Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ibrahima Ba

Showing results (21-30 of 40) with videos related to

Pageof 4
Sort By:
ERJ Open Research|October 29, 2025
Is <i>MUC5B</i> rs35705950 promoter polymorphism associated with chronic lung allograft dysfunction?Adèle Sandot, Ibrahima Ba, Clément R Massonnaud, et al.
Respirology (Carlton, Vic.)|October 3, 2025
Molecular Investigation in Early-Onset Interstitial Lung Disease: Results From 699 Unrelated PatientsCamille Louvrier, Nadia Nathan, Vincent Cottin, et al.
ERJ Open Research|April 9, 2026
Efficacy and safety of danazol for pulmonary fibrosis or bone-marrow failure associated with telomere-related gene mutationFlore Sicre de Fontbrune, Stéphane Jouneau, Vincent Cottin, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|July 11, 2021
A large epidemic of a necrotic skin infection in the Democratic Republic of São Tomé and Principe: an epidemiological studyLorenzo Subissi, Andreza Sousa, Ibrahima Ba, et al.
Genes & Development|September 4, 2024
Heterozygous <i>RPA2</i> variant as a novel genetic cause of telomere biology disordersRima Kochman, Ibrahima Ba, Maïlyn Yates, et al.
ERJ Open Research|January 21, 2026
Adult male patients with <i>DKC1</i> mutations present early-onset pulmonary fibrosis and severe prognosisOphélie Evrard, Quentin Philippot, Caroline Kannengiesser, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Human Molecular Genetics|January 28, 2020
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndromeManame Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, et al.
British Journal of Haematology|September 16, 2024
Haematological features of telomere biology disorders diagnosed in adulthood: A French nationwide study of 127 patientsFrançois Maillet, Jacques-Emmanuel Galimard, Raphaël Borie, et al.
Annals of Epidemiology|July 11, 2026
Defining strata of women at risk for HIV in sub-Saharan Africa: A pooled latent class analysisKatherine Rucinski, Yuanqi Mi, Kaitlyn Atkins, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
ERJ Open Research|October 29, 2025
Is <i>MUC5B</i> rs35705950 promoter polymorphism associated with chronic lung allograft dysfunction?Adèle Sandot, Ibrahima Ba, Clément R Massonnaud, et al.
Respirology (Carlton, Vic.)|October 3, 2025
Molecular Investigation in Early-Onset Interstitial Lung Disease: Results From 699 Unrelated PatientsCamille Louvrier, Nadia Nathan, Vincent Cottin, et al.
ERJ Open Research|April 9, 2026
Efficacy and safety of danazol for pulmonary fibrosis or bone-marrow failure associated with telomere-related gene mutationFlore Sicre de Fontbrune, Stéphane Jouneau, Vincent Cottin, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|July 11, 2021
A large epidemic of a necrotic skin infection in the Democratic Republic of São Tomé and Principe: an epidemiological studyLorenzo Subissi, Andreza Sousa, Ibrahima Ba, et al.
Genes & Development|September 4, 2024
Heterozygous <i>RPA2</i> variant as a novel genetic cause of telomere biology disordersRima Kochman, Ibrahima Ba, Maïlyn Yates, et al.
ERJ Open Research|January 21, 2026
Adult male patients with <i>DKC1</i> mutations present early-onset pulmonary fibrosis and severe prognosisOphélie Evrard, Quentin Philippot, Caroline Kannengiesser, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Human Molecular Genetics|January 28, 2020
NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndromeManame Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, et al.
British Journal of Haematology|September 16, 2024
Haematological features of telomere biology disorders diagnosed in adulthood: A French nationwide study of 127 patientsFrançois Maillet, Jacques-Emmanuel Galimard, Raphaël Borie, et al.
Annals of Epidemiology|July 11, 2026
Defining strata of women at risk for HIV in sub-Saharan Africa: A pooled latent class analysisKatherine Rucinski, Yuanqi Mi, Kaitlyn Atkins, et al.
Pageof 4