Zobrazeno 1 - 10
of 19
pro vyhledávání: '"R I, Markowitz"'
Publikováno v:
RadioGraphics. 16:871-893
Cystic fibrosis (CF), the most common lethal autosomal recessive disease in white populations, is characterized by dysfunctional chloride ion transport across epithelial surfaces. Although recurrent pulmonary infections and pulmonary insufficiency ar
Publikováno v:
Radiology. 181:813-818
Hemangioendotheliomas and arteriovenous malformations (AVMs) of the liver often cause congestive heart failure in babies, but embolization of the hepatic artery is not always effective. Six newborns and infants (four with hemangioendotheliomas and tw
Autor:
K W, Gripp, C A, Stolle, D M, McDonald-McGinn, R I, Markowitz, S P, Bartlett, J A, Katowitz, M, Muenke, E H, Zackai
Publikováno v:
American journal of medical genetics. 78(4)
We present a patient with pansynostosis, hydrocephalus, seizures, extreme proptosis with luxation of the eyes out of the lids, apnea and airway obstruction, intestinal non-rotation, and severe developmental delay. His skeletal abnormalities include b
Autor:
R I, Markowitz
Publikováno v:
Seminars in roentgenology. 33(2)
Publikováno v:
American journal of medical genetics. 73(4)
We report on a fetus with tetramelic campomelia, polysplenia, multicystic dysplastic kidneys, and cervical lymphocele. This condition is similar to the autosomal recessive condition described by Cumming et al. [1986: Am J Med Genet 25:783-790] and is
Autor:
J S Meyer, R I Markowitz
Publikováno v:
AJR. American journal of roentgenology. 169(6)
OBJECTIVE: Our objective is to report how an inexpensive computer database program (Filemaker Pro, version 3.0, for Macintosh) can be used to manage work schedules and optimize staff use in a radiology department. CONCLUSION: Using this report in con
Autor:
J E, Ming, D M, McDonald-McGinn, T E, Megerian, D A, Driscoll, E R, Elias, B M, Russell, M, Irons, B S, Emanuel, R I, Markowitz, E H, Zackai
Publikováno v:
American journal of medical genetics. 72(2)
Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs,
Publikováno v:
American journal of medical genetics. 70(2)
Osteopathia striata with cranial sclerosis (OS-CS) is a bone dysplasia characterized by hypertelorism, macrocephaly, frontal bossing, broad nasal bridge, palate anomalies, hearing deficits, and mental retardation. The radiographic findings include cr
Publikováno v:
Pediatrics. 88(3)
While testifying in child abuse cases, physicians have been frustrated by the lawyer who asks, "Doctor, how did this injury happen?" The medical records and radiographs of 215 children younger than the age of 3 with fractures evaluated by a pediatric
Publikováno v:
The Journal of trauma. 30(12)
The overall approach to blunt abdominal trauma resulting in hematoma and intestinal obstruction has been variable and controversial. Recent reports recommend conservative nonoperative management. We reviewed six cases of duodenal and jejunal hematoma