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Türk Pediatri Arşivi

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https://www.readbyqxmd.com/read/29485139/erratum
#1
(no author information available yet)
[This corrects the article on p. 165 in vol. 52, PMID: 29062251.].
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29485137/erratum
#2
(no author information available yet)
[This corrects the article on p. 133 in vol. 52, PMID: 29062246.].
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483808/re-neonatal-grave-s-disease-a-caution-while-treating
#3
Selim Kurtoğlu, Ahmet Özdemir
No abstract text is available yet for this article.
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483807/neonatal-grave-s-disease-a-caution-while-treating
#4
COMMENT
Devi Dayal, Anshita Aggarwal
No abstract text is available yet for this article.
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483806/evaluation-of-two-non-myasthenic-patients-with-ptosis
#5
Serkan Kırık, Olcay Güngör, Sedat Işıkay, Can Acıpayam, Yasemin Çoban, Emre Çelik
Decreased height of the eyelid or the narrowing of the lid is called ptosis. Ptosis has several causes. Malignancy-related conditions such as Horner's syndrome, which causes unilateral ptosis in the pediatric age group, and patients with malignancy receiving chemotherapeutic treatment, are often secondary to these drugs and ptosis is a clue of underlying diseases. Underlying pathologies can lead to different clinical conditions such as cognitive impairment from coma, the presence of ptosis should be cautionary...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483805/a-rare-cause-of-vomiting-annular-pancreas
#6
Yasin Şahin, Yusuf Doğan, Hasret Ayyıldız Civan, Şenol Emre, Osman Uzunlu, Gonca Topuzlu Tekant, Hatice Arıöz Habibi, İbrahim Adaletli, Fügen Çullu Çokuğraş, Tufan Kutlu, Tülay Erkan
Annular pancreas is a rare congenital anomaly that consists of a ring of pancreatic tissue partially or completely encircling the second part of the duodenum. It can affect anyone from neonates to adults, and is difficult to diagnose because it can present in a wide range of clinical conditions. Although cases have also been reported in adults, symptomatic cases are often referred in infancy or early childhood. A 17-year-old female patient who was diagnosed as having annular pancreas is reported. The patient had had non-bilious vomiting accompanied by abdominal pain, especially 5-10 minutes after meals, for seven years...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483804/two-patients-with-apert-syndrome-with-different-mutations-the-importance-of-early-diagnosis
#7
Esra Işık, Tahir Atik, Hüseyin Onay, Ferda Özkınay
Apert syndrome is an autosomal dominant craniosynostosis syndrome accompanied by limb anomalies. The fibroblast growth factor receptor 2 ( FGFR2 ) gene is responsible for the disease and two different heterozygous mutations, p.Pro253Arg and p.Ser252Trp, have been defined as responsible in the majority of cases of Apert syndrome. In this case report, two patients with Apert syndrome with two different FGFR2 gene mutations are presented. Case-1, a 4-month-old boy with craniosynostosis and syndactyly was referred to pediatric genetic clinic...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483803/a-case-of-donohue-syndrome-leprechaunism-with-a-novel-mutation-in-the-insulin-receptor-gene
#8
Birgül Kirel, Özkan Bozdağ, Pelin Köşger, Sultan Durmuş Aydoğdu, Eylem Alıncak, Neslihan Tekin
Donohue syndrome (Leprechaunism) is characterized by severe insulin resistance, hyperinsulinemia, postprandial hyperglycemia, preprandial hypoglycemia, intrauterine and postnatal growth retardation, dysmorphic findings, and clinical and laboratory findings of hyperandrogenemia due to homozygous or compound heterozygous inactivating mutations in the insulin receptor gene. A female newborn presented with lack of subcutaneous fat tissue, bilateral simian creases, hypertrichosis, especially on her face, gingival hypertrophy, cliteromegaly, and prominent nipples...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483802/evaluation-of-patients-with-orbital-infections
#9
Deniz Aygün, Cezmi Doğan, Mustafa Hepokur, Osman Şevki Arslan, Haluk Çokuğraş, Yıldız Camcıoglu
