IRIS
DE BERARDINIS, TERESA
 Distribuzione geografica
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Continente #
NA - Nord America 611
EU - Europa 323
AS - Asia 152
Totale 1.086
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Nazione #
US - Stati Uniti d'America 603
IT - Italia 109
UA - Ucraina 109
SG - Singapore 91
CN - Cina 53
DE - Germania 37
FI - Finlandia 36
IE - Irlanda 16
GB - Regno Unito 13
CA - Canada 8
HK - Hong Kong 4
CH - Svizzera 2
TR - Turchia 2
ID - Indonesia 1
IN - India 1
SE - Svezia 1
Totale 1.086
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Città #
Chandler 137
Jacksonville 103
Singapore 76
Napoli 37
Princeton 35
Boston 34
Millbury 28
Ashburn 20
Nanjing 18
Wilmington 15
Kronberg 13
Pozzuoli 12
Nanchang 10
Santa Clara 9
Ottawa 7
Giugliano In Campania 6
Norwalk 6
Sant'antonio Abate 6
Ann Arbor 5
Beijing 5
Changsha 5
Naples 5
Shenyang 5
Des Moines 4
Dublin 4
Woodbridge 4
Jiaxing 3
Orange 3
Acerra 2
Casapulla 2
Hebei 2
Paterno 2
Pontassieve 2
Saliceto 2
Solothurn 2
Tianjin 2
Varese 2
Verona 2
Bari 1
Brescia 1
Catania 1
Falls Church 1
Fremont 1
Hangzhou 1
Indiana 1
Kunming 1
Lappeenranta 1
Milan 1
New York 1
Pune 1
Shanghai 1
Villaricca 1
Washington 1
Totale 650
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Nome #
Cerebellar Atrophy in Congenital Fibrosis of the Extraocular Muscles Type 1 72
Congenital fibrosis of the extraocular muscles type 1 (CFEOM1), additional CFEOM1 families, and a reduction of the critical region on chromosome 12. 56
Isolated hereditary congenital ptosis can be caused by defects of craniofacial development 51
IDENTIFICATION OF KIF21A MUTATIONS AS A RARE CAUSE OF CONGENITAL FIBROSIS OF THE EXTRAOCULAR MUSCLES TYPE 3 (CFEOM3). 48
Pharmacological denervation in the treatment of sixth cranial nerve palsy. 48
Oftalmoplegia Congenita Esterna: conferma della presenza di un locus genetico sul cromosoma 12. 44
Classificazione,valutazione e trattamento delle blefaroptosi in età pediatrica 39
: BMC Genet. 2002;3(1):3. Epub 2002 Mar 06. CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX. 37
Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1). 36
Clinical and surgical data of affected members of a classic CFEOM 1 family. 35
Genetic, clinical and surgical data of affected members of a classic CFEOM 1 family 35
Molecular and clinical characterization of albinism in a large cohort of Italian patients. 34
Pharmacological denervation in the treatment of sixth cranial nerve palsy. 32
Treatment of blepharospasm with botulinum neurotoxin type A: long-term results. 31
Le Varietà di strabismo sensibili al trattamento con tossina botulinica 31
Genetic, clinical and surgical data of affected members of a classic CFEOM 1 family 31
Clinical and genetic data of two (classic) CFEOM1 families and one atypical CFEOM family. 31
Oftalmoplegie familiari ad insorgenza precoce e tardiva. 29
Clinical and genetic data of two (classic) CFEOM1 families and one atypical CFEOM family. 29
Clinical and surgical data of affected members of a classic CFEOM 1 family. 28
Clinical and surgical data of affected members of a classic CFEOM 1 family. 28
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX. 27
Oftalmoplegia congenita esterna:conferma della presenza di un locus genetico sul cromosoma 12. 27
CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX. 27
(1998). Classificazione, valutazione e trattamento delle blefaroptosi in età pediatrica. 27
Surgical treatment of ptosis in chronic progressive external ophthalmoplegia. 24
Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance. 23
Risk factors for spread of primary adult onset blepharospasm: a multicentre investigation of the Italian movement disorders study group 21
Surgical treatment of ptosis in chronic progressive external ophthalmoplegia. 20
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. 20
Oftalmoplegie familiari ad insorgenza precoce e tardiva. BOLLETTINO DI OCULISTICA, vol. 78 suppl. 3, p. 21-28, ISSN: 0006-67 20
Analysis of foveation duration and repeatability at different gaze positions in patients affected by congenital nystagmus. 19
Possible risk factors for primary adult onset dystonia: a case-control investigation by the Italian Movement Disorders Study Group. 18
Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly. 18
Studio del metabolismo mitocondriale (curva lattato ed enzimi mitocondriali su piastrine ) in 4 pazienti affetti da oftalmoplegia congenita esterna cronica progressiva ad esordio infantile 14
null 11
Totale 1.121
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Categoria #
all - tutte 4.931
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 4.931
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202060 0 0 0 0 22 0 0 0 1 1 11 25
2020/2021173 0 22 12 22 22 25 26 0 23 0 21 0
2021/2022138 0 0 0 1 5 2 0 7 13 15 17 78
2022/2023263 41 23 14 10 45 33 0 29 48 0 18 2
2023/2024127 8 28 12 19 5 5 1 17 0 0 23 9
2024/2025107 45 57 1 0 4 0 0 0 0 0 0 0
Totale 1.121