Publications by authors named "Hussein Daoud"

63Publications

Impact of Sex Differences on Outcomes of Peripheral Artery Disease Intervention (From a Nationwide Sample).

Am J Cardiol 2020 Nov 17. Epub 2020 Nov 17.

University of Massachusetts Medical School, Worcester, MA, USA.

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http://dx.doi.org/10.1016/j.amjcard.2020.11.003DOI Listing
November 2020

Giant right atrium: a long-term complication of rheumatic heart disease.

Oxf Med Case Reports 2020 Feb 28;2020(2):omaa011. Epub 2020 Feb 28.

Department of Cardiology, Jackson Memorial Hospital/University of Miami, FL 33136, USA.

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http://dx.doi.org/10.1093/omcr/omaa011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588348PMC
February 2020

National Trends of Outcomes in Transcatheter Aortic Valve Replacement (TAVR) Through Transapical Versus Endovascular Approach: From the National Inpatient Sample (NIS).

Cardiovasc Revasc Med 2020 Aug 15;21(8):964-970. Epub 2020 May 15.

Advocate Illinois Masonic Medical Center, Chicago, IL, United States of America; University of California, San Francisco, San Francisco, CA, United States of America.

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http://dx.doi.org/10.1016/j.carrev.2020.05.010DOI Listing
August 2020

Lime-induced phytophotodermatitis.

Oxf Med Case Reports 2019 Nov 9;2019(11):470-472. Epub 2019 Dec 9.

Department of Internal Medicine, Advocate Illinois Masonic Medical Center, Chicago, IL, USA.

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http://dx.doi.org/10.1093/omcr/omz113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6902619PMC
November 2019

Acute Coronary Syndrome (ACS) due to Coronary Artery Embolism in a Patient with Atrial Fibrillation.

Case Rep Cardiol 2019 10;2019:9347198. Epub 2019 Oct 10.

Department of Cardiology, Advocate Illinois Masonic Medical Center, 836 W Wellington Ave., Chicago, IL 60657, USA.

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http://dx.doi.org/10.1155/2019/9347198DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811972PMC
October 2019

Infective endocarditis and brain abscess secondary to Aggregatibacter aphrophilus.

IDCases 2019 17;17:e00561. Epub 2019 May 17.

Department of Internal Medicine, Advocate Illinois Masonic Medical Center, 836 W Wellington Ave., Chicago, IL, 60657, USA.

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http://dx.doi.org/10.1016/j.idcr.2019.e00561DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535683PMC
May 2019

Chronic Type A Aortic Dissection: Rare Presentation of Incidental Pericardial Effusion.

Case Rep Cardiol 2019 2;2019:3562871. Epub 2019 May 2.

Department of Internal Medicine, Advocate Illinois Masonic Medical Center, 836 W Wellington Avenue, Chicago, IL 60657, USA.

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http://dx.doi.org/10.1155/2019/3562871DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525833PMC
May 2019

Adopting High-Resolution Allele Frequencies Substantially Expedites Variant Interpretation in Genetic Diagnostic Laboratories.

J Mol Diagn 2019 07 25;21(4):602-611. Epub 2019 Apr 25.

Department of Genetics, CHEO, Ottawa, Ontario, Canada; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jmoldx.2019.02.009DOI Listing
July 2019

Genetic Diagnostic Testing for Inherited Cardiomyopathies: Considerations for Offering Multi-Gene Tests in a Health Care Setting.

J Mol Diagn 2019 05 4;21(3):437-448. Epub 2019 Feb 4.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jmoldx.2019.01.004DOI Listing
May 2019

Spontaneous Celiac Artery Dissection Presenting With Splenic Infarction: A Case Report.

Gastroenterology Res 2018 Oct 1;11(5):379-382. Epub 2018 Oct 1.

Department of Internal Medicine, Advocate Illinois Masonic Medical Center, 836 W Wellington Ave., Chicago, IL 60657, USA.

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http://dx.doi.org/10.14740/gr1065wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188032PMC
October 2018

Isolated Superior Mesenteric Artery Dissection: A Case Report and Literature Review.

Gastroenterology Res 2018 Oct 1;11(5):374-378. Epub 2018 Oct 1.

Department of Internal Medicine, Advocate Illinois Masonic Medical Center, 836 W Wellington Ave., Chicago, IL 60657, USA.

