Başlık için Dahili Tıp Bilimleri Bölümü listeleme
Toplam kayıt 3863, listelenen: 2433-2452
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Natural History Of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey
(Oxford Univ Press, 2016)Context: Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near-total lack of body fat. Objective: We aimed to study natural history and disease burden of various subtypes ... -
Natural History Of T1N0M0 Hepatocellular Carcinoma: Large-Scale Study In The United States
(Karger, 2017)Background: Hepatocellular carcinoma (HCC) prognosis depends on clinicopathological features in addition to the treatment provided. We aimed to assess the natural history of TNM stage I HCC tumors which received different ... -
Naturally Acquired Hepatitis a Antibodies After Haematopoetic Stem Cell Transplantation
(Cambridge University Press, 2011)Haematopoietic stem cell transplant (HSCT) recipients lose immune memory of exposure to infectious agents and vaccines accumulated throughout their lifetime and therefore need to be revaccinated. We aimed to evaluate the ... -
Nazofarenks Kanseri Tedavisinde Indüksiyon Tedavilerinin Retrospektif Değerlendirilmesi
(Tıp Fakültesi, 2013)The standard treatment of local advanced nasopharyngeal cancer is chemoradiotherapy. Opinions regarding induction theraphy differ. In this study we retrospectively examined patients treated in our clinic and administered ... -
Nazofarinks Kanserli Hastalarda Radyoterapi Sonrası MRG'de Klivustaki Medüller Intensite Değişiklikleri
(Tıp Fakültesi, 2014)Clivus is commonly involved in nasopharyngeal carcinoma (NPC) and the intensity changes in the bone marrow can persist after the radiation therapy (RT) even after the disappearance of the mucosal soft tissue mass. Furthermore ... -
Nbeal2 Is Mutated In Gray Platelet Syndrome And Is Required For Biogenesis Of Platelet Alpha-Granules
(2011)Gray Platelet Syndrome (GPS) is an autosomal recessive bleeding disorder with large platelets that lack α-granules. We found that mutations of NBEAL2 (neurobeachin-like 2), encoding a BEACH/ARM/WD40 domain protein, cause ... -
Necrotizing Fasciitis Secondary To Bevacizumab Treatment For Metastatic Rectal Adenocarcinoma
(2014)Bevacizumab is a recombinant humanized monoclonal antibody that selectively blocks the activity of vascular endothelial growth factor (VEGF) receptor and it is used in metastatic colorectal patients. We present here a case ... -
Necrotizing Pneumonia Caused By Streptococcus Pneumoniae Serotype 3 Despite Pcv13
(2019)Streptococcus pneumoniae is the most common cause of complicated pneumonia. Pneumococcal necrotizing pneumonia (PNP) is a rare and serotype related complication. Serotypes 1, 3, 14, 15, 19A and 33 were the most reported ... -
Need For Comprehensive Hormonal Workup In The Management Of Adrenocortical Tumors In Children
(2014)Objective: Clinical findings do not reflect the excess hormonal status in adrenocortical tumors (ACTs) in children. Identification of abnormal hormone secretion may help provide the tumor marker and delineate those ... -
Needlestick Injury To A Patient
(2008) -
NEFRİN MUTASYONU OLAN KONJENİTAL NEFROTİK SENDROMLU HASTALARDA NEFREKTOMİNİN HASTA SAĞKALIM ÜZERİNE ETKİSİNİN RETROSPEKTİF ARAŞTIRILMASI
(Tıp Fakültesi, 2024-02-19)Congenital nephrotic syndrome is a glomerular disease characterized by protein loss from the kidneys. The onset of the disease occurs in the antenatal period, and patients are diagnosed within the first three months of ... -
Neisseria Meningitidis Serogroup X St-5799 (St-22 Complex) In Turkey: A Unique Pediatric Case
(Taylor & Francis Inc, 2018)Although outbreaks of Neisseria meningitidis serogroup X occured in a couple of African countries, a limited number of serogroup X meningococcal cases were reported in America and Europe as well as Turkey. Additionally, ... -
Neoadjuvant Chemotherapy Improves Survival In Patients With Locally Advanced Nasopharyngeal Carcinoma
(2019)This study aimed to evaluate survival in patients with locally advanced nasopharyngeal carcinoma. The records of 407 patients with locally advanced nasopharyngeal carcinoma treated retrospectively reviewed. Patients were ... -
Neocentric Small Supernumerary Marker Chromosomes (Ssmc) - Three More Cases And Review Of The Literature
(Karger, 2007)Here we report on three new patients with neocentric small supernumerary marker chromosomes (sSMC) derived from chromosome 2, 13 and 15, respectively. The sSMC( 13) and sSMC( 15) had inverted duplicated shapes and the sSMC( ... -
Neodymium:Yttrium-Aluminum-Garnet Lazer ve Fraksiyonel Karbondioksit Lazerin Saçlı Deride Yerleşen Alopesi Areata'daki Etkilerini Araştıran Karşılaştırmalı ve Kontrollü, Prospektif Klinik Çalışma
(Tıp Fakültesi, 2013)Alopesi areata (AA) is an autoimmune disease that causes hair loss. There is a need for effective and safe treatment options. Whether lasers might be a treatment option for alopecia is a topic of debate. This comparative, ... -
Neonatal Adrenal Insufficiency: Turkish Neonatal And Pediatric Endocrinology And Diabetes Societies Consensus Report
(2018)It is difficult to make a diagnosis of adrenal insufficiency in the newborn, because the clinical findings are not specific and the normal serum cortisol level is far lower compared to children and adults. However, ... -
Neonatal Assessment In The Delivery Room – Trial To Evaluate A Specified Type Of Apgar (Test-Apgar)
(2015)Background Since an objective description is essential to determine infant’s postnatal condition and efficacy of interventions, two scores were suggested in the past but weren’t tested yet: The Specified-Apgar uses the 5 ... -
Neonatal Effects Of Thyroid Diseases In Pregnancy And Approach To The Infant With Increased Tsh: Turkish Neonatal And Pediatric Endocrinology And Diabetes Societies Consensus Report
(2018)Thyroid functions in the fetus and newborn carry importance in terms of the baby’s health and development of the central nervous system. Maternaliodine deficiency, exposure to iodine, thyroid diseases (Hashimoto thyroiditis, ... -
Neonatal Screening For Congenital Adrenal Hyperplasia In Turkey: A Pilot Study With 38,935 Infants
(2019)Objective: Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. ...