28 91 90 137 65 39
2021/20221.849 18 108 195 43 206 26 58 194 114 134 317 436
2022/20231.748 342 389 61 150 243 156 19 100 148 35 86 19
2023/20241.065 57 119 24 58 72 229 48 72 20 162 92 112
Totale 9.967