Results 121 to 130 of about 5,131 (199)

Hereditary spherocytosis and allied disorders

HemaSphere, 2019
Roberta Russo, Immacolata Andolfo
doaj   +1 more source

Optimal Corticosteroid Therapy Based on Liver Biopsy for Severe Immune-Mediated Hepatitis During Pembrolizumab Treatment: A Case Report. [PDF]

Cureus
Esaki K, Horikoshi H, Awashima M, Nakayama S, Kichikawa Y.   +4 more
europepmc   +1 more source

Hereditary Spherocytosis due to an SPTA1 Nonsense Mutation Coinherited With α spectrin^LELY in Trans. [PDF]

Am J Hematol
Molina-Arrebola MA, Bain BJ.
europepmc   +1 more source

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

Front Pediatr
Qing X, Zhu J, Zhu X, Zhang Y, Deng J, Tang B.   +5 more
europepmc   +1 more source

Hereditary spherocytosis concomitant with JAK2V617F-positive primary myelofibrosis: a case report. [PDF]

Front Oncol
Qiu CE, Lei L, Jiang G, Huang X, Li Y.
europepmc   +1 more source

Genotype/phenotype correlation in hereditary spherocytosis

Haematologica, 2008
Achille Iolascon, Rosa Anna Avvisati
doaj   +1 more source

Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children. [PDF]

Front Pediatr
Duowen H, Xia G, Ju G.
europepmc   +1 more source

A flow cytometric assay of murine erythrocyte osmotic fragility. [PDF]

PLoS One
Zhang P, Zhang L, Chen S, Chen Y, Zhu X, Shen R, Lei Y.   +6 more
europepmc   +1 more source

Clinical course and pregnancy outcomes in women with hereditary spherocytosis: Insights from a case series. [PDF]

Obstet Med
Pegu B, Sivaranjani P, Subbaiah M, Murugesan A.   +3 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