Osteoarticular manifestations in sickle-cell disorders

scientific article published on December 1984

Osteoarticular manifestations in sickle-cell disorders is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1007/BF02031264
P698PubMed publication ID6396021

P2093author name stringP Kaklamanis
P2860cites workChronic synovitis with early cartilage destruction in sickle cell diseaseQ33551197
Sickle cell disease associated with uric acid deposition diseaseQ33552624
A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobinQ33969344
Fetal haemoglobin in homozygous sickle cell diseaseQ34054912
Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemiaQ34277661
Salmonella osteomyelitis in childhood. A report of 63 cases seen in Nigerian children of whom 57 had sickle cell anaemiaQ35114099
Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell diseaseQ37019479
Serum urate concentrations in homozygous sickle cell diseaseQ37087974
Pathology in 700-year-old Nigerian bones. Query: sickle-cell infarctsQ38586209
Haemoglobinopathies including thalassaemia. Part 3. Sickle cell anaemia in tropical AfricaQ39195656
Polyarthritis and positive LE preparation in sickle hemoglobinopathies: A report of two casesQ39573470
Radiographic changes of the skull in sickle cell anemiaQ39652798
Radiological changes in 127 patients with sickle cell anemiaQ39767885
Necrosis of the femoral head associated with sickle-cell anemia and its genetic variants. A review of the literature and study of thirteen cases.Q39977483
The critically ill child: sickle cell disease crises and their management.Q40002094
Bacterial infection and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literatureQ40004574
Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severityQ40107001
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjectsQ40108760
Comparative evaluation of fifteen anti-sickling agentsQ40146100
Gout and hyperuricemia associated with sickle-cell AnemiaQ40154591
The intracellular polymerization of sickle hemoglobin and its relevance to sickle cell diseaseQ40319551
Sternal cupping: a new finding in childhood sickle cell anemiaQ40338783
Sickle cell anemiaQ76143598
Unusual Bone Changes in Sickle-Cell Disease in ChildhoodQ76458843
Dactylitis and Growth DisordersQ76466510
Gout and blood dyscrasiasQ78666274
S-C hemoglobin: a clinical studyQ79063218
The bone changes in sickle cell anaemia and its genetic variantsQ79316084
Hemoglobin S-C diseaseQ79344494
The handfoot syndrome in sickle-cell disease in young childrenQ79706119
Roentgen findings in sickle-cell anemiaQ80632961
Haemoglobin SC diseaseQ87314857
Acute infarction of long bones in children with sickle cell anemiaQ40843005
The Natural History of Urate Overproduction in Sickle Cell AnemiaQ41537090
Calcaneal abnormalities and erosive bone disease associated with sickle cell anemiaQ41638087
Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severityQ41643285
Cerebrovascular disease in sickle cell anemia: a clinical, pathological and radiological correlationQ42441425
Acute long bone diaphyseal infarcts in sickle cell diseaseQ44089326
Sickle Cell Anemia and HyperuricemiaQ44703049
Hemoglobinopathic salmonella osteomyelitis. Orthopedic aspectsQ45018141
Ischemic necrosis of bone in sickle cell traitQ46281907
The treatment of severely ill patients with sickle cell anemia and associated septic arthritisQ46463643
Arthritis of sickle cell anemia.Q46674438
RADIOGRAPHIC MANIFESTATIONS OF SICKLE CELL ANEMIAQ46983400
Joint manifestations of sickle cell diseaseQ47861322
Avascular Necrosis and Erythrocytosis in Sickle-Cell TraitQ47892815
Bilateral pelvic osteomyelitis in children with sickle-cell anemia. Report of four cases.Q50213564
Orthopedic aspects of sickle cell anemia and allied hemoglobinopathiesQ50224477
Septic arthritis in sickle-cell thalassemia. Pathophysiology of impaired response to infectionQ50228959
Salmonella Paravertebral Abscess and Cervical Osteomyelitis in Sickle-Thalassemia DiseaseQ50240988
Deficiency of pneumococcal serum opsonizing activity in sickle-cell diseaseQ50246000
Salmonella osteitis in Nigerian childrenQ50279020
Arthritis during sickle-cell crisis.Q53745872
Arthropathy in sickle-cell disease.Q53950887
Pneumococcal and other infections in children with sickle cell-hemoglobin C (SC) diseaseQ57097709
Abnormal epiphyses in the sickling disordersQ66953204
The Hand-Foot Syndrome in Sickle Cell β-Thalassemia DiseaseQ67022752
The technetium phosphate bone scan in the diagnosis of osteomyelitis in childhoodQ67277534
Management of osteonecrosis in sickle-cell anemia and its genetic variantsQ67316541
Systemic lupus erythematosus and sickle-cell anaemiaQ67443131
Bone Marrow Scan Evaluation of Arthropathy in Sickle Cell DisordersQ67447571
Absence of increased frequency of bone and joint disease with hemoglobin AS and ACQ67545154
Prospective study of sickle cell anemia in infancyQ67758319
Sickle Cell Dactylitis: Histopathologic ObservationsQ69394840
The pathogenesis of hyperuricemia and gout in sickle cell anemiaQ69926141
An abnormality of the alternate pathway of complement activation in sickle-cell diseaseQ70034822
Deficiency of plasma prostacyclin or PGI2 regenerating ability in sickle cell anaemiaQ70174482
Bone marrow infarction in sickle cell anemia: correlation with hematologic profilesQ70507076
Uric acid excretion in sickle cell anemiaQ70568614
Serratia Osteomyelitis In Sickle Cell DiseaseQ70572278
Orbital infarction in sickle cell diseaseQ70773737
Sickle cell-thalassemia presenting as arthritis of the hipQ71463179
Hemarthrosis and sickle cell traitQ71630307
Exophthalmos in hemoglobin SC diseaseQ71728559
Hand-foot syndrome in sickle-cell thalassemiaQ71747089
Aseptic necrosis of the femoral heads in sickle-A hemoglobin diseaseQ72274704
Bone and joint lesions in sickle-cell diseaseQ72283042
Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell diseaseQ72656097
Long survival in sickle cell anemiaQ72675361
A re-evaluation of the "fish vertebra" sign in sickle cell hemoglobinopathyQ72821892
Aseptic necrosis of bone in Caucasians with chronic hemolytic anaemia due to combined sickling and thalassemia traitsQ73334221
Dental bone changes occurring in sickle-cell diseases and abnormal hemoglobin traitsQ73860497
P433issue4
P304page(s)419-434
P577publication date1984-12-01
P1433published inClinical RheumatologyQ15754927
P1476titleOsteoarticular manifestations in sickle-cell disorders
P478volume3

Search more.