Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Cox, HC"'
Autor:
Menon, S.1, Cox, HC2, Kuwahata, M.2, Quinlan, S.2, MacMillan, JC3, Haupt, LM2, Lea, RA4, Griffiths, LR2
Publikováno v:
Cephalalgia. Feb2011, Vol. 31 Issue 3, p264-270. 7p.
Autor:
Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, Gray NA, Rastaldi MP, Parnham A, Gianfrancesco F, Griffiths LR.
Publikováno v:
Human molecular genetics
(2013).
info:cnr-pdr/source/autori:Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, Gray NA, Rastaldi MP, Parnham A, Gianfrancesco F, Griffiths LR./titolo:Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene./doi:/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
(2013).
info:cnr-pdr/source/autori:Esposito T, Lea RA, Maher BH, Moses D, Cox HC, Magliocca S, Angius A, Nyholt DR, Titus T, Kay T, Gray NA, Rastaldi MP, Parnham A, Gianfrancesco F, Griffiths LR./titolo:Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene./doi:/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
Focal segmental glomerulosclerosis (FSGS) is the consequence of a disease process that attacks the kidney's filtering system, causing serious scarring. More than half of FSGS patients develop chronic kidney failure within 10 years, ultimately requiri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::2658802f4ed103680446076a7de80497
http://www.cnr.it/prodotto/i/224081
http://www.cnr.it/prodotto/i/224081
Autor:
Bansal, GS, Cox, HC, Marsh, S, Gomm, JJ, Yiangou, C, Luqmani, Y, Coombes, RC, Johnston, CL, Bansal, G S, Cox, H C, Gomm, J J, Coombes, R C, Johnston, C L
Publikováno v:
British Journal of Cancer; Jun1997, Vol. 75 Issue 11, p1567-1574, 8p
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Autor:
Hatton JN; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA., Frone MN; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA., Cox HC; PreventionGenetics LLC, Marshfield, Wisconsin, USA., Crowley SB; Invitae Corporation, San Francisco, California, USA., Hiraki S; GeneDx, Gaithersburg, Maryland, USA., Yokoyama NN; Ambry Genetics, Aliso Viejo, California, USA., Abul-Husn NS; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Amatruda JF; Cancer and Blood Disease Institute, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California, USA., Anderson MJ; Invitae Corporation, San Francisco, California, USA., Bofill-De Ros X; RNA Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA., Carr AG; Weststat, Inc, Rockville, Maryland, USA., Chao EC; Ambry Genetics, Aliso Viejo, California, USA.; Division of Genetics and Genomics, Department of Pediatrics, University of California, Irvine, California, USA., Chen KS; Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas, USA., Gu S; RNA Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, USA., Higgs C; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA., Machado J; Exact Sciences Laboratories, Madison, Wisconsin, USA., Ritter D; Baylor College of Medicine, Houston, Texas, USA., Schultz KA; Cancer and Blood Disorders, Children's Minnesota, International Pleuropulmonary Blastoma/DICER1 Registry, Minneapolis, Minnesota, USA., Soper ER; Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, New York, USA., Wu MK; Cancer and Blood Disease Institute, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California, USA., Mester JL; GeneDx, Gaithersburg, Maryland, USA., Kim J; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA., Foulkes WD; Department of Human Genetics, McGill University, Montreal, Quebec, Canada., Witkowski L; Department of Human Genetics, McGill University, Montreal, Quebec, Canada., Stewart DR; Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Publikováno v:
Human mutation [Hum Mutat] 2023; Vol. 2023. Date of Electronic Publication: 2023 Mar 29.
Autor:
Yau J; Department of Pharmacy Services, University of Virginia Health System, Charlottesville, Virginia., Dann J; Department of Pharmacy Services, University of Virginia Health System, Charlottesville, Virginia., Geyston J; Department of Pharmacy Services, University of Virginia Health System, Charlottesville, Virginia., Hall HC; Department of Pharmacy Services, University of Virginia Health System, Charlottesville, Virginia., Pelletier S; Division of Transplantation Surgery, Department of Surgery, University of Virginia Health System, Charlottesville, Virginia., Sifri CD; Division of Infectious Diseases & International Health, Department of Medicine, University of Virginia Health System, Charlottesville, Virginia.
Publikováno v:
Antimicrobial stewardship & healthcare epidemiology : ASHE [Antimicrob Steward Healthc Epidemiol] 2022 Jan 24; Vol. 2 (1), pp. e13. Date of Electronic Publication: 2022 Jan 24 (Print Publication: 2022).