Profil bibliographique

Monique Elmaleh

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

225Publications signalées

4529Citations signalées

1Affiliations récentes

Institutions déclarées

Hôpital Robert-Debré

Domaines associés

Fetal and Pediatric Neurological DisordersNeonatal and fetal brain pathologyHemoglobinopathies and Related DisordersHead and Neck AnomaliesEar Surgery and Otitis Media

Publications récentes

Accès ouvert 2026 articleOpenAlex

Identification of predictive factors for reversal of cerebral vasculopathy in an original longitudinal cohort study in newborns with sickle cell anaemia

Julie Sommet, Priscilla Boizeau, Zinédine Haouari, Bérengère Koehl et autres

0 citationsBritish Journal of Haematology

Accès ouvert 2026 articleOpenAlex

Better 10‐Year Cerebrovascular Outcome After Transplant Than on Standard‐Care in Sickle Cell Anemia: DREPAGREFFE Trial

Francoise Bernaudin, Suzanne Verlhac, Elisabeth Ducros-Miralles, Cécile Arnaud et autres

2 citationsAmerican Journal of Hematology

Accès ouvert 2025 articleOpenAlex

Investigating Cerebral Anomalies in Preterm Infants and Associated Risk Factors With Magnetic Resonance Imaging at Term-Equivalent Age

Nicolas Elbaz, Valérie Biran, Chloé Ghozland, Laurie Devisscher et autres

2 citationsPediatric Neurology

Accès ouvert 2025 articleOpenAlex

Vestibular Deficit in Patients with Waardenburg Syndrome

Mathilde Benifla, Margaux Serey‐Gaut, E. Bois, S. Jbyeh et autres

0 citationsBiomedicines

Accès ouvert 2025 articleOpenAlex

Neuroimaging insights into brain mechanisms of early-onset restrictive eating disorders

Clara Moreau, Anaël Ayrolles, Christopher R. K. Ching, Robin Bonicel et autres

5 citationsNature Mental Health

Accès ouvert 2025 articleOpenAlex

Pattern of Deep Grey Matter Undersizing Boosts MRI ‐Based Diagnostic Classifiers in Fetal Alcohol Spectrum Disorders

Eliot Kerdreux, Justine Fraize, Alexandra Ntorkou, Pauline Garzón et autres

1 citationHuman Brain Mapping

Accès ouvert 2025 articleOpenAlex

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption

Caroline Nava, Benjamin Cogné, Elsa Leitão, François Lecoquierre et autres

49 citationsNature Genetics

Accès ouvert 2025 articleOpenAlex

Assessing the diagnostic performance of investigations in pediatric myoclonic epilepsies: A retrospective cohort study

Blandine Dozières‐Puyravel, Hala Nasser, Monique Elmaleh, François‐Xavier Mauvais et autres

1 citationEpilepsia

Accès ouvert 2025 articleOpenAlex

A biallelic variant in GORASP1 causes a novel Golgipathy with glycosylation and mitotic defects

Sophie Lebon, Arnaud Bruneel, Séverine Drunat, Alexandra Albert et autres

3 citationsLife Science Alliance

Accès ouvert 2024 articleOpenAlex

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

Thomas B. Smith, Robert Kopajtich, Leigh Demain, Alessandro Rea et autres

9 citationsThe American Journal of Human Genetics

2024 articleOpenAlex

Outcome of Cerebral Vasculopathy and Cognitive Performances 10 Years Post-Enrollment in the Drepagreffe Trial Comparing Allogeneic Stem Cell Transplantation to Standard-Care in Children with Sickle Cell Anemia and History of Abnormal Cerebral Velocities

Françoise Bernaudin, Suzanne Verlhac, Elisabeth Ducros-Miralles, Cécile Arnaud et autres

0 citationsBlood

Accès ouvert 2024 articleOpenAlex

Hearing loss and vestibular dysfunction in congenital CMV infection: Could it be due to endolymphatic pressure anomaly? A preliminary study

Laureline Kahn, Guillaume Poillon, Monique Elmaleh, Luca Litman-Roventa et autres

1 citationInternational Journal of Pediatric Otorhinolaryngology

Profil ORCID Notice OpenAlex

BNTIC News n’est pas le producteur de ces données. Recherche à la demande dans Crossref et Europe PMC, sans clé ; OpenAlex reste optionnel. Aucun service payant requis, aucune réponse conservée. Sources et limites.