CATALOGO DEI PRODOTTI DELLA RICERCA

CAMILOT, Marta
 Distribuzione geografica
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Continente #
NA - Nord America 1.463
EU - Europa 1.097
AS - Asia 550
OC - Oceania 5
SA - Sud America 4
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 3
Totale 3.125
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Nazione #
US - Stati Uniti d'America 1.456
CN - Cina 358
GB - Regno Unito 308
SG - Singapore 147
SE - Svezia 136
IE - Irlanda 109
RU - Federazione Russa 104
FR - Francia 103
IT - Italia 98
FI - Finlandia 88
DE - Germania 84
UA - Ucraina 28
BE - Belgio 14
KR - Corea 13
CA - Canada 7
JP - Giappone 7
NL - Olanda 7
AU - Australia 5
ID - Indonesia 5
LV - Lettonia 5
PL - Polonia 5
CH - Svizzera 4
IN - India 4
PH - Filippine 4
VN - Vietnam 4
A2 - ???statistics.table.value.countryCode.A2??? 2
AR - Argentina 2
CL - Cile 2
PT - Portogallo 2
TG - Togo 2
TR - Turchia 2
AM - Armenia 1
BD - Bangladesh 1
EU - Europa 1
HU - Ungheria 1
IQ - Iraq 1
KG - Kirghizistan 1
LK - Sri Lanka 1
SK - Slovacchia (Repubblica Slovacca) 1
SL - Sierra Leone 1
TM - Turkmenistan 1
Totale 3.125
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Città #
Chandler 350
Southend 280
Jacksonville 236
Woodbridge 162
Singapore 122
Dublin 109
Beijing 86
Ann Arbor 77
Houston 71
Ashburn 61
New York 55
Wilmington 38
Lawrence 37
Princeton 37
Jinan 29
Helsinki 28
Shenyang 28
Verona 26
Nanjing 24
Sindelfingen 17
Brussels 14
Hebei 13
Tianjin 12
Changsha 10
Frankfurt am Main 10
Ningbo 10
Santa Clara 10
Seoul 10
Zhengzhou 10
Bologna 9
Milan 9
Nanchang 9
Taizhou 9
Boardman 8
Jiaxing 8
Kent 8
Los Angeles 8
Redmond 8
Hangzhou 7
Seattle 7
Tokyo 7
Guangzhou 6
Redwood City 6
Taiyuan 6
Haikou 5
Jakarta 5
Lanzhou 5
Fairfield 4
Lancaster 4
Moscow 4
Norwalk 4
Caloocan City 3
Clearwater 3
Dallas 3
Detroit 3
Munich 3
Riga 3
Toronto 3
Auburn Hills 2
Buenos Aires 2
Bussolengo 2
Camogli 2
Dong Ket 2
Genoa 2
Kiel 2
Lappeenranta 2
Lomé 2
Montréal 2
Nuremberg 2
Pergine Valsugana 2
Riva 2
San Diego 2
San Francisco 2
Sigillo 2
Sydney 2
Venezia 2
Zurich 2
Aarau 1
Agordo 1
Ashgabat 1
Atlanta 1
Bishkek 1
Bratislava 1
Cerea 1
Cicciano 1
Cormeilles-en-Parisis 1
Dalian 1
Des Moines 1
Dongguan 1
Düsseldorf 1
Freetown 1
Fuzhou 1
Gazipur 1
Guiyang 1
Hanover 1
Hilla 1
Hongtong 1
Latina 1
Magione 1
Manila 1
Totale 2.200
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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. 125
L. Inibina B in bambini prepuberi con pregresso criptorchidismo: indice di disfunzione testicolare? 118
Idiopathic Juvenile Osteoporosis: Clinical Experience from a Single Centre and Screening of LRP5 and LRP6 Genes 112
Neonatal screening for congenital errors of metabolism in Northeast Italy: retrospective study of the years 1978-1997 97
Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern italian neonatal screening 96
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations. 93
Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes. 91
Characterizatin of phenyalanine hydroxylase alleles in North-East Italy: a preliminary investigation 91
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 90
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. 90
Polymorphisms of the TSH Receptor gene in children with resistance to TSH and in helthy young controls 89
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 87
Congenital hypothyroidism with delayed TSH elevation in low-birth-weight infants: incidence, diagnosis and management 87
Circulating ghrelin levels in girls with central precocious puberty are reduced during treatment with LHRH analog. 86
Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? 86
Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up 85
Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program. 83
Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor? 83
Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation 81
A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis 81
Effect of early thyroid scanning on levothyroxine dosage and neuropsychological development in congenital hypothyroidism. 81
High-protein goat's milk diet identified through newborn screening: clinical warning of a potentially dangerous dietetic practice 80
Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children 79
Functional studies of new TSH receptor (TSHr) mutations identified in patients affected by hypothyroidism or isolated hyperthyrotrophinaemia 75
Risultati del follow-up a lungo termine di pz con ipotiroidismo congenito: l'etiologia condiziona il trattamento 74
L-Thyroxine stored in the hair of congenital hypothyroidism newborns at time of diagnosis. An evidence of placental crossing 73
Role of genotype in the diagnosis of children with 21-hydroxylase deficiency 73
Growth Hormone Deficiency and Lysinuric Protein Intolerance: Case Report and Review of the Literature 71
Multiple acyl-COA dehydrogenase deficiency in elderly carriers 69
Possible andrologic markers in elevated neonatal 17-hydroxyprogesterone 66
Incidence of inborn errors of metabolism: results of newborn screening program in North-East Italy 65
Thyroxine hair content in congenital hypothyroidism and hyperthyroidism. 62
Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy 61
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 58
Newborn Screening for Biotinidase Deficiency. The Experience of a Regional Center in Italy 57
Benefits of rescreening newborns of mothers affected by autoimmune hypothyroidism 56
The Effects of Iodine Supplementation in Pregnancy on Iodine Status, Thyroglobulin Levels and Thyroid Function Parameters: Results from a Randomized Controlled Clinical Trial in a Mild-to-Moderate Iodine Deficiency Area 52
A Gain-of-Function Mutation on BCKDK Gene and Its Possible Pathogenic Role in Branched-Chain Amino Acid Metabolism 51
20 {YEARS} {OF} {NEONATAL} {SCREENING} {FOR} {CONGENITAL} {ADRENAL} {HYPERPLASIA} {IN} {NORTH}-{EASTERN} {ITALY}: {ROLE} {OF} {LC}-{MS}/{MS} {AS} A {SECOND} {TIER} {TEST} 45
Vitamin B12 Administration by Subcutaneous Catheter Device in a Cobalamin A (cblA) Patient 31
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 26
Totale 3.156
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Categoria #
all - tutte 11.652
article - articoli 10.814
book - libri 0
conference - conferenze 838
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 23.304
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020272 0 0 0 0 36 27 40 34 17 50 27 41
2020/2021306 18 56 20 40 47 31 6 21 20 10 32 5
2021/2022284 24 92 4 28 6 0 3 18 12 8 23 66
2022/2023829 48 106 57 193 72 179 8 46 96 1 12 11
2023/2024388 14 33 39 34 34 72 20 16 5 22 74 25
2024/2025315 40 49 47 164 15 0 0 0 0 0 0 0
Totale 3.156