Catalogo dei prodotti della ricerca

LULLI, Patrizia
 Distribuzione geografica
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Continente #
NA - Nord America 2.102
EU - Europa 870
AS - Asia 448
AF - Africa 31
SA - Sud America 23
Totale 3.474
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Nazione #
US - Stati Uniti d'America 2.088
IT - Italia 388
SG - Singapore 219
IN - India 140
SE - Svezia 132
UA - Ucraina 130
CN - Cina 84
FI - Finlandia 74
DE - Germania 53
TG - Togo 25
GB - Regno Unito 22
AR - Argentina 20
IE - Irlanda 19
BG - Bulgaria 17
CA - Canada 13
BE - Belgio 12
FR - Francia 8
RU - Federazione Russa 6
NL - Olanda 5
ZA - Sudafrica 3
CL - Cile 2
TR - Turchia 2
BO - Bolivia 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
ID - Indonesia 1
IR - Iran 1
JP - Giappone 1
MA - Marocco 1
MX - Messico 1
NA - Namibia 1
RO - Romania 1
SC - Seychelles 1
SM - San Marino 1
Totale 3.474
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Città #
Fairfield 279
Chandler 210
Singapore 171
Woodbridge 168
Ann Arbor 126
Ashburn 124
Houston 94
Wilmington 88
Seattle 86
Cambridge 76
Princeton 74
Plano 64
Beijing 63
Jacksonville 56
Rome 55
Santa Clara 47
Boston 37
Lomé 25
Millbury 25
San Paolo di Civitate 23
Lawrence 22
Federal 20
Dearborn 19
Dublin 19
San Diego 18
Sofia 16
Andover 15
Helsinki 15
Milan 14
Boardman 13
Manassas 12
Toronto 11
Brussels 10
New York 9
Norwalk 8
Bremen 7
Denver 6
Des Moines 6
Bühl 5
Falkenstein 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
London 3
Macomer 3
Muizenberg 3
Reggio Calabria 3
Salerno 3
Bari 2
Bono 2
Cachan 2
Capri 2
Chaoyang 2
Genoa 2
Gloucester 2
Gurgaon 2
Istanbul 2
Kunming 2
Littleton 2
Livorno 2
Los Angeles 2
Lucca 2
Mestre 2
Mondragone 2
Montechiarugolo 2
Montréal 2
Naples 2
Napoli 2
Palermo 2
Parma 2
Pasian Di Prato 2
Portland 2
Redmond 2
Rogliano 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
Totale 2.274
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Nome #
Varianti alleliche del gene notch3 in un paziente con sospetto cadasil 256
Caratterizzazione molecolare di pazienti italiani affetti da Atassia con Aprassia Oculomotoria di tipo 1 (AOA1) 134
Lack of evidence for post-vaccine onset of autoimmune/lymphoproliferative disorders, during a nine-month follow-up in multiply vaccinated Italian military personnel 127
A mouse monoclonal antibody detecting the allospecificity HLA-A3 103
Cytotoxic T lymphocyte antigen 4 polymorphism 49 (A>G) and migraine. 91
A cytotoxic anti HLA-AB monoclonal antibody which in dilution becomes specific to HLA-A3 crossreacting group 89
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 87
Mre11 mutations and impaired ATM-dependent responses in an Italian family with ataxia telangiectasia-like disorder 80
Genetics of migraine and pharmacogenomics: Some considerations 79
Tumor necrosis factor gene polymorphism in migraine 77
HLA-DQ and risk gradient for celiac disease 72
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 63
Bone marrow transplantation and thymopoietin pentapeptide treatment in two infants with immunodeficiency with predominant T-cell defects 63
Osteoporosis (OP) and human leukocyte antigen (HLA) 62
Chromosome 6p- encoded HLA DR2 determinant discriminates migraine without aura from migraine with aura 59
HLA and complement factors alleles sharing in italian couples with recurrent spontaneous abortions 59
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds. 59
HLA-DRB1 and -DQB1 loci in three west African ethnic groups: genetic relationship with sub-Saharan African and European populations 55
p53 centrosomal localization diagnoses AtaxiaTelangiectasia homozygotes and heterozygotes 54
Il ruolo dell’Apratassina (APTX) nel riparo delle rotture del DNA a singolo filamento 54
