CATALOGO DEI PRODOTTI DELLA RICERCA

TEOFOLI, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 829
EU - Europa 612
AS - Asia 220
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 2
SA - Sud America 2
Totale 1.667
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Nazione #
US - Stati Uniti d'America 827
CN - Cina 193
GB - Regno Unito 185
SE - Svezia 88
IT - Italia 78
IE - Irlanda 70
FR - Francia 59
FI - Finlandia 51
DE - Germania 44
UA - Ucraina 17
KR - Corea 12
RU - Federazione Russa 6
BE - Belgio 5
VN - Vietnam 4
NL - Olanda 3
PH - Filippine 3
TR - Turchia 3
AU - Australia 2
CA - Canada 2
CL - Cile 2
IN - India 2
PL - Polonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BD - Bangladesh 1
CH - Svizzera 1
EU - Europa 1
IQ - Iraq 1
KG - Kirghizistan 1
LV - Lettonia 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 1.667
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Città #
Chandler 220
Southend 170
Jacksonville 132
Woodbridge 87
Dublin 70
Beijing 53
Ann Arbor 46
New York 38
Ashburn 36
Houston 28
Lawrence 24
Princeton 24
Wilmington 24
Shenyang 20
Verona 20
Helsinki 19
Jinan 17
Nanjing 15
Bologna 9
Seoul 9
Sindelfingen 8
Taizhou 8
Zhengzhou 8
Tianjin 7
Hebei 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
Dong Ket 2
Kiel 2
Norwalk 2
Nuremberg 2
Pergine Valsugana 2
Sigillo 2
Sydney 2
Bishkek 1
Boardman 1
Bratislava 1
Cerea 1
Clearwater 1
Des Moines 1
Dongguan 1
Fuzhou 1
Gazipur 1
Hanover 1
Hilla 1
Latina 1
Los Angeles 1
Magione 1
Muenster 1
Mumbai 1
Napoli 1
Newark 1
Porto 1
Poznan 1
Redwood City 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 1.213
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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. 117
L. Inibina B in bambini prepuberi con pregresso criptorchidismo: indice di disfunzione testicolare? 108
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. 85
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations. 82
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. 79
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls 77
Congenital hypothyroidism with delayed TSH elevation in low-birth-weight infants: incidence, diagnosis and management 77
Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? 76
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 76
Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program. 75
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis 72
Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor? 72
Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up 71
Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children 68
Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia 68
High-protein goat's milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice 67
Role of genotype in the diagnosis of children with 21-hydroxylase deficiency 65
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 61
Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy 57
Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved. 46
Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy 43
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 42
A Gain-of-Function Mutation on BCKDK Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid Metabolism 36
20 {YEARS} {OF} {NEONATAL} {SCREENING} {FOR} {CONGENITAL} {ADRENAL} {HYPERPLASIA} {IN} {NORTH}-{EASTERN} {ITALY}: {ROLE} {OF} {LC}-{MS}/{MS} {AS} A {SECOND} {TIER} {TEST} 35
Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient 21
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 14
Totale 1.690
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Categoria #
all - tutte 5.583
article - articoli 5.357
book - libri 0
conference - conferenze 226
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 11.166
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20196 0 0 0 0 0 0 0 0 0 0 5 1
2019/2020209 18 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
2023/2024199 8 23 30 17 20 53 14 12 3 16 3 0
Totale 1.690