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Haematologica|January 14, 2011
New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 childrenNathalie Aladjidi, Guy Leverger, Thierry Leblanc, et al.
The Journal of Allergy and Clinical Immunology|September 19, 2012
Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiencyFabian Hauck, Clotilde Randriamampita, Emmanuel Martin, et al.
American Journal of Human Genetics|April 7, 2022
Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiationMarion Coolen, Nami Altin, Karthyayani Rajamani, et al.
The Journal of Pediatrics|September 18, 2010
Isolated congenital asplenia: a French nationwide retrospective survey of 20 casesNizar Mahlaoui, Veronique Minard-Colin, Capucine Picard, et al.
The Journal of Clinical Investigation|October 3, 2003
A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiencyGilles Courtois, Asma Smahi, Janine Reichenbach, et al.
Pediatrics|December 14, 2011
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic reviewSandrine Leroy, Despina Moshous, Olivier Cassar, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 20, 2023
Chronic Aichi Virus Infection As a Cause of Long-Lasting Multiorgan Involvement in Patients With Primary Immune DeficienciesJacques Fourgeaud, Mathilde M Lecuit, Philippe Pérot, et al.
Blood|February 3, 2005
Failure of SCID-X1 gene therapy in older patientsAdrian J Thrasher, Salima Hacein-Bey-Abina, H Bobby Gaspar, et al.
Nature Medicine|June 18, 2021
Retrieval of vector integration sites from cell-free DNADaniela Cesana, Andrea Calabria, Laura Rudilosso, et al.
Blood|March 16, 2013
Outcomes of transplantation using various hematopoietic cell sources in children with Hurler syndrome after myeloablative conditioningJaap Jan Boelens, Mieke Aldenhoven, Duncan Purtill, et al.
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