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  1. Book ; Online: Land Use Change from Non-urban to Urban Areas

    González-Jaramillo, Víctor Hugo / Novelli, Antonio

    Problems, Challenges and Opportunities

    2022  

    Keywords Research & information: general ; Geography ; land use/land cover change ; water recharge ; flooding ; meteorological forecast ; hydrological response ; IWRM ; best management practices ; watershed management ; experimental watershed study design ; municipal watershed ; adaptive management ; functional urban land ; urban space ; urban land use/cover change ; urbanization ; Changchun ; urban hydrology ; impervious surfaces ; land use scenarios ; urban surface growth ; hydrological model ; flood flows ; construction land development intensity ; construction land use benefit ; coupling and coordination relationship ; spatiotemporal evolution ; Lanzhou-Xining urban agglomeration ; land cover ; land use change ; downscaling approach ; Switzerland ; geographic information system ; aerial photo interpretation ; topographic map ; inverse distance weighting ; expert system ; village ; strategy ; development priorities ; land use ; land take ; urban agriculture ; land use planning ; zoning ; GI products ; integrated water resources management ; territory management ; future scenarios ; prospective analysis ; decision support system ; urban growth boundaries (UGBs) ; LULC change simulation ; multi-source big data ; SD model ; PLUS model ; county area ; Xinxing County
    Language English
    Size 1 electronic resource (184 pages)
    Publisher MDPI - Multidisciplinary Digital Publishing Institute
    Publishing place Basel
    Document type Book ; Online
    Note English
    HBZ-ID HT030379071
    ISBN 9783036557922 ; 303655792X
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  2. Book ; Online ; E-Book: Marine neurotoxins

    Novelli, Antonello

    (Advances in Neurotoxicology ; 6)

    2021  

    Author's details edited by Antonello Novelli [and three others]
    Series title Advances in Neurotoxicology ; 6
    Keywords Neurotoxic agents/Physiological effect ; Neurotoxicology
    Subject code 615.9
    Language English
    Size 1 online resource (332 pages)
    Publisher Academic Press
    Publishing place Cambridge, MA
    Document type Book ; Online ; E-Book
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    ISBN 0-12-822015-5 ; 0-12-822014-7 ; 978-0-12-822015-3 ; 978-0-12-822014-6
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  3. Article ; Online: Letter: The ROTA-CUT randomised trial: push the button harder.

    Novelli, Laura / Colombo, Antonio / Mangieri, Antonio

    EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology

    2024  Volume 20, Issue 4, Page(s) e268

    Language English
    Publishing date 2024-02-19
    Publishing country France
    Document type Journal Article
    ZDB-ID 2457174-X
    ISSN 1969-6213 ; 1774-024X
    ISSN (online) 1969-6213
    ISSN 1774-024X
    DOI 10.4244/EIJ-D-23-00937
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 6680: Show issues Location:
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    Zs.MO 571: Show issues

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  4. Article: Editorial: Unravelling the basis of non-invasive prenatal screening results.

    De Falco, Luigia / Pelo, Elisabetta / Qi, Zhongxia / Novelli, Antonio

    Frontiers in genetics

    2023  Volume 14, Page(s) 1247764

    Language English
    Publishing date 2023-07-17
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2023.1247764
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Clinical refinement of the SETD5-associated phenotype in a child displaying novel features and KBG syndrome-like appearance.

    Pascolini, Giulia / Gnazzo, Maria / Novelli, Antonio / Grammatico, Paola

    American journal of medical genetics. Part A

    2022  Volume 188, Issue 5, Page(s) 1623–1625

    MeSH term(s) Abnormalities, Multiple/genetics ; Bone Diseases, Developmental/genetics ; Facies ; Humans ; Intellectual Disability/diagnosis ; Intellectual Disability/genetics ; Methyltransferases/genetics ; Phenotype ; Tooth Abnormalities/genetics
    Chemical Substances Methyltransferases (EC 2.1.1.-) ; SETD5 protein, human (EC 2.1.1.-)
    Language English
    Publishing date 2022-02-07
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 2108614-X
    ISSN 1552-4833 ; 0148-7299 ; 1552-4825
    ISSN (online) 1552-4833
    ISSN 0148-7299 ; 1552-4825
    DOI 10.1002/ajmg.a.62679
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 1376/A: Show issues Location:
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    Jg. 1995 - 2021: Lesesall (1.OG)
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  6. Article ; Online: How to predict conduction disturbances after transcatheter aortic valve replacement.

