IRIS
BUKVIC, NENAD
 Distribuzione geografica
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Continente #
NA - Nord America 267
EU - Europa 76
AS - Asia 32
Totale 375
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Nazione #
US - Stati Uniti d'America 266
SE - Svezia 27
CN - Cina 23
IT - Italia 19
FI - Finlandia 7
GB - Regno Unito 7
FR - Francia 5
DE - Germania 4
VN - Vietnam 4
IN - India 3
BE - Belgio 2
RU - Federazione Russa 2
SG - Singapore 2
SI - Slovenia 2
CR - Costa Rica 1
IE - Irlanda 1
Totale 375
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Città #
Chandler 34
Fairfield 32
Ashburn 25
Woodbridge 24
Nyköping 22
Wilmington 20
Ann Arbor 16
Houston 16
Cambridge 15
Seattle 9
Beijing 8
Helsinki 6
Lawrence 6
Nanjing 6
Roxbury 6
Dearborn 5
New York 5
Bari 4
Dong Ket 4
Jacksonville 3
Pune 3
Shenyang 3
Barletta 2
Brooklyn 2
Brussels 2
Inglewood 2
Ljubljana 2
Munich 2
Singapore 2
Valenzano 2
Albenga 1
Altopascio 1
Boardman 1
Changsha 1
Des Moines 1
Dublin 1
Hebei 1
Hounslow 1
Kunming 1
London 1
Milan 1
Mt. Pleasant 1
Napoli 1
Paris 1
Princeton 1
Quanzhou 1
San Francisco 1
San José 1
Shanghai 1
Stimigliano 1
Toulouse 1
Trieste 1
Zhengzhou 1
Totale 311
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Nome #
Accurate classification of NF1 gene variants in 84 Italian patients with neurofibromatosis type 1 114
Familly with two different cases of post- and pre-natal L1 syndrome; When hydrocephaly become "multidisciplinary headache" 96
OSTEOGENIC DIFFERENTIATION AND GENE EXPRESSION OF DENTAL PULP STEM CELLS UNDER LOW-LEVEL LASER IRRADIATION: A GOOD PROMISE FOR TISSUE ENGINEERING. 62
The first case of congenital myasthenic syndrome caused by a large homozygous deletion in the cterminal region of colq (Collagen like tail subunit of asymmetric acetylcholinesterase) protein 54
The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate 45
Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants 29
What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis 8
First report of whole CFTR gene duplication in a healthy newborn carrying R74W and V855I variants on the same allele 2
Impact of High-to-Moderate Penetrance Genes on Genetic Testing: Looking over Breast Cancer 1
De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature 1
Totale 412
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Categoria #
all - tutte 2.147
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 2.147
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202071 8 1 2 7 4 8 6 5 8 6 8 8
2020/202194 3 6 2 11 10 3 22 6 6 11 3 11
2021/202247 1 1 2 2 1 7 1 5 6 5 6 10
2022/202392 13 22 4 4 6 11 2 8 17 1 3 1
2023/202447 1 8 0 11 9 13 0 1 2 1 0 1
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 412