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Hacettepe Üniversitesi Hastaneleri Kan Bankası Aferez Ünitesi'nde Gerçekleştirilen Tedavi Amaçlı Aferez İşlemlerinin Değerlendirilmesi
(Tıp Fakültesi, 2002)
Apheresis is the process of separation and collection of blood components. A study was carried out to evaluate the safety and efficacy of therapeutic apheresis procedures performed in Hacettepe University Hospitals Blood ...
Tıp Akademisyenlerinin Elektronik Veri Tabanı ve Elektronik Dergi Kullanımları: Hacettepe Üniversitesi Örneği
(Sosyal Bilimler Enstitüsü, 2007)
As a result of the rapid development of Internet and Internet technologies, electronic information sources have become widely available. Such developments have impact on information seeking behaviours of the users. Researchers ...
Effect of Breastfeeding on Asthma, Lung Function and Bronchial Hyperreactivity in Isaac Phase Ii
(European Respiratory Soc Journals Ltd, 2009)
The association between breastfeeding and wheezing, lung function and atopy was evaluated in the International Study of Asthma and Allergy in Childhood (ISAAC) Phase II. Cross-sectional studies were performed in 27 centres ...
Extensive Scanning Of The Calpain-3 Gene Broadens The Spectrum Of Lgmd2A Phenotypes
(B M J Publishing Group, 2005)
Background: The limb girdle muscular dystrophies ( LGMD) are a heterogeneous group of Mendelian disorders highlighted by weakness of the pelvic and shoulder girdle muscles. Seventeen autosomal loci have been so far identified ...
Evidence From Autoimmune Thyroiditis Of Skewed X-Chromosome Inactivation In Female Predisposition To Autoimmunity
(Nature Publishing Group, 2006)
The etiologic factors in the development of autoimmune thyroid diseases (AITDs) are not fully understood. We investigated the role of skewed X-chromosome inactivation (XCI) mosaicism in female predisposition to AITDs. One ...
Human Osteoclast-Poor Osteopetrosis With Hypogammaglobulinemia Due To Tnfrsf11A (Rank) Mutations
(Cell Press, 2008)
Autosomal-Recessive Osteopetrosis (ARO) comprises a heterogeneous group of bone diseases for which mutations in five genes are known as causative. Most ARO are classified as osteoclast-rich, but recently a subset of ...
Homozygous Inactivating Mutations In The Nkx3-2 Gene Result In Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
(Cell Press, 2009)
Spondylo-megaepiphyseal-metaphyseal dysplasia (SMMD) is a rare skeletal dysplasia with only a few cases reported in the literature. Affected individuals have a disproportionate short stature with a short and stiff neck and ...
Histological Response To Injected Gluteraldehyde Cross-Linked Bovine Collagen Based Implant In A Rat Model
(2006)
Background The aim of present study is to investigate the short and long term histopathological alterations caused by submucosal injection of gluteraldehyde cross-linked bovine collagen based on an experimental rat model. ...
Mutations In A Gene Encoding A Novel Sh3/Tpr Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy
(Univ Chicago Press, 2003)
Charcot-Marie-Tooth disease type 4C (CMT4C) is a childhood-onset demyelinating form of hereditary motor and sensory neuropathy associated with an early-onset scoliosis and a distinct Schwann cell pathology. CMT4C is inherited ...