HLA DR and DQ alleles in Italian patients with melanoma. 54
A study of HLA Class II antigens in an Italian paediatric population with Coeliac Disease 53
Sharing at the Major Histocompatibility Complex affects the secondary sex ratio in differing ways 53
Alleli HLA e predisposizione all'osteoporosi nei maschi 53
Modifications of nuclear architecture and chromatin organization in ataxia telangiectasia cells are coupled to changes of gene transcription 53
Caratterizzazione molecolare di pazienti italiani affetti da Atassia con Aprassia Oculomotoria di tipo 1 (AOA1) 51
[Distribution of isoantigens (HLA) in multiple sclerosis]. 48
Comet Assay nello studio della radiosensibilità in pazienti con Atassia Telangiectasia (AT), Atassia Telangiectasia Variante (ATLD) e Nijmegen Breakage Sindrome (NBS). 48
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. 47
Analysis of HLA class II loci polymorphism in three West African ethnic groups showing different immune response to Plasmodium falciparum malaria 46
High prevalence of vitamin D deficiency and insufficiency in patients with rheumatic diseases 46
Immunogenicity of viral vaccines in the italian military 46
TUMOR NECROSIS FACTOR B GENE POLYMORPHISM CONTRIBUTES TO SUSCEPTIBILITY TO MIGRAINE WITHOUT AURA 45
[Anti-HLA-DR antibodies in the sera of multigravidae in labor]. 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
Autosomal dominant pure cerebellar ataxia. Neurological and genetic study 43
Studio preliminare sull’influenza del gene ESR1 alpha nell’osteoporosi primaria e secondaria ad artrite reumatoide 42
. Il ruolo dell’apratassina (APTX) nel riparo delle rotture del dna a singolo filamento 41
HLA alleles and susceptibility to osteoporosis in men 40
[Anti-HLA-A, B, C antibodies in the sera of multigravidae in labor and after labor]. 39
Aprataxin Mutations in Italian Patients with Ataxia and Oculomotor Apraxia (AOA) 36
COMET ASSAY NELLO STUDIO DELLA RADIOSENSIBILITÀ IN PAZIENTI CON ATASSIA TELANGIECTASIA(AT), ATASSIA TELANGIECTASIA VARIANTE (ATLD) E NIJMEGEN BREAKAGE SINDROME (NBS) 36
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
ST1 in two Italian families 35
Molecular HLA typing and risk of coeliac disease in Italy 35
Clinical and cellular phenotype of two Italian sibs with ATLD 34
Cutaneous venous malformation due to krit1 mutation: a case report 33
Anticardiolipin antibodies: their relationship with HLA-DR antigens in systemic lupus erythematosus. 33
The Gene for Spinal Cerebellar Ataxia 1 is Flanked by Two Closely Linked Highly Polymorphic Microsatellite Loci 33
Founder Effects for ATM Gene Mutations in Italian Ataxia Telangiectasia Families 32
HLA antigens and aging. 32
Studio dei loci HLA-DRB1 e –DQB1 in tre gruppi etnici africani: distanza genetica tra popolazioni africane sub-sahariane ed europee 31
HLA antigens and antigliadin antibodies in coeliac disease. 28
[HLA and hypo-responsivity to anti-HBV vaccination (genetic study of non-responder subjects to anti-hepatitis B viral vaccine)]. 27
HLA antigens in Italian patients with systemic lupus erythematosus: Evidence for the association of DQw2 with the autoantibody response to extractable nuclear antigens 26
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 22
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. 15
Fenotipo clinico e cellulare di una fratria con ATLD (Ataxia Telangiectasia-Like Disorder) 14
Totale 3.518
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Categoria #
all - tutte 10.090
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 10.090
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020398 0 0 0 0 0 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
2024/2025291 28 131 26 9 61 36 0 0 0 0 0 0
Totale 3.518