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  1. Article: Cryptosepalum korupense Burgt, sp. nov. (Leguminosae, Caesalpinioideae), a tree species from the Southwest Region in Cameroon

    Van Der Burgt, Xander M / Poundje Maguy / Sene Olivier

    Adansonia. 2014 June, v. 36, no. 1

    2014  

    Abstract: The tree species Cryptosepalum korupense Burgt, sp. nov. (Leguminosae: Caesalpinioideae) is ...

    Abstract The tree species Cryptosepalum korupense Burgt, sp. nov. (Leguminosae: Caesalpinioideae) is described and illustrated. Cryptosepalum korupense, sp. nov. is related to C. staudtii Harms. Cryptosepalum korupense, sp. nov. has (10-)14-21(-26) pairs of leaflets; C. staudtii has 10-14(-16) pairs of leaflets. The placement of the midvein of the small, emarginate leaflets of C. korupense, sp. nov. distinguishes the species from all other West and Central African Caesalpinioideae species. Cryptosepalum korupense, sp. nov. trees can grow to 44 m high and 88 cm trunk diameter. The new species presents ballistic seed dispersal and grows gregariously; a map of a group of 14 trees is presented. Cryptosepalum korupense, sp. nov. is endemic to the Southwest Region in Cameroon. In southern Korup National Park 18 trees over 10 cm trunk diameter were found during the mapping of c. 11.2 km² of forest. Of the trees over 50 cm trunk diameter, one tree out of c. 3100 trees is C. korupense, sp. nov. The new species was also found along the banks of the Idu River near the village Besingi, and in the lowland forests northwest of Mount Cameroon. Cryptosepalum korupense, sp. nov. is assessed as Endangered (EN) and C. staudtii as Least Concern (LC) under the criteria of the IUCN.
    Keywords Cryptosepalum ; lowland forests ; national parks ; new species ; rivers ; scientific illustration ; seed dispersal ; taxon descriptions ; trees ; villages ; Cameroon
    Language English
    Dates of publication 2014-06
    Size p. 73-81.
    Publishing place National Museum of Natural History
    Document type Article
    ISSN 1280-8571
    DOI 10.5252%2Fa2014n1a7
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Serum

    Moran, Alan B / Elgood-Hunt, Georgia / van der Burgt, Yuri E M / Wuhrer, Manfred / Mesker, Wilma E / Tollenaar, Rob A E M / Spencer, Daniel I R / Lageveen-Kammeijer, Guinevere S M

    Biomolecules

    2023  Volume 13, Issue 6

    Abstract: A newly developed analytical strategy was applied to profile the total ... ...

    Abstract A newly developed analytical strategy was applied to profile the total serum
    MeSH term(s) Humans ; Glycosylation ; Chromatography, Reverse-Phase ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods ; Polysaccharides/chemistry ; Colorectal Neoplasms/surgery
    Chemical Substances Polysaccharides
    Language English
    Publishing date 2023-05-27
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom13060896
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Book: Weinstadt Dillenburg

    May, Hartmut

    eine kleine Weinchronik über Weintrinken und Weinanbau in Dillenburg

    (Schriften zur Weingeschichte ; 110)

    1994  

    Author's details von Hartmut May
    Series title Schriften zur Weingeschichte ; 110
    Collection
    Keywords Dillenburg ; Wein ; Geschichte 1451-1990 ; Oranje-Nassau, Willem van ; Geschichte 1561 ; Weinbau
    Subject Weinanbau ; Rebbau ; Weine
    Language German
    Size 40 S. : Ill., Kt.
    Publisher Ges. für Geschichte des Weines
    Publishing place Wiesbaden
    Publishing country Germany
    Document type Book
    HBZ-ID HT006537469
    Database Catalogue ZB MED Nutrition, Environment, Agriculture

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    In stock of ZB MED Bonn / Germany

    Shelf markLoan statusLocation
    958/236 available for loan (reading room) Freihandmagazin (U1)

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  4. Book ; Online: Bedrijfseconomische prestaties van bodemmaatregelen

    Bijker, William / van der Burgt, Eva / van den Berg, Wim / Selin-Norén, Isabella

    opbrengstabiliteit en kosten-batenverhouding van bodemmaatregelen

    2022  

    Abstract: Het rapport geeft inzicht in de economische aspecten van bodemmaatregelen in combinatie met ... verschillende grondbewerkingstechnieken. Middels twee methodes zijn de economische prestaties van de maatregelen ... in kaart gebracht namelijk via 1) opbrengststabiliteit door het berekenen van de variatiecoëfficiënt en 2 ...

