IRIS
MOIA, STEFANIA
 Distribuzione geografica
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Continente #
EU - Europa 337
NA - Nord America 274
AS - Asia 92
Totale 703
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Nazione #
US - Stati Uniti d'America 272
IE - Irlanda 103
DE - Germania 77
SE - Svezia 65
UA - Ucraina 37
HK - Hong Kong 28
CN - Cina 26
IT - Italia 24
FI - Finlandia 23
IN - India 13
IR - Iran 11
VN - Vietnam 8
SG - Singapore 6
RU - Federazione Russa 4
FR - Francia 3
CA - Canada 2
GB - Regno Unito 1
Totale 703
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Città #
Dublin 103
Jacksonville 72
Dearborn 43
Hong Kong 28
Wilmington 16
Piemonte 13
Beijing 12
Bremen 12
Lawrence 12
Princeton 12
San Mateo 12
Chandler 8
Dong Ket 8
Zanjan 7
Andover 6
Ashburn 6
Ann Arbor 5
Cassano Magnago 3
Monmouth Junction 3
Norwalk 3
Singapore 3
Turin 3
Ardabil 2
Chicago 2
Düsseldorf 2
Hefei 2
Henderson 2
Munich 2
Boardman 1
Changsha 1
Chaoyang 1
Chongqing 1
Fort Worth 1
Guangzhou 1
Hebei 1
Helsinki 1
Kunming 1
Leawood 1
Nanjing 1
Ningbo 1
Portland 1
Sabz 1
Sacramento 1
Toronto 1
Volga 1
Winnipeg 1
Wuhan 1
Totale 421
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Nome #
Adiponectin oligomers are similarly distributed in adequate-for-gestational-age obese children irrespective of feeding in their first year 74
A novel HESX1 splice mutation causes isolated GH deficiency by interfering with mRNA processing 73
Endocrine disorders in childhood and adolescence. Natural history of subclinical hypothyroidism in children and adolescents and potential effects of replacement therapy: a review. 67
Unacylated, acylated ghrelin and obestatin levels are differently inhibited by oral glucose load in pediatric obesity: Association with insulin sensitivity and metabolic alterations. 63
Pediatric obesity and vitamin D deficiency: a proteomic approach identifies multimeric adiponectin as a key link between these conditions. 61
Obestatin levels are associated with C-peptide and anti-insulin antibodies at the onset whereas unacylated and acylated ghrelin levels are not predictive of long-term metabolic control in children with type 1 diabetes. 61
The W520X mutation in the TSHR gene brings on subclinical hypothyroidism through an haploinsufficiency mechanism. 60
Isolated GHD: investigation and implication of JAK/STAT related genes before and after rhGH treatment. 57
Tourette syndrome in a patient with resistance to thyroid hormone syndrome. 54
Interictal ghrelin levels in adult patients with epilepsy. 53
Compound heterozygosity for two GHR missense mutations in a patient affected by Laron Syndrome: A case report 53
Involvement of genes related to inflammation and cell cycle in Idiopathic Short Stature. 48
Totale 724
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Categoria #
all - tutte 3.516
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 3.516
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020157 0 0 13 0 28 25 28 9 14 27 13 0
2020/202192 12 0 12 0 12 5 12 0 12 4 15 8
2021/2022100 3 5 9 12 9 0 6 3 6 4 19 24
2022/2023213 15 14 18 0 16 17 6 8 104 0 8 7
2023/202470 15 2 3 3 12 0 8 0 0 0 23 4
2024/20252 0 2 0 0 0 0 0 0 0 0 0 0
Totale 724