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International Journal of Molecular Sciences|December 24, 2021
Investigating Pathogenicity and Virulence of Staphylococcus pettenkoferi: An Emerging PathogenNour Ahmad-Mansour, Lucile Plumet, Sylvaine Huc-Brandt, et al.
Orphanet Journal of Rare Diseases|September 4, 2012
Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3Tobias Eisenberger, Rima Slim, Ahmad Mansour, et al.
American Journal of Ophthalmology Case Reports|October 16, 2024
Multifocal vitelliform lesions associated with mitochondrial retinopathyMaurizio Battaglia Parodi, Alessio Antropoli, Lorenzo Bianco, et al.
International Journal of Molecular Sciences|December 23, 2022
Phenotypic and Genotypic Virulence Characterisation of Staphylococcus pettenkoferi Strains Isolated from Human Bloodstream and Diabetic Foot InfectionsChloé Magnan, Nour Ahmad-Mansour, Cassandra Pouget, et al.
Diagnostics (Basel, Switzerland)|May 28, 2022
Artificial Intelligence in the Diagnosis of Oral Diseases: Applications and PitfallsShankargouda Patil, Sarah Albogami, Jagadish Hosmani, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|March 17, 2020
Comparison of Loading Doses of Ziv-Aflibercept and Aflibercept in Neovascular Age-Related Macular DegenerationApoorva Ayachit, Sumit Randhir Singh, Anand Subramanyam, et al.
Biomedicine Hub|June 25, 2026
Occult Tuberculosis in Dialysis Patients Is Rarely Straightforward: Retrospective Case SeriesSalah K Essa, Mahmoud Sami Mohammed, Mohamed Salah Essa, et al.
Frontiers in Cellular and Infection Microbiology|January 1, 2025
Deciphering pathogenicity and virulence of the first Staphylococcus debuckii isolate from diabetic foot osteomyelitisCynthia N Abi Najem, Chloé Magnan, Lucile Plumet, et al.
The British Journal of Oral & Maxillofacial Surgery|November 18, 2025
Treatment options for radiation-induced xerostomia in patients with head and neck cancer: a systematic review and meta-analysisOadi N Shrateh, Ashna Habib, Hammad Ur Rehman Shamsi, et al.
American Journal of Human Genetics|April 29, 2014
Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndromeNisha Patel, Arif O Khan, Ahmad Mansour, et al.
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