    Abstract Het rapport geeft inzicht in de economische aspecten van bodemmaatregelen in combinatie met verschillende grondbewerkingstechnieken. Middels twee methodes zijn de economische prestaties van de maatregelen in kaart gebracht namelijk via 1) opbrengststabiliteit door het berekenen van de variatiecoëfficiënt en 2) een kosten-batenvergelijking. De methodes zijn toegepast op data komend van de systeemproeven op dalgrond (Bodemkwaliteit Veenkoloniën) in Valthermond en op zandgrond (Bodemkwaliteit op zand) in Vredepeel. Uit de analyse kunnen een aantal conclusies getrokken worden: 1. Tagetes heeft een positief effect in zetmeelaardappels op zowel opbrengststabiliteit als de kosten-batenverhouding. In een veenkoloniaal bouwplan is dit hierdoor een toepasbare maatregel, 2. Voldoende organische stofaanvoer via mest kan zorgen voor een verbeterde opbrengststabiliteit en behoud van opbrengsten op zandgrond, 3. Niet-kerende grondbewerking is een economisch haalbare maatregel in beide proeven, met een licht positief bedrijfsresultaat voor de kosten-batenvergelijking op zandgrond maar niet op dalgrond, 4. Het aanvoeren van extra compost is een economisch haalbare maatregel, met een licht positief of licht negatief bedrijfsresultaat op bouwplanniveau, 5. Steenmeel en de Ca/Mg-methode dragen niet bij aan een hoger bedrijfsresultaat of een verbeterde opbrengststabiliteit. De uitkomsten van dit onderzoek helpen telers, adviseurs en beleidsmakers inzicht geven in de economische haalbaarheid van de onderzochte bodemmaatregelen.
    Keywords Life Science
    Language Dutch
    Publisher Wageningen Plant Research
    Publishing country nl
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism.

    Sihombing, Nydia Rena Benita / Winarni, Tri Indah / van Bokhoven, Hans / van der Burgt, Ineke / de Leeuw, Nicole / Faradz, Sultana M H

    American journal of medical genetics. Part A

    2020  Volume 182, Issue 11, Page(s) 2731–2736

    Abstract: We present a family with three girls presenting similar dysmorphic features, including overgrowth, intellectual disability, macrocephaly, prominent forehead, midface retrusion, strabismus, and scoliosis. Both parents were unaffected, suggesting the ... ...

    Abstract We present a family with three girls presenting similar dysmorphic features, including overgrowth, intellectual disability, macrocephaly, prominent forehead, midface retrusion, strabismus, and scoliosis. Both parents were unaffected, suggesting the presence of an autosomal recessive syndrome. Following exome sequencing, a heterozygous nonsense variant was identified in the NFIX gene in all three siblings. The father appeared to have a low-grade (7%) mosaicism for this variant in his blood. Previously, de novo pathogenic variants in NFIX have been identified in Marshall-Smith syndrome and Malan syndrome, which share distinctive phenotypic features shared with the patients of the present family. This case emphasizes the importance of further molecular analysis especially in familial cases, to exclude the possibility of parental mosaicism.
    MeSH term(s) Adult ; Developmental Disabilities/genetics ; Developmental Disabilities/pathology ; Female ; Growth Disorders/genetics ; Growth Disorders/pathology ; Humans ; Intellectual Disability/genetics ; Intellectual Disability/pathology ; Male ; Mosaicism ; Mutation ; NFI Transcription Factors/genetics ; Pedigree ; Phenotype ; Siblings ; Young Adult
    Chemical Substances NFI Transcription Factors ; NFIX protein, human
    Language English
    Publishing date 2020-09-18
    Publishing country United States
    Document type Case Reports ; Research Support, Non-U.S. Gov't
    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.61835
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 1376/A: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  6. Article ; Online: First-year growth in children with Noonan syndrome: Associated with feeding problems?

    Croonen, Ellen A / Draaisma, Jos M T / van der Burgt, Ineke / Roeleveld, Nel / Noordam, Cees

    American journal of medical genetics. Part A

    2018  Volume 176, Issue 4, Page(s) 951–958

    Abstract: Children with Noonan syndrome show rapid decline of growth in the first year of life and feeding problems are present in over 50%. The aim of this study was to explore whether growth decelerates because of feeding problems or other Noonan syndrome- ... ...

