CRIS Current Research Information System

PIRAZZOLI, PIERO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 2.362
NA - Nord America 2.206
EU - Europa 1.691
AF - Africa 140
SA - Sud America 101
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.512
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.162
VN - Vietnam 899
CN - Cina 510
SG - Singapore 504
GB - Regno Unito 399
DE - Germania 288
SE - Svezia 222
IT - Italia 185
HK - Hong Kong 158
UA - Ucraina 131
FR - Francia 111
IN - India 97
RU - Federazione Russa 86
BR - Brasile 68
IE - Irlanda 58
NL - Olanda 50
JP - Giappone 44
FI - Finlandia 38
ZA - Sudafrica 37
CA - Canada 32
KR - Corea 31
CI - Costa d'Avorio 30
NG - Nigeria 30
TG - Togo 23
BG - Bulgaria 21
EE - Estonia 21
CH - Svizzera 19
BE - Belgio 18
AR - Argentina 16
IL - Israele 14
JO - Giordania 14
PH - Filippine 14
AT - Austria 11
TR - Turchia 11
AU - Australia 10
SC - Seychelles 9
IQ - Iraq 8
TH - Thailandia 8
ES - Italia 7
MX - Messico 7
PL - Polonia 7
TW - Taiwan 7
ID - Indonesia 6
PK - Pakistan 6
EC - Ecuador 5
IR - Iran 5
MA - Marocco 5
AE - Emirati Arabi Uniti 4
RO - Romania 4
BD - Bangladesh 3
CO - Colombia 3
EG - Egitto 3
LT - Lituania 3
MY - Malesia 3
NO - Norvegia 3
PE - Perù 3
UZ - Uzbekistan 3
CL - Cile 2
CR - Costa Rica 2
GR - Grecia 2
KG - Kirghizistan 2
LB - Libano 2
MK - Macedonia 2
NP - Nepal 2
OM - Oman 2
PT - Portogallo 2
PY - Paraguay 2
SA - Arabia Saudita 2
BO - Bolivia 1
CG - Congo 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
EU - Europa 1
KH - Cambogia 1
KM - Comore 1
LU - Lussemburgo 1
LY - Libia 1
MD - Moldavia 1
MM - Myanmar 1
NI - Nicaragua 1
PS - Palestinian Territory 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 6.512
Salva come PNG Salva come JPEG
Città #
Southend 355
Singapore 351
Ho Chi Minh City 226
Chandler 224
Ashburn 219
Hanoi 190
Hong Kong 149
San Jose 148
Dong Ket 118
Fairfield 113
Santa Clara 107
Jacksonville 93
Hefei 92
Houston 83
Princeton 79
Ann Arbor 77
Beijing 73
Wilmington 67
Woodbridge 60
Dublin 56
Seattle 48
Boardman 41
Tokyo 38
Cambridge 36
Los Angeles 35
Lauterbourg 34
Westminster 34
Bologna 32
Munich 31
Nanjing 31
Turin 31
Abidjan 30
Padova 30
Abeokuta 27
Frankfurt am Main 27
Helsinki 27
Da Nang 26
Berlin 25
Haiphong 25
Lomé 23
Redwood City 23
Seoul 22
Sofia 21
Medford 20
Saint Petersburg 18
Jinan 17
Mülheim 17
Brussels 16
Shenyang 16
Buffalo 15
Amman 14
Bern 14
Guangzhou 14
New York 14
San Diego 13
Hải Dương 12
Tianjin 12
Can Tho 11
Chennai 11
Tacoma 11
Turku 11
Bengaluru 10
Falkenstein 10
São Paulo 10
Toronto 10
Vienna 10
Chicago 9
Dallas 9
Dearborn 9
Düsseldorf 9
Ha Long 9
Nanchang 9
Biên Hòa 8
Brookhaven 8
Bắc Ninh 8
Changsha 8
Dortmund 8
Falls Church 8
Rishon LeTsiyyon 8
Hagen 7
Hebei 7
Mahé 7
Mountain View 7
Orem 7
Warsaw 7
Milan 6
Ninh Bình 6
Olalla 6
Quận Mười 6
Thái Nguyên 6
Washington 6
Ankara 5
Bremen 5
Burlington 5
Bắc Giang 5
Hangzhou 5
Johannesburg 5
Leawood 5
Melle 5
Ramat Gan 5
Totale 4.116
Salva come PNG Salva come JPEG
Nome #
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 509
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 398
Turner syndrome, insulin sensitivity and growth hormone treatment 269
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 256
Active and total ghrelin concentrations in the newborn 236
Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations. 226
Mutational spectrum of SHOX gene in 25 Italian pediatric patients with Lèri-Weill dyschondrosteosis (LWD). 218
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 205
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 202
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 199
Determination of BMP15 gene dosage in a woman with TS and spontaneous menarche. 188
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 187
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 179
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 173
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. 170
ORTICARIA ACUTA IN BAMBINI CHE AFFERISCONO IN PRONTO SOCCORSO 169
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY 169
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 167
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. 165
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 164
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 155
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 154
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 148
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism 142
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. 138
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy 136
McCune-Albright syndrome in a boy may present with a monolateral macroorchidism as an early and isolated clinical manifestation. 133
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 130
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 130
HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype. 130
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 129
The SHOX gene: a new indication for GH treatment 127
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 126
Rare Syndromes and Hormones Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy 126
FINAL HEIGHT IN A PATIENT WITH LARON SYNDROME AFTER LONG TERM THERAPY WITH rhIGF-1 AND SHORT TERM THERAPY WITH LHRH-ANALOGUE AND OXANDROLONE DURING PUBERTY. 69
Helicobacter pylori and type 1 diabetes mellitus in children 64
Helicobacter pylori and type 1 diabetes mellitus in children 63
null 42
Totale 6.591
Salva come PNG Salva come JPEG
Categoria #
all - tutte 14.869
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 14.869
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021181 0 0 0 0 0 0 0 0 0 24 24 133
2021/2022794 131 33 47 84 53 44 18 37 29 33 164 121
2022/2023892 92 125 51 104 73 78 18 44 160 23 84 40
2023/2024241 11 36 36 24 19 39 14 10 14 24 5 9
2024/2025904 32 164 64 83 126 54 33 37 4 79 34 194
2025/20262.161 405 256 163 142 215 104 222 131 397 126 0 0
Totale 6.591