نتایج جستجو برای: new syndrome

تعداد نتایج: 2405747  

بزرگ‌مهری, خاطره, کاظمی, ملیحه‌السادات, گل‌پرور, محسن,

Objectives: This research was administered with the aim of studying the relationship between retirement syndrome components with general health symptoms in retired adults in Esfahan city. Methods & Materials: This research carried out in descriptive and correlational method. Research statistical population was the retired adults in Esfahan city, among them, 461 persons for participating to r...

1999
Klaus-Dieter Thoben Frithjof Weber

The availability of information is a key success factor for effective Concurrent Engineering (CE). However, in day-to-day practice, missing information is the bottleneck in many product development projects. One of the major reasons for this is the insufficient planning of information and communication structures (ICS). Within the scope of a CE research project, from which different methods and...

Journal: :iranian journal of child neurology 0
ravish singhal* pg resident, department of pediatrics, government multispecialty hospital, sector-16, chandigarh, india sadbhavna pandit head of the department pediatrics, government multispeciality hospital, sector-16, chandigarh, india ashok saini government multispeciality hospital, sector-16, chandigarh paramjit singh medical officer, pediatrics, government multispecialty hospital, sector-16, chandigarh, india neeraj dhawan medical officer, pediatrics, government multispecialty hospital, sector-16, chandigarh, india

how to cite this article: singhal r, pandit s, saini a, singh p, dhawan n. the acrocallosal syndrome in a neonate with further widening of phenotypic expression. iran j child neurol. 2014 spring;8(2):60-64.   the presentation of the typical characteristics of the acrocallosal syndrome (acls) are hypoplasia/agenesis of corpus callosum, moderate to severe mental retardation, characteristic cranio...

Alireza Zeinaddini Mahin Aflatoonian Maryam Khalili Rahim Ahmadi Simin Shamsi Meymandi

PHACES syndrome (Posterior Fossa Malformations, Hemangioma, Arterial Anomalies, Cardiac Defects and Coarctation of the Aorta, Eye Abnormalities, and Sternal Abnormalities or Ventral Developmental Defects) is a rare neurocutaneous syndrome, which characteristic feature is large segmental hemangioma. Extracutaneous involvement is an important cause of morbidity in this syndrome.<br /...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شهید مدنی آذربایجان - دانشکده ادبیات و علوم انسانی 1392

ii abstract the legend of human being’s refulgence was distorted completely in the age of modernity. this new age, had some drastic negative effects, besides its positive qualities. one significant negative effect of it was the emergence of neurosis in human beings. aldous huxley’s brave new world was one of the novels of the 02 th century that contained the prophecy of criticizing ...

Journal: :iranian journal of child neurology 0
marjan shakiba assistant professor of pediatric pediatric endocrinology, mofid children hospital, shahid beheshti university of medical sciences, tehran, iran habibe nezhad bieglari pediatrician mohammad reza alaee associate professor of pediatric endocrinology, mofid children hospital, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: shakiba m, nejad biglari h, alaee mr. digital and dental malformation and short stature in a patient with neurological problems: a variant of the oculodentodigital dysplasia syndrome or a new syndrome?iran j child neurol autumn 2012; 6(4): 51-54.   abstract several syndromes have been recognized with digital abnormality and cns involvement such as oculodentodigital dys...

Aghil Esmaeili-Bandboni, Alireza Sharafshah, Arash Davoudi, Fereshteh Fallahabadi, Forozan Milani, Parvaneh Keshavarz, Sara Afzali,

The common causes of 18p deletion syndrome are spontaneous errors in the chromosomal structure in the early stages of human embryonic development. In this study, a 29-year-old girl was introduced with the features of deletion of chromosome 18. In addition, GTG banding karyotype revealed that this case had a deletion involving the short arm of chromosome 18. In comparison with the usual phenotyp...

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