Search Results - "HENN, WOLFRAM"
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A classification of the aims of vaccination and its relevance to transgenerational justice
Published in Journal of global health (01-06-2020)“…[...]neglect or refusal to be vaccinated for non-medical reasons in countries where safe and efficient measles vaccines are easily available, does not only…”
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Left ventricular systolic dysfunction in asymptomatic Marfan syndrome patients is related to the severity of gene mutation: insights from the novel three dimensional speckle tracking echocardiography
Published in PloS one (22-04-2015)“…In asymptomatic Marfan syndrome (MFS) patients we evaluated the relationship between the types of fibrillin-1 (FBN1) gene mutation and possible altered left…”
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Allocation criteria for an initial shortage of a future SARS-CoV-2 vaccine and necessary measures for global immunity
Published in Vaccine (22-07-2020)“…Any shortage of vital goods bears severe ethical challenges, as it generates distribution conflicts that can amount to antisocial behavior at the individual as…”
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Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants
Published in Human genetics (01-03-2006)“…Single base substitutions in DNA mismatch repair genes which are predicted to lead either to missense or silent mutations, or to intronic variants outside the…”
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The fetus in the age of the genome
Published in Human genetics (01-05-2022)“…Due to a number of recent achievements, the field of prenatal medicine is now on the verge of a profound transformation into prenatal genomic medicine. This…”
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Application of oncogenetic trees mixtures as a biostatistical model of the clonal cytogenetic evolution of meningiomas
Published in International journal of cancer (01-10-2007)“…Meningiomas are mostly benign tumors that originate from the coverings of brain and spinal cord. Typically, they reveal a normal karyotype or monosomy for…”
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Predictive value of progression-associated chromosomal aberrations for the prognosis of meningiomas : a retrospective study of 198 cases
Published in Journal of neurosurgery (01-10-2001)“…The goal of this study was to determine whether in meningiomas cytogenetic findings are suitable as a predictive parameter relevant to prognosis. Between 1992…”
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General Cognitive Abilities and Psychosocial Development in Children and Adolescents Having a Co-Twin with Down Syndrome
Published in The Journal of pediatrics (01-05-2021)“…To examine the general cognitive and psychosocial development in children and adolescents having a co-twin with Down syndrome. A case control study with an…”
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Deletion of Chromosome 1p and Loss of Expression of Alkaline Phosphatase Indicate Progression of Meningiomas
Published in Clinical cancer research (01-11-1999)“…Meningiomas are cytogenetically characterized by loss of one chromosome 22 as a typical primary aberration and progression-associated secondary chromosome…”
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An offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis
Published in Nature reviews. Genetics (01-08-2009)Get full text
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Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene: A lesson for differential diagnosis of alopecia universalis
Published in Journal of the American Academy of Dermatology (01-10-2002)“…Background: Atrichia with papular lesions (APL) is a rare, autosomal recessive form of total alopecia in which mutations in the hairless (HR) gene have been…”
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To know or not to know the genomic sequence of a fetus
Published in Nature reviews. Genetics (01-10-2012)Get full text
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Behavioral and psychological features in girls and women with triple‐X syndrome
Published in American journal of medical genetics. Part A (01-11-2018)“…Triple‐X syndrome is a common sex chromosome aneuploidy, which appears in 1 out of 1,000 females. The aim of our study was to describe the behavioral features…”
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Whole-Genome Sequencing in Diagnostic Medicine: Too Much Information for Doctors and Patients?
Published in Transfusion medicine and hemotherapy (2009)Get full text
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Early postnatal high-dose fat-soluble enteral vitamin A supplementation for moderate or severe bronchopulmonary dysplasia or death in extremely low birthweight infants (NeoVitaA): a multicentre, randomised, parallel-group, double-blind, placebo-controlled, investigator-initiated phase 3 trial
Published in The lancet respiratory medicine (01-07-2024)“…Vitamin A plays a key role in lung development, but there is no consensus regarding the optimal vitamin A dose and administration route in extremely low…”
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Reply: Non-invasive prenatal diagnosis: an ethical imperative
Published in Nature reviews. Genetics (01-10-2009)Get full text
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Kommentar I zum Fall: „Gibt es eine elterliche Pflicht zum genetischen Wissen?
Published in Ethik in der Medizin (01-12-2013)Get full text
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Proliferation enhancement by spontaneous multiplication of chromosome 7 in rheumatic synovial cells in vitro
Published in Human genetics (01-12-1995)“…Mosaic trisomy of chromosome 7 is known to occur in a variety of non-neoplastic hyperproliferative disorders. In long-term cell cultures established from…”
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Auf dem Weg zum Designerbaby?: Der Rede wert
Published in gynäkologie + geburtshilfe (01-04-2014)Get full text
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Ethics watch: an offer you can't refuse? Ethical implications of non-invasive prenatal diagnosis
Published in Nature reviews. Genetics (01-08-2009)Get full text
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