Results 111 to 120 of about 28,210 (227)

Inherited hemolytic disorders with high occurrence of b-thalassemia in Sindhi community of Jabalpur town in Madhya Pradesh, India [PDF]

, 2010
Hereditary hemolytic disorders such as hemoglobin disorders, β-thalassemia syndrome, G6PD deficiency, and ABO and Rhesus blood groups are the most common public health problems in India.
Balgir, RS
core   +1 more source

Sickled erythrocytes in urine as a clue to the diagnosis of sickle cell trait

Saudi Journal of Kidney Diseases and Transplantation, 2017
Sickled erythrocytes in patients of sickle cell trait with microscopic hematuria have rarely been reported so far. A 30-year-old female underwent delivery of a healthy full-term baby by cesarean section. However, postcesarean, she had pain in abdomen and
Shanu Srivastava, Rashmi Srivastava, K G Ghorpade   +2 more
doaj  

Spartan Daily, February 21, 1989 [PDF]

, 1989
Volume 92, Issue 18https://scholarworks.sjsu.edu/spartandaily/7808/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core   +1 more source

Serum Lactate Dehydrogenase in Children with Sickle cell disease.

Nigerian Journal of Paediatrics
Summary: Measurement of scrum LDH is frequently employed diagnostically in disease states associated with tissue destructions of various types. Since children with sickle cell disease suffer from chronic red cell destruction and associated necrosis of ...
Adebonojo Festus O.
doaj  

Differential sensitivity to hypoxia enables shape‐based classification of sickle cell disease and trait blood samples at point of care

Bioengineering & Translational Medicine
Red blood cells (RBCs) become sickle‐shaped and stiff under hypoxia as a consequence of hemoglobin (Hb) polymerization in sickle cell anemia. Distinguishing between sickle cell disease and trait is crucial during the diagnosis of sickle cell disease ...
Claudy D'Costa, Oshin Sharma, Riddha Manna, Minakshi Singh, Samrat Singh, Srushti Singh, Anish Mahto, Pratiksha Govil, Sampath Satti, Ninad Mehendale, Yazdi Italia, Debjani Paul   +11 more
doaj   +1 more source

Prevalence Of Common Hemoglobinopathies in Gujarat: An Analysis of a Large Population Screening Program

National Journal of Community Medicine, 2012
Objectives: To determine prevalence and geographical distribution of ß-thalassemia trait and sickle cell trait in Gujarat Methods: The present study includes 3, 17,539 persons who were screened for hemoglobinopathies from September 2004 to November ...
Ashwin P Patel , Madhuben R Naik , Nilam M Shah , Narmadeshwar P Sharma , Prakash H Parmar   +4 more
doaj  

Sickle-cell disease: a call to action [PDF]

, 2015
Piel, FB, Weatherall, DJ
core   +1 more source

A Case of Sickle Cell Trait Presenting With Stroke. [PDF]

Cureus
Thanigasalan M.
europepmc   +1 more source

Sickle Cell Trait: Is It Always Benign? [PDF]

J Hematol, 2023
Brown TS, Lakra R, Master S, Ramadas P.
europepmc   +1 more source

When sickle cell trait is not just trait: risk of VTE. [PDF]

Hematology Am Soc Hematol Educ Program
Naik RP, Pawlinski R, Key NS.
europepmc   +1 more source