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https://www.karger.com/Article/Pdf/448879
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http://www.gastrores.org/index.php/Gastrores/article/view/10
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http://dx.doi.org/10.14740/gr1056wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6188040PMC
October 2018

Mosaic KRAS mutation in a patient with encephalocraniocutaneous lipomatosis and renovascular hypertension.

Am J Med Genet A 2018 11 5;176(11):2523-2527. Epub 2018 Oct 5.

Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong.

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http://doi.wiley.com/10.1002/ajmg.a.40349
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http://dx.doi.org/10.1002/ajmg.a.40349DOI Listing
November 2018

Reinterpretation of sequence variants: one diagnostic laboratory's experience, and the need for standard guidelines.

Genet Med 2018 Mar 14;20(3):365-368. Epub 2017 Dec 14.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1038/gim.2017.191DOI Listing
March 2018

Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.

CMAJ 2016 Aug 30;188(11):E254-E260. Epub 2016 May 30.

Department of Genetics (Daoud, Luco, Beaulieu, Jarinova, Carson, Nikkel, Graham, Richer, Armour, Boycott, Dyment) and Department of Pediatrics (Bulman, Chakraborty, Geraghty, Lines, Lacaze-Masmonteil), Children's Hospital of Eastern Ontario, Ottawa, Ont.; McGill University (Li, Bareke, Majewski) and Genome Quebec Innovation Centre (Li, Bareke, Majewski), Montréal, Que.

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http://dx.doi.org/10.1503/cmaj.150823DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4978597PMC
August 2016

CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.

Nat Commun 2016 Apr 15;7:11253. Epub 2016 Apr 15.

Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Macquarie University, Sydney, New South Wales 2109, Australia.

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http://dx.doi.org/10.1038/ncomms11253DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835537PMC
April 2016

Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature.

BMC Med Genet 2016 Feb 27;17:15. Epub 2016 Feb 27.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, K1H 8L1, Canada.

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http://dx.doi.org/10.1186/s12881-016-0276-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769499PMC
February 2016

Resolution of refractory hypotension and anuria in a premature newborn with loss-of-function of ACE.

Am J Med Genet A 2015 Nov 26;167A(11):2867. Epub 2015 Aug 26.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37270DOI Listing
November 2015

Investigation of C9orf72 repeat expansions in Parkinson's disease.

Neurobiol Aging 2013 Jun 27;34(6):1710.e7-9. Epub 2012 Dec 27.

Centre of Excellence in Neuroscience of Université de Montréal (CENUM), CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.11.025DOI Listing
June 2013

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.

Neurobiol Aging 2013 Apr 10;34(4):1311.e1-2. Epub 2012 Oct 10.

Centre of Excellence in Neuroscience of Université de Montréal, CHUM Research Center and the Department of Medicine, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.09.001DOI Listing
April 2013

Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia.

Eur J Hum Genet 2013 Feb 27;21(2):237-9. Epub 2012 Jun 27.

Centre of Excellence in Neurosciences of Université de Montréal, CHUM Research Center, Montreal, Québec, Canada.

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http://dx.doi.org/10.1038/ejhg.2012.135DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3548267PMC
February 2013

UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Sep 3;33(9):2230.e1-2230.e5. Epub 2012 May 3.

Centre of Excellence in Neuroscience of Université de Montréal (CENUM), CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.03.015DOI Listing
September 2012

Analysis of the SORT1 gene in familial amyotrophic lateral sclerosis.

Neurobiol Aging 2012 Aug 22;33(8):1845.e7-9. Epub 2012 Feb 22.

Centre of Excellence in Neurosciences of Université de Montréal, CHUM Research Center, Montreal, QC H2L 4M1, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.01.011DOI Listing
August 2012

Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis.

Arch Neurol 2012 May;69(5):653-6

Centre of Excellence in Neurosciences of Université de Montréal, Montreal, Quebec, Canada.

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http://archneur.jamanetwork.com/article.aspx?doi=10.1001/arc
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http://dx.doi.org/10.1001/archneurol.2011.2499DOI Listing
May 2012

Exome sequencing reveals SPG11 mutations causing juvenile ALS.

Neurobiol Aging 2012 Apr 10;33(4):839.e5-9. Epub 2011 Dec 10.

Centre of Excellence in Neuroscience of Université de Montréal, CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.11.012DOI Listing
April 2012

A role for ubiquilin 2 mutations in neurodegeneration.

