Frontiers | Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease
Jean-Paul Marie (@MARIEJeanPaul7) / Twitter
Bilateral Otomastoiditis in a 8 Month-Old Child with Orofacial Cleft
ORL, chirurgie cervico-faciale
IJERPH | Free Full-Text | Change in University Student Health Behaviours after the Onset of the COVID-19 Pandemic
Evidence for high breakpoint variability in 46, XX, SRY‐positive testicular disorder and frequent ARSE deletion that may be associated with short stature - Capron - 2022 - Andrology - Wiley Online Library
Invivox - Prof. Jean-Paul Marie
PDF) A Review of Treatment of Bilateral Vocal Fold Movement Impairment
Workshop Pr JP MARIE - Laryngeal Reinnervation Course - MTC
Jean-Paul MARIE email address & phone number | NOVUS VIA, LLC BusinessandFinance Consultant contact information - RocketReach
Au CHU de Rouen, le chef de service ORL remporte un prix de l'innovation médicale - Paris-Normandie
Jean-Paul MARIE email address & phone number | INVIVOX Faculty in ENT Surgery contact information - RocketReach
Reparer la voix avec le professeur Jean-Paul Marie du CHU de Rouen
Jean-Paul MARIE | Head of Department | MD, PhD | Otorhinolaryngology, Head and Neck Surgery, Expérimental Surgery Laboratory, EA 3830 GRHV, Institute of Biomédical Research in Normandy | Research profile
Jean-Paul MARIE | Head of Department | MD, PhD | Otorhinolaryngology, Head and Neck Surgery, Expérimental Surgery Laboratory, EA 3830 GRHV, Institute of Biomédical Research in Normandy | Research profile
Liste des stations du TEOR et du tramway de Rouen — Wikipédia
Jean-Paul MARIE - Faculty in ENT Surgery - INVIVOX | LinkedIn
Scientific council - ELSOC
Workshop Pr JP MARIE - Laryngeal Reinnervation Course - MTC
New insights into the genetic etiology of Alzheimer's disease and related dementias | Nature Genetics
Prof. Marie Introduces Unilateral & Bilateral Laryngeal Reinnervation Workshop - YouTube
IRIB Normandy Rouen
Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French severe congenital neutropenia registry – topic of research paper in Clinical medicine. Download scholarly article PDF and read
