Zobrazeno 1 - 10
of 945
pro vyhledávání: '"Hendson, G."'
Autor:
Di Francesco D; MD Undergraduate Program, University of British Columbia, Vancouver, British Columbia, Canada., Swenerton A; Provincial Medical Genetics Program, B.C. Women's Hospital, Vancouver, British Columbia, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada., Li WL; Breakthrough Genomics, Irvine, California, USA., Dunham C; Department of Pathology and Laboratory Medicine, University of British Columbia and BC Children's Hospital, Vancouver, British Columbia, Canada., Hendson G; Department of Pathology and Laboratory Medicine, University of British Columbia and BC Children's Hospital, Vancouver, British Columbia, Canada., Boerkoel CF; Provincial Medical Genetics Program, B.C. Women's Hospital, Vancouver, British Columbia, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2023 Dec; Vol. 191 (12), pp. 2903-2907. Date of Electronic Publication: 2023 Sep 04.
Autor:
Zhang L; Faculty of Medicine, University of British Columbia, Vancouver, Canada. Electronic address: lcjzhang@student.ubc.ca., Delisle MF; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada., Hendson G; Department of Anatomic Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada., Liauw J; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, Canada.
Publikováno v:
Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC [J Obstet Gynaecol Can] 2023 Nov; Vol. 45 (11), pp. 101785. Date of Electronic Publication: 2021 Jul 22.
Autor:
Oliwa A; Undergraduate Medical School, College of Medical, Veterinary & Life Sciences, University of Glasgow, Glasgow, UK., Hendson G; Division of Neuropathology, Department of Pathology, University of British Columbia, Vancouver, British Columbia, Canada., Longman C; West of Scotland Regional Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK., Synnes A; Division of Neonatology, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada., Seath K; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada., Barnicoat A; Clinical Genetics Department, Great Ormond Street Hospital, London, UK., Hall JG; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada., Patel MS; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2023 Feb; Vol. 191 (2), pp. 546-553. Date of Electronic Publication: 2022 Nov 01.
Autor:
Hasselblatt M; Institute of Neuropathology, University Hospital Münster, Münster, Germany., Thomas C; Institute of Neuropathology, University Hospital Münster, Münster, Germany., Federico A; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.; Division of Paediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany., Bens S; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany., Hellström M; Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden., Casar-Borota O; Department of Immunology, Genetics and Pathology, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.; Department of Clinical Pathology, Uppsala University Hospital, Uppsala, Sweden., Kordes U; Department of Pediatric Hematology and Oncology, University Medical Center, Hamburg, Germany., Neumann JE; Institute of Neuropathology, University Medical Center, Hamburg, Germany.; Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Dottermusch M; Institute of Neuropathology, University Medical Center, Hamburg, Germany.; Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany., Rodriguez FJ; Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Lo AC; Radiation Oncology, British Columbia Cancer and University of British Columbia, Vancouver, Canada., Cheng S; Division of Hematology, Oncology and BMT, Department of Pediatrics, University of British Columbia, Vancouver, Canada., Hendson G; Department of Pathology, BC Women and Children's Hospital, Vancouver, Canada., Hukin J; Division of Hematology, Oncology and BMT, Department of Pediatrics, University of British Columbia, Vancouver, Canada., Hartmann C; Department of Neuropathology, Institute of Pathology, Hannover Medical School, Hannover, Germany., Koch A; Department of Neuropathology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany., Capper D; Department of Neuropathology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.; German Cancer Consortium (DKTK), Partner Site Berlin, German Cancer Research Center (DKFZ), Heidelberg, Germany., Siebert R; Institute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany., Paulus W; Institute of Neuropathology, University Hospital Münster, Münster, Germany., Nemes K; Pediatric and Adolescent Medicine, Swabian Childrens' Cancer Center, University Childrens' Hospital Medical Center Augsburg and EU-RHAB Registry, Augsburg, Germany., Johann PD; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.; Division of Paediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany.; Pediatric and Adolescent Medicine, Swabian Childrens' Cancer Center, University Childrens' Hospital Medical Center Augsburg and EU-RHAB Registry, Augsburg, Germany., Frühwald MC; Pediatric and Adolescent Medicine, Swabian Childrens' Cancer Center, University Childrens' Hospital Medical Center Augsburg and EU-RHAB Registry, Augsburg, Germany., Kool M; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany.; Division of Paediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK), Heidelberg, Germany.; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Publikováno v:
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2022 Jun; Vol. 48 (4), pp. e12797. Date of Electronic Publication: 2022 Feb 18.
