Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Michael, Nadjari"'
Autor:
Yael, Adler-Levy, Simcha, Yagel, Michael, Nadjari, Yaakov, Bar-ziv, Natalia, Simanovsky, Nurith, Hiller
Publikováno v:
The Israel Medical Association journal : IMAJ. 17(1)
Sonographic evaluation of congenital skeletal dysplasias is often challenging. Ultrasound may be limited in demonstrating the skeleton and may overlook specific signs of skeletal abnormality. Computed tomography (CT) with 3D reconstruction was propos
Autor:
Michael Nadjari, Yossef Ezra, David Shveiky, Nathan Rojansky, Vered H. Eisenberg, Arnon Samueloff, Ella Ophir
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 84:432-435
Background. Intensive management and elective delivery between 32 and 35 weeks of monoamniotic twin pregnancies were suggested as improving perinatal outcome. We sought to evaluate this management as viewed by the outcome of monoamniotic twin pregnan
Ultrasonographic prenatal diagnosis of microcephalic osteodysplastic primordial dwarfism types I/III
Autor:
Jacob Bar-Ziv, Uriel Elchalal, Ilana Ariel, Sozos J. Fasouliotis, Annick Raas-Rothschild, Michael Nadjari
Publikováno v:
Prenatal Diagnosis. 20:666-669
Microcephalic osteodysplastic primordial dwarfism is a rare disease characterized by unique clinical appearance and specific radiographic findings, and distinctive brain abnormalities. We describe the prenatal diagnosis of two siblings with microceph
Publikováno v:
Journal of Ultrasound in Medicine. 16:509-512
Publikováno v:
Pediatric Radiology. 36:138-140
We report a case of hemimegalencephaly diagnosed by prenatal MRI with an emphasis on its appearance on diffusion-weighted images. This case shows that in this condition the enlarged hemisphere may show restricted diffusion on prenatal MRI. In our opi
Autor:
Ephrat Levy-Lahad, Michal Inbar-Feigenberg, Shamir Zenvirt, Orly Elpeleg, Rachel Michaelson-Cohen, Avraham Shaag, Ziva Ben-Neriah, Michael Nadjari, Sharon Zeligson
Publikováno v:
American journal of medical genetics. Part A. (11)
Diaphonospondylodysostosis (DSD) is a rare, recessively inherited, lethal skeletal dysplasia, characterized by severe spinal ossification, segmentation defects, and renal cystic dysplasia with nephrogenic rests. We hereby present three affected indiv
Autor:
Uriel Elchalal, Michael Nadjari, Sagui Gavri, Azaria J.J.T. Rein, Amiram Nir, Dror Mevorach, Zeev Perles
Publikováno v:
Circulation. 120
We thank Guettrot-Imbert et al for their comments. They question whether all cases of first-degree atrioventricular block (AVB) were necessarily pathological and in need of treatment. They also question our 8.6% incidence of first-degree AVB versus t
Autor:
Yossef, Ezra, David, Shveiky, Ella, Ophir, Michael, Nadjari, Vered H, Eisenberg, Arnon, Samueloff, Nathan, Rojansky
Publikováno v:
Acta obstetricia et gynecologica Scandinavica. 84(5)
Intensive management and elective delivery between 32 and 35 weeks of monoamniotic twin pregnancies were suggested as improving perinatal outcome. We sought to evaluate this management as viewed by the outcome of monoamniotic twin pregnancies in our
Autor:
Gila Shazberg, Yaacov Akerman, Jonathan Moise, Aharon Klar, Michael Nadjari, Arie Levy, Shoshana Revel-Vilk, David Branski, Talia Israeli, Gabriel Katz, Haggit Hurvitz, Yaacov Berkun, Anat Ben Ami
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 40(4)
Objective: Evaluation and follow-up of infants with cholelithiasis and pseudolithiasis in a pediatric ward. Patients & Methods: Prospective study from April 1990 to October 2003 identified hospitalized infants younger than 2 years with ultrasonograph
Publikováno v:
The Journal of reproductive medicine. 47(3)
Caudal regression syndrome (CRS) is a rare anomaly of the lower body pole that represents a continuum of congenital malformations ranging from isolated sacral agenesis to absence of the lumbosacral spine and major visceral anomalies. While the exact