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News
Medicine, through the looking glass - The Globe and Mail
www.theglobeandmail.com
Quebec family with rare mirror-movement trait provides key to discoveries about how the human nervous system develops
Discovery Reveals Brain Abnormality And Mirror Movement Link ...neurosciencenews.com › mirror-movement-brain-abnormality-6186
neurosciencenews.com
Mar 2, · ... Annalisa Paolino, Kate Pope, Florence Riant, Gail A Robinson, Megan Spencer-Smith, Myriam Srour, Sarah E M Stephenson, Rick Tankard, ...
Getting the wires crossed: New research identifies cause of mirror...
www.thechildren.com
By Christine Zeindler
Molecular Mechanisms Offer Hope for New Pain Treatments
www.newswise.com
By working with individuals suffering from a severe disorder that causes sensory neurons to degenerate, researchers at the University of Montreal Hospital and...
Network Profiles
LinkedIn: Myriam Srour | LinkedIn
View Myriam Srour's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Myriam Srour discover inside ...
pinterest.com: Myriam Srour
32 Pins • 5 Followers
pinterest.com: Myriam Zoghbi Srour
13 Pins • 10 Followers
Interests
Discovery of a gene that causes Joubert Syndrome | EurekAlert!...
www.eurekalert.org
C5ORF42 was identified as the gene that causes Joubert Syndrome in a number of families in the Lower St. Lawrence region of Quebec where the causal gene had...
Gene that causes Joubert Syndrome discovered -- ScienceDaily
www.sciencedaily.com
Joubert Syndrome is a condition that affects brain development and manifests itself through delayed psychomotor development, abnormal coordination of eye...
Homozygous deletion of Tenascin-R in a patient with intellectual...
jmg.bmj.com
Myriam Srour 1, 2; 1 Division of Pediatric Neurology, Departments of Neurology/Neurosurgery, McGill University, Montreal Children's Hospital-McGill ...
Mirror, mirror: Scientists find cause of involuntary EurekAlert!www.eurekalert.org › pub_releases › uom-mms
www.eurekalert.org
Apr 29, · ... people affected with mirror movements," explains first author Dr. Myriam Srour, a pediatric neurologist and a doctoral student at the Université ...
Employees
Myriam Srour, MD CM, FRCP(C), PhD | Montreal Children's Hospitalwww.thechildren.com › departments-and-staff › staff › myriam-srour-md-c...
www.thechildren.com
Myriam Srour, MD CM, FRCP(C), PhD. Pediatrics, Neurology & Neurosurgery. Fun fact about me. I have lived in 5 different countries. I love working with children ...
Meet the Team | Srour Lab: Genetics of Neurodevelopmental ...www.mcgill.ca › geneneurodisorderslab › team
www.mcgill.ca
Myriam Srour MDCM, PhD. Pediatric Neurologist Clinician-Scientist at Montreal Children's Hospital. Assistant Professor, Departments of Pediatrics, Neurology and Neurosurgery, McGill University. Director of the Neurogenetics and Brain Malformations Clinics. McGill Pediatric Neurogenetics Fellowship program director.
Education
classmates: Myriam Srour
Western Canada High School, Calgary, AB,
classmates: Myriam Srour
Western Canada High School, Calgary, AB,
Books & Literature
bokus.com: Measures for Children with Developmental Disability - Annette...
Pris: kr. Inbunden, Skickas inom vardagar. Köp Measures for Children with Developmental Disability av Annette Majnemer på Bokus.com.
Antenatal corticosteroid administration and early PLOS Medicinejournals.plos.org › plosmedicine › article › authors › journal.pmed
journals.plos.org
Dec 7, · Myriam Srour. Roles Conceptualization, Formal analysis, Funding acquisition, Writing – review & editing. Affiliation Departments of Pediatrics ...
Neurodevelopmental Disabilities: Clinical and Scientific Foundations...
books.google.de
Neurodevelopmental disabilities are a common problem in child health. This book takes a comprehensive approach to addressing these often challenging clinical...
Rosenberg's Molecular and Genetic Basis of Neurological and...
books.google.de
Rosenberg’s Molecular and Genetic Basis of Neurologic and Psychiatric Disease, Fifth Edition provides a comprehensive introduction and reference to the...