Aim: Orbital tissue infections are common infections of childhood that can lead to severe complications. Herein, we aimed to evaluate the etiologic factors, diagnosis, follow-up, and treatment procedures in pediatric patients with orbital infections. Material and Methods: This study was performed retrospectively between January 2014 and December 2015 in Cerrahpasa Medical Faculty Pediatric Infectious Disease Unit. Patients were studied for age, ophthalmologic examination features, laboratory and radiology results, treatment modalities, and the response to these treatments...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483801/evaluation-of-febrile-neutropenic-attacks-of-pediatric-hematology-oncology-patients
#10
Yeter Düzenli Kar, Zeynep Canan Özdemir, Özcan Bör
Aim: Febrile neutropenia is an important cause of mortality and morbidity in hematology-oncology patients undergoing chemotherapy. The objective of this study was to evaluate febrile neutropenic episodes in children with malignancy. Material and Methods: Sixty-eight children who received chemotherapy for malignancy between 2010 and 2015 were retrospectively reviewed. The demographic characteristics, laboratory data, infection foci, and frequency of microorganisms grown in culture were examined...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483800/levels-of-inflammatory-cytokines-from-peripheral-blood-mononuclear-cells-of-children-with-cow-s-milk-protein-allergy
#11
Maria D'Apolito, Angelo Campanozzi, Ida Giardino, Massimo Pettoello-Mantovani
Aim: The aim of the study was to investigate the level of cytokines in cultures of cow's milk protein- stimulated peripheral blood mononuclear cells of patients with cow's milk protein allergy. Material and Methods: Eleven children with cow's milk protein allergy and 11 non-allergic controls were studied. Their peripheral blood mononuclear cells were cultured alone and in the presence of cow's milk α-lactalbumin; β-lactoglobulin; αS 1, αS 2, β, and κ-casein fraction mixtures; and a cow's protein mixture from whole milk...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483799/the-effect-of-phototherapy-on-sister-chromatid-exchange-with-different-light-density-in-newborn-hyperbilirubinemia
#12
Hayriye Gözde Kanmaz, Nilüfer Okur, Dilek Dilli, Ahmet Yeşilyurt, Şerife Suna Oğuz
Aim: Concerns of possible genotoxic effects of hyperbilirubinemia and phototherapy were raised from experimental and observational studies in neonates. The purpose of this study was to assess the effect of hyperbilirubinemia and phototherapy with three different methods on DNA damage by investigating sister chromatid exchange frequency. Material and Methods: Patients whose gestational ages were >37 weeks and bilirubin levels above phototherapy limits were enrolled into three groups and each group was planned to receive 25 babies...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483798/electrocardiographic-changes-in-children-with-diabetic-ketoacidosis-and-ketosis
#13
Deniz Aygün, Fatih Aygün, Kemal Nişli, Firdevs Baş, Agop Çıtak
Aim: We aimed to study electrocardiographic changes in children with diabetic ketoacidosis and ketosis and to evaluate the relation of the changes with serum electrolyte levels and ketosis. Material and Methods: This study was performed in Istanbul Medical Faculty, Pediatric Emergency and Intensive Care Department between May 2008 and May 2009. The electrocardiographic parameters and QT length of children with diabetic ketoacidosis and ketosis were evaluated at diagnosis and after the treatment...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29483797/vascular-toxicity-of-urea-a-new-old-player-in-the-pathogenesis-of-chronic-renal-failure-induced-cardiovascular-diseases
#14
REVIEW
Ida Giardino, Maria D'Apolito, Michael Brownlee, Angela Bruna Maffione, Anna Laura Colia, Michele Sacco, Pietro Ferrara, Massimo Pettoello-Mantovani
Chronic kidney disease in children is an irreversible process that may lead to end-stage renal disease. The mortality rate in children with end-stage renal disease who receive dialysis increased dramatically in the last decade, and it is significantly higher compared with the general pediatric population. Furthermore, dialysis and transplant patients, who have developed end-stage renal disease during childhood, live respectively far less as compared with age/race-matched populations. Different reports show that cardiovascular disease is the leading cause of death in children with end-stage renal disease and in adults with childhood-onset chronic kidney disease