Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Edward B. Blau"'
Autor:
Lysette Mutkus, Gina Bonavita, Edward B. Blau, Ulrike A. Mau, Gabriel Núñez, Naohiro Inohara, Gerard Tromp, Charlene J. Williams, Helena Kuivaniemi, Xiaoju Wang
Publikováno v:
Arthritis & Rheumatism. 46:3041-3045
Objective To analyze the CARD15 gene in families with heritable multi-organ granulomatoses, including the original Blau syndrome kindred as well as other families with related granulomatous conditions. Methods Linkage mapping was performed in 10 fami
Publikováno v:
American journal of diseases of children (1960). 147(8)
• Objective. —To determine whether HLA and autoimmunity contribute to the pathogenesis of Blau syndrome (familial granulomatous arthritis, uveitis, and rash) and evaluate whether this condition is related to sarcoidosis. Design. —Large family s
Autor:
Edward B. Blau, Teresa Silberman
Publikováno v:
The American journal of pediatric hematology/oncology. 14(3)
Hyponatremia and malignant hypertension are rare manifestations of Wilms' tumor. Hyponatremia associated with malignant hypertension of any cause is not explained. We present a patient with hyponatremia, malignant hypertension, Wilms' tumor, and an e
Autor:
Edward B. Blau
Publikováno v:
The Journal of Pediatrics. 133:322-323
Autor:
Edward B. Blau, Jody R. Gross
Publikováno v:
Pediatric Nephrology. 11:361-362
A woman with a renal transplant developed a systemic cytomegalovirus infection. She recovered and 3 years later she became pregnant. She had 3 days of fever in the first trimester. She delivered an infant severely affected with congenital cytomegalov
Autor:
Edward B. Blau
Publikováno v:
The Journal of Pediatrics. 107:689-693
Eleven family members over four generations have had granulomatous disease of the skin, eyes, and joints. Ten have had arthritis; two had skin, eye, and joint involvement; one had skin and joint disease, and one had iritis only. The disease is transm
Publikováno v:
Pediatrics. 60:227-234
Polyarteritis in the older child is thought to be a rare disease. This study describes 11 children, 3 to 12 years of age, with polyarteritis seen over a five-year period. Fever, abdominal pain, hypertension, and leukocytosis were found in almost all.
Publikováno v:
American Journal of Medical Genetics. 26:729-732
Publikováno v:
Pediatrics. 67:862-870
Clinical and pathologic data of 13 children, aged 5 to 16 years, with acute interstitial nephritis (AIN) are presented. The cause of AIN in these children was assessed as being related to infection in ten and methicillin in one; no infection, drug, o
Publikováno v:
American journal of diseases of children (1960). 122(1)
A child who survived with probable unilateral renal cortical necrosis is presented. The kidney that was not as severely involved by cortical necrosis was chronically obstructed at the uteropelvic junction. Chronic uteropelvic obstruction protected ra