Catalogo dei prodotti della ricerca

LULLI, Patrizia
 Distribuzione geografica
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Continente #
NA - Nord America 2.071
EU - Europa 840
AS - Asia 395
AF - Africa 30
SA - Sud America 22
Totale 3.358
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Nazione #
US - Stati Uniti d'America 2.057
IT - Italia 374
SG - Singapore 168
IN - India 140
SE - Svezia 132
UA - Ucraina 130
CN - Cina 84
FI - Finlandia 68
DE - Germania 48
TG - Togo 25
AR - Argentina 20
GB - Regno Unito 19
IE - Irlanda 19
BG - Bulgaria 17
CA - Canada 13
BE - Belgio 11
FR - Francia 8
RU - Federazione Russa 6
NL - Olanda 5
ZA - Sudafrica 3
CL - Cile 2
TR - Turchia 2
CH - Svizzera 1
JP - Giappone 1
MX - Messico 1
NA - Namibia 1
RO - Romania 1
SC - Seychelles 1
SM - San Marino 1
Totale 3.358
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Città #
Fairfield 279
Chandler 210
Woodbridge 168
Ann Arbor 126
Ashburn 123
Singapore 120
Houston 94
Wilmington 88
Seattle 86
Cambridge 76
Princeton 74
Plano 64
Beijing 63
Jacksonville 56
Rome 55
Boston 37
Lomé 25
Millbury 25
San Paolo di Civitate 23
Lawrence 22
Santa Clara 22
Federal 20
Dearborn 19
Dublin 19
San Diego 18
Sofia 16
Andover 15
Milan 14
Boardman 13
Manassas 12
Toronto 11
Brussels 9
Helsinki 9
New York 9
Norwalk 8
Bremen 7
Denver 6
Des Moines 6
Bühl 5
Mannheim 5
Nanjing 5
Falls Church 4
Marigliano 4
Messina 4
Auburn Hills 3
Aversa 3
Brembate di Sopra 3
Brescia 3
Fontenay-sous-bois 3
Fremont 3
Hefei 3
Macomer 3
Muizenberg 3
Salerno 3
Bari 2
Bono 2
Cachan 2
Capri 2
Chaoyang 2
Genoa 2
Gurgaon 2
Istanbul 2
Kunming 2
Littleton 2
London 2
Lucca 2
Mestre 2
Mondragone 2
Montechiarugolo 2
Montréal 2
Naples 2
Napoli 2
Palermo 2
Pasian Di Prato 2
Portland 2
Redmond 2
San Francisco 2
Siena 2
Taormina 2
Venezia 2
Villanovafranca 2
Waanrode 2
Acton 1
Adelfia 1
Ancona 1
Aosta 1
Atina 1
Azzate 1
Bagneux 1
Bergamo 1
Bibbona 1
Bologna 1
Bolzano 1
Borgonovo Val Tidone 1
Buffalo 1
Cagliari 1
Calolziocorte 1
Capoterra 1
Castrovillari 1
Catania 1
Totale 2.178
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Nome #
Varianti alleliche del gene notch3 in un paziente con sospetto cadasil 253
Lack of evidence for post-vaccine onset of autoimmune/lymphoproliferative disorders, during a nine-month follow-up in multiply vaccinated Italian military personnel 124
Caratterizzazione molecolare di pazienti italiani affetti da Atassia con Aprassia Oculomotoria di tipo 1 (AOA1) 121
A mouse monoclonal antibody detecting the allospecificity HLA-A3 100
Cytotoxic T lymphocyte antigen 4 polymorphism 49 (A>G) and migraine. 89
A cytotoxic anti HLA-AB monoclonal antibody which in dilution becomes specific to HLA-A3 crossreacting group 87
Tetanus-diphtheria vaccination in adults. the long-term persistence of antibodies is not dependent on polyclonal B-cell activation and the defective response to diphtheria toxoid re-vaccination is associated to HLADRB1∗01 85
Mre11 mutations and impaired ATM-dependent responses in an Italian family with ataxia telangiectasia-like disorder 80
Genetics of migraine and pharmacogenomics: Some considerations 75
Tumor necrosis factor gene polymorphism in migraine 75
HLA-DQ and risk gradient for celiac disease 71
Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster. 70
HLA antigens and rheumatoid arthritis. 66
HLA-DR association in rheumatoid arthritis patients and the shared susceptibility epitope hypothesis 65
Immunogenicity of meningococcal polysaccharide ACWY vaccine in primary immunized or revaccinated adults 62
Bone marrow transplantation and thymopoietin pentapeptide treatment in two infants with immunodeficiency with predominant T-cell defects 61
Osteoporosis (OP) and human leukocyte antigen (HLA) 60
HLA and complement factors alleles sharing in italian couples with recurrent spontaneous abortions 58
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds. 58
Chromosome 6p- encoded HLA DR2 determinant discriminates migraine without aura from migraine with aura 57
Sharing at the Major Histocompatibility Complex affects the secondary sex ratio in differing ways 53
Il ruolo dell’Apratassina (APTX) nel riparo delle rotture del DNA a singolo filamento 53
HLA-DRB1 and -DQB1 loci in three west African ethnic groups: genetic relationship with sub-Saharan African and European populations 53
HLA DR and DQ alleles in Italian patients with melanoma. 53
