Zobrazeno 1 - 10
of 148
pro vyhledávání: '"Marjorie, Hertz"'
Autor:
John P. Blandy
Publikováno v:
British Journal of Surgery. 61:671-671
Autor:
Fredric N. Silverman
Publikováno v:
Pediatrics. 59:487-487
The volume is divided into three parts: the first is a general consideration of the subject, and the second and third parts show, primarily in atlas form, the author's experience with cystourethrography in children and in adults. There is a good bibl
Autor:
Blandy, John
Publikováno v:
British Journal of Surgery; August 1974, Vol. 61 Issue: 8 p671-671, 1p
Publikováno v:
The British Journal of Radiology. 85:753-757
The aim was to evaluate whether enlargement of the spleen on CT in a post-partum female with fever is a common phenomenon.In this retrospective institutional review board-approved study, the spleen was measured by CT in 77 females (average age 30.7 y
Publikováno v:
Acta Radiologica. 51:539-542
Background: The iliopsoas compartment can be involved in many different disease processes with a wide variety of symptoms that may simulate avascular necrosis (AVN) of the femoral head. The psoas muscle merges with the iliacus to form a checkmark (
Autor:
Gabriela Gayer, Larisa Guranda, Eli Konen, Sara Apter, Zippy Erlich, Marjorie Hertz, Uri Rimon, Orith Portnoy, Michal Amitai
Publikováno v:
Abdominal Imaging. 35:99-105
Purpose: To assess the CT features of sealed rupture of abdominal aortic aneurysm. Patients and methods: We reviewed the CT scans of six index cases obtained over a 3 year period with a sealed rupture of an abdominal aortic aneurysm and those reporte
Publikováno v:
Clinical Genetics. 5:223-229
Publikováno v:
Clinical Genetics. 17:437-442
Two Jewish Ashkenazi male sibs are reported as having a new syndrome consisting of a white forelock, distinct facial features associated with congenital malformations involving the eye, cardio-pulmonary and skeletal systems. It is postulated that the
Publikováno v:
Clinical Genetics. 28:61-68
A detailed account is given of a 5-year-old girl with the facio-audio-symphalangism syndrome. This genetic disorder has been known previously by other names, including the WL syndrome. The reasons for suggesting this new descriptive term are given, a
Publikováno v:
Clinical Genetics. 26:342-355
A new camptodactyly syndrome is described in a 16-year-old Sephardic Jewish girl consisting of unusual facies with multiple eye anomalies, short stature, scoliosis, and joint contractures. Parental consanguinity is suggestive of an autosomal recessiv