M. Törehan Aslan

M. Törehan Aslan
Istanbul University · Istanbul Faculty of Medicine

Doctor of Medicine
Tekirdağ Namık Kemal University Faculty of Medicine, Department of Pediatrics, Division of Neonatology

About

31
Publications
5,138
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39
Citations
Citations since 2017
29 Research Items
39 Citations
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2017201820192020202120222023051015
Introduction
Mustafa Törehan Aslan is currently working as a neonatologist at Tekirdağ Namık Kemal University Faculty of Medicine, Department of Pediatrics, Division of Neonatology.
Additional affiliations
December 2018 - December 2021
Istanbul University
Position
  • Fellow

Publications

Publications (31)
Article
Full-text available
Objective: Stenotrophomonas maltophilia is a pathogen, which may cause serious outbreak, particularly in neonatal intensive care units, with increasing importance at present. The aim of this study was to assess the epidemiological and clinical features of S. maltophilia epidemic that we encountered in our neonatal intensive care unit and outbreak m...
Article
Full-text available
COVID-19 disease caused by a novel type coronavirus (2019-nCoV / SARS-CoV-2) infection is more severe and symptomatic in older people and people with an additional disease, unlike children and young people without additional disease. However, there is not yet sufficient evidence about the transition routes to the fetus, the clinical course of the v...
Article
Full-text available
The epidemic that emerged in recent months and related to severe acute respiratory syndrome coronavirus-2 (SARSCoV-2) caused a global threat. When ineffective treatment methods and the lack of vaccines were considered, these issues caused a serious international concern (1). 80% of people who have had COVID-19 disease as a result of SARS-CoV-2 infe...
Article
Full-text available
The first mesenchymal stem cells (MSC) described in 1999 were derived from human bone marrow, but now they can be obtained from many tissues such as umbilical cord blood, adipose tissue [1]. MSC therapy, one of the new and promising treatment methods, is currently used for many diseases, including bronchopulmonary dysplasia (BPD). Our case had seve...
Chapter
Full-text available
Metabolic diseases develop due to problems in food metabolism and/or cellular basic functions. Most, if not all, show autosomal recessive inheritance. They may present with different clinical findings in a age range period from the intrauterine period to adulthood. Since life-threatening metabolic crises may develop in the newborn period, the use o...
Preprint
Long QT syndrome (LQTS) is a serious condition that can cause sudden cardiac death. Subsequently, a heterozygous mutation of KCNH2 was identified. This has led to the hypothesis that the use of maternal tacrolimus may cause LQTS or have an effect that may facilitate the early occurrence of congenital LQTS.
Conference Paper
Full-text available
Yenidoğanlarda Serum 25-OH Vitamin D, Vitamin B12 ve Folat Düzeyleri İle İlişkili Faktörler Tekirdağ Namık Kemal Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Neonatoloji Bilim Dalı Giriş: Annedeki serum vitamin düzeyleri yanı sıra, yenidoğanlardaki düşük vitamin düzeyleri de önemli sağlık sorunlarına yol açabilmektedir...
Article
Full-text available
The novel coronavirus disease (COVID-19), which was accepted as a pandemic by the World Health Organization (WHO) in 2020, has aected millions of people all over the world and caused deaths. Examining the pathophysiology of radiological lesions is perhaps the key in understanding this endless disease for which early diagnosis is crucial due to its...
Article
Full-text available
Holoprosencephaly is a complex brain malformation caused by the inability of the prosencephalon to divide to form the cerebral hemispheres. Central diabetes insipidus (CDI), as a result of a defect in vasopressin release, may be seen due to the abnormal hypothalamic infundibular region. CDI developing secondary to holoprosencephaly in the early neo...
Article
Full-text available
Since its emergence in China in December 2019, a novel coronavirus disease (COVID19) has rapidly spread all over the world and has been a major public health concern. This disease was pronounced as a pandemic by World Health Organization (WHO) and this highly contagious virus is named severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Al...
Conference Paper
Full-text available
İTP Tanılı Anne Bebekleri: Yenidoğanda Trombositopeni ve İlişkili Morbiditeler Öngörülebilir mi? Mustafa Törehan Aslan1, Zeynep İnce1, Leyla Bilgin1, Çiğdem Kunt İşgüder2, Asuman Çoban1 1İstanbul Üniversitesi, İstanbul Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Neonatoloji Bilim Dalı, İstanbul 2İstanbul Üniversitesi, İstanbul Tı...
Article
Full-text available
COVID-19 is a new type of respiratory infection and might lead to serious pneumonia causing acute respiratory distress syndrome (ARDS). Most people infected with SARSCoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) manifest as having asymptomatic or mild to moderate upper respiratory tract disease. However, a minority of all can have severe...
Conference Paper
Full-text available
