Solvent effects on aggregation and spectra of iron(III) porphyrins.

Autor: Cole, SJ, Curthoys, GC, Magnusson, EA

Publikováno v: Australian Journal of Chemistry; 1971, Vol. 24 Issue: 9 p1967-1970, 4p

Triceps Surae Lengthening in Foot and Ankle Trauma: A Survey of OTA and AOFAS Members.

Autor: Patterson JT; Department of Orthopaedic Surgery, Keck School of Medicine of University of Southern California, Los Angeles, CA, USA., Campbell ST; Department of Orthopaedic Surgery, UC Davis Medical Center, Sacramento, CA, USA., Wallace SJ; Summit Orthopaedics, Lake Oswego, OR, USA., Magnusson EA; Proliance Orthopaedics & Sports Medicine, Bellevue, WA, USA., Elliott IS; Optum Care Orthopaedics and Spine, Las Vegas, NV, USA., Mertz K; Department of Orthopaedic Surgery, Keck School of Medicine of University of Southern California, Los Angeles, CA, USA., Benirschke SK; Department of Orthopaedics and Sports Medicine, University of Washington, Seattle, WA, USA.

Publikováno v: Foot & ankle orthopaedics [Foot Ankle Orthop] 2022 Sep 30; Vol. 7 (3), pp. 24730114221126719. Date of Electronic Publication: 2022 Sep 30 (Print Publication: 2022).

What happens at the L5/S1 facet joint when implants are placed across the sacroiliac joint?

Autor: Schiffman CJ; University of Washington Department of Orthopaedics & Sports Medicine, Seattle, WA, United States. Electronic address: cjschif@uw.edu., Telfer S; University of Washington Department of Orthopaedics & Sports Medicine, Seattle, WA, United States. Electronic address: telfers@uw.edu., Magnusson EA; University of Washington Department of Orthopaedics & Sports Medicine, Seattle, WA, United States. Electronic address: emagnus@uw.edu., Firoozabadi R; University of Washington Department of Orthopaedics & Sports Medicine, Seattle, WA, United States. Electronic address: rezaf2@uw.edu.

Publikováno v: Injury [Injury] 2022 Jun; Vol. 53 (6), pp. 2121-2125. Date of Electronic Publication: 2022 Feb 05.

Does a Medial Malleolar Osteotomy or Posteromedial Approach Provide Greater Surgical Visualization for the Treatment of Talar Body Fractures?

Autor: Magnusson EA; Department of Orthopaedic Surgery, University of Washington, Seattle, Washington., Telfer S, Jackson M, Githens MF

Publikováno v: The Journal of bone and joint surgery. American volume [J Bone Joint Surg Am] 2021 Dec 15; Vol. 103 (24), pp. 2324-2330.

De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome.

Autor: Jansen S; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Geuer S; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Pfundt R; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Brough R; Cancer Research UK Gene Function Laboratory and Breast Cancer Now Research Centre, Institute of Cancer Research, London SW3 6JB, UK., Ghongane P; Cancer Research UK Gene Function Laboratory and Breast Cancer Now Research Centre, Institute of Cancer Research, London SW3 6JB, UK., Herkert JC; Department of Genetics, University Medical Center Groningen, University of Groningen, PO Box 30.001, 9700 RB Groningen, the Netherlands., Marco EJ; Departments of Neurology, Pediatrics, and Psychiatry, University of California, San Francisco, 675 Nelson Rising Lane, Suite 405, San Francisco, CA 94143, USA., Willemsen MH; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Kleefstra T; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Hannibal M; Division of Pediatric Genetics, Metabolism & Genomic Medicine, University of Michigan Medical School, D5257 Medical Professional Building, 1500 East Medical Center Drive, Ann Arbor, MI 48109-5718, USA., Shieh JT; Division of Medical Genetics, Department of Pediatrics, UCSF Benioff Children's Hospital, Institute for Human Genetics, University of California, San Francisco, San Francisco, CA 94143-0793, USA., Lynch SA; Clinical Genetics, Children's University Hospital, Temple Street, Dublin 1, Ireland; Academic Centre on Rare Diseases, School of Medicine and Medical Sciences, University College Dublin, Dublin 1, Ireland., Flinter F; Department of Clinical Genetics, Guy's and St. Thomas' NHS Foundation Trust, Great Maze Pond, London SE1 9RT, UK., FitzPatrick DR; Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road South, Edinburgh EH4 2XU, UK., Gardham A; North West Thames Regional Genetic Service (Kennedy Galton Centre), North West London Hospitals, Watford Road, London HA1 3UJ, UK., Bernhard B; North West Thames Regional Genetic Service (Kennedy Galton Centre), North West London Hospitals, Watford Road, London HA1 3UJ, UK., Ragge N; Faculty of Health and Life Sciences, Oxford Brookes University, Gipsy Lane, Oxford OX3 0BP, UK; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham B15 2TG, UK., Newbury-Ecob R; Department of Clinical Genetics, University Hospitals Bristol NHS Foundation Trust, St. Michael's Hospital, Southwell Street, Bristol BS2 8EG, UK., Bernier R; Center on Human Development and Disability, University of Washington, PO Box 357920, Seattle, WA 98195-7920, USA., Kvarnung M; Department of Clinical Genetics, Karolinska University Hospital Solna, Karolinska Institutet, 171 77 Stockholm, Sweden., Magnusson EA; Department of Medicine and Neurology, Habilitation Organization, Region Skåne, 291 89 Kristianstad, Sweden., Wessels MW; Department of Clinical Genetics, Erasmus Medical Center, PO Box 2040, 3000 CA Rotterdam, the Netherlands., van Slegtenhorst MA; Department of Clinical Genetics, Erasmus Medical Center, PO Box 2040, 3000 CA Rotterdam, the Netherlands., Monaghan KG; GeneDx, Gaithersburg, MD 20877, USA., de Vries P; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., Veltman JA; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands; Department of Clinical Genetics, Maastricht University Medical Centre, Universiteitssingel 50, 9229 ER Maastricht, the Netherlands., Lord CJ; Cancer Research UK Gene Function Laboratory and Breast Cancer Now Research Centre, Institute of Cancer Research, London SW3 6JB, UK., Vissers LE; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands., de Vries BB; Department of Human Genetics, Donders Centre for Neuroscience, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands. Electronic address: bert.devries@radboudumc.nl.

Publikováno v: American journal of human genetics [Am J Hum Genet] 2017 Apr 06; Vol. 100 (4), pp. 650-658. Date of Electronic Publication: 2017 Mar 23.