GIOVANNIELLO, TERESA
 Distribuzione geografica
Continente #
NA - Nord America 503
EU - Europa 235
AS - Asia 135
AF - Africa 16
SA - Sud America 11
OC - Oceania 1
Totale 901
Nazione #
US - Stati Uniti d'America 493
IT - Italia 89
CN - Cina 55
SG - Singapore 47
UA - Ucraina 36
SE - Svezia 34
IN - India 28
FI - Finlandia 21
DE - Germania 14
TG - Togo 14
CA - Canada 9
AR - Argentina 8
CZ - Repubblica Ceca 7
GB - Regno Unito 6
IE - Irlanda 6
BE - Belgio 5
CH - Svizzera 3
NL - Olanda 3
RU - Federazione Russa 3
TR - Turchia 3
CO - Colombia 2
ES - Italia 2
ID - Indonesia 2
NO - Norvegia 2
SC - Seychelles 2
AL - Albania 1
AT - Austria 1
CL - Cile 1
EE - Estonia 1
MX - Messico 1
NZ - Nuova Zelanda 1
RO - Romania 1
Totale 901
Città #
Chandler 62
Fairfield 60
Houston 33
Singapore 30
Woodbridge 30
Ann Arbor 27
Beijing 26
Rome 26
Ashburn 25
Seattle 21
Wilmington 20
Santa Clara 19
Princeton 17
Cambridge 16
Plano 16
Lomé 14
Torre del Greco 14
Boston 12
Jacksonville 10
Lawrence 9
Federal 8
Brno 7
Falkenstein 7
Millbury 7
Boardman 6
New York 6
Dublin 5
Helsinki 5
San Paolo di Civitate 5
Toronto 4
Andover 3
Brussels 3
Moscow 3
Norwalk 3
Ottawa 3
Sivas 3
Agotnes 2
Capannelle 2
Dearborn 2
Des Moines 2
Elgin 2
Elk Grove Village 2
Falls Church 2
Jakarta 2
Mahé 2
Montreal 2
Naples 2
San Mateo 2
Santiago de Cali 2
Waanrode 2
Wenzhou 2
Auburn Hills 1
Baotou 1
Bari 1
Benisa 1
Bern 1
Bremen 1
Caserta 1
Cesana Brianza 1
Chongqing 1
Christchurch 1
Dallas 1
Frankfurt am Main 1
Greystones 1
Harbin 1
Indiana 1
Kunming 1
Laurel 1
Los Angeles 1
Madrid 1
Mannheim 1
Mexico City 1
Milan 1
Monsampolo Del Tronto 1
Munich 1
Nanjing 1
Nuremberg 1
Orange 1
Phoenix 1
Redmond 1
Romola 1
Rotkreuz 1
San Diego 1
San Giorgio 1
Santiago 1
Shijiazhuang 1
Tallinn 1
Tirana 1
Vienna 1
Vigevano 1
Washington 1
Wuhan 1
Wuxi 1
Zurich 1
Totale 638
Nome #
Molecular analysis of PKU-associated PAH mutations: a fast and simple genotyping test 113
A New Tyrosine Hydroxylase Genotype Associated With Early-Onset Severe Encephalopathy 77
A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia. 75
A novel missense mutation pattern of the GCH1 gene in dopa-responsive dystonia 70
Determinazione dell’attività dell’enzima guanidinoacetato metiltrasferasi (GAMT) mediante ESI-MS/MS. 56
Newborn screening of galactosemia by tandem mass spectrometry (MS/MS): a pilot study. 53
The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylanine hydroxylase deficiency. 50
A NOVEL TYROSINE HYDROXYLASE GENOTYPE ASSOCIATED WITH EARLY ONSET ENCEPHALOPATY. 44
The relationship between glicated hemoglobin and polymorphonuclear leukocytes leukotriene B4 release in people with diabetes mellitus 43
MUTATION ANALYSIS OF PHENYLALANINE HYDROXYLATION (PAH) GENE BY DHPLC 42
3-Methylglutaconic Aciduria Type I Due to AUH Defect: The Case Report of a Diagnostic Odyssey and a Review of the Literature 42
Dopa-responsive dystonias/dyskinesias (DRDS): diagnosis and monitoring of the treatment 40
NEOPTERIN EXCRETION IN URINE AS POSSIBLE PERIPHERAL MARKER OF SEGAWA DISEASE 36
Two new mutations on tyrosine hydroxylase gene (TH) presenting as late onset dystonic-dyskinetic syndrome 35
null 32
null 32
Outcome in short chain acyl-CoA dehydrogenase deficiency (SCADD) detected by newborn screening (NBS) 24
Genotype-phenotype correlation study through protein model of 3- methylcrotonyl-CoA carboxylase 22
null 21
Transient hyperphenylalaninemia due to heterozygous mutation in pyruvoyltetrahydropterin synthase (PTS) gene 19
Totale 926
Categoria #
all - tutte 2.936
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 2.936


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202093 0 0 0 0 0 12 15 14 11 28 12 1
2020/202160 8 9 15 5 2 3 1 4 3 4 6 0
2021/2022157 1 9 14 6 18 4 2 12 18 15 24 34
2022/2023202 30 36 7 40 37 14 0 7 16 5 10 0
2023/202480 5 17 3 6 6 9 0 6 0 12 9 7
2024/2025119 15 12 7 31 34 20 0 0 0 0 0 0
Totale 926