Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eitan Ben-David"'
Autor:
Mordechai Shemesh, Eitan Ben-David
Publikováno v:
Biology of Reproduction. 42:131-138
We have previously reported that the steroidogenic activity of the bovine placentome is stimulated by a calcium-mediated, cyclic nucleotide-independent mechanism and that this steroidogenesis is limited by the availability of sterol substrate to the
Publikováno v:
Journal of the American Academy of Dermatology. 31:1058-1060
Autor:
Arieh Kuritzky, Mati Shaklai, Nelly Avissar, Aida Inbal, Eitan Ben-David, Abel Schejter, Ben-Zion Garty, Sara Shanske
Publikováno v:
American journal of medical genetics. 55(3)
We describe 2 sibs (brother and sister) with myopathy, sideroblastic anemia, lactic acidosis, mental retardation, microcephaly, high palate, high philtrum, distichiasis, and micrognathia. Very low levels of cytochromes a, b, and c were detected in th
Publikováno v:
Brain : a journal of neurology. 116
Twenty-two Jewish patients, belonging to 15 families, 11 of them from Iran and three possibly of Iranian stock, suffered from progressive muscle weakness and wasting. The initial symptom was usually distal leg muscle weakness, appearing in the third
Autor:
Eitan Ben-David, Mordechai Shohat, Michael David, Ben-Zion Garty, Israel Kremer, Arieh Ingber, Sasson Nakar, Emmilia Hodak
Publikováno v:
American journal of medical genetics. 43(5)
We present 2 sibs with a local junctional type of epidermolysis bullosa associated with enamel defect of the teeth, dystrophic nails of the feet, and mental retardation. Subluxation of the lenses was evident in 1 of them. This combination found in a
Publikováno v:
Postgraduate medical journal. 68(797)
Summary A 46 year old woman had a relapsing-remitting course of hemiparesis, disorientation, paraparesis and seizures, followed by progressive dementia, spasticity and ataxia. Computed tomography at onset showed a parietotemporal hypodense area with
Publikováno v:
Developmental medicine and child neurology. 34(2)
SUMMARY The authors describe a 25-year-old woman with giant axonal neuropathy (GAN) and severe CNS involvement. She had been admitted to hospital with generalized seizures, and had had gait disturbances followed by progressive mental deterioration si
Autor:
Ilana Nissenkorn, Raphael Weitz, Gertrude Kohn, Eitan Ben-David, Israel Kramer, Yehuda Shapira
Publikováno v:
Braindevelopment. 12(5)
A 15-month-old boy, thought to have a congenital myopathy, was subsequently diagnosed as having mucolipidosis type IV, with typical membranous inclusions in muscle fibers. Involvement of skeletal muscle in this lysosomal storage disease may explain t
Autor:
Miriam Sandbank, Eitan Ben-David
Publikováno v:
International Journal of Dermatology. 18:50-54
Biopsy material in early and late stages of cutaneous lishmaniasis was obtained. The ultra-structural study using acid phosphatase reaction as a marker for lysosomes showed that in early stages parasites proliferate undisturbed within macrophage cyto
Publikováno v:
Journal of Neurochemistry. 29:561-578
— Two membrane fractions were obtained from electric organ tissue of the electric eel by sucrose gradient centrifugation of tissue homogenates. Electron microscopic examination showed that both fractions contained mainly vesicular structures (micro