CATALOGO DEI PRODOTTI DELLA RICERCA

TEOFOLI, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 846
EU - Europa 660
AS - Asia 267
SA - Sud America 3
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
Totale 1.780
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Nazione #
US - Stati Uniti d'America 844
CN - Cina 210
GB - Regno Unito 185
SE - Svezia 88
IT - Italia 79
IE - Irlanda 72
FR - Francia 59
FI - Finlandia 51
RU - Federazione Russa 47
DE - Germania 45
SG - Singapore 23
UA - Ucraina 17
KR - Corea 12
JP - Giappone 6
BE - Belgio 5
NL - Olanda 4
VN - Vietnam 4
PH - Filippine 3
PL - Polonia 3
TR - Turchia 3
AU - Australia 2
CA - Canada 2
CL - Cile 2
IN - India 2
LV - Lettonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
BD - Bangladesh 1
CH - Svizzera 1
EU - Europa 1
IQ - Iraq 1
KG - Kirghizistan 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TM - Turkmenistan 1
Totale 1.780
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Città #
Chandler 220
Southend 170
Jacksonville 132
Woodbridge 87
Dublin 72
Beijing 63
Ann Arbor 46
Ashburn 39
New York 38
Houston 28
Lawrence 24
Princeton 24
Wilmington 24
Shenyang 20
Verona 20
Helsinki 19
Jinan 17
Nanjing 15
Singapore 11
Bologna 9
Seoul 9
Sindelfingen 8
Taizhou 8
Zhengzhou 8
Tianjin 7
Boardman 6
Hebei 6
Kent 6
Tokyo 6
Brussels 5
Changsha 5
Hangzhou 5
Jiaxing 5
Milan 5
Nanchang 5
Seattle 5
Haikou 4
Lanzhou 4
Ningbo 4
Taiyuan 4
Caloocan City 3
Fairfield 3
Guangzhou 3
Redmond 3
Auburn Hills 2
Bussolengo 2
Camogli 2
Dallas 2
Dong Ket 2
Kiel 2
Norwalk 2
Nuremberg 2
Pergine Valsugana 2
Sigillo 2
Sydney 2
Ashgabat 1
Bishkek 1
Bratislava 1
Buenos Aires 1
Cerea 1
Clearwater 1
Des Moines 1
Dongguan 1
Frankfurt am Main 1
Fuzhou 1
Gazipur 1
Hanover 1
Hilla 1
Latina 1
Los Angeles 1
Magione 1
Moscow 1
Muenster 1
Mumbai 1
Napoli 1
Newark 1
Pisa 1
Porto 1
Poznan 1
Redwood City 1
Riga 1
Saint Louis 1
San Diego 1
San Francisco 1
San Martino Buon Albergo 1
Santa Clara 1
Seveso 1
Strasbourg 1
Szczecin 1
Toronto 1
Utrecht 1
Venezia 1
Totale 1.264
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Nome #
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns. 120
L. Inibina B in bambini prepuberi con pregresso criptorchidismo: indice di disfunzione testicolare? 114
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. 86
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations. 85
Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center. 84
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls 83
Congenital hypothyroidism with delayed TSH elevation in low-birth-weight infants: incidence, diagnosis and management 82
Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program. 80
Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? 80
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism 80
Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up 78
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis 77
Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor? 76
Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children 75
High-protein goat's milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice 73
Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia 71
Role of genotype in the diagnosis of children with 21-hydroxylase deficiency 67
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 63
Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy 59
Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved. 49
Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience 48
Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy 47
A Gain-of-Function Mutation on BCKDK Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid Metabolism 43
20 {YEARS} {OF} {NEONATAL} {SCREENING} {FOR} {CONGENITAL} {ADRENAL} {HYPERPLASIA} {IN} {NORTH}-{EASTERN} {ITALY}: {ROLE} {OF} {LC}-{MS}/{MS} {AS} A {SECOND} {TIER} {TEST} 39
Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient 24
Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up,Influenza della morfologia tiroidea sullo sviluppo psicomotorio di bambini affetti da ipotiroidismo congenito durante 8 anni di follow-up 20
Totale 1.803
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Categoria #
all - tutte 6.476
article - articoli 6.212
book - libri 0
conference - conferenze 264
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.952
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020191 0 3 2 12 24 17 25 19 16 27 21 25
2020/2021188 12 34 14 25 31 18 3 11 9 7 19 5
2021/2022167 14 51 4 19 3 0 2 12 7 3 11 41
2022/2023516 29 71 33 118 43 110 6 27 62 1 7 9
2023/2024263 8 23 30 17 20 53 14 12 3 16 51 16
2024/202549 26 23 0 0 0 0 0 0 0 0 0 0
Totale 1.803