Related Documents
Pediatric Psychopharmacology: Psychopharmacology of Tic Disorders...
www.pdfsearch.io
Pediatric Psychopharmacology: Psychopharmacology of Tic Disorders Myriam Srour MD1, Paul Lespérance MD1, Francois Richer PhD1, Sylvain Chouinard ...
EBSCOhost | | Homozygous deletion of Tenascin-R in a patient...
web.b.ebscohost.com
intellectual disability. David Dufresne,1,2 Fadi F Hamdan,3 Jill A Rosenfeld,4 Beth Torchia,4. Bernard Rosenblatt,. 1,2. Jacques L Michaud,. 3. Myriam Srour. 1, 2.
Identification of a homozygous splice site mutation in the dynein...
www.deepdyve.com
Mehrnaz Ohadi · Huda Mahmood · Guy A. Rouleau · Attya Bhatti · Muhammad Ayub · Myriam Srour ·. Peter John · John B. Vincent. Received: 4 April
Mutations in TMEM231 cause Joubert syndrome in French Canadians -...
www.proquest.com
Myriam Srour,1 Fadi F Hamdan,1 Jeremy A Schwartzentruber,2 Lysanne Patry,1. Luis H Ospina,3 Michael I Shevell,4 Valérie Désilets,5 Sylvia Dobrzeniecka,1.
Scientific Publications
An Instructive Case of an 8-Year-Old Boy With Intellectual Disability...
www.sciencedirect.com
Seminars in Pediatric Neurology, Volume 15, Issue 4, Pages , December 2008, Authors:Myriam Srour, MD CM; Bassam A. Bejjani, MD; Emily A. Rorem, ...
Rare diseases in ICD11: making rare diseases visible in health...
ojrd.biomedcentral.com
Because of their individual rarity, genetic diseases and other types of rare diseases are under-represented in healthcare coding systems; this contributes to a...
Discovery of a Gene that Causes Joubert Syndrome : Health & Medicine...
www.scienceworldreport.com
May 10, · According to Myriam Srour, a doctoral student and co-author of the study, the mutations likely spread in the population along these migration routes.
A single genetic fault makes one hand mirror the other’s movements
www.nationalgeographic.com
Clench your left hand into a fist. What happened to your right hand when you did it? If you’re like most people, the answer is nothing. But, surprisingly, not...
Publications
Myriam Srour | PubFactswww.pubfacts.com › author › Myriam+Srour
www.pubfacts.com
Publications by authors named "Myriam Srour". 67 Publications. Page 1 of 3; Next Page. © PubFacts. About PubFacts · Privacy Policy · Sitemap.
Diagnostic Approach to Cerebellar Hypoplasia | SpringerLink
link.springer.com
Feb 3, · Diagnostic Approach to Cerebellar Hypoplasia. Andrea Accogli,; Nassima Addour-Boudrahem &; Myriam Srour. The Cerebellum (2021)Cite ...
Association of intronic variants of the BTBD9 gene with Tourette...
www.biomedsearch.com
... Myriam Srour / ; Marc Thibault / ; Sylvie Toupin / ; Isabelle Tremblay / ; Mijouk Vézina
Publications Authored by Myriam Srour | PubFacts
www.pubfacts.com
Publications Authored by Myriam Srour
Reports & Statements
Google Blogs: A single genetic fault makes one hand mirror the other's movements ...
Now, Myriam Srour from the University of Montreal has found that a single faulty gene can cause the condition. She studied a large French Canadian family with four generations of members who had been making mirror ...
Age-related injury responses of human oligodendrocytes to Naturewww.nature.com › communications biology › articles › article
www.nature.com
Jan 4, · Myriam Srour participated in design of pediatric studies and writing of manuscript. Charles Couturier participated in design and analysis of the ...
The mirror movement mutation | Mo Costandi
neurophilosophy.wordpress.com
A single genetic mutation causes involuntary movements that mirror those of the limb on the opposite side of the body
Miscellaneous
Myriam Srour | LinkedIn
www.linkedin.com
View Myriam Srour's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Myriam Srour discover inside ...
Geometry.Net - Health_Conditions: Hereditary Sensory Motor Neuropathy
www.geometry.net
... Myriam Srour, B.Sc., Giovanna Pari , M.D., F.R.C.P.(C.), George Karpati , M.D., F.R.C.P.(C.), and G. Jackson Snipes , M.D., Ph.D.