    Novelli, Laura / Jamie, Gulrays / Regazzoli, Damiano / Reimers, Bernhard / Frontera, Antonio / Mangieri, Antonio

    Kardiologia polska

    2023  Volume 81, Issue 4, Page(s) 330–337

    Abstract: Transcatheter aortic valve replacement (TAVI) has evolved into the gold standard management option for high-risk patients with severe aortic stenosis. Despite identifying procedural, electrocardiographic, and clinical predictors of important post- ... ...

    Abstract Transcatheter aortic valve replacement (TAVI) has evolved into the gold standard management option for high-risk patients with severe aortic stenosis. Despite identifying procedural, electrocardiographic, and clinical predictors of important post-procedural conduction disturbances (left bundle branch block and high-degree atrioventricular block) and despite continuous technological refinement of transcatheter aortic valves, the rate of post-procedural conduction disturbance remains high and challenging to manage. New strategies are required to reduce the overall rate of post-procedural permanent pacemaker implantations. In this article, we will review the incidence, predictive factors, and clinical implications of conduction disturbances after TAVI.
    MeSH term(s) Humans ; Transcatheter Aortic Valve Replacement/adverse effects ; Pacemaker, Artificial/adverse effects ; Treatment Outcome ; Aortic Valve Stenosis/surgery ; Atrioventricular Block/therapy ; Aortic Valve/surgery ; Heart Valve Prosthesis/adverse effects
    Language English
    Publishing date 2023-02-06
    Publishing country Poland
    Document type Journal Article
    ZDB-ID 411492-9
    ISSN 1897-4279 ; 0022-9032
    ISSN (online) 1897-4279
    ISSN 0022-9032
    DOI 10.33963/KP.a2023.0039
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.B 598: Show issues Location:
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    Zs.MO 474: Show issues

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  7. Article ; Online: Will GWAS eventually allow the identification of genomic biomarkers for COVID-19 severity and mortality?

    Colona, Vito Luigi / Biancolella, Michela / Novelli, Antonio / Novelli, Giuseppe

    The Journal of clinical investigation

    2021  Volume 131, Issue 23

    Abstract: GWAS involve testing genetic variants across the genomes of many individuals to identify genotype-phenotype associations. GWAS have enabled the identification of numerous genomic biomarkers in various complex human diseases, including infectious ones. ... ...

    Abstract GWAS involve testing genetic variants across the genomes of many individuals to identify genotype-phenotype associations. GWAS have enabled the identification of numerous genomic biomarkers in various complex human diseases, including infectious ones. However, few of these studies are relevant for clinical practice or at the bedside. In this issue of the JCI, Nakanishi et al. characterized the clinical implications of a major genetic risk factor for COVID-19 severity and its age-dependent effect, using individual-level data in a large international multicenter consortium. This study indicates that a common COVID-19 genetic risk factor (rs10490770) associates with increased risks of morbidity and mortality, suggesting potential implications for future clinical risk management. How can the genomic biomarkers identified by GWAS be associated with the clinical outcomes of an infectious disease? In this Commentary, we evaluate the advantages and limitations of this approach.
    MeSH term(s) Biomarkers, Tumor ; COVID-19 ; Genome-Wide Association Study ; Genomics ; Humans ; SARS-CoV-2
    Chemical Substances Biomarkers, Tumor
    Language English
    Publishing date 2021-10-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 3067-3
    ISSN 1558-8238 ; 0021-9738
    ISSN (online) 1558-8238
    ISSN 0021-9738
    DOI 10.1172/JCI155011
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Fetal First-trimester Cystic Hygroma as the Prenatal Presenting Feature of ASCC1-Related Spinal Muscular Atrophy with Bone Fractures 2.