    Abstract Children with Noonan syndrome show rapid decline of growth in the first year of life and feeding problems are present in over 50%. The aim of this study was to explore whether growth decelerates because of feeding problems or other Noonan syndrome-related factors. We performed a retrospective, longitudinal cohort study of clinically and genetically diagnosed subjects with Noonan syndrome (n = 143). Questionnaires about the phenotypic-genotypic profile and reported feeding problems were sent to eligible subjects. Data on first-year growth was obtained from growth charts. Ninety-one participants were excluded because of different criteria. A total of 52 subjects with Noonan syndrome were included. The largest decline in weight and length standard deviation score (SDS) occurred in the first 2.5 months after birth (-1.93 and -1.15, respectively), with feeding problems causing a decline of 0.57 SDS in the remaining months. At 1 year, children with feeding problems were on average 290 g lighter and 0.8 cm shorter than children without feeding problems. Weight gain was also negatively influenced by having a PTPN11 mutation (n = 39) and a higher gestational age, whereas children of parents with Noonan syndrome and with a higher birth weight gained more weight. Growth in length was reduced by having cardiac surgery and a higher gestational age, but positively influenced by birth length and maternal height. Growth in children with Noonan syndrome is impaired right after birth and only partially associated with feeding problems. In addition, several specific Noonan syndrome-related factors seem to influence growth in the first year.
    MeSH term(s) Alleles ; Child ; Child, Preschool ; Feeding Behavior ; Female ; Genotype ; Growth Charts ; Humans ; Infant ; Longitudinal Studies ; Male ; Mutation ; Noonan Syndrome/diagnosis ; Noonan Syndrome/epidemiology ; Noonan Syndrome/genetics ; Odds Ratio ; Phenotype ; Retrospective Studies ; Surveys and Questionnaires ; Time Factors
    Language English
    Publishing date 2018-02-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1493479-6
    ISSN 1552-4833 ; 1552-4825
    ISSN (online) 1552-4833
    ISSN 1552-4825
    DOI 10.1002/ajmg.a.38649
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Book ; Online: Prof. Richard Kranenburg

    van Kranenburg, R.

    Bacteriën als fabriekjes van de bio-economie

    2017  

    Abstract: Video over micro-organismen in de biobased ... ...

    Abstract Video over micro-organismen in de biobased economy
    Keywords bacteria ; biobased economy ; enzymes ; genetic change ; industrial microbiology ; microbial degradation ; research ; bacteriën ; enzymen ; genetische verandering ; industriële microbiologie ; microbiële afbraak ; onderzoek
    Language Dutch
    Publisher Wageningen University & Research
    Publishing country nl
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Variable phenotypic expression in a large Noonan syndrome family segregating a novel SOS1 mutation.

    van Trier, Dorothée C / Rinne, Tuula / Noordam, Kees / Draaisma, Jos M / van der Burgt, Ineke

    American journal of medical genetics. Part A

    2017  Volume 173, Issue 11, Page(s) 2968–2972

    Abstract: Noonan syndrome (NS) is an autosomal dominant multisystem condition with a variable phenotype. The most characteristic features are short stature, congenital heart defects, and recognizable facial features. Mutations in SOS1 are found in 10-20% of ... ...

    Abstract Noonan syndrome (NS) is an autosomal dominant multisystem condition with a variable phenotype. The most characteristic features are short stature, congenital heart defects, and recognizable facial features. Mutations in SOS1 are found in 10-20% of patients with NS. Different genotype-phenotype studies mention correlations between SOS1 mutations and some features, such as ectodermal abnormalities and specific facial features. We present a large NS family with a novel pathogenic mutation; SOS1 c.3134C>G, p.Pro1045Arg. Ten family members with NS are included with genetically confirmed mutation and clinical evaluation. The phenotype shows a broad spectrum from only few suggestive features for NS in the older generation to typical features in the youngest generation. We report on a novel pathogenic mutation in the SOS1 gene and a large clinical spectrum in a NS family with ten genetically confirmed affected individuals.
    MeSH term(s) Adolescent ; Adult ; Aged ; Child ; Female ; Genetic Association Studies ; Heart Defects, Congenital/complications ; Heart Defects, Congenital/genetics ; Heart Defects, Congenital/physiopathology ; Heterozygote ; Humans ; Male ; Middle Aged ; Mutation ; Noonan Syndrome/complications ; Noonan Syndrome/genetics ; Noonan Syndrome/physiopathology ; Pedigree ; Phenotype ; SOS1 Protein/genetics ; Young Adult
    Chemical Substances SOS1 Protein
    Language English
    Publishing date 2017-09-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1493479-6
    ISSN 1552-4833 ; 1552-4825
    ISSN (online) 1552-4833
    ISSN 1552-4825
    DOI 10.1002/ajmg.a.38466
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era.

