Zobrazeno 1 - 10
of 105
pro vyhledávání: '"John M. Kissane"'
Autor:
John M. Kissane, Lauren V. Ackerman
Publikováno v:
The Journal of the Faculty of Radiologists. Faculty of Radiologists (Great Britain). 7(2)
Summary A case interpreted as an example of maturation by a relatively undifferentiated tumour of the sympathetic nervous system is presented. The patient was found at age 2 years to have an inoperable intrathoracic tumour, histologically a poorly di
Autor:
Kenneth M. Ludmerer, John M. Kissane
Publikováno v:
The American Journal of Medicine. 103:441-447
Autor:
Kenneth M. Ludmerer, John M. Kissane
Publikováno v:
The American Journal of Medicine. 103:318-327
Autor:
Kenneth M. Ludmerer, John M. Kissane
Publikováno v:
The American Journal of Medicine. 102:310-315
Autor:
Kenneth M. Ludmerer, John M. Kissane
Publikováno v:
The American Journal of Medicine. 101:111-117
Autor:
Jose L. Manes, Rosa M. Davila, John M. Kissane, Mary A. Rudloff, Richard S. Larson, Helen Liapis
Publikováno v:
Pediatric Nephrology. 9:594-598
Renal dysplasia has been reported in association with a number of anatomical abnormalities, including pancreatic dysgenesis and hepatic anomalies. The combination of renal, hepatic, and pancreatic dysplasia (RHPD), also known as Ivemark syndrome, is
Autor:
Kenneth M. Ludmerer, John M. Kissane
Publikováno v:
The American Journal of Medicine. 98:291-302
Publikováno v:
American Journal of Physiology-Renal Physiology. 268:F258-F265
The degree of glomerular inflammation and injury during immune-mediated glomerulonephritis is felt to be critical to the eventual development of glomerulosclerosis, although the relative contributions of acute and chronic inflammation are uncertain.
Publikováno v:
American Journal of Kidney Diseases. 23:743-746
The association of Hodgkin's disease and minimal-change nephrotic syndrome is well established. We describe a gentleman who developed Hodgkin's disease that was treated successfully. Two years later, he developed minimal-change nephrotic syndrome tha
Autor:
Mary A. Foulkes, Louis A. Gilula, Mark Nesbit, Gene P. Siegal, Susan J. Maygarden, B A Janice Schoppe, Frederic B. Askin, John M. Kissane
Publikováno v:
Cancer. 71:2109-2118
Background. Nineteen patients with Ewing sarcoma of bone, each younger than 3 years of age at the time of initial presentation, are reported. These children represent an unusually young age group for documented Ewing sarcoma and represent 2.6% of all