Nat Rev Neurol 2011 Oct 11;7(11):599-600. Epub 2011 Oct 11.

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http://dx.doi.org/10.1038/nrneurol.2011.163DOI Listing
October 2011

Association of long ATXN2 CAG repeat sizes with increased risk of amyotrophic lateral sclerosis.

Arch Neurol 2011 Jun;68(6):739-42

Centre for Excellence in Neuromics, CHUM Research Center, Université de Montréal, 2099 Alexandre De-Seve St, Montreal, QC H2L 2W5, Canada.

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http://dx.doi.org/10.1001/archneurol.2011.111DOI Listing
June 2011

De novo SYNGAP1 mutations in nonsyndromic intellectual disability and autism.

Biol Psychiatry 2011 May 15;69(9):898-901. Epub 2011 Jan 15.

Centre of Excellence in Neuromics of Université de Montréal and Synapse to Disease, S2D, Group, Centre Hospitalier Universitaire Sainte-Justine Research Center, Montréal, Canada.

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http://dx.doi.org/10.1016/j.biopsych.2010.11.015DOI Listing
May 2011

Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis.

Arch Neurol 2011 May 10;68(5):587-93. Epub 2011 Jan 10.

Centre of Excellence in Neuromics, Centre hospitalier de l'Université de Montréal Research Center, 2099 Alexandre De-Seve St., Montreal, QC, Canada.

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http://dx.doi.org/10.1001/archneurol.2010.351DOI Listing
May 2011

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

J Hum Genet 2011 Mar 16;56(3):247-9. Epub 2010 Dec 16.

Center of Excellence in Neuromics of Université de Montréal, CHUM Research Center, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1038/jhg.2010.162DOI Listing
March 2011

Analysis of OPTN as a causative gene for amyotrophic lateral sclerosis.

Neurobiol Aging 2011 Mar 11;32(3):555.e13-4. Epub 2010 Nov 11.

Centre of Excellence in Neuromics of Université de Montréal, CHUM Research Center, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2010.10.001DOI Listing
March 2011

Exploring the 7p22.1 chromosome as a candidate region for autism.

J Biomed Biotechnol 2010 18;2010:423894. Epub 2010 Apr 18.

Laboratoire de Génétique Humaine, Faculté de Médecine de Tunis, 15 rue Djebel Lakhdhar La Rabta, 1007 Tunis, Tunisia.

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http://www.hindawi.com/journals/bmri/2010/423894/
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http://dx.doi.org/10.1155/2010/423894DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2856063PMC
July 2010

Analysis of DPP6 and FGGY as candidate genes for amyotrophic lateral sclerosis.

Amyotroph Lateral Scler 2010 Aug;11(4):389-91

Centre of Excellence in Neuromics, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.3109/17482960903358857DOI Listing
August 2010

Genetics of motor neuron disorders: new insights into pathogenic mechanisms.

Nat Rev Genet 2009 Nov 13;10(11):769-82. Epub 2009 Oct 13.

Centre Hospitalier Universitaire Sainte-Justine Research Center, Centre of Excellence in Neuromics, Universit de Montral, Quebec H2L 2W5, Canada.

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http://dx.doi.org/10.1038/nrg2680DOI Listing
November 2009

Recent advances in the genetics of amyotrophic lateral sclerosis.

Curr Neurol Neurosci Rep 2009 May;9(3):198-205

Center of Excellence in Neuromics of the CHUMResearch Center and the Department of Medicine,University of Montreal, 1560 Sherbrooke Street East, Room Y-3633, Montreal QCH2L4M1, Canada.

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http://dx.doi.org/10.1007/s11910-009-0030-9DOI Listing
May 2009

The creatine transporter gene paralogous at 16p11.2 is expressed in human brain.

Comp Funct Genomics 2008 :609684

Human Genetics Laboratory, Faculty of Medicine of Tunis, 15 rue Djebel Lakdhar La Rabta, Tunis 1007, Tunisia.

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http://dx.doi.org/10.1155/2008/609684DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2396218PMC
June 2010

De novo balanced translocation t (7;16) (p22.1; p11.2) associated with autistic disorder.

J Biomed Biotechnol 2008 ;2008:231904

Laboratoire de Génétique Humaine, Faculté de Médecine de Tunis, 15 rue Djebel Lakhdhar La Rabta, Tunis 1007, Tunisia.

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http://dx.doi.org/10.1155/2008/231904DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373955PMC
July 2008