Results 191 to 200 of about 75,157 (240)
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Pediatrics in Review, 2015
On the basis of observational studies, the most common cause of nephrotic syndrome in school-aged children is minimal change disease. On the basis of research evidence and consensus, corticosteroids are considered first-line therapy for treatment of nephrotic syndrome.
Tecile Prince, Andolino +1 more
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On the basis of observational studies, the most common cause of nephrotic syndrome in school-aged children is minimal change disease. On the basis of research evidence and consensus, corticosteroids are considered first-line therapy for treatment of nephrotic syndrome.
Tecile Prince, Andolino +1 more
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Pediatric Clinics of North America, 2019
Nephrotic syndrome is characterized by edema, proteinuria, hypoalbuminemia, and hyperlipidemia. Minimal change disease, the most common cause in childhood, generally responds to corticosteroids, although most patients experience disease relapses. Focal segmental glomerulosclerosis is usually resistant to corticosteroids and carries a significant risk ...
Chia-Shi, Wang, Larry A, Greenbaum
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Nephrotic syndrome is characterized by edema, proteinuria, hypoalbuminemia, and hyperlipidemia. Minimal change disease, the most common cause in childhood, generally responds to corticosteroids, although most patients experience disease relapses. Focal segmental glomerulosclerosis is usually resistant to corticosteroids and carries a significant risk ...
Chia-Shi, Wang, Larry A, Greenbaum
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Primary Care: Clinics in Office Practice, 1979
The nephrotic syndrome appears to be an expression of a number of complex disease processes. The supportive, as well as the definitive, management of the nephrotic syndrome patient requires considerable knowledge of disease pathophysiology, drugs, and drug interactions. Therapy of any degree cannot be undertaken lightly for fear of further compromising
D, Nagar, R L, Wathen
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The nephrotic syndrome appears to be an expression of a number of complex disease processes. The supportive, as well as the definitive, management of the nephrotic syndrome patient requires considerable knowledge of disease pathophysiology, drugs, and drug interactions. Therapy of any degree cannot be undertaken lightly for fear of further compromising
D, Nagar, R L, Wathen
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The American Journal of Medicine, 1974
Abstract Systematic pedigree information was obtained from 70 patients with idiopathic nephrotic syndrome; 16 patients were found to have familial nephrotic syndrome including 1 pair of affected monozygotic twins, 5 affected sibling pairs, 2 affected first cousins from a consanguineous family and 2 patients with sporadic cases from consanguineous ...
P I, Bader +3 more
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Abstract Systematic pedigree information was obtained from 70 patients with idiopathic nephrotic syndrome; 16 patients were found to have familial nephrotic syndrome including 1 pair of affected monozygotic twins, 5 affected sibling pairs, 2 affected first cousins from a consanguineous family and 2 patients with sporadic cases from consanguineous ...
P I, Bader +3 more
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Pediatric Nephrology, 2001
A female infant born at 34 weeks' gestation after several days of ruptured membranes had a Potter-like face and compression-induced limb posture consistent with oligohydramnios. Oedema developed on day 2; initial investigations showed massive proteinuria, hypoalbuminaemia, hyponatraemia, acidosis and marked renal insufficiency. The infant was intubated
A, Koziell +4 more
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A female infant born at 34 weeks' gestation after several days of ruptured membranes had a Potter-like face and compression-induced limb posture consistent with oligohydramnios. Oedema developed on day 2; initial investigations showed massive proteinuria, hypoalbuminaemia, hyponatraemia, acidosis and marked renal insufficiency. The infant was intubated
A, Koziell +4 more
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Journal of Perinatology, 2021
Congenital nephrotic syndrome (CNS), a challenging form of nephrotic syndrome, is characterized by massive proteinuria, hypoalbuminemia, and edema. Extensive leakage of plasma proteins is the main feature of CNS. Patients can be diagnosed in utero or during the first few weeks of life, usually before three months.
Asmaa S. AbuMaziad +2 more
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Congenital nephrotic syndrome (CNS), a challenging form of nephrotic syndrome, is characterized by massive proteinuria, hypoalbuminemia, and edema. Extensive leakage of plasma proteins is the main feature of CNS. Patients can be diagnosed in utero or during the first few weeks of life, usually before three months.
Asmaa S. AbuMaziad +2 more
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Archives of Internal Medicine, 1964
Patients have been observed who have had one or more recurrences of the nephrotic syndrome after long periods of complete freedom from the disease. 1,2 Such recurrences are an occasional manifestation of lipoid nephrosis (also known as pure, true, membranous, idiopathic, Ellis type 2) and ordinarily do not occur in nephrotic syndrome of other cause ...
M A, SHEARN, W H, TU, C F, PIEL
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Patients have been observed who have had one or more recurrences of the nephrotic syndrome after long periods of complete freedom from the disease. 1,2 Such recurrences are an occasional manifestation of lipoid nephrosis (also known as pure, true, membranous, idiopathic, Ellis type 2) and ordinarily do not occur in nephrotic syndrome of other cause ...
M A, SHEARN, W H, TU, C F, PIEL
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New England Journal of Medicine, 1998
The nephrotic syndrome is defined by a urinary protein level exceeding 3.5 g per 1.73 m2 of body-surface area per day. At the turn of the century, clinicians distinguished a nephritic syndrome of inflammatory origin and a nephrotic syndrome of presumed degenerative origin.
S R, Orth, E, Ritz
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The nephrotic syndrome is defined by a urinary protein level exceeding 3.5 g per 1.73 m2 of body-surface area per day. At the turn of the century, clinicians distinguished a nephritic syndrome of inflammatory origin and a nephrotic syndrome of presumed degenerative origin.
S R, Orth, E, Ritz
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Congenital nephrotic syndromes
Current Opinion in Genetics & Development, 2001Many acquired and familial renal diseases in man lead to kidney dysfunction and nephrotic syndrome. These diseases share a common pathological fate in the form of glomerular dysfunction and proteinuria. Classification of the disease is difficult because the onset of pathological appearance in congenital nephrotic syndrome (CNS) varies considerably ...
J, Khoshnoodi, K, Tryggvason
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Clinics in Perinatology, 1981
Children with congenital nephrotic syndrome have a clinical course that differs markedly from and is less favorable than that for the idiopathic nephrotic syndrome of childhood. Pathologic findings, pathogenesis, and management are detailed.
J R, Hoyer, C E, Anderson
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Children with congenital nephrotic syndrome have a clinical course that differs markedly from and is less favorable than that for the idiopathic nephrotic syndrome of childhood. Pathologic findings, pathogenesis, and management are detailed.
J R, Hoyer, C E, Anderson
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