IDIOPATHIC PAROXYSMAL MYOGLOBINURIA is a rare syndrome consisting basically of the spontaneous onset of muscle pa in and swelling followed by myoglobinuria and frequently com-plicated by oliguria or anur ia due to myoglobin-induced renal damage. T h e muscles most fre-quent ly affected are the muscles of the calf and the thigh, b u t abdominal, thoracic, cervical, masseter, and u p p e r extremity muscle groups have also been involved. Associated symptoms in some cases include fever, chills, abdominal pain, diarrhea, vomiting, and pseudoparalysis of the affected muscle groups. Almost all of the repor ted cases have shown some degree of renal involvement, varying from albuminur ia, cylin-druria, and oliguria to the passage of red cell casts,...
To evaluate the proportion of cases of myoglobinuria that can be ascribed to specific metabolic defe...
A case of serologically documented influenza A infection associated with myoglobinuria is described....
Background. Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disease of the blood system, ...
-•- pathic or paralytic myoglobinuria and re-current rhabdomyolysis, is a rare disease, 56 cases hav...
THE occurrence of myoglobin in the urine has been well-established in various con-ditions. These inc...
Os autores registram um caso de mioglobinúria confirmada pela eletroforese de proteínas da urina. A ...
MUSCLE PARESIS OR PARALYSIS is infrequently associated with hyperkalemia (1-3). Th i s relat ionship...
A case of myoglobinuria with acute renal failure in a 29-year-old male is presented. The attack foll...
Idiopathic paroxysmal rhabdomyolysis indicating a classical triad of symptoms consisting of muscle p...
Rhabdomyolysis is the breakdown of striated muscle cells resulting in leakage of cell matter into th...
Myoglobinuria is a frequent complication of metabolic myopathies and may also occur in Duchenne and ...
MYOGLOBINURIA has been considered to be a relatively rare disease and has been observed only in the ...
Three new cases of carnitine palmityl transferase deficiency are described. The syndrome consists of...
McArdle’s disease (Glycogen storage disease type V) is a rare inherited autosomal recessive disease ...
Rhabdomyolysis, a term used to describe the rapid breakdown of striated muscle, is characterized by ...
To evaluate the proportion of cases of myoglobinuria that can be ascribed to specific metabolic defe...
A case of serologically documented influenza A infection associated with myoglobinuria is described....
Background. Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disease of the blood system, ...
-•- pathic or paralytic myoglobinuria and re-current rhabdomyolysis, is a rare disease, 56 cases hav...
THE occurrence of myoglobin in the urine has been well-established in various con-ditions. These inc...
Os autores registram um caso de mioglobinúria confirmada pela eletroforese de proteínas da urina. A ...
MUSCLE PARESIS OR PARALYSIS is infrequently associated with hyperkalemia (1-3). Th i s relat ionship...
A case of myoglobinuria with acute renal failure in a 29-year-old male is presented. The attack foll...
Idiopathic paroxysmal rhabdomyolysis indicating a classical triad of symptoms consisting of muscle p...
Rhabdomyolysis is the breakdown of striated muscle cells resulting in leakage of cell matter into th...
Myoglobinuria is a frequent complication of metabolic myopathies and may also occur in Duchenne and ...
MYOGLOBINURIA has been considered to be a relatively rare disease and has been observed only in the ...
Three new cases of carnitine palmityl transferase deficiency are described. The syndrome consists of...
McArdle’s disease (Glycogen storage disease type V) is a rare inherited autosomal recessive disease ...
Rhabdomyolysis, a term used to describe the rapid breakdown of striated muscle, is characterized by ...
To evaluate the proportion of cases of myoglobinuria that can be ascribed to specific metabolic defe...
A case of serologically documented influenza A infection associated with myoglobinuria is described....
Background. Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disease of the blood system, ...