    Guadagnolo, Daniele / Mastromoro, Gioia / Hashemian, Nader Khaleghi / Orlando, Valeria / Lepri, Francesca Romana / D'Alberti, Elena / Giancotti, Antonella / Novelli, Antonio / Pizzuti, Antonio

    Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC

    2023  Volume 45, Issue 8, Page(s) 558–559

    MeSH term(s) Pregnancy ; Female ; Humans ; Lymphangioma, Cystic/diagnostic imaging ; Pregnancy Trimester, First ; Muscular Atrophy, Spinal ; Fractures, Bone ; Ultrasonography, Prenatal ; Carrier Proteins
    Chemical Substances ASCC1 protein, human ; Carrier Proteins
    Language English
    Publishing date 2023-05-17
    Publishing country Netherlands
    Document type Letter
    ZDB-ID 2171082-X
    ISSN 1701-2163
    ISSN 1701-2163
    DOI 10.1016/j.jogc.2023.05.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    Zs.A 6445: Show issues Location:
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  9. Article ; Online: First Case of a Dominant De Novo

    Minale, Elia Marco Paolo / De Falco, Alessandro / Agolini, Emanuele / Novelli, Antonio / Russo, Roberta / Andolfo, Immacolata / Iolascon, Achille / Piscopo, Carmelo

    Genes

    2024  Volume 15, Issue 1

    Abstract: Cranio-lenticulo-sutural dysplasia (CLSD, OMIM #607812) is a rare genetic condition characterized by late-closing fontanels, skeletal defects, dysmorphisms, and congenital cataracts that are caused by bi-allelic or monoallelic variants in ... ...

    Abstract Cranio-lenticulo-sutural dysplasia (CLSD, OMIM #607812) is a rare genetic condition characterized by late-closing fontanels, skeletal defects, dysmorphisms, and congenital cataracts that are caused by bi-allelic or monoallelic variants in the
    MeSH term(s) Male ; Humans ; Child ; Vesicular Transport Proteins/genetics ; Vesicular Transport Proteins/metabolism ; Intellectual Disability/genetics ; Intellectual Disability/metabolism ; Mutation, Missense ; Endoplasmic Reticulum/metabolism ; Golgi Apparatus/metabolism
    Chemical Substances Vesicular Transport Proteins ; SEC23A protein, human
    Language English
    Publishing date 2024-01-20
    Publishing country Switzerland
    Document type Review ; Case Reports ; Journal Article
    ZDB-ID 2527218-4
    ISSN 2073-4425 ; 2073-4425
    ISSN (online) 2073-4425
    ISSN 2073-4425
    DOI 10.3390/genes15010130
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Case report: A new

    Minotti, Chiara / Graziani, Ludovico / Sallicandro, Ester / Digilio, Maria Cristina / Falasca, Roberto / Alesi, Viola / Novelli, Giuseppe / Dentici, Maria Lisa / Loddo, Sara / Novelli, Antonio

    Frontiers in genetics

    2024  Volume 14, Page(s) 1315291

    Abstract: Interstitial deletions involving 6q chromosomal region are rare. Less than 30 patients have been described to date, and fewer have been characterized by high-resolution techniques, such as chromosomal microarray. Deletions involving 6q21q22.1 region are ... ...

    Abstract Interstitial deletions involving 6q chromosomal region are rare. Less than 30 patients have been described to date, and fewer have been characterized by high-resolution techniques, such as chromosomal microarray. Deletions involving 6q21q22.1 region are associated with an extremely wide and heterogeneous clinical spectrum, thus genotype-phenotype correlation based on the size of the rearranged region and on the involved genes is complex, even among individuals with overlapping deletions. Here we describe the phenotypic and molecular characterization of a new 6q interstitial deletion in a girl with developmental delay, intellectual disability, cerebellar vermis hypoplasia, facial peculiar characteristics, ataxia and ocular abnormalities. Microarray analysis of the proposita revealed a 7.9 Mb interstitial
    Language English
    Publishing date 2024-02-06
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2606823-0
    ISSN 1664-8021
    ISSN 1664-8021
    DOI 10.3389/fgene.2023.1315291
    Database MEDical Literature Analysis and Retrieval System OnLINE

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