Autor:
Chin HL; Department of Medical Genetics and Provincial Medical Genetics Program, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada.; Khoo Teck Puat-National University Children's Medical Institute, National University Hospital, Singapore, Singapore., Huynh S; Department of Medical Genetics and Provincial Medical Genetics Program, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada., Ashkani J; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada., Castaldo M; Division of Neonatology, Department of Pediatrics, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada., Dixon K; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada., Selby K; Division of Neurology, Department of Pediatrics, University of British Columbia and Children's Hospital of British Columbia, Vancouver, British Columbia, Canada., Shen Y; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada., Wright M; Division of Respirology, Department of Pediatrics, University of British Columbia and Children's Hospital of British Columbia, Vancouver, British Columbia, Canada., Boerkoel CF; Department of Medical Genetics and Provincial Medical Genetics Program, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada., Hendson G; Department of Pathology, BC Children's Hospital, BC Women's Hospital and Health Centre, Vancouver, British Columbia, Canada., Jones SJM; Department of Medical Genetics and Provincial Medical Genetics Program, University of British Columbia and Women's Hospital of British Columbia, Vancouver, British Columbia, Canada.; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2022 Mar; Vol. 188 (3), pp. 926-930. Date of Electronic Publication: 2021 Nov 26.
Autor:
Chang CA; Department of Medical Genetics, BC Women and Children's Hospital, Vancouver, British Columbia, Canada., Perrier R; Department of Medical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada., Kurek KC; Department of Pathology, Alberta Children's Hospital, Calgary, Alberta, Canada., Estrada-Veras J; Medical Genetics Service, Walter Reed National Military Medical Center, Henry M. Jackson Foundation for the Advancement of Military Medicine, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA., Lehman A; Department of Medical Genetics, BC Women and Children's Hospital, Vancouver, British Columbia, Canada., Yip S; Department of Pathology & Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada., Hendson G; Department of Pathology, BC Women and Children's Hospital, Vancouver, British Columbia, Canada., Diamond C; Department of Hematology-Oncology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Pinchot JW; Department of Interventional Radiology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Tran JM; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Arkin LM; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Drolet BA; Department of Dermatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA., Napier MP; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, Ontario, Canada., O'Neill SA; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, Ontario, Canada., Balci TB; Medical Genetics Program of Southwestern Ontario, London Health Sciences Centre, London, Ontario, Canada., Keppler-Noreuil KM; Division of Genetics and Metabolism, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2021 Sep; Vol. 185 (9), pp. 2829-2845. Date of Electronic Publication: 2021 May 30.
Autor:
Oliveira, Ricardo Cunha de1,2 (AUTHOR) oliveira.ca.ricardo@gmail.com, Cavalcante, Giovanna C.1,2 (AUTHOR) giovannaccavalcante@gmail.com, Soares-Souza, Giordano B.1,3 (AUTHOR) giovannaccavalcante@gmail.com
Publikováno v:
International Journal of Molecular Sciences. Dec2024, Vol. 25 Issue 23, p12585. 21p.
Autor:
Fakhroo, Fatima A.1 (AUTHOR) Fatima.am.md.fakhroo@live.com, Almutairi, Meshari2 (AUTHOR), Baeshen, Salem2 (AUTHOR), Almutairi, Othman2 (AUTHOR), Alkhalidi, Hisham3 (AUTHOR), Ajlan, Abdulrazaj4 (AUTHOR)
Publikováno v:
Egyptian Journal of Neurosurgery. 11/27/2024, Vol. 39 Issue 1, p1-4. 4p.
Autor:
Morimoto, M, Yu, Z, Stenzel, P, Clewing, JM, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, JG, Gormley, AK, Saraiva, JM
BACKGROUND: Arteriosclerosis and emphysema develop in individuals with Schimke immuno-osseous dysplasia (SIOD), a multisystem disorder caused by biallelic mutations in SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1504::60366d38e1aa5c31c8f412fd5cb91de4
https://hdl.handle.net/10400.4/1491
https://hdl.handle.net/10400.4/1491
Autor:
Morimoto, M, Yu, ZX, Stenzel, P, Clewing, JM, Najafian, B, Mayfield, C, Hendson, G, Weinkauf, JG, Gormley, AK, Parham, DM, Ponniah, U, Andre, JL, Asakura, Y, Basiratnia, M, Bogdanovic, R, Bokenkamp, A, Bonneau, D, Buck, A, Charrow, J, Cochat, P, Cordeiro, I, Deschenes, G, Fenkci, MS, Frange, P, Frund, S, Fryssira, H, Guillen-Navarro, E, Keller, K, Kirmani, S, Kobelka, C, Lamfers, P, Levtchenko, E, Lewis, DB, Massella, L, McLeod, DR, Milford, DV, Nobili, F, Saraiva, JM, Semerci, CN, Shoemaker, L, Stajic, N, Stein, A, Taha, D, Wand, D, Zonana, J, Lucke, T, Boerkoel, CF
Background: Arteriosclerosis and emphysema develop in individuals with Schimke immuno-osseous dysplasia (SIOD), a multisystem disorder caused by biallelic mutations in SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of chromat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2702258ce3ba6587e983173a38b00185
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13721
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/13721