Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tal Nachlieli"'
Autor:
Sarit Cohen, Ines Verner, Tal Nachlieli, Hadas Shoshani, Joseph N Mehrabi, Ofir Artzi, Hadas Prag Naveh
Publikováno v:
Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]. 45(5)
Microneedling fractional radiofrequency (FRF) and chemical peels are widely used for skin rejuvenation.The authors aimed at evaluating the efficacy and safety of FRF and trichloroacetic acid 20% (TCA20%) peel in different combinations for determining
Autor:
Alon Binnun, Yitzhak Ramon, Yehuda Ulman, Yedidia Bentur, Yitzhak J. Peled, Oren Shoshani, Yosef Berger, Tal Nachlieli, Arek Tabak
Publikováno v:
Journal of Toxicology: Clinical Toxicology. 36:707-711
Phenol is a general protoplastic poison which has been in use in medicine and industry for decades. It is readily absorbed through the skin causing both local and systemic toxicity.A 47-year-old male had 90% phenol spilled over his left foot and shoe
Publikováno v:
Aesthetic plastic surgery. 24(4)
The widespread use of antibacterial agents for prophylaxis has altered surgical practice markedly in the past 20 years and now represents one of the most frequent uses of antibiotics in hospitals, accounting for as many as half of all antibiotics pre
Publikováno v:
American journal of medical genetics. 44(3)
Two infants with cystic kidney dysplasia and polydactyly were born to consanguineous parents. One infant died at age 2 months, and the other is currently 3.5 years old. A third pregnancy was terminated following ultrasonographic visualization of larg
Autor:
Tal Nachlieli, Ruth Gershoni-Baruch
Publikováno v:
American journal of medical genetics. 42(4)
We report on an infant (born to consanguineous parents) with an unusual face, microphthalmia, cleft palate, dextrocardia, choreoathetosis, and mental retardation. This child has many traits in common with an infant recently described by Aughton [1990
Publikováno v:
Child's Nervous System. 7
A case of Apert's syndrome with posterior (occipital) encephalocele and absence of corpus callosum is described. This is a rare combination. The mechanisms involved are discussed.