Modifications of nuclear architecture and chromatin organization in ataxia telangiectasia cells are coupled to changes of gene transcription 53
p53 centrosomal localization diagnoses AtaxiaTelangiectasia homozygotes and heterozygotes 51
Alleli HLA e predisposizione all'osteoporosi nei maschi 51
A study of HLA Class II antigens in an Italian paediatric population with Coeliac Disease 50
Caratterizzazione molecolare di pazienti italiani affetti da Atassia con Aprassia Oculomotoria di tipo 1 (AOA1) 50
[Distribution of isoantigens (HLA) in multiple sclerosis]. 47
Comet Assay nello studio della radiosensibilità in pazienti con Atassia Telangiectasia (AT), Atassia Telangiectasia Variante (ATLD) e Nijmegen Breakage Sindrome (NBS). 47
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. 45
TUMOR NECROSIS FACTOR B GENE POLYMORPHISM CONTRIBUTES TO SUSCEPTIBILITY TO MIGRAINE WITHOUT AURA 44
Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: Report of a novel mutation of the PCNT gene 44
Further heterogeneity of HLA-B5 43
[Anti-HLA-DR antibodies in the sera of multigravidae in labor]. 43
Studio preliminare sull’influenza del gene ESR1 alpha nell’osteoporosi primaria e secondaria ad artrite reumatoide 42
Immunogenicity of viral vaccines in the italian military 42
High prevalence of vitamin D deficiency and insufficiency in patients with rheumatic diseases 41
Autosomal dominant pure cerebellar ataxia. Neurological and genetic study 40
. Il ruolo dell’apratassina (APTX) nel riparo delle rotture del dna a singolo filamento 39
[Anti-HLA-A, B, C antibodies in the sera of multigravidae in labor and after labor]. 38
Analysis of HLA class II loci polymorphism in three West African ethnic groups showing different immune response to Plasmodium falciparum malaria 37
HLA alleles and susceptibility to osteoporosis in men 37
Tumor necrosis factor (TNF) –B gene polymorphysm contributes to the susceptibility to migraine without aura 35
TNF A gene: the –308 promoter polymorphysm in migraine 35
Aprataxin Mutations in Italian Patients with Ataxia and Oculomotor Apraxia (AOA) 35
ST1 in two Italian families 34
COMET ASSAY NELLO STUDIO DELLA RADIOSENSIBILITÀ IN PAZIENTI CON ATASSIA TELANGIECTASIA(AT), ATASSIA TELANGIECTASIA VARIANTE (ATLD) E NIJMEGEN BREAKAGE SINDROME (NBS) 34
Molecular HLA typing and risk of coeliac disease in Italy 34
Clinical and cellular phenotype of two Italian sibs with ATLD 33
Founder Effects for ATM Gene Mutations in Italian Ataxia Telangiectasia Families 32
Anticardiolipin antibodies: their relationship with HLA-DR antigens in systemic lupus erythematosus. 31
The Gene for Spinal Cerebellar Ataxia 1 is Flanked by Two Closely Linked Highly Polymorphic Microsatellite Loci 31
HLA antigens and aging. 30
Cutaneous venous malformation due to krit1 mutation: a case report 30
Studio dei loci HLA-DRB1 e –DQB1 in tre gruppi etnici africani: distanza genetica tra popolazioni africane sub-sahariane ed europee 29
HLA antigens and antigliadin antibodies in coeliac disease. 27
HLA antigens in Italian patients with systemic lupus erythematosus: Evidence for the association of DQw2 with the autoantibody response to extractable nuclear antigens 25
[HLA and hypo-responsivity to anti-HBV vaccination (genetic study of non-responder subjects to anti-hepatitis B viral vaccine)]. 25
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds. 23
Genetic Heterogeneity between Migraine with Aura and Migraine without Aura Is HLA-DR2-Linked 20
DHPLC screening of ATM gene in Italian patients affected by ataxia-telangiectasia: Fourteen novel ATM mutations 20
Frequenza degli alleli HLA nei pazienti affetti da epatite cronica HCV-correlata e predisposizione alla comparsa della patologia tiroidea immuno-mediata dopo trattamento antivirale. 14
Fenotipo clinico e cellulare di una fratria con ATLD (Ataxia Telangiectasia-Like Disorder) 12
Totale 3.402
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Categoria #
all - tutte 9.035
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 9.035
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020492 0 0 11 33 50 65 67 74 47 62 63 20
2020/2021218 24 35 6 17 14 18 4 21 32 31 14 2
2021/2022587 5 42 48 24 81 11 8 59 58 54 65 132
2022/2023675 123 127 48 72 67 72 29 32 55 8 26 16
2023/2024323 28 50 19 44 26 37 14 8 0 29 34 34
2024/2025175 28 131 16 0 0 0 0 0 0 0 0 0
Totale 3.402