CRIS Current Research Information System

BARONIO, FEDERICO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 3.366
NA - Nord America 2.752
EU - Europa 2.197
AF - Africa 213
SA - Sud America 138
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.670
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 2.715
VN - Vietnam 1.119
SG - Singapore 814
CN - Cina 780
GB - Regno Unito 477
IT - Italia 455
DE - Germania 288
SE - Svezia 235
HK - Hong Kong 224
FR - Francia 155
RU - Federazione Russa 137
IN - India 133
UA - Ucraina 121
BR - Brasile 92
KR - Corea 81
IE - Irlanda 78
JP - Giappone 62
NL - Olanda 59
CI - Costa d'Avorio 56
FI - Finlandia 53
ZA - Sudafrica 53
TG - Togo 44
NG - Nigeria 28
CH - Svizzera 27
EE - Estonia 24
AR - Argentina 22
JO - Giordania 22
BG - Bulgaria 21
PH - Filippine 21
IQ - Iraq 20
CA - Canada 17
TH - Thailandia 15
PL - Polonia 14
AT - Austria 13
SC - Seychelles 13
TR - Turchia 12
MX - Messico 11
ID - Indonesia 10
LT - Lituania 10
ES - Italia 9
PK - Pakistan 9
BD - Bangladesh 8
BE - Belgio 7
CL - Cile 7
IR - Iran 7
EG - Egitto 6
CO - Colombia 4
LB - Libano 4
MY - Malesia 4
PY - Paraguay 4
DO - Repubblica Dominicana 3
EC - Ecuador 3
PE - Perù 3
SA - Arabia Saudita 3
SY - Repubblica araba siriana 3
TW - Taiwan 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 2
ET - Etiopia 2
GR - Grecia 2
JM - Giamaica 2
KE - Kenya 2
KG - Kirghizistan 2
MA - Marocco 2
OM - Oman 2
RS - Serbia 2
UG - Uganda 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
CG - Congo 1
CR - Costa Rica 1
CY - Cipro 1
CZ - Repubblica Ceca 1
DJ - Gibuti 1
DK - Danimarca 1
DZ - Algeria 1
GT - Guatemala 1
HU - Ungheria 1
LU - Lussemburgo 1
LV - Lettonia 1
LY - Libia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
RO - Romania 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
YE - Yemen 1
Totale 8.670
Salva come PNG Salva come JPEG
Città #
Singapore 578
Southend 406
Ashburn 338
Chandler 300
Ho Chi Minh City 248
San Jose 247
Hong Kong 212
Hanoi 198
Hefei 165
Fairfield 147
Dong Ket 143
Santa Clara 121
Princeton 103
Beijing 92
Jacksonville 89
Wilmington 82
Dublin 78
Seattle 77
Seoul 75
Woodbridge 66
Bologna 63
Lauterbourg 58
Tokyo 58
Abidjan 56
Boardman 53
Ann Arbor 52
Houston 50
Los Angeles 49
Cambridge 46
Helsinki 45
Lomé 44
Nanjing 43
Westminster 42
Turin 41
Padova 37
Da Nang 35
Haiphong 35
Council Bluffs 34
Milan 33
Berlin 30
Munich 30
Saint Petersburg 29
Abeokuta 27
Frankfurt am Main 27
Medford 26
Jinan 25
Buffalo 23
Amman 21
Sofia 21
Bern 20
Nanchang 20
Dallas 19
Shanghai 19
Mülheim 18
New York 17
Rome 17
Bengaluru 16
Redondo Beach 16
Tianjin 16
Naples 14
Shenyang 14
Johannesburg 13
São Paulo 13
Changsha 12
Guangzhou 12
The Dalles 12
Mahé 11
Florence 10
Nuremberg 10
Quận Bình Thạnh 10
Warsaw 10
Amsterdam 9
Bremen 9
Can Tho 9
Hebei 9
Hải Dương 9
Roubaix 9
San Diego 9
San Francisco 9
Zhengzhou 9
Biên Hòa 8
Dearborn 8
Des Moines 8
Falkenstein 8
London 8
Olalla 8
Redwood City 8
Bắc Ninh 7
Cascina 7
Denver 7
Düsseldorf 7
Jiaxing 7
Phoenix 7
Baghdad 6
Bari 6
Brooklyn 6
Catania 6
Chengdu 6
Kunming 6
Montreal 6
Totale 5.438
Salva come PNG Salva come JPEG
Nome #
Quando non trascurare la splenomegalia nel lattante un insegnamento dalla pratica clinica 326
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 254
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 206
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 202
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 202
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 201
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 200
Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature 187
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 187
Diagnostic features of thyroid nodules in pediatrics 183
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study 183
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 179
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 179
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 179
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs 175
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough 174
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 171
Body Mass Index (BMI) evaluation in survivors from childhood cancer 171
Il bambino oncologico "guarito": quali alterazioni endocrinologiche temere? 170
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening 168
