review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1007/BF02031264 |
P698 | PubMed publication ID | 6396021 |
P2093 | author name string | P Kaklamanis | |
P2860 | cites work | Chronic synovitis with early cartilage destruction in sickle cell disease | Q33551197 |
Sickle cell disease associated with uric acid deposition disease | Q33552624 | ||
A specific chemical difference between the globins of normal human and sickle-cell anaemia haemoglobin | Q33969344 | ||
Fetal haemoglobin in homozygous sickle cell disease | Q34054912 | ||
Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia | Q34277661 | ||
Salmonella osteomyelitis in childhood. A report of 63 cases seen in Nigerian children of whom 57 had sickle cell anaemia | Q35114099 | ||
Abnormal adherence of sickle erythrocytes to cultured vascular endothelium: possible mechanism for microvascular occlusion in sickle cell disease | Q37019479 | ||
Serum urate concentrations in homozygous sickle cell disease | Q37087974 | ||
Pathology in 700-year-old Nigerian bones. Query: sickle-cell infarcts | Q38586209 | ||
Haemoglobinopathies including thalassaemia. Part 3. Sickle cell anaemia in tropical Africa | Q39195656 | ||
Polyarthritis and positive LE preparation in sickle hemoglobinopathies: A report of two cases | Q39573470 | ||
Radiographic changes of the skull in sickle cell anemia | Q39652798 | ||
Radiological changes in 127 patients with sickle cell anemia | Q39767885 | ||
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 literature | Q40004574 | ||
Clinical diversity of sickle cell anemia: genetic and cellular modulation of disease severity | Q40107001 | ||
Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects | Q40108760 | ||
Comparative evaluation of fifteen anti-sickling agents | Q40146100 | ||
Gout and hyperuricemia associated with sickle-cell Anemia | Q40154591 | ||
The intracellular polymerization of sickle hemoglobin and its relevance to sickle cell disease | Q40319551 | ||
Sternal cupping: a new finding in childhood sickle cell anemia | Q40338783 | ||
Sickle cell anemia | Q76143598 | ||
Unusual Bone Changes in Sickle-Cell Disease in Childhood | Q76458843 | ||
Dactylitis and Growth Disorders | Q76466510 | ||
Gout and blood dyscrasias | Q78666274 | ||
S-C hemoglobin: a clinical study | Q79063218 | ||
The bone changes in sickle cell anaemia and its genetic variants | Q79316084 | ||
Hemoglobin S-C disease | Q79344494 | ||
The handfoot syndrome in sickle-cell disease in young children | Q79706119 | ||
Roentgen findings in sickle-cell anemia | Q80632961 | ||
Haemoglobin SC disease | Q87314857 | ||
Acute infarction of long bones in children with sickle cell anemia | Q40843005 | ||
The Natural History of Urate Overproduction in Sickle Cell Anemia | Q41537090 | ||
Calcaneal abnormalities and erosive bone disease associated with sickle cell anemia | Q41638087 | ||
Erythrocyte adherence to endothelium in sickle-cell anemia. A possible determinant of disease severity | Q41643285 | ||
Cerebrovascular disease in sickle cell anemia: a clinical, pathological and radiological correlation | Q42441425 | ||
Acute long bone diaphyseal infarcts in sickle cell disease | Q44089326 | ||
Sickle Cell Anemia and Hyperuricemia | Q44703049 | ||
Hemoglobinopathic salmonella osteomyelitis. Orthopedic aspects | Q45018141 | ||
Ischemic necrosis of bone in sickle cell trait | Q46281907 | ||
The treatment of severely ill patients with sickle cell anemia and associated septic arthritis | Q46463643 | ||
Arthritis of sickle cell anemia. | Q46674438 | ||
RADIOGRAPHIC MANIFESTATIONS OF SICKLE CELL ANEMIA | Q46983400 | ||
Joint manifestations of sickle cell disease | Q47861322 | ||
Avascular Necrosis and Erythrocytosis in Sickle-Cell Trait | Q47892815 | ||
Bilateral pelvic osteomyelitis in children with sickle-cell anemia. Report of four cases. | Q50213564 | ||
Orthopedic aspects of sickle cell anemia and allied hemoglobinopathies | Q50224477 | ||
Septic arthritis in sickle-cell thalassemia. Pathophysiology of impaired response to infection | Q50228959 | ||
Salmonella Paravertebral Abscess and Cervical Osteomyelitis in Sickle-Thalassemia Disease | Q50240988 | ||
Deficiency of pneumococcal serum opsonizing activity in sickle-cell disease | Q50246000 | ||
Salmonella osteitis in Nigerian children | Q50279020 | ||
Arthritis during sickle-cell crisis. | Q53745872 | ||
Arthropathy in sickle-cell disease. | Q53950887 | ||
Pneumococcal and other infections in children with sickle cell-hemoglobin C (SC) disease | Q57097709 | ||
Abnormal epiphyses in the sickling disorders | Q66953204 | ||
The Hand-Foot Syndrome in Sickle Cell β-Thalassemia Disease | Q67022752 | ||
The technetium phosphate bone scan in the diagnosis of osteomyelitis in childhood | Q67277534 | ||
Management of osteonecrosis in sickle-cell anemia and its genetic variants | Q67316541 | ||
Systemic lupus erythematosus and sickle-cell anaemia | Q67443131 | ||
Bone Marrow Scan Evaluation of Arthropathy in Sickle Cell Disorders | Q67447571 | ||
Absence of increased frequency of bone and joint disease with hemoglobin AS and AC | Q67545154 | ||
Prospective study of sickle cell anemia in infancy | Q67758319 | ||
Sickle Cell Dactylitis: Histopathologic Observations | Q69394840 | ||
The pathogenesis of hyperuricemia and gout in sickle cell anemia | Q69926141 | ||
An abnormality of the alternate pathway of complement activation in sickle-cell disease | Q70034822 | ||
Deficiency of plasma prostacyclin or PGI2 regenerating ability in sickle cell anaemia | Q70174482 | ||
Bone marrow infarction in sickle cell anemia: correlation with hematologic profiles | Q70507076 | ||
Uric acid excretion in sickle cell anemia | Q70568614 | ||
Serratia Osteomyelitis In Sickle Cell Disease | Q70572278 | ||
Orbital infarction in sickle cell disease | Q70773737 | ||
Sickle cell-thalassemia presenting as arthritis of the hip | Q71463179 | ||
Hemarthrosis and sickle cell trait | Q71630307 | ||
Exophthalmos in hemoglobin SC disease | Q71728559 | ||
Hand-foot syndrome in sickle-cell thalassemia | Q71747089 | ||
Aseptic necrosis of the femoral heads in sickle-A hemoglobin disease | Q72274704 | ||
Bone and joint lesions in sickle-cell disease | Q72283042 | ||
Haematological factors associated with avascular necrosis of the femoral head in homozygous sickle cell disease | Q72656097 | ||
Long survival in sickle cell anemia | Q72675361 | ||
A re-evaluation of the "fish vertebra" sign in sickle cell hemoglobinopathy | Q72821892 | ||
Aseptic necrosis of bone in Caucasians with chronic hemolytic anaemia due to combined sickling and thalassemia traits | Q73334221 | ||
Dental bone changes occurring in sickle-cell diseases and abnormal hemoglobin traits | Q73860497 | ||
P433 | issue | 4 | |
P304 | page(s) | 419-434 | |
P577 | publication date | 1984-12-01 | |
P1433 | published in | Clinical Rheumatology | Q15754927 |
P1476 | title | Osteoarticular manifestations in sickle-cell disorders | |
P478 | volume | 3 |
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