Results 91 to 100 of about 5,131 (194)

Poster Sessions

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Publication Only

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Additional file 1: of A de novo ANK1 mutation associated to hereditary spherocytosis: a case report

open access: yes, 2019
Timeline of this case. of a de novo ANK1 mutation associated to hereditary spherocytosis: a case report.
Yun-Bi Lin (6374768)   +10 more
core   +1 more source

Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert's syndrome

open access: yes, 2011
In this article the authors present a case of pathological neonatal jaundice resistant to phototherapy in a baby with a family history of Gilbert's syndrome and hereditary spherocytosis.
A. Q. T. Ismail   +5 more
core   +1 more source

Open heart surgery in presence of hereditary spherocytosis

open access: yes, 1995
A patient with ostium secundum atrial septal defect was operated upon despite having hereditary spherocytosis, without any hemolytic effects of cardiopulmonary bypass.

core  

Coexistence of Gilbert Syndrome and Hereditary Spherocytosis in a Child Presenting with Extreme Jaundice

open access: yes, 2014
Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is characterized by intermittent episodes of jaundice in the absence of hepatocellular disease or hemolysis.
이재희(조선대학교); 문경래(조선대학교)
core  

[Laparoscopic splenectomy in children with hereditary spherocytosis]

open access: yes, 2008
Based on the positive international experience with laparoscopic splenectomy on a large number of patients since 1991, we treated two teenagers with symptomatic hereditary spherocytosis and moderate splenomegaly. Both operations and postoperative courses
Jess, Per   +2 more
core  

Hereditary spherocytosis.

open access: yesKathmandu 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

Stuttering priapism associated with hereditary spherocytosis.

open access: yes, 2007
Stuttering priapism is a clinical phenomenon that occurs commonly in certain patient populations, including sickle cell anemia and other hematologic dyscrasias. Although the mechanism is still not completely understood, treatment is focused on prevention
Smaldone, Marc C   +3 more
core  

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