Growth patterns in children treated for Acute Lymphoblastic Leukemia (ALL): Relationship with cranial irradiation 166
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 164
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three NR3C2 gene SNPs 163
Focal nodular hyperplasia of the liver after intensive treatment for pediatric cancer: is hematopoietic stem cell transplantation a risk factor? 160
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) 157
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study 149
Fanconi-Bickel syndrome: a mild form associated with GLUT2 mutation 149
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 148
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 148
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis 146
Maternal PKU: Defining phenylalanine tolerance and its variation during pregnancy, according to genetic background 145
Obesity in children and adolescents: an increasing metabolic problem. 144
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 143
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 143
Height as a risk factor for osteosarcoma. 141
Height outcome and pubertal development in CYP21 genotyped CAH male patients 141
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 141
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. 138
Genotyping Patients with Differences of Sex Development: 25 Years of Investigation of an Italian Population of 308 Cases (194 46,XY and 114 46,XX) 137
Severe hypercholesterolaemia in a paediatric patient with congenital analbuminaemia 137
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis 135
Prevalence and ultrasound patterns of testicular adrenal rest tumors in adults with congenital adrenal hyperplasia 134
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
The SHOX gene: a new indication for GH treatment 127
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 123
Hemophagocytic lymphohistiocytosis and lysinuric protein intolerance:case report 123
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 122
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 121
Intratesticular Doppler Flow and Gonadal Status in Male Survivors of a Childhood Malignancy 117
Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria 94
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report 89
Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center 85
Longitudinal evaluation with quantitative ultrasound of bone marrow transplantation-associated bone loss in a series of 28 children 83
Omocisteina alta? Quello che il pediatra deve sapere 82
Radiological and Neuroradiological Features in Pediatric Mucopolysaccharidoses: A Retrospective Case Series from the Emilia-Romagna Regional Referral Center 54
Enzymatic Evolution and Longitudinal Recovery in Biotinidase Deficiency: Genotypic and Clinical Insights from the Follow-Up of a Newborn-Screened Cohort in Emilia-Romagna, Italy 54
Understanding Glycogen Storage Disease Type IX: A Systematic Review with Clinical Focus—Why It Is Not Benign and Requires Vigilance 53
Tachycardiomyopathy-like presentation in neonatal MCAD deficiency: A novel cardiac phenotype 42
Transition in inherited metabolic diseases: the dietitians, pediatricians and adult physicians’ point of view: the results of an Italian survey 41
Glucose dynamics in glycogen storage disease type IXa with novel PHKA2 variants: insights from our experience and a comprehensive review of the disease spectrum 38
Does Basal Morning Luteinizing Hormone (bLH) Predict Central Precocious Puberty (CPP) in Girls? 33
Early-Onset Inherited Metabolic Diseases: When Clinical Symptoms Precede Newborn Screening—Insights from Emilia-Romagna (Italy) 32
Clinical Implications and Preventive Strategies for Neonatal and Infant Hypovitaminosis D: Analysis and Comparison of Current Evidence 32
Primary ovarian insufficiency in Classic Galactosemia: a systematic review 22
Totale 8.823
Salva come PNG Salva come JPEG
Categoria #
all - tutte 21.215
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 21.215
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021314 0 0 0 0 0 0 0 0 0 21 20 273
2021/2022865 113 28 48 53 66 51 11 56 22 48 203 166
2022/20231.153 105 186 69 142 70 93 29 51 230 15 103 60
2023/2024290 9 56 21 43 19 49 11 26 10 16 7 23
2024/20251.372 61 176 89 128 191 58 80 58 30 94 102 305
2025/20263.369 383 286 255 225 343 206 387 227 806 251 0 0
Totale 8.823