نتایج جستجو برای: congenital absence of skin

تعداد نتایج: 21198095  

Journal: :Archives of Disease in Childhood - Fetal and Neonatal Edition 2005

2018
Joel Canosa Vicenç Martí

The aim of this study is the application of a software tool to the design of stripping columns to calculate the removal of trihalomethanes (THMs) from drinking water. The tool also allows calculating the rough capital cost of the column and the decrease in carcinogenic risk indeces associated with the elimination of THMs and, thus, the investment to save a human life. The design of stripping co...

Journal: :iranian journal of child neurology 0
bita bozorgmehr kariminejad &najmabadi genetic center ariana kariminejad kariminejad & najmabadi genetic center, tehran, iran shahriar nafissi shariati hospital, tehran, iran bita jebelli pediatric neurologist, tehran, iran urtizberea andoni hospital marin, paris, france corine gartoux 5. upmc univ paris 06, ifr14, paris, f-75013, france 6. cnrs, umr7215, paris, f-75013, france 7. inserm, u974, paris, f-75013, france 8. institut de myologie, paris, f-75013, france

how to cite this article: bozorgmehr b, kariminejad a, nafissi sh, jebelli b, andoni u, gartioux c, ledeuil c, allamand y, richard p, kariminejad mh. ullrich congenital muscular dystrophy (ucmd):clinical and genetic correlations. iran j child neurol. 2013 summer; 7(3): 15-22.   obj ective: ullrich congenital muscular dystrophy (ucmd) corresponds to the severe end of the clinical spectrum of neu...

Journal: :Srpski Arhiv Za Celokupno Lekarstvo 2023

Introduction. Microtia presents a congenital ear deformity ranging from minor and barely visible defect to complete absence of the ear. Currently, there are three options for reconstruction: autologous costal cartilage, silicon prothesis prosthetic Ear reconstruction with cartilage is usually performed in two stages. During first stage cartilaginous framework fabricated placed under skin, anato...

Journal: :Saudi medical journal 2003
Pradeep J Chopra Samir S Hussein

We report a rare case of agenesis of the gallbladder, which was misdiagnosed as cholecystitis. This is the first reported case from the Middle East. Despite advances in biliary imaging, the diagnosis is usually made at surgery. Like most patients, our patient became asymptomatic after the surgery. Extensive dissection to exclude the presence of gallbladder in an ectopic site is discouraged.

Acharya N Prasad, Prasad P, Sharma Sharma N SharmaU Singh M Singh SK

Background: Mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene can cause congenital bilateral absence of vas deferens. Yet, the spectrum and frequency of CFTR mutations in Indian males with congenital absence of vas deferens (CAVD) is unknown. Materials and Methods: We investigated 50 Indian males, diagnosed with unilateral or bilateral absence of vas deferens at t...

2005
F M Kiessling P Gille

A combined process for temperature measurements in THM growth systems is described including the preparation of the source material as well as the liquid solution zone in one and the same ampoule. Using starting compositions with an excess of that component to act as the solvent the solution zone is formed during the travelling heater procedure. With thermocouples attached to the slightly modif...

Journal: :Australian and New Zealand Journal of Ophthalmology 1986

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