Results 111 to 120 of about 6,512 (195)

Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis

Altres ajuts: This work was generated within the European Reference Network on Rare Hematological Diseases (ERN-EuroBloodNet) - FPA No. 739541Hereditary spherocytosis (HS) originates from defective anchoring of the cytoskeletal network to the ...
Van Wijk, R., Huisjes, R., Petkova-Kirova, P., Bogdanov, A., Pignatelli, S., Schiffelers, R.M., Mañu Pereira, Mª del Mar, Makhro, A., Hertz, L., Vives Corrons, Juan Luís, Rab, M.A.E., Van Solinge, W.W., Kaestner, L., Universitat Autònoma de Barcelona, Llaudet-Planas, Esther, Verhagen, L.P., Seiler, E.   +16 more
core  

Case Report: Abnormally low hemoglobin A1c in a diabetic patient with <i>SLC4A1</i> gene mutation. [PDF]

Front Endocrinol (Lausanne)
Ye L, Ren Q, Ba T, Wu J, Han X, Ji L.
europepmc   +1 more source

Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression. [PDF]

Childs Nerv Syst
Yan L, Lu X, Yang B, Ma Y.
europepmc   +1 more source

Editorial: Recent advances in pediatric red blood cells disorders

Frontiers in Pediatrics
Gabriele Canciani, Gabriele Canciani, Giuseppe Palumbo, Giuseppe Palumbo, John Brewin, Francesca Rossi, Giulia Ceglie   +6 more
doaj   +1 more source

From Splenectomy to Partial Splenic Embolization, Which is Better for Hereditary Spherocytosis? [PDF]

J Blood Med
Si M, Yang S, Chen Z, Dou A.
europepmc   +1 more source

Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review. [PDF]

Int J Mol Sci
Vives-Corrons JL, Krishnevskaya E.
europepmc   +1 more source

De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review. [PDF]

Ann Hematol
Qin Y, Lu L, Huang X, Li W, Qin Y, Tang S, Wei S.   +6 more
europepmc   +1 more source

Parvovirus B19-Induced Aplastic Crisis and Hemophagocytic Lymphohistiocytosis in a Child With Hereditary Spherocytosis. [PDF]

Cureus
Oyama M, Sakamoto K, Okura E, Saito S, Nakazawa Y.   +4 more
europepmc   +1 more source

Case Report: Clinical and genetic analysis of a family with hereditary spherocytosis combined with familial chylomicronemia syndrome. [PDF]

Front Genet
Qin Y, Liu Y, Li K, Deng Y, Li H, Chen X, Pan X, Huang X, Xie M, Long X, Tang S.   +10 more
europepmc   +1 more source

Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children. [PDF]

Mol Genet Genomic Med
Li Y, Wang Y, Liu T, Xiao L, Huang L, Zhang Y, Xiang Y, Yu J.   +7 more
europepmc   +1 more source