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Presse Medicale (Paris, France : 1983)|August 24, 2019
[Biological diagnosis of mature B cell malignancies]Sophie Kaltenbach, Ludovic Lhermitte
Pediatric Dermatology|October 3, 2020
Dermatofibrosarcoma protuberans, fibrosarcomatous variant: A rare tumor in childrenMatthieu Chicaud, Annonciade Frassati-Biaggi, Sophie Kaltenbach, et al.
Annual Review of Genomics and Human Genetics|February 5, 2024
PIK3CA-Related Disorders: From Disease Mechanism to Evidence-Based TreatmentsGabriel M Morin, Lola Zerbib, Sophie Kaltenbach, et al.
Blood|June 19, 2010
NUP98-MLL fusion in human acute myeloblastic leukemiaSophie Kaltenbach, Gwendoline Soler, Carole Barin, et al.
American Journal of Medical Genetics. Part A|September 3, 2021
PIEZO1-gene gain-of-function mutations with lower limb lymphedema onset in an adult: Clinical, scintigraphic, and noncontrast magnetic resonance lymphography findingsStéphane Vignes, Sophie Kaltenbach, Loïc Garçon, et al.
European Journal of Human Genetics : EJHG|June 6, 2025
First report of successful pregnancies after treatment with alpelisib for PIK3CA-related overgrowth spectrumGabriel Morin, Antoine Fraissenon, Caroline Chopinet, et al.
Annales De Pathologie|March 22, 2026
[High-grade B-cell lymphoma with 11q aberration: A case report]George Terinte-Balcan, Pierre Isnard, Sophie Kaltenbach, et al.
British Journal of Haematology|October 20, 2010
Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemiaBenoîte Pérez, Olivier Kosmider, Bruno Cassinat, et al.
American Journal of Medical Genetics. Part A|July 23, 2021
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactylyAhmed El Mouatani, Géraldine Van Winckel, Khaoula Zaafrane-Khachnaoui, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|December 10, 2013
Small intestinal CD4+ T-cell lymphoma is a heterogenous entity with common pathology featuresGeorgia Malamut, Bertrand Meresse, Sophie Kaltenbach, et al.
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