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Small (Weinheim an Der Bergstrasse, Germany)|June 27, 2017
High Aspect Ratio Sub-Micrometer Channels Using Wet Etching: Application to the Dynamics of Red Blood Cell Transiting through Biomimetic Splenic SlitsPriya Gambhire, Scott Atwell, Cécile Iss, et al.
Sub-Cellular Biochemistry|September 26, 2025
Genetics and cancer-related Laminopathies: Involvement of Lamins and Lamin-Chromatin InteractionsCamille Desgrouas, Diane Frankel, Nathalie Bonello-Palot, et al.
European Journal of Medical Genetics|July 6, 2019
Congenital Sodium Diarrhea by mutation of the SLC9A3 geneGeorges Dimitrov, Sarah Bamberger, Chloe Navard, et al.
Journal of Clinical Pathology|May 26, 2010
Neonatal screening for sickle cell disease in France: evaluation of the selective processIsabelle Thuret, Jacques Sarles, Françoise Merono, et al.
Clinical Hemorheology and Microcirculation|November 20, 2020
HbF-promoting polymorphisms may specifically reduce the residual risk of cerebral vasculopathy in SCA children with alpha-thalassemiaPhilippe Joly, Nathalie Bonello-Palot, Catherine Badens, et al.
Haematologica|July 28, 2011
Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the diseaseCatherine Badens, Philippe Joly, Imane Agouti, et al.
Annales De Biologie Clinique|January 7, 2017
Diagnostic approach to hemoglobins with high oxygen affinity: experience from France and Belgium and review of the literatureCorentin Orvain, Philippe Joly, Serge Pissard, et al.
European Journal of Medical Genetics|November 28, 2017
Missense mutation of TTC7A mimicking tricho-hepato-enteric (SD/THE) syndrome in a patient with very-early onset inflammatory bowel diseaseJoão Farela Neves, Isabel Afonso, Luis Borrego, et al.
Journal of Clinical Medicine|March 28, 2026
Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare DiseaseSarah Szepetowski, Audrey Benoit, Julie Berbis, et al.
American Journal of Medical Genetics. Part A|February 1, 2018
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two familiesAlexandre Fabre, Laetitia-Marie Petit, Lars F Hansen, et al.
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