Başlık için Dahili Tıp Bilimleri Bölümü Makale Koleksiyonu listeleme
Toplam kayıt 2912, listelenen: 2760-2779
-
Turkish League Against Rheumatism Consensus Report: Recommendations For Management Of Axial Spondyloarthritis
(Turkish League Against Rheumatism, 2018)Objectives: This study aims to update 2011 Turkish League Against Rheumatism SpondyloArthritis Recommendations, and to compose a national expert opinion on management of axial spondyloarthritis under guidance of current ... -
Turkish Pediatric Atypical Hemolytic Uremic Syndrome Registry: Initial Analysis Of 146 Patients
(2017)Background Atypical hemolytic uremic syndrome (aHUS) is a devastating disease with significant morbidity and mortality. Its genetic heterogeneity impacts its clinical presentation, progress, and outcome, and there is no ... -
Türk Neonatoloji Derneği Yenidoğan Döneminde Ağrı Ve Tedavisi Rehberi
(2018)Pain control is an important ethical issue to be considered and constitutes the basis of treatment in premature and term newborns. The inadequacy of pain control in these infants in neonatal intensive care units leads to ... -
Türkiye Psoriasis Biyolojik Ajan Kullanım Kılavuzu
(Deri Zuhrevi Hastaliklar Dernegi, 2008) -
Two cases of glutaric aciduria type II: how to differentiate from inflammatory myopathies?
(Taylor and Francis, 2018-11-19)Muscle weakness is a nonspecific finding of myopathy of any etiology that include iatrogenic, toxic, endocrinological, infectious, immunologic, and metabolic disorders. Among the metabolic myopathies glutaric aciduria type ... -
Two New Cases with Pearson Syndrome and Review of Hacettepe Experience
(2008)SUMMARY: Topaloğlu R, Lebre AS, Demirkaya E, Kuşkonmaz B, Coşkun T, Orhan D, Gürgey A, Gümrük F. Two new cases with Pearson syndrome and review of Hacettepe experience. Turk J Pediatr 2008; 50: 572-576. Pearson syndrome ... -
Two New Loci For Autosomal Recessive Ichthyosis On Chromosomes 3P21 And 19P12-Q12 And Evidence For Further Genetic Heterogeneity
(Univ Chicago Press, 2000)Autosomal recessive ichthyosis (ARI) includes a heterogeneous group of disorders of keratinization characterized by desquamation over the whole body. Two forms largely limited to the skin have been defined: lamellar ... -
Two Otolaryngologic Cases Of Munchausen'S Syndrome
(Ortadogu Ad Pres & Publ Co, 2012)Munchausen's Syndrome is characterized by repeated attempts to be hospitalized following an extremely credible and dramatic representation of physical symptoms. This syndrome is commonly known as a factitious disorder. ... -
Type 3B Malrotation Presented With Acute Appendicitis As Left Renal Colic
(2012)Midgut malrotation is a rare anatomic anomaly that complicates the diagnosis and managemant of acute abdominal pain. It is a congenital anomaly that arises from incomplete rotation or abnormal position of the midgut during ... -
Type I Ifn-Related Netosis In Ataxia Telangiectasia And Artemis Deficiency
(Mosby-Elsevier, 2018)Background: Pathological inflammatory syndromes of unknown etiology are commonly observed in ataxia telangiectasia (AT) and Artemis deficiency. Similar inflammatory manifestations also exist in patients with STING-associated ... -
Type Of Setting For The Inpatient Adolescent With An Eating Disorder: Are Specialized Inpatient Clinics A Must Or Will The Pediatric Ward Do?
(Turkish J Pediatrics, 2016)There are a range of different services for treating adolescent eating disorders (ED) but there is no clinical consensus and a paucity of research indicating which type of treatment setting is the best. Although it would ...