Amaç Bu çalışmada kliniğimizde gebelik takibi ve doğumu gerçekleştirilen idiyopatik trombositopenik purpura (ITP) tanısı almış gebelerin maternal ve neonatal sonuçlarını ortaya koymayı amaçladık. Yöntem: Çalışmamızda İstanbul Tıp Fakültesi Kadın Hastalıkları ve Doğum Kliniği’nde 01.01.201301.05.2020 tarihleri arasında gebelik takibi, doğumu gerçekl...
Article
Full-text available
The novel coronavirus infection (SARS-CoV-2 infection), which appeared in the Wuhan region of China in late 2019, spread rapidly in a short time. A few months later, it was accepted as pandemic by the WHO (World Health Organization) and became an important threat to public health. The death rate in cases occurring in China was around 2%. Although i...
Article
Full-text available
Neonatal sepsis remains an important global problem, with little progress despite great efforts. Currently there is no recognized international consensus on the definition, diagnosis, and treatment of neonatal sepsis. The developments regarding the definition, incidence, etiology, pathophysiology, risk factors, clinical signs and symptoms, diagnosi...
Article
Full-text available
The epidemic that emerged in recent months and related to severe acute respiratory syndrome coronavirus-2 (SARSCoV-2) caused a global threat. When ineffective treatment methods and the lack of vaccines were considered, these issues caused a serious international concern (1). 80% of people who have had COVID-19 disease as a result of SARS-CoV-2 infe...
Article
Full-text available
COVID-19 d sease caused by a novel type coronavrus (2019-nCoV / SARS-CoV-2) nfecton s more severe and symptomatc n older people and people wth an addtonal d sease, unl ke ch ldren and young people wthout addtonal d sease. However, there s not yet su cent evdence about the transton routes to the fetus, the clncal course of the vrus, laboratory chang...
Article
Background: There is no data regarding the prevalence of malignancies in patients with primary immunodeficiency (PID) in Turkey. Along with the prevalence of malignancy, we aimed to present the types of malignancy and define the underlying immune deficiency of the patients. Method: Between the years 1992 and 2018 years, from 5 tertiary immunolog...
Article
Full-text available
Hemolytic disease of the newborn is mostly caused by the hemolysis of fetal erythrocytes by maternal and placental antibodies. Antigens in this group are Kell, Duffy, Kidd, MNSs and the E, e, C, c found in the Rh system. They are responsible for 3-5% of hemolytic disease of the newborn. In cases of minor blood group incompatibility, clinical pictur...
Presentation
Full-text available
Özet: Hipoksik iskemik ensefalopati (HİE), neonatal ölüm, serebral palsi ve ileri dönemlerde daha da belirginleşen gelişimsel gerilikle sonuçlanabilen santral sinir sistemindeki kalıcı hasarın en önemli sebeplerinden birisidir. HİE’de günümüzdeki en etkin tedavi yöntemi tüm vücut soğutma (Hipotermi) tedavisidir ve hipoksik olaydan etkilenen bebekle...
Article
Full-text available
Mastocytosis, first described by Nettleship and Tay in 1869 as cutaneous mast cell disease, is characterized by the proliferation and accumulation of mast cells in primarily skin and bone marrow and various other tissues e.g. the liver, spleen and lymph nodes. The abnormal increase and activity of mast cells in different tissues leads to different...
Article
Suçiçeği, insan herpes virüsleri arasında yer alan varisella zoster virü- sünün (VZV) birincil bir hastalığıdır. Suçiçeği enfekte olan kişiden hava yolu, damlacık ve direkt temas ile kolaylıkla bulaşabilir bir hastalıktır. Suçiçeği enfeksiyonu sonrası deri lezyonlarının stafilokok ya da strep- tokoklarla ikincil enfeksiyonu hastalığın en sık görüle...
Article
Full-text available
Datura stramonium, also known as pipe flower or angel’s trumpet, is a toxic plant member of the belladonna family containing several alkaloids. All parts of Datura plants contain tropane alkaloids at dangerous levels, such as atropine, hyaline and scopolamine, classified as deliriums or anticholinergics. High amounts of datura stramonium ingestion...
Chapter
Full-text available
25. Bölüm Yazarlığı: “Besin Alerjisi olan Hastaların ve Ailelerinin Eğitimi Nasıl Olmalıdır ?”
Article
Full-text available
Varicella is a primary disease of varicella zoster virus (VZV), which is among the human herpes viruses. Chickenpox is a disease that can be easily transmitted by airway, droplet and direct contact to the infected person. Skin lesions after varicella infection are the most common complication of staphylococcal or streptococcal secondary infections....
Article
Full-text available
Juvenile dermatomyositis (JDM) is an inflammatory myopathy with specific skin lesions. The prevalence rate is 10/10,000,000 while the prevalence rate in children is 3.2/10,000,000. Although the etiology is not fully understood, tissue compatibility antigens, environmental factors (viruses, drugs, etc.) and autoimmunity are often responsible. In adu...
Article
Full-text available
Introduction: Osteogenesis imperfecta (OI) is a hereditary disease that impairs the quality of life by frequent bone fractures. The objective of our study is to retrospectively evaluate patients diagnosed with OI and to come up with helpful data that will assist developing new diagnosis and treatment protocols. Materials and Methods: Twenty-eight c...

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