Tara Montgomery

Tara Montgomery

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Tara Montgomery

Tara Montgomery

Publications by authors named "Tara Montgomery"

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Integration of Real-Time Electronic Health Records and Wireless Technology in a Mobile Stroke Unit.

J Stroke Cerebrovasc Dis 2019 Sep 12;28(9):2530-2536. Epub 2019 Jul 12.

University of Colorado School of Medicine, Aurora, Colorado. Electronic address:

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http://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2019.06.008DOI Listing
September 2019

Promoting Trust Between Patients and Physicians in the Era of Artificial Intelligence.

JAMA 2019 Jul 15. Epub 2019 Jul 15.

Department of Medicine, University of California, San Francisco.

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http://dx.doi.org/10.1001/jama.2018.20563DOI Listing
July 2019

Clinical and molecular characterization of -related severe early-onset epilepsy.

Neurology 2018 01 1;90(1):e55-e66. Epub 2017 Dec 1.

From Molecular Neurosciences (A.M., E.M., A., A.N., M.A.K.), Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health; Department of Neurology (A.M., A., A.N., C.E., J.H.C., M.A.K.) and Neuroradiology (W.K.C.), Great Ormond Street Hospital for Children, London, UK; Florey Institute of Neuroscience and Mental Health (U.N., E.V.G., I.E.S., S.P.), Melbourne, Australia; Department of Biological Sciences (S.M., M.T.), Institute of Structural and Molecular Biology, Birkbeck College, University of London; Regional Molecular Genetics Laboratory (N.T., R.H.S.), North East Thames Regional Genetics Service, and Department of Clinical Genetics (A.V.K., R.H.S.), Great Ormond Street Hospital, London, UK; Department of Paediatric Neurology (S.A.), Red Cross War Memorial Children's Hospital, Cape Town, South Africa; Department of Paediatric Neurology (G.A.), Addenbrooke's Hospital, Cambridge; Roald Dahl EEG Unit (R.A.), Department of Neurology, and Department of Neurology (R.K.), Alder Hey Children's Hospital, Liverpool; Department of Paediatric Neurology (A.D.), Sheffield Children's Hospital; Clinical Neurosciences (C.E., J.H.C.), Developmental Neurosciences, UCL Great Ormond Street Institute of Child Health, London; Institute of Infection and Global Health (R.K.), University of Liverpool; Department of Paediatric Neurology (K.L.), Evelina Children's Hospital, Guys and St. Thomas' NHS Foundation Trust, London; Department of Clinical Genetics (T.M.), Northern Genetics Service; Department of Pediatric Neurology (V.R.), Great North Children's Hospital, Newcastle Upon Tyne; Department of Paediatric Neurology (R.S.), University Hospital Leicester Children's Hospital; Department of Paediatric Neurology (J.T.), Royal Manchester Children's Hospital; Department of Paediatric Neurology (W.W.), Nottingham University Hospitals NHS Trust, UK; Epilepsy Genetics Program (A. Poduri), Department of Neurology, Boston Children's Hospital; Department of Neurology (A. Poduri), Harvard Medical School, Boston, MA; University of Melbourne (I.E.S.), Austin Health and Royal Children's Hospital, Australia; and Department of Medicine (S.P.), Royal Melbourne Hospital, University of Melbourne, Australia. Dr. Malhotra is currently at the Department of Biochemistry, University of Cambridge, UK.

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http://dx.doi.org/10.1212/WNL.0000000000004762DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754647PMC
January 2018

Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.

PLoS One 2014 15;9(1):e85600. Epub 2014 Jan 15.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America ; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085600PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893250PMC
December 2014

Delineation of the 3p14.1p13 microdeletion associated with syndromic distal limb contractures.

Am J Med Genet A 2014 Dec 24;164A(12):3027-34. Epub 2014 Sep 24.

Fédération Hospitalo-Universitaire TRANSLAD et Centre de Génétique et Centre de Référence «Anomalies du Développement et Syndromes Malformatifs» du Grand Est, Hôpital d'Enfants, CHU Dijon, Dijon, France; Université de Bourgogne, Dijon, France.

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http://dx.doi.org/10.1002/ajmg.a.36751DOI Listing
December 2014

TUBA1A mutation-associated lissencephaly: case report and review of the literature.

Pediatr Neurol 2012 Feb;46(2):127-31

Department of Pediatric Neurology, Great North Children's Hospital, Newcastle-upon-Tyne, UK.

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http://dx.doi.org/10.1016/j.pediatrneurol.2011.11.017DOI Listing
February 2012

22q11 Deletion in children with cleft lip and palate--is routine screening justified?

J Plast Reconstr Aesthet Surg 2008 17;61(2):130-2. Epub 2007 Aug 17.

Cleft Lip & Palate Service, Royal Victoria Infirmary, Queen Victoria Road, Newcastle-upon-Tyne, NE1 4LP, UK.

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http://dx.doi.org/10.1016/j.bjps.2007.06.018DOI Listing
March 2008

SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders.

Hum Mutat 2005 Sep;26(3):176-83

Institute for Human Genetics and Anthropology, Universität Freiburg, Freiburg, Germany.

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http://dx.doi.org/10.1002/humu.20215DOI Listing
September 2005