Results 81 to 90 of about 7,739 (202)

Сlinical case of hemolytic anemia combined with secondary chronic pyelonephritis and intracellular infection in a 7-year-old child

Zdorovʹe Rebenka, 2017
Hemolytic anemias are group of diseases that are characterized by decreased lifetime of erythrocytes due to their accelerated destruction caused by membrane and enzymopathies of red blood cells, defects in globin synthesis or external factors such as ...
I.G. Samoylenko, V.V. Dolinsky, M.V. Karpovich, E.N. Pavlov, E.V. Tkachenko   +4 more
doaj   +1 more source

Pitting of malaria parasites and spherocyte formation [PDF]

, 2006
Background A high prevalence of spherocytes was detected in blood smears of children enrolled in a case control study conducted in the malaria holoendemic Lake Victoria basin.
Gichuki Charity W, Schrier Stanley L, Anyona Samuel B, Waitumbi John N   +3 more
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A Case of Hereditary Spherocytosis Initially Manifested as an Aplastic Crisis Caused by Parvovirus B19 Infection

Clinical Pediatric Hematology-Oncology, 2020
Hereditary spherocytosis (HS) is the most common inherited red cell membrane disorder. Its main laboratory finding is anemia with reticulocytosis. However, in the case of an aplastic crisis, there may be no reticulocytosis, making the diagnosis of HS ...
Hyungsuk Jin, Ji Won Lee, Hee Young Ju, Hee Won Cho, Ju Kyung Hyun, Ki Woong Sung, Hong Hoe Koo, Hee-Jin Kim, Keon Hee Yoo   +8 more
doaj   +1 more source

Numerical Model for the Determination of Erythrocyte Mechanical Properties and Wall Shear Stress in vivo From Intravital Microscopy. [PDF]

, 2019
The mechanical properties and deformability of Red Blood Cells (RBCs) are important determinants of blood rheology and microvascular hemodynamics. The objective of this study is to quantify the mechanical properties and wall shear stress experienced by ...
Cabrales, Pedro, Jani, Vinay P, Jani, Vivek P, Lucas, Alfredo, Munoz, Carlos, Ortiz, Daniel, Williams, Alexander T, Yalcin, Ozlem   +7 more
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Human parvovirus infection and aplastic crisis in hereditary spherocytosis

Current Medicine Research and Practice, 2011
Parvovirus B19 is usually associated with an acute, self-limiting disease. In patients with congenital haemolytic anaemia, infection with this virus can cause an aplastic crisis.
A Gogia, A Kakar, S P Byotra, U Parakh, M Bhargava   +4 more
doaj  

Laparoscopic splenectomy experience in the University Hospital ‘‘Dr. José Eleuterio González’’ [PDF]

, 2015
To present the laparoscopic splenectomy (LS) experience at the ‘‘Dr. José E. González’’ University Hospital from January 2008 to October 2014. Methods: Retrospective and descriptive analysis of clinical and surgical aspects of all patients who underwent ...
Akwari, Balague, Castillo, Cusick, Delaitre, Franklin, Habermalz, Martínez Ferro, Owera, Pace, Patel, Pekolj, Reddy, Rosen, Targarona, Trias, Velanovich   +16 more
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Risk of hereditary spherocytosis misdiagnosis due to limited effective diagnostic methods

Revista Cubana de Medicina Militar
Introduction: Hereditary spherocytosis is a prevalent congenital hemolytic erythrocyte membranopathy. Laboratory diagnosis is traditionally based on erythrocyte morphology, yet 20% of cases may lack visible spherocytes, leading to misdiagnosis.
Hien Thanh Dao, Triet Hy Van, Tuyet Thi Bach Tran, Dat Quoc Ngo, Anh Thi Mai Nguyen   +4 more
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Simultaneous gallbladder-preserving cholecystolithotomy and laparoscopic splenectomy as a surgical option for hereditary spherocytosis in a child: A case report

Journal of Pediatric Surgery Case Reports, 2017
For hereditary spherocytosis complicated by cholelithiasis, cholecystectomy is simultaneously performed with splenectomy. However, jaundice promptly disappears after removing the spleen, and the risk for recurrent cholelithiasis decreases in majority of ...
Yutaka Yamada, Akinori Sekioka, Akiyoshi Nomura, Kei Oyama, Toshiaki Takahashi, Masaya Yamoto, Koji Fukumoto, Naoto Urushihara   +7 more
doaj   +1 more source

Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3 [PDF]

, 2000
Absence of band 3, associated with the mutation Coimbra (V488M) in the homozygous state, caused severe hereditary spherocytosis in a young child. Although prenatal testing was made available to the parents, it was declined.
Alliosio, N, Almeida, H, Bey-Cabet, F, Delaunay, J, Gomes, C, Lemos, C, Mimoso, G, Morlé, L, Ribeiro, ML, Rudigoz, RC, Tamagnini, G, Texier, P   +11 more
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Esplenectomias não traumáticas em adultos e crianças: um estudo comparativo. [PDF]

, 2002
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis ...
Bez, Carolina Moreira
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