نتایج جستجو برای: 22 and

تعداد نتایج: 16857492  

2016
Muhammad Babar Khawar Fareeha Azam Nadeem Sheikh Khawaja Abdul Mujeeb

Interleukin-22 (IL-22) is a pluripotent T cell-derived cytokine which is a member of IL-10 cytokine family. It is the only interleukin produced by immune cells but does not target immune system components. IL-22 is mainly produced by dendritic cells (DCs) and TH17, TH22, NK, and NKT cells and targets a number of body tissues including liver, pancreas, and other epithelial tissues. It provokes a...

Journal: :Journal of medical genetics 1977
F Mollica G Sorge L Pavone

A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitution. This is the first reported case of a trisome 22 phenotype with such a mosaic karyotype.

2012
Pascal Gelebart Raymond Lai

2010

Four randomised controlled trials (RCTs) and one RCT metaanalysis are featured in the Journal this month. The latter is a review of trials of newer-generation antidepressants and cognitive–behavioural therapy (CBT) for adolescent depression (Dubicka et al, pp. 433–440). In an area of clinical practice plagued by controversy, the authors of this review were able to contribute the finding that ad...

Journal: :Clinical dysmorphology 2004
Johannes H Merks Nicolaas Ceelie Huib N Caron Raoul C Hennekam

We report a family with co-occurring disorders including neuroblastoma in the first child conceived by in-vitro fertilization with history of sodium valproate use by the mother during pregnancy and mosaic trisomy 22 in the third child. We discuss the possibility of an association between the disorders but conclude that no firm aetiological connection can be established between the different dis...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان کرمانشاه 1370

cml in breif cml is characterized by the proliferation of large numbers of immature wbc in the blood and bone marrow. in most of the patients , it is a clonal disorder in which all cell lines, express the philadelphia chromosome)q/22 translocation(it accounts for 20 of all leukemias and most cases occur over 25 yrs of age. the disease usually begins insidiously,but symptoms referable to anemia ...

Journal: :iranian red crescent medical journal 0
maryam jalessi ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran mohammad farhadi ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran seyyed kamran kamrava ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran ebrahim amintehran ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran alimohammad asghari ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran; ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran. tel: +98-2166504294, fax: +98-2166504294 mohsen rezaei hemami ent-head and neck research center and department, hazrat rasoul akram hospital, tehran university of medical sciences, tehran, ir iran

conclusions the persian version of snot 22 questionnaire is a valid and reliable instrument for accessing sinonasal diseases in persian-speaking people. results thirty adults with nasal septal deviation need surgical correction and 30 healthy volunteers were included (mean age 30.4 ± 7.1 vs. 33 ± 6.7, p value = 0.148). the questionnaire was introduced to subjects two times with a two-week-perio...

2008
Kimberlie Dean

Three papers in the Journal this month consider issues related to measuring, understanding and treating mental ill health in childhood. Baron-Cohen et al (pp. 500–509) undertook a study to establish the prevalence of autism-spectrum conditions in Cambridgeshire using two case ascertainment methods. First, a survey of individuals on the Special Educational Needs register and second, a screening ...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

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