نتایج جستجو برای: ellis
تعداد نتایج: 4036 فیلتر نتایج به سال:
ANALYTICAL STANDARD. D. L. Cook, M. Wadhwa, A. M. Davis, and R. N. Clayton, Department of the Geophysical Sciences, The University of Chicago, 5734 S. Ellis Ave., Chicago, IL 60637 ([email protected]), Chicago Center for Cosmochemistry, 5640 S. Ellis Ave., Chicago, IL 60637, Department of Geology, The Field Museum, 1400 S. Lake Shore Dr., Chicago, IL, 60605, Enrico Fermi Institute, The Univ...
Three new iridoids, Gardenal-I (1), Gardenal-II (2) and Gardenal-III (3), together with nine known iridoid glycosides; geniposide (4), 6-β-hydroxy geniposide (5), 6-α-hydroxy geniposide (6), 6-α-methoxy geniposide (7), feretoside (8), genipin-1-β-gentiobioside (9), shanzhiside (10), lamalbidic acid (11) and picrocrocinic acid (12) were isolated from EtOH extract of G. gasminoides. The structure...
chondroectodermal dysplasia (ellis-van creveld syndrome) is a rare autosomal recessive congenital abnormality. this syndrome is characterized by a spectrum of clinical findings, among which chondrodystrophy, polydactyly, ectodermal dysplasia, and congenital cardiac anomalies are the most common. it is imperative to not overlook the cardiac complications in patients with this syndrome during den...
چکیده برای دو دهه مطالعات بر روی فرصت تمهید و نقش آن در عملکرد گفتاری زبان آموزان نشان داده است که فرصت برای تمهید جهت انجام کار ((task عموما گفتار فراگیران را بهبود می بخشد (ellis, 2005). فرض بر این است که فرصت تمهید بار ذهنی را در خلال پردازش زبانی کاهش داده و به فراگیران اجازه میدهد تا به جنبه های مختلف زبان توجه کنند و این توجه تسهیل شده در عوض منتج به عملکرد کار موفق تر میشود. پژوهشگرا...
ellis-van creveld syndrome is transmitted as an autosomal recessive trait. this syndrome is accompanied in 60% of cases with congenital heart disease, mostly single atrium or large asd. patients are mostly symptomatic, but in this rare case despite 68 years of age, the patient was free of symptoms except for complete heart block for which pacemaker was inserted
Ellis-Van Creveld syndrome is a very rare congenital disorder which its principal features are polysyndactyly, chondrodysplasia, cardiac abnormalities and ectodermal dysplasia. We report a 10-year-old girl with major manifestations of this syndrome who also had multiple brownish macules and patches on trunk and extremities with aortic and pulmonary stenosis in echocardiographic evaluations.
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