Results 71 to 80 of about 3,937 (163)

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Hereditary spherocytosis.

Kathmandu University medical journal (KUMJ), 2005
Hereditary spherocytosis is a congenital haemolytic anaemia due to defect in spectrin-a RBC membrane protein and is transmitted as autosomal dominant. Due to this defect there is presence of characteristic spherical cell in peripheral blood smear and osmotic fragility is increased.
B L, Bajracharya, A, Giri, M R, Baral
openaire   +1 more source

Hereditary Spherocytosis

Zamora EA, Schaefer CA.
europepmc   +2 more sources

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

A novel <i>ANK1</i> gene mutation associated with hereditary spherocytosis: a case report. [PDF]

Front Pediatr
Lai M, Luo Z, Yang Z, Pan R, Huang W, Zhang W, Ma G, Chen R.   +7 more
europepmc   +1 more source

In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis. [PDF]

Br J Haematol
de Wilde JRA, Kuppens GZL, Boesveld ME, van Vuren AJ, van Solinge WW, Waanders E, van Beers EJ, Rab MAE, Bartels M, van Wijk R.   +9 more
europepmc   +1 more source

Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report. [PDF]

Cureus
Becerra-Carrillo RI, Mendoza-Maldonado C, Rendón-Aguilar H, Torres-Hernández M, Ochoa-Ramírez L.   +4 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

Cognitive impairment in hereditary spherocytosis. [PDF]

Br J Haematol
Tartaglione I, Paturzo MG, Picazio S, Malvone C, De Biasio D, Roberti D, Di Gennaro F, Contieri M, Librizzi G, Pirozzi MA, Esposito F, Perrotta S, Manara R.   +12 more
europepmc   +1 more source