Search Results - "Krüger, Gabriele"

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    Standardization and quality assurance in skeletal landmark placement and osteometry by Liebenberg, Leandi, Krüger, Gabriele C.

    Published in Forensic science international (01-03-2020)
    “…•This study addressed modifications to commonly used osteometric standards.•Several measurements differed significantly using the modified…”
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    Journal Article
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    Veldt fires in South Africa: Implications on osteometry and the biological profile by Liebenberg, Maritza, Liebenberg, Leandi, Krüger, Gabriele C., L'Abbé, Ericka N.

    Published in Journal of forensic sciences (01-03-2023)
    “…Standard operating procedures for forensic anthropological analyses dictate that thermally altered remains should not be measured, hindering the creation of a…”
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    Journal Article
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    Postcraniometric sex and ancestry estimation in South Africa: a validation study by Liebenberg, Leandi, Krüger, Gabriele C., L’Abbé, Ericka N., Stull, Kyra E.

    Published in International journal of legal medicine (01-01-2019)
    “…With the acceptance of the Daubert criteria as the standards for best practice in forensic anthropological research, more emphasis is being placed on the…”
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    Journal Article
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    Sex estimation from the long bones of modern South Africans by Krüger, Gabriele C., L’Abbé, Ericka N., Stull, Kyra E.

    “…Best scientific practice for sex estimation incorporates accurate techniques that employ appropriate standards and population- and period-specific data. Single…”
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    Journal Article
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    Physical Activity and Quality of Life in People With Visual Impairments: A Systematic Review by Caputo, Eduardo L., Porcellis da Silva, Rafael B., Leal da Cunha, Larissa, Krüger, Gabriele R., Reichert, Felipe F.

    Published in Journal of visual impairment & blindness (01-01-2022)
    “…Objective This systematic review aimed to investigate the relationship between physical activity and quality of life (QOL) in people with visual impairments…”
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    Journal Article
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    Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E by Klopocki, Eva, Hennig, Bianca P., Dathe, Katarina, Koll, Randi, de Ravel, Thomy, Baten, Emiel, Blom, Eveline, Gillerot, Yves, Weigel, Johannes F.W., Krüger, Gabriele, Hiort, Olaf, Seemann, Petra, Mundlos, Stefan

    Published in American journal of human genetics (12-03-2010)
    “…Autosomal-dominant brachydactyly type E (BDE) is a congenital limb malformation characterized by small hands and feet predominantly as a result of shortened…”
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    Journal Article
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    Motor skills of children with autism spectrum disorder by Kruger, Gabriele Radünz, Silveira, Jennifer Rodrigues, Marques, Alexandre Carriconde

    “…Abstract The objective of this study is to describe variables of life habits associated with motor skills of children with autism spectrum disorder aged 8-10…”
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    Journal Article
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    The Pretoria Bone Collection: A 21st Century Skeletal Collection in South Africa by L’Abbé, Ericka N., Krüger, Gabriele C., Theye, Charlotte E. G., Hagg, Alieske C., Sapo, Okuhle

    Published in Forensic sciences (Basel, Switzerland) (08-12-2021)
    “…The Pretoria Bone Collection (PBC) began in 1942 with the opening of a medical school at the University of Pretoria (UP) in Pretoria, South Africa, where this…”
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    Journal Article
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    Sexual dimorphism in cranial morphology among modern South Africans by Krüger, Gabriele Christa, L’Abbé, Ericka N., Stull, Kyra E., Kenyhercz, Michael W.

    Published in International journal of legal medicine (01-07-2015)
    “…Pattern expressions of morphoscopic cranial traits vary across populations with classification accuracies being highly dependent on the reference collection to…”
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    Journal Article
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    A morphoscopic exploration of cranial sexual dimorphism among modern South Africans using computed tomography scans by Krüger, Gabriele Christa, Jantz, Richard L., van der Walt, Elizabeth, Lockhat, Zarina I., L’Abbé, Ericka N.

    Published in International journal of legal medicine (01-11-2024)
    “…Continual re-evaluation of standards for forensic anthropological analyses are necessary, particularly as new methods are explored or as populations change…”
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    Journal Article
  13. 13

    Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome by Seifert, Wenke, Meinecke, Peter, Krüger, Gabriele, Rossier, Eva, Heinritz, Wolfram, Wüsthof, Achim, Horn, Denise

    Published in BMC genetics (30-11-2014)
    “…Floating-Harbor syndrome is a rare autosomal dominant short stature syndrome with retarded speech development, intellectual disability and dysmorphic facial…”
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    Journal Article
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    Características das instalações e equipamentos para a prática de atividade física em escolas da zona rural de Pelotas, Rio Grande do Sul by Müller, Werner de Andrade, Krüger, Gabriele Radünz, Domingues, Marlos Rodrigues

    Published in Atividade física & saúde (08-10-2019)
    “…O objetivo do estudo foi descrever as instalações e equipamentos para atividade física nas escolas da zona rural de Pelotas, Rio Grande do Sul. Trata-se de um…”
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    Journal Article
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    Comparison of Sexually Dimorphic Patterns in the Postcrania of South Africans and North Americans by Krüger, Gabriele Christa

    Published 01-01-2014
    “…Recently, a multivariate approach to sex estimation using the postcrania achieved higher accuracies than the commonly used cranium, recommending…”
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    Dissertation
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    O efeito de um programa de atividades rítmicas na interação social e na coordenação motora em crianças com transtorno do espectro autista by Krüger, Gabriele Radünz, Garcias, Luciana Maia, Hax, Gabriela Padilha, Marques, Alexandre Carriconde

    Published in Atividade física & saúde (25-03-2019)
    “…Este estudo tem como objetivo verificar o efeito de um programa de atividades rítmicas na interação social e coordenação motora de crianças com…”
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    Journal Article
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    Intronic mutations in the L1CAM gene may cause X-linked hydrocephalus by aberrant splicing by Hübner, Christian A., Utermann, Barbara, Tinschert, Sigrid, Krüger, Gabriele, Ressler, Bernadette, Steglich, Cordula, Schinzel, Albert, Gal, Andreas

    Published in Human mutation (01-05-2004)
    “…L1 disease is a clinically heterogeneous X‐chromosomal neurodevelopmental disorder that is frequently associated with mental retardation and congenital…”
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    Journal Article
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