Başlık için Dahili Tıp Bilimleri Bölümü Makale Koleksiyonu listeleme
Toplam kayıt 2912, listelenen: 1147-1166
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G-CSF Treatment of Healthy Pediatric Donors Affects Their Hematopoietic Microenvironment Through Changes in Bone Marrow Plasma Cytokines and Stromal Cells
(2021-03)Although G-CSF mobilized peripheral blood stem cell (PBSC) transplantation is commonly used in adults, bone marrow (BM) is still the preferred stem cell source in pediatric stem cell transplantation. Despite the fact that ... -
Gadolinium Leakage Into Subarachnoid Space And Cystic Metastases
(Turkish Soc Radiology, 2013)Subarachnoid space (SAS) and cystic metastatic lesions of brain parenchyma appear hypointense on fluid-attenuated inversion-recovery (FLAIR) and T1-weighted magnetic resonance imaging (MRI) unless there is a hemorrhage or ... -
Gastric Volvulus: A Rare Diagnosis Of Abdominal Pain
(2019)Gastric volvulus (GV) is a rare but life-threatening condition in case of delay in diagnosis and treatment. Herein, we presented a case of GV due to Morgagni hernia presenting to the emergency department with complaints ... -
Gastroenteropancreatic Neuroendocrine Tumors: Recommendations Of Turkish Multidisciplinary Neuroendocrine Tumor Study Group On Diagnosis, Treatment And Follow-Up
(2017)Gastroenteropancreatic neuroendocrine tumors (GEPNETs) are a relatively rare, heterogeneous group of diseases in which important advances have been observed in the diagnosis and treatment as well as in our understanding ... -
Gastrointestinal Involvement In Poems Syndrome: A Novel Clinical Manifestation
(BMJ, 2005)POEMS syndrome ( polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes) is characterised by a rare multisystem disorder of unknown pathogenesis. Although its pathophysiology is not well ... -
Gaucher Disease: New Developments In Treatment And Etiology
(W J G Press, 2008)Gaucher disease (GD) is an autosomal recessive disease which if undiagnosed or diagnosed late results in devastating complications. Because of the heterozygous nature of GD, there is a wide spectrum of clinical presentation. ... -
Gemcitabine Combined With The Monoclonal Antibody Nimotuzumab Is An Active First-Line Regimen In Kras Wildtype Patients With Locally Advanced Or Metastatic Pancreatic Cancer: A Multicenter, Randomized Phase Iib Study
(Oxford Univ Press, 2017)Background: This randomized study was designed to investigate the superiority of gemcitabine (gem) plus nimotuzumab (nimo), an anti-epidermal growth factor receptor monoclonal antibody, compared with gem plus placebo as ... -
Gender Differences In Defense Mechanisms, Ways Of Coping With Stress And Sense Of Identity In Adolescent Suicide Attempts
(Turkish J Pediatrics, 2016)The main aim of this study was to investigate the gender differences in defense mechanisms, ways of coping with stress and identity formation in relation to adolescent suicidal behavior. This study involved 64 adolescents ... -
Generalised Periodic Epileptiform Discharges: Clinical Features, Neuroradiological Evaluation And Prognosis In 37 Adult Patients
(W B Saunders Co Ltd, 2003)Generalised periodic epileptiform discharges (GPEDs) are very rare patterns and are classified as periodic short-interval diffuse discharges (PSIDDs), periodic long-interval diffuse discharges (PLIDDs) and suppression-burst ... -
Generation Of Chimeric “Abs Nanohemostat” Complex And Comparing Its Histomorphological In Vivo Effects To The Traditional Ankaferd Hemostat In Controlled Experimental Partial Nephrectomy Model
(2013)Purpose. Using the classical Ankaferd Blood Stopper (ABS) solution to create active hemostasis during partial nephrectomy (PN) may not be so effective due to insufficient contact surface between the ABS hemostatic liquid ... -
Generic Imatinib Mesylate Is As Effective As Original Glivec In The Clinical Management Of Cml
(Akad Doktorlar Yayınevi, 2015)Unsustainable drug prices in chronic myeloid leukemia (CML) and cancer may be causing harm to patients. The aim of this multi-center study is to assess the efficacy of generic imatinib mesylate (IM) over Glivec in terms ... -
Genes For Spinocerebellar Ataxia With Blindness And Deafness (Scabd/Scar3, Mim# 271250 And Scabd2)
(Nature Publishing Group, 2016)Ataxia is a symptom that is often associated with syndromic inherited diseases. We previously reported the linkage of a novel syndrome, ataxia with blindness and deafness (SCAR3/SCABD, OMIM# 271250), to chromosome 6p21-p23 ... -
Genes That Affect Brain Structure And Function Identified By Rare Variant Analyses Of Mendelian Neurologic Disease
(Cell Press, 2015)Development of the human nervous system involves complex interactions among fundamental cellular processes and requires a multitude of genes, many of which remain to be associated with human disease. We applied whole exome ... -
Genetic Architecture Distinguishes Systemic Juvenile Idiopathic Arthritis From Other Forms Of Juvenile Idiopathic Arthritis: Clinical And Therapeutic Implications
(2017)Objectives Juvenile idiopathic arthritis (JIA) is a heterogeneous group of conditions unified by the presence of chronic childhood arthritis without an identifiable cause. Systemic JIA (sJIA) is a rare form of JIA characterised ... -
Genetic Basis Of Cystinosis In Turkish Patients: A Single-Center Experience
(Springer, 2012)We report the molecular findings for the CTNS gene in 12 Turkish cystinosis patients aged 7-29 years. All presented initially with severe failure to thrive, polyuria, and polydipsia. Cystinosis was diagnosed at age 1 month ...