    Stuurman, Kyra E / Joosten, Marieke / van der Burgt, Ineke / Elting, Mariet / Yntema, Helger G / Meijers-Heijboer, Hanne / Rinne, Tuula

    Journal of medical genetics

    2019  Volume 56, Issue 10, Page(s) 654–661

    Abstract: Background: This study evaluates 6 years of prenatal rasopathy testing in the Netherlands, updates on previous data and gives recommendations for prenatal rasopathy testing.: Methods: 424 fetal samples, sent in for prenatal rasopathy testing in 2011- ... ...

    Abstract Background: This study evaluates 6 years of prenatal rasopathy testing in the Netherlands, updates on previous data and gives recommendations for prenatal rasopathy testing.
    Methods: 424 fetal samples, sent in for prenatal rasopathy testing in 2011-2016, were collected. Cohort 1 included 231 samples that were sequenced for 1-5 rasopathy genes. Cohort 2 included 193 samples that were analysed with a 14-gene next generation sequencing (NGS) panel. For all mutation-positive samples in both cohorts, the referring physician provided detailed ultrasound findings and postnatal follow-up. For 168 mutation-negative samples in cohort 2, solely clinical information on the requisition form was collected.
    Results: In total, 40 (likely) pathogenic variants were detected (9.4%). All fetuses showed a variable degree of involvement of prenatal findings: increased nuchal translucency (NT)/cystic hygroma, distended jugular lymph sacs (JLS), hydrops fetalis, polyhydramnios, pleural effusion, ascites, cardiac defects and renal anomalies. An increased NT was the most common finding. Eight fetuses showed solely an increased NT/cystic hygroma, which were all larger than 5.5 mm. Ascites and renal anomalies appeared to be poor predictors of pathogenic outcome.
    Conclusion: Fetuses with a rasopathy show in general multiple ultrasound findings. The larger the NT and the longer it persists, the more likely it is to find a pathogenic variant. Rasopathy testing is recommended when the fetus shows an isolated increased NT ≥5.0 mm or when NT of ≥3.5 mm and at least one of the following ultrasound anomalies is present: distended JLS, hydrops fetalis, polyhydramnios, pleural effusion, ascites, cardiac defects and renal anomalies.
    MeSH term(s) Cohort Studies ; Female ; Fetus ; Genetic Testing ; High-Throughput Nucleotide Sequencing ; Humans ; Lymphangioma, Cystic/genetics ; Mutation ; Netherlands ; Noonan Syndrome/diagnosis ; Noonan Syndrome/genetics ; Pregnancy ; Prenatal Diagnosis ; Sequence Analysis, DNA
    Language English
    Publishing date 2019-04-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 220881-7
    ISSN 1468-6244 ; 0022-2593
    ISSN (online) 1468-6244
    ISSN 0022-2593
    DOI 10.1136/jmedgenet-2018-105746
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 177: Show issues Location:
    Je nach Verfügbarkeit (siehe Angabe bei Bestand)
    bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular
    Jg. 1995 - 2021: Lesesall (1.OG)
    ab Jg. 2022: Lesesaal (EG)

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  10. Article: Nachruf für Prof. Dr. rer. nat. Dr. med. Wolfgang Müller-Schauenburg

    Burchert, Wolfgang / van den Hoff, Jörg / Ziegler, Sibylle / Geworski, Lilli

    Nuklearmedizin - NuclearMedicine

    2021  Volume 60, Issue 05, Page(s) 383–384

    Language German
    Publishing date 2021-10-01
    Publisher Georg Thieme Verlag KG
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 2030804-8
    ISSN 2567-6407 ; 0029-5566
    ISSN (online) 2567-6407
    ISSN 0029-5566
    DOI 10.1055/a-1616-9342
    Database Thieme publisher's database

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