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Translocation Renal Cell Carcinoma t(6;11)(p21;q12) and Sickle Cell Anemia: First Report and Review of the Literature

Chaste D, Vian E, Verhoest G, Blanchet P

Translocation renal cell carcinoma (RCC) is a family of rare tumors recently identified in the pediatric and young adult population. We report the first case of a young woman from...
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Salmonella Typhi Osteomyelitis in a Non-sickle Cell Patient: Three Cases Report

Shin KH, Youn KH, Jahng JS

Salmonella osteomyelitis is uncommon and it often develops in patients with sickle cell anemia and other hemoglobinopathy. Especially, osteomyelitis caused Salmonella typhi in a nonsickle cell patients is a very...
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A Case of Sickle Cell Anemia with a Lack of High Frequency Red Blood Cell Antigen

Lee HJ, Shin KH, Kim H, Jeong S, Kong SG, Kim HH

Patients with sickle cell anemia are chronically transfused. Therefore, it is important to prevent the alloimmunization of RBC antigens. The authors identified a high frequency antigen-negative blood group in patients...
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Genotypic influence of alpha-deletions on the phenotype of Indian sickle cell anemia patients

Pandey S, Pandey S, Mishra RM, Sharma M, Saxena R

BACKGROUND: Some reports have shown that co-inheritance of alpha-thalassemia and sickle cell disease improves hematological parameters and results in a relatively mild clinical picture for patients; however, the exact molecular...
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Epidural anesthesia for laparoscopic cholecystectomy in a patient with sickle cell anemia, beta thalassemia, and Crohn's disease: A case report

Bas SS, Ozlu O

A 37-year-old woman diagnosed with sickle cell anemia (SCA), beta (+) thalassemia, Crohn's disease, and liver dysfunction was scheduled for laparoscopic cholecystectomy (LC) due to acute cholecystitis with gall bladder....
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Effective sickle hemoglobin reduction by automated red cell exchange using Spectra Optia in three Emirati patients with sickle cell disease before allogeneic hematopoietic stem cell transplantation

Choi SJ, Cho H, Eom KS, Lee JW, Kim Y, Lim J

No abstract available.
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BCL11A rs1427407 Genotypes in Sickle Cell Anemia Patients Undergo to Stroke Problems in Sudan

Hassan FM, Al-zahrani FM

BACKGROUND: Sickle cell disease is an autosomal recessive condition that results from the presence of a mutated form of hemoglobin. Some genetic variants of BCL11A are amenable to therapeutic manipulation....
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Treatment and Management of Late Complications in Hereditary Hemolytic Anemia

Chueh HW

Hereditary hemolytic anemia is a very heterogeneous disorder in which abnormalities of red blood cell structural protein, globin protein, or enzyme defect lead to shortened life span. There has been...
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Precision of SPECT/CTAllows the Diagnosis of a Hidden Brodie's Abscess of the Talus in a Patient with Sickle Cell Disease

Al-Jafar H, Al-Shemmeri E, Al-Shemmeri J, Aytglu L, Afzal U, Al-Enizi S

Brodie's abscess is a rare subacute osteomyelitis that can be found in sickle cell disease along with other bone complications. A 21-year-old female with sickle cell disease was presenting frequently...
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Chlorpromazine-Induced Priapism

An JH, Yoo SJ, Choi S, Kim JC, Rhew HY

  • KMID: 1851759
  • J Korean Androl Soc.
  • 1994 Dec;12(2):155-159.
Priapism may be primary(idiopathic) or secondary to sickle cell anemia, trauma, leukemia, drugs, venous thromboembolic disease, and other less common disorders. It has become more common with the development...
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Recurrent Priapism Associated with Splenectomy

Lee HI, Kim DG, Seo YJ, Ha DB, Lee KS

  • KMID: 2292665
  • Korean J Urol.
  • 2002 Aug;43(8):720-722.
Priapism is a prolonged erection of the corpus cavernosum that is unaccompanied by sexual desire. It has been classified into 2 main groups: primary (idiopathic) or secondary. The common conditions...
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Segmental Testicular Infarction Masquerading as Testicular Neoplasm

Nam JS, Kim DS, Lee ST, Lee YG, Cho ST, Kim KK

  • KMID: 2293838
  • Korean J Urol.
  • 2005 Nov;46(11):1228-1230.
Segmental testicular infarction is an uncommon and usually idiopathic phenomenon. Some case reports have linked segmental infarction to sickle cell anemia, hypersensitivity angiitis, polycythemia, and an idiopathic cause. Magnetic resonance...
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Segmental Testicular Infarction: Radiologic Diagnosis and Conservative Management

Jung SG, Park SW, Park HJ, Kim S, Lee SD

  • KMID: 2311992
  • Korean J Urol.
  • 2008 Jun;49(6):574-578.
Segmental testicular infarction is a rare cause of an acute scrotum. The etiology can be related to sickle cell anemia, hypersensitivity angiitis and polycythemia in some cases, but the condition...
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A case of back pain caused by Salmonella spondylitis: A case report

Choi YS, Cho WJ, Yun SH, Lee SY, Park SH, Park JC, Jang EH, Shin HY

Salmonella spondylitis is a rare illness, and it generally occurs in patients who have already had sickle cell anemia, and it is even rarer in patients who are without sickle...
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MicroRNAs in Human Diseases: From Lung, Liver and Kidney Diseases to Infectious Disease, Sickle Cell Disease and Endometrium Disease

Ha TY

MicroRNAs (miRNAs) are a class of naturally occurring small non-coding RNAs of about 22 nucleotides that have recently emerged as important regulators of gene expression at the posttranscriptional level. Recent...
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A Case Report of Priapism

Kim JK, Kim JS

  • KMID: 1911349
  • Korean J Urol.
  • 1981 Aug;22(4):489-492.
Priapism is the condition of persistent penile erection, most often accompanied by pain and unaccompanied by sexual desire. The most common form is idiopathic priapism in the adult but sickle...
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Red Blood Cell Alloimmunization in Pediatric Sickle Cell Disease Population of Puerto Rico: An Observational Study

Balbuena-Merle RI, Nazario-Delgado CM, Rosario-Rosado RV, Millán-Tapia D, Climent-Peris C

No abstract available.
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Biochemical effects and safety of Gum arabic (Acacia Senegal) supplementation in patients with sickle cell anemia

Kaddam LA, Fdl-Elmula I, Eisawi OA, Abdelrazig HA, Elnimeiri , Saeed AM

BACKGROUND: Sickle cell anemia (SCA) is a hereditary chronic hemolytic anemia with several clinical consequences. Intravascular sickling of red blood cells leads to multi-organ dysfunction. Moreover, several biochemical abnormalities have...
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A Case of Splenic Infarction and Rupture in Chronic Pancreatitis with Pseudocyst

Cho YG, Lim YC, Han BH, Kim CK, Lim HS, Sim YW, Song GY

  • KMID: 2085012
  • Korean J Gastroenterol.
  • 2001 Dec;38(6):457-460.
Splenic infarction is not common disease which is caused by occlusion of the main splenic artery or any of its branches. It is mainly caused by emboli that arise from...
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Salmonella Spondylitis Concomitant Infected Aortic Aneurysm: A Case Report

Ha KY, Kim YH, Lee JS

  • KMID: 2105981
  • J Korean Orthop Assoc.
  • 2003 Apr;38(2):209-212.
With increasing number of the elderly persons, the incidence of aortic aneurysm is increasing too. Infected aneurysm is considered as a lesion of the arterial wall due to bacterial contamination,...
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