Bölüm "İstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı" Diğer Yayınlar Koleksiyonu için listeleme
Toplam kayıt 28, listelenen: 1-20
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Adölesan hastada efor dispnesi ve siyanozun nadir bir nedeni: Pulmoner arteriyovenöz malformasyon ve başarılı tedavisi
(Turkish Society of Cardiology, 2019)On üç yaşında kız son 1.5yılda giderek artan beş yıldır çabuk yorulma, görmede bulanıklık, baş ağrısı, zaman zaman konuşma bozukluğu, eforla dudaklarda ve tırnaklarda morarma, öksürük ve kilo alamama yakınmaları ile çocuk ... -
Aortik kros klemp ile myokard iskemisi yaratmadan konjenital düzeltilmiş büyük arter transpozisyonlu asendan aortu hipoplazik tip A kesintili aortik arkı olan hastanın tedavisi
(Dokuz Eylül Üniversitesi, 2022)İnterrupted aortik ark tedavisi karmaşık bir süreçtir. Cerrahi rekonstrüksiyon genellikle myokard iskemisine neden olan aortik kros klempleme, kalbin durdurulması ve hatta kansız operasyon sahası için derin hipotermi ... -
Benign infantil hidrosefali: Hangi çocukta, ne zaman düşünelim, ne yapalım?
(İstanbul Üniversitesi, 2022)Makrosefalinin en sık sebeplerinden biri olan benign infantil hidrosefali, beyin omurilik sıvısının emiliminden sorumlu araknoid villusun olgunlaş mamasından kaynaklandığı düşünülen kendini sınırlayan bir klinik durum dur. ... -
Brucella infection associated with complete atrioventricular block
(Aves, 2016)Background: The clinical spectrum of Brucella infection is quite diverse and characterized by multi-system involvement. Patients present with myocarditis, endocarditis, or pericarditis. Infective endocarditis is the most ... -
A child with a severe headache: Answers
(Springer Science and Business Media Deutschland GmbH, 2021)1) What is your suspected diagnosis of acute severe headache in this patient? We report here an adolescent girl who presented with severe headache while receiving acute sinusitis treatment and was found to have bilateral ... -
A child with a severe headache: Questions
(Springer, 2021)A 12-year-old girl presented with complaint of severe headache lasting 10 days, nausea and vomiting for 1 day. The headache was localized in the right fronto-occipital region with spread to the neck and shoulders. In her ... -
The clinical spectrum of reactions developed based on paraphenylenediamine hypersensitivity two pediatric cases
(Termedia Publishing House, 2015)Paraphenylenediamine (PPD) is a blue-black aniline dye commonly used in hair dyes. It is also used in textile and fur dyes, wool dye, dark cosmetics, temporary tattoo hennas, photo baths, and photocopy and printing ink. ... -
COVID-19 infection in children with cancer and stem cell transplant recipients in Turkey: A nationwide study
(Wiley, 2021)To the Editor: Adults with cancer are reported to have a higher risk for coronavirus disease (COVID-19) infection and more severe disease and mortality than the general population.1, 2 Although children seem to be at a ... -
Durable remissions in TCF3-HLF positive acute lymphoblastic leukemia with blinatumomab and stem cell transplantation
(Ferrata Storti Foundaition, 2019)TCF3-HLF-positive leukemia represents a rare subtypeof childhood acute lymphoblastic leukemia (ALL), characterized by a high rate of treatment failure despite treatment intensification and allogeneic stem cell transplantation ... -
Inflammatory bowel disease and guillain barre syndrome in FCHO1 deficiency
(Springer, 2021)To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, ... -
Laryngeal web associated with chromosome 22q11 deletion in a preterm infant
(Editions Medecine et Hygiene, 2015)... -
Management of paediatric arrhythmias in Europe
(Oxford University Press, 2015)We read with great interest the EP wire report entitled ‘How are arrhythmias managed in the paediatric population in Europe? Results of the European Heart Rhythm Survey’ by HernandezMadrid et al. 1 On behalf of the Arrhythmias ... -
Marfan sendromu hastada non-koroner sinüs valsalvanın dev anevrizması
(Dokuz Eylül Üniversitesi Tıp Fakültesi, 2022)Valsalva sinüslerinin anevrizmaları, aort anulusu ile sinotubüler bileşke arasındaki aort kök bölgesinin dilatasyonu olarak tanımlanır. Valsalva sinüsünün izole anevrizmaları nadir görülen kardiovasküler patolojilerdir. ... -
Nadir bir anafilaksi nedeni: Soğuk maruziyeti
(Dr Behçet Uz Çocuk Hastalıkları ve Cerrahisi, 2018)Fiziksel ürtikerin bir formu olan soğuk ürtikeri, cildin soğuk ile teması sonrası mast hücrelerinden histamin ve diğer proinflamatuvar mediatörlerin salınımı ile oluşmaktadır (1). Tüm fiziksel ürtikerler arasında soğuk ... -
Non-invasive ventilation for children with chronic lung disease
(Frontiers Media S.A., 2020)Advances in medical care and supportive care options have contributed to the survival of children with complex disorders, including children with chronic lung disease. By delivering a positive pressure or a volume during ... -
Patolojik tibiya kırığı olan yenidoğan: osteofibroz displazi
(2013)Osteofibroz displazi, uzun kemiklerin çok nadir görülen tümör benzeri gelişimsel fibroosöz durumudur (1). Bildiğimiz kadarıyla literatürde yenidoğan döneminde toplam sekiz, patolojik kırığı olan üç osteofibroz displazi ... -
Posterior reversible encephalopathy syndrome secondary to acute post-streptococcal glomerulonephritis
(Sociedade Brasileira de Medicina Tropical, 2023)A previously healthy 11-year-old boy presented to the emergency department with generalized tonic-clonic seizures. One week prior, he had complained of headaches, blurry vision, nausea, and vomiting. Once the seizures were ... -
Primary antibody deficiencies in Turkey: molecular and clinical aspects (Oct, 10.1007/s12026-021-09242-z, 2021)
(Humana Press Inc, 2022)The original published version of this article contained a mistake in one of the afliations. The correct afliation of author Manolya Kara (7) should read. -
A rare association with suffered cardiac arrest, long qt interval, and syndactyly: Timothy syndrome (LQT-8)
(Turkish Society of Cardiology, 2015)Timothy syndrome (TS), also referred to as syndactylyassociated long QT syndrome (LQTS) or LQT8, is a multi-system disorder characterized by developmental defects causing dysmorphic facial features, congenital heart ... -
A rare coronary anomaly with masked diagnosis: Anomalous left circumflex artery from right pulmonary artery
(Turkish Society of Cardiology, 2015)Anomalous origin of the circumflex coronary artery from the pulmonary artery is a rare congenital cor- onary anomaly. While it generally follows an asymptom- atic course, if undiagnosed it may lead to severe clinical ...