Search Results - "Burggraf, Siegfried"

Verification of lateral flow antigen tests for SARS-CoV-2 by qPCR directly from the test device.

Authors: Czibere, Ludwig Burggraf, Siegfried Becker, Marc et al.

Source: Dental Materials. Jun2022, Vol. 38 Issue 6, pe155-e159. 5p.

Subjects: COVID-19 testing, Point-of-care testing, COVID-19 pandemic, Dental emergencies, Amplification reactions, Medical screening

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Quality considerations and major pitfalls for high throughput DNA-based newborn screening for severe combined immunodeficiency and spinal muscular atrophy.

Authors: Bzdok, Jessica Czibere, Ludwig Burggraf, Siegfried et al.

Source: PLoS ONE. 6/28/2024, Vol. 19 Issue 6, p1-18. 18p.

Fast and cost-effective screening for SARS-CoV-2 variants in a routine diagnostic setting.

Authors: Durner, Jürgen Burggraf, Siegfried Czibere, Ludwig et al.

Source: Dental Materials. Mar2021, Vol. 37 Issue 3, pe95-e97. 3p.

Subjects: SARS-CoV-2, Clinical indications, Medical personnel

Geographic Terms: United Kingdom, South Africa

Type-Specific Detection of Human Papillomaviruses in a Routine Laboratory Setting--Improved Sensitivity and Specificity of PCR and Sequence Analysis Compared to Direct Hybridisation.

Authors: Kösel, Siegfried Burggraf, Siegfried Mommsen, Jens et al.

Source: Clinical Chemistry & Laboratory Medicine. Jun2003, Vol. 41 Issue 6, p787-791. 5p. 1 Chart, 1 Graph.

A Modular Genetic Approach to Newborn Screening from Spinal Muscular Atrophy to Sickle Cell Disease—Results from Six Years of Genetic Newborn Screening.

Authors: Bzdok, Jessica Czibere, Ludwig Burggraf, Siegfried et al.

Source: Genes. Nov2024, Vol. 15 Issue 11, p1467. 12p.

Fast and simple high-throughput testing of COVID 19.

Authors: Durner, Jürgen Burggraf, Siegfried Czibere, Ludwig et al.

Source: Dental Materials. May2020, Vol. 36 Issue 5, pe141-e142. 2p.

Subjects: Messenger RNA, Spinal muscular atrophy

Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.

Authors: Vill, Katharina Schwartz, Oliver Blaschek, Astrid et al.

Source: Orphanet Journal of Rare Diseases. 3/31/2021, Vol. 16 Issue 1, p1-10. 10p.

Occurrence and role of di-myo-inositol-1,1'-phosphate in Methanococcus igneus

Authors: Stetter, Karl O. Roberts, MaryF. Ciulla, Rose Anne et al.

Source: Applied & Environmental Microbiology. Oct1994, Vol. 60 Issue 10, p3660. 0p.

Subjects: Temperature effect

Identifying members of the domain Archaea with rRNA-targeted oligonucleotide probes

Authors: Stetter, Karl O. Woese, Carl R. Schadhauser, Sibylle et al.

Source: Applied & Environmental Microbiology. Sep1994, Vol. 60 Issue 9, p3112. 0p.

Subjects: Archaebacteria, Bacteria

Pyrobaculum aerophilum sp. nov., a novel nitrate-reducing hyperthermophilic archaeon

Authors: Stetter, Karl O. Huber, Robert Trincone, Antonio et al.

Source: Applied & Environmental Microbiology. Sep1993, Vol. 59 Issue 9, p2918. 0p.

Newbornscreening SMA - From Pilot Project to Nationwide Screening in Germany.

Authors: Müller-Felber W Blaschek A Schwartz O et al.

Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2023; Vol. 10 (1), pp. 55-65.

Publication Type: Journal Article

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 101649948 Publication Model: Print Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE

Spinal Muscular Atrophy - Is Newborn Screening Too Late for Children with Two SMN2 Copies?

Authors: Schwartz O Kölbel H Blaschek A et al.

Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2022; Vol. 9 (3), pp. 389-396.

Publication Type: Journal Article

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 101649948 Publication Model: Print Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE

High Throughput Newborn Screening for Sickle Cell Disease - Application of Two-Tiered Testing with a qPCR-Based Primary screen.

Transliterated Title: Hochdurchsatz-Neugeborenenscreening auf Sichelzellkrankheit – Anwendung einer zweistufigen Analytik mit einem qPCR-basierten Primärscreening.

Authors: Janda J Hegert S Bzdok J et al.

Source: Klinische Padiatrie [Klin Padiatr] 2023 Nov; Vol. 235 (6), pp. 366-372. Date of Electronic Publication: 2023 Sep 25.

Publication Type: Journal Article

Journal Info: Publisher: Ferdinand Enke Verlag Country of Publication: Germany NLM ID: 0326144 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1439-3824 (Electronic) Linking ISSN: 03008630 NLM ISO Abbreviation: Klin Padiatr Subsets: MEDLINE

Erratum to "Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening - Opportunity or Burden?"

Authors: Müller-Felber W Vill K Schwartz O et al.

Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2021; Vol. 8 (2), pp. 335-336.

Publication Type: Published Erratum

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 101649948 Publication Model: Print Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE; PubMed not MEDLINE

Next generation sequencing as second-tier test in high-throughput newborn screening for nephropathic cystinosis.

Authors: Fleige T Burggraf S Czibere L et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Feb; Vol. 28 (2), pp. 193-201. Date of Electronic Publication: 2019 Sep 30.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Infants Diagnosed with Spinal Muscular Atrophy and 4 SMN2 Copies through Newborn Screening - Opportunity or Burden?

Authors: Müller-Felber W Vill K Schwartz O et al.

Source: Journal of neuromuscular diseases [J Neuromuscul Dis] 2020; Vol. 7 (2), pp. 109-117.

Publication Type: Journal Article

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 101649948 Publication Model: Print Cited Medium: Internet ISSN: 2214-3602 (Electronic) Linking ISSN: 22143599 NLM ISO Abbreviation: J Neuromuscul Dis Subsets: MEDLINE

High-throughput genetic newborn screening for spinal muscular atrophy by rapid nucleic acid extraction from dried blood spots and 384-well qPCR.

Authors: Czibere L Burggraf S Fleige T et al.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 Jan; Vol. 28 (1), pp. 23-30. Date of Electronic Publication: 2019 Jul 30.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE