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[PDF] Top 20 Primary Hyperparathyroidism Mimicking Vaso-occlusive Crises in Sickle Cell Disease

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Primary Hyperparathyroidism Mimicking Vaso-occlusive Crises in Sickle Cell Disease

Primary Hyperparathyroidism Mimicking Vaso-occlusive Crises in Sickle Cell Disease

... of primary hyperparathyroidism, may still reflect the natural evolution of sickle cell disease in this ...with primary hyperparathyroidism was successfully prevented in ... See full document

5

Hematological parameters in Ghanaian sickle cell disease patients

Hematological parameters in Ghanaian sickle cell disease patients

... in vaso-occlusive crises (VOC), and 34 HbSC patients in ...packed cell volume, red blood cell (RBC) concentration, mean corpuscular Hb, mean cell volume, mean corpuscular Hb ... See full document

7

Study of vaso occlusive (pain) crises in patients of sickle cell disease (SCD) – one year TMH experience

Study of vaso occlusive (pain) crises in patients of sickle cell disease (SCD) – one year TMH experience

... pain crises for female patients as against other studies which showed male ...Acute Sickle Cell Painful Episodes” in 2005, where the average length of stay for an acute painful episode, was ... See full document

8

The challenge of differentiating vaso-occlusive crises from osteomyelitis in children with sickle cell disease and bone pain: A 15-year retrospective review

The challenge of differentiating vaso-occlusive crises from osteomyelitis in children with sickle cell disease and bone pain: A 15-year retrospective review

... 22. Peltola H, Pääkkönen M, Kallio P, et al. Short- versus long-term antimicrobial treatment for acute hematogenous osteomyelitis of childhood: prospective, randomized trial on 131 culture-positive cases. Pediatr Infect ... See full document

8

Intravenous Magnesium Sulfate for Vaso-occlusive Episodes in Sickle Cell Disease

Intravenous Magnesium Sulfate for Vaso-occlusive Episodes in Sickle Cell Disease

... 25. Rogovik AL, Li Y, Kirby MA, Friedman JN, Goldman RD. Admission and length of stay due to painful vasoocclusive crisis in chil- dren. Am J Emerg Med. 2009;27(7):797 – 801 26. Panepinto JA, Brousseau DC, Hillery CA, ... See full document

10

Haemostatic Disorders in Sickle Cell Disease Subjects in Nigeria: A Review of Literature

Haemostatic Disorders in Sickle Cell Disease Subjects in Nigeria: A Review of Literature

... Chronic haemolysis with the release of plasma free haemoglobin results in scavenging of NO with consequent endothelial dysfunction, which may favour sickle cell adherence. It has also been found to play a ... See full document

7

Amelioration of Sickle Cell Pain after Parathyroidectomy in Two Patients with Concurrent Hyperparathyroidism: An Interesting Finding

Amelioration of Sickle Cell Pain after Parathyroidectomy in Two Patients with Concurrent Hyperparathyroidism: An Interesting Finding

... Sickle cell disease (SCD) is a genetic disorder which affects approximately 100,000 Americans ...This disease is char- acterized by production of an abnormal hemoglobin (Hb) molecule which ... See full document

7

Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode

Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode

... The primary study objective of feasibility and tolerability of QST following VOE was determined using the following measures: 1) recruitment into this phase of the study, defined by the proportion of patients ... See full document

9

Assessment of the direct cost associated with the management of major sickle cell syndromes in the pediatric department of the yalgado ouédraogo university hospital

Assessment of the direct cost associated with the management of major sickle cell syndromes in the pediatric department of the yalgado ouédraogo university hospital

... Vaso-occlusive crises (VOC) due to tissue ischemia are one of the most common acute manifestations of the disease and the leading cause of hospitalization (Girot, 2007; Fosdal, ...severe ... See full document

5

Knowledge, Attitudes and Practices of Parents in the Vaso Occlusive Crises of the Sick Children in Brazzaville

Knowledge, Attitudes and Practices of Parents in the Vaso Occlusive Crises of the Sick Children in Brazzaville

... of sickle cell disease. The means of preventing sickle-cell anemia cited by the parents were: the obligation of the pre- nuptial assessment 222 cases ... See full document

10

Cytokine profiles in sickle cell anemia: Pathways to be unraveled

Cytokine profiles in sickle cell anemia: Pathways to be unraveled

... 2013 Altered levels of pro-inflammatory cytokines in sickle cell disease patients during vaso-occlusive crises and the steady state condition.. European Cytokine Network.[r] ... See full document

7

Serum Biomarkers for Identifying Acute Chest Syndrome Among Patients Who Have Sickle Cell Disease and Present to the Emergency Department

Serum Biomarkers for Identifying Acute Chest Syndrome Among Patients Who Have Sickle Cell Disease and Present to the Emergency Department

... with sickle cell disease presenting to the pediatric ED with vaso-occlusive crises or fever in which we compared levels of secretory phospholipase A2 (sPLA2), endothe- lin-1, ... See full document

8

Low-dose methotrexate in sickle-cell disease: a pilot study with rationale borrowed from rheumatoid arthritis

Low-dose methotrexate in sickle-cell disease: a pilot study with rationale borrowed from rheumatoid arthritis

... SCD: sickle cell disease; MTX: methotrexate; VOC: vasoocclusive pain crises; QOL: quality of life; AVN: avascular osteonecrosis; ROS: reactive oxygen species; TLR4: toll‑like ... See full document

11

Study of Prognostic Factors of Death in Children with Sickle Cell Diseases Followed at the Albert Royer National Children's Hospital Center, Dakar, Senegal

Study of Prognostic Factors of Death in Children with Sickle Cell Diseases Followed at the Albert Royer National Children's Hospital Center, Dakar, Senegal

... On the other hand, some variables do not seem to provide explanatory power to the model in the presence of the other covariates: hydroxyurea intake, the existence of generalized infection in the last year of follow-up, ... See full document

11

Examining the validity and reliability of the Activities Specific Balance Confidence Scale 6 (ABC 6) in a diverse group of older adults

Examining the validity and reliability of the Activities Specific Balance Confidence Scale 6 (ABC 6) in a diverse group of older adults

... for sickle cell anemia (Walters et ...with vaso-occlusive pain, ...a disease with both psychosocial and physiological complications (Edwards et ... See full document

105

Prevention practices influencing frequency of occurrence of vaso-occlusive crisis among sickle cell patients in Abeokuta South Local Government Area of Ogun State, Nigeria

Prevention practices influencing frequency of occurrence of vaso-occlusive crisis among sickle cell patients in Abeokuta South Local Government Area of Ogun State, Nigeria

... of sickle cell crisis amongst the participants is similar to what has been reported in previous studies [17–19] which reveals that there is overall increase in frequency of vaso occlusive ... See full document

7

EXPRESSION THE CONCEPT OF PAIN IN PATIENTS WITH SICKLE CELL ANEMIA (A QUALITATIVE STUDY)

EXPRESSION THE CONCEPT OF PAIN IN PATIENTS WITH SICKLE CELL ANEMIA (A QUALITATIVE STUDY)

... Sickle Cell Anemia is a chronic disease which affects the quality of life 19 ...of crises is not necessarily related to vessels blockage, it can also appear as a result of venous necrosis in ... See full document

6

THE CRITICALLY ILL CHILD: SICKLE CELL DISEASE CRISES AND THEIR MANAGEMENT

THE CRITICALLY ILL CHILD: SICKLE CELL DISEASE CRISES AND THEIR MANAGEMENT

... XVI: Sudden death during sickle cell crises in young chil-. dren[r] ... See full document

9

Cholecystitis and Cholelithiasis Masking as Abdominal Crises in Sickle Cell Disease

Cholecystitis and Cholelithiasis Masking as Abdominal Crises in Sickle Cell Disease

... Some physicians and pediatricians believe that (1) cholelithiasis and cholecystitis are uncommon in sickle cell disease; (2) the complications of gallstones are not significant; (3) the [r] ... See full document

9

Lung vaso-occlusion in sickle cell disease mediated by arteriolar neutrophil-platelet microemboli

Lung vaso-occlusion in sickle cell disease mediated by arteriolar neutrophil-platelet microemboli

... pulmonary vaso-occlusion stems primarily from histological studies of lungs in SCD mice, which reveal the presence of blood cell aggregates in the lung micro-vessels following challenge with ... See full document

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