CRIS Current Research Information System

BARONIO, FEDERICO
 Distribuzione geografica
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Continente #
NA - Nord America 4.643
AS - Asia 3.414
EU - Europa 2.293
AF - Africa 213
SA - Sud America 159
Continente sconosciuto - Info sul continente non disponibili 157
OC - Oceania 3
Totale 10.882
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Nazione #
US - Stati Uniti d'America 4.584
VN - Vietnam 1.119
SG - Singapore 828
CN - Cina 786
IT - Italia 544
GB - Regno Unito 478
DE - Germania 288
SE - Svezia 236
HK - Hong Kong 234
FR - Francia 155
RU - Federazione Russa 137
IN - India 133
UA - Ucraina 121
BR - Brasile 109
KR - Corea 81
IE - Irlanda 78
JP - Giappone 62
NL - Olanda 60
CI - Costa d'Avorio 56
FI - Finlandia 53
ZA - Sudafrica 53
TG - Togo 44
CH - Svizzera 31
NG - Nigeria 28
BD - Bangladesh 26
CA - Canada 25
AR - Argentina 24
EE - Estonia 24
JO - Giordania 22
BG - Bulgaria 21
PH - Filippine 21
IQ - Iraq 20
TH - Thailandia 15
MX - Messico 14
PL - Polonia 14
AT - Austria 13
SC - Seychelles 13
TR - Turchia 12
ID - Indonesia 10
LT - Lituania 10
ES - Italia 9
PK - Pakistan 9
BE - Belgio 7
CL - Cile 7
IR - Iran 7
EG - Egitto 6
CO - Colombia 5
JM - Giamaica 5
EC - Ecuador 4
LB - Libano 4
MY - Malesia 4
PY - Paraguay 4
DO - Repubblica Dominicana 3
NI - Nicaragua 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
HN - Honduras 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
AG - Antigua e Barbuda 1
AZ - Azerbaigian 1
BB - Barbados 1
BH - Bahrain 1
BS - Bahamas 1
BZ - Belize 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 10.726
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Città #
Singapore 590
Southend 406
Ashburn 381
Chandler 300
San Jose 286
Ho Chi Minh City 248
Hong Kong 222
Hanoi 198
Hefei 165
Fairfield 148
Dong Ket 143
Santa Clara 129
Princeton 108
Beijing 96
Jacksonville 92
Wilmington 84
Dublin 78
Seattle 77
Seoul 75
Bologna 71
Council Bluffs 66
Woodbridge 66
Los Angeles 65
Houston 58
Lauterbourg 58
Tokyo 58
Abidjan 56
Boardman 53
Ann Arbor 52
Cambridge 47
Helsinki 45
Lomé 44
Nanjing 43
Turin 42
Westminster 42
Milan 39
New York 38
Padova 37
Da Nang 35
Haiphong 35
Berlin 31
Munich 30
Saint Petersburg 29
Abeokuta 27
Buffalo 27
Frankfurt am Main 27
Dallas 26
Medford 26
Rome 26
São Paulo 26
Jinan 25
Amman 21
Sofia 21
Bern 20
Nanchang 20
Phoenix 20
Shanghai 20
Mülheim 18
San Diego 17
Bengaluru 16
Naples 16
Redondo Beach 16
Tianjin 16
Denver 15
Atlanta 14
Shenyang 14
Johannesburg 13
Philadelphia 13
Changsha 12
Guangzhou 12
The Dalles 12
Dearborn 11
Florence 11
Mahé 11
Washington 11
Chicago 10
Nuremberg 10
Quận Bình Thạnh 10
San Francisco 10
Warsaw 10
Amsterdam 9
Bremen 9
Brooklyn 9
Can Tho 9
Cleveland 9
Des Moines 9
Hebei 9
Hải Dương 9
Roubaix 9
Zhengzhou 9
Biên Hòa 8
Charlotte 8
Falkenstein 8
Las Vegas 8
London 8
Miami 8
Montreal 8
Olalla 8
Redwood City 8
Rimini 8
Totale 5.766
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Nome #
Quando non trascurare la splenomegalia nel lattante un insegnamento dalla pratica clinica 1.920
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 261
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 209
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 209
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 207
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 204
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 202
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 197
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 193
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study 189
Diagnostic features of thyroid nodules in pediatrics 186
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 183
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 183
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 182
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 179
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough 178
Body Mass Index (BMI) evaluation in survivors from childhood cancer 176
Il bambino oncologico "guarito": quali alterazioni endocrinologiche temere? 176
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 175