Étudiants à l'honneur - Programmes de biologie moléculaire
biomol.umontreal.ca
Myriam Srour « Mutations in C5ORF42 cause Joubert syndrome in the french canadian population » (Affiche) PRIX ASTRAZENECA. Shanti Rojas-Sutterlin « Hematopoietic stem
ChemFeeds - Myriam Srour
www.chemfeeds.com
Authors called Myriam Srour. 1. +1. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical ...
Myriam Srour, MD CM, FRCP(C), PhD | Hopital de Montreal pour ...www.hopitalpourenfants.com › personnel › myriam-sr...
www.hopitalpourenfants.com
Myriam Srour, MD CM, FRCP(C), PhD. Neurologie pediatrique et neurophysiologie. Pediatrics, Neurology & Neurosurgery. Fait amusant. J'ai vécu dans 5 pays ...
Myriam Srour (myriamsrour) - Profile | Pinterestwww.pinterest.ca › myriamsrour
www.pinterest.ca
- Earrings are made of polymer clay and are super light on the ears. The clay is very durable… Myriam SrourEar rings.
Selected syndromes every neurologist should know Myriam Srourslidetodoc.com › selected-syndromes-every-neurologist-should-know-myri...
slidetodoc.com
Selected syndromes every neurologist should know Myriam Srour, Pediatric Neurologist September 25, Retts syndrome. Classical Retts- main clinical ...
Child Neurology: Andersen-Tawil syndrome | Neurology
n.neurology.org
Mohammed Almuqbil, MD and Myriam Srour, MD, FRCPC; From the Division of Pediatric Neurology (M.A., M.S.), Montreal Children's Hospital-McGill ...
McGill Department of Neurology
neurology.mcgill.ca
Name: Myriam Srour McGill title: Assistant Professor Hospital title: Office phone: Fax: E-mail: Areas of clinical expertise/research interests: Back to faculty list
Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian...
www.infona.pl
Myriam Srour. Centre of Excellence in Neurosciences, Université de Montréal and Sainte-Justine Hospital Research Center, Montréal H3T ...
De Novo Mutations in Moderate or Severe Intellectual Disability
journals.plos.org
De Novo Mutations in Moderate or Severe Intellectual Disability Myriam Srour, Jose-Mario Capo-Chichi, Hussein Daoud, Christina Nassif, Lysanne Patry, ...
C5orf42
www.labome.org
Species, Research Topics, Scientific Experts, Publications, Genomes and Genes about C5orf42
Rare Mutation That Causes Mirror Movements Reflects Nervous System's...
www.scientificamerican.com
Scientific American is the essential guide to the most awe-inspiring advances in science and technology, explaining how they change our understanding of the...
De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive...
cris.maastrichtuniversity.nl
author = "Jae-Ran Lee and Myriam Srour and Doyoun Kim and Hamdan, {Fadi. F.} and So-Hee Lim and Catherine Brunel-Guitton and Jean-Claude Decarie and ...
Descubren la causa genética de los 'movimientos espejo'
www.infosalus.com
Investigadores canadienses han identificado la causa genética de los 'movimientos espejo', aquellos que afectan a las personas que son incapaces de mover una...
Mutations in DCC cause isolated agenesis of the corpus callosum ...www.x-mol.com › paper
en.x-mol.com
Apr 1, · ... Annalisa Paolino, Kate Pope, Florence Riant, Gail A Robinson, Megan Spencer-Smith, Myriam Srour, Sarah E M Stephenson, Rick Tankard, ...
Paeds Reads - Envokee1.envoke.com › ...
e1.envoke.com
7 days ago · Departmental Acknowledgment. Myriam Srour, MDCM, PhD - Research Institute of the McGill University Health Centre -. Hi Everyone.
La vie avec une microcéphalie - La Presse+
plus.lapresse.ca
On entend par microcéphalie une boîte crânienne anormalement petite. « Si le périmètre crânien est inférieur au 2e percentile sur l’échelle de courbe de...
SLC45A1 - Collect information about clinic management and ...humandiseasegenes.nl › ...
humandiseasegenes.nl
Myriam Srour, MD CM, FRCP (C), PhD, Division of Pediatric Neurology, Departments of Pediatrics and Neurology & Neurosurgery, McGill University, Montreal, ...
Living life seizure-free | Montreal Children's Hospital
www.thechildren.com
Imagine living with seizures so frequent, they happened every hour. Right before he underwent major brain surgery just over a year ago, 3-year old Cédric...
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