Detalhe da pesquisa
1.
Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
J Allergy Clin Immunol
; 141(3): 1036-1049.e5, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29241729
2.
Outcome of haematopoietic stem cell transplantation in dyskeratosis congenita.
Br J Haematol
; 183(1): 110-118, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29984823
3.
Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study.
Br J Haematol
; 177(5): 751-758, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28444729
4.
Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others.
Eur J Pediatr
; 161(7): 368-72, 2002 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12111187