Growth patterns in children treated for Acute Lymphoblastic Leukemia (ALL): Relationship with cranial irradiation 172
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 170
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening 170
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study 167
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 166
Focal nodular hyperplasia of the liver after intensive treatment for pediatric cancer: is hematopoietic stem cell transplantation a risk factor? 162
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) 159
Omocisteina alta? Quello che il pediatra deve sapere 152
Obesity in children and adolescents: an increasing metabolic problem. 152
Fanconi-Bickel syndrome: a mild form associated with GLUT2 mutation 152
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 151
Diagnosis, treatment, and follow-up of a case of Wolman disease with hemophagocytic lymphohistiocytosis 150
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 150
Maternal PKU: Defining phenylalanine tolerance and its variation during pregnancy, according to genetic background 150
Prevalence and ultrasound patterns of testicular adrenal rest tumors in adults with congenital adrenal hyperplasia 150
Height as a risk factor for osteosarcoma. 149
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 148
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 146
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 146
Height outcome and pubertal development in CYP21 genotyped CAH male patients 145
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) 142
Severe hypercholesterolaemia in a paediatric patient with congenital analbuminaemia 141
A NOVEL FRAME-SHIFT MUTATION IN THE SHOX GENE IN A SUBJECT WITH LERI-WEIL DYSCHONDROSTEOSIS. 140
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis 136
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. 135
The SHOX gene: a new indication for GH treatment 133
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 128
Hemophagocytic lymphohistiocytosis and lysinuric protein intolerance:case report 125
Intratesticular Doppler Flow and Gonadal Status in Male Survivors of a Childhood Malignancy 124
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 124
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 123
Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria 97
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report 91
Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center 90
Radiological and Neuroradiological Features in Pediatric Mucopolysaccharidoses: A Retrospective Case Series from the Emilia-Romagna Regional Referral Center 86
Longitudinal evaluation with quantitative ultrasound of bone marrow transplantation-associated bone loss in a series of 28 children 86
Understanding Glycogen Storage Disease Type IX: A Systematic Review with Clinical Focus—Why It Is Not Benign and Requires Vigilance 64
Tachycardiomyopathy-like presentation in neonatal MCAD deficiency: A novel cardiac phenotype 62
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 62
Glucose dynamics in glycogen storage disease type IXa with novel PHKA2 variants: insights from our experience and a comprehensive review of the disease spectrum 59
Transition in inherited metabolic diseases: the dietitians, pediatricians and adult physicians’ point of view: the results of an Italian survey 57
Does Basal Morning Luteinizing Hormone (bLH) Predict Central Precocious Puberty (CPP) in Girls? 46
Clinical Implications and Preventive Strategies for Neonatal and Infant Hypovitaminosis D: Analysis and Comparison of Current Evidence 46
Early-Onset Inherited Metabolic Diseases: When Clinical Symptoms Precede Newborn Screening—Insights from Emilia-Romagna (Italy) 42
Primary ovarian insufficiency in Classic Galactosemia: a systematic review 27
Totale 10.882
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Categoria #
all - tutte 25.403
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 25.403
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022752 0 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
2025/20265.267 383 286 255 225 343 206 387 227 806 303 1.715 131
2026/2027161 121 40 0 0 0 0 0 0 0 0 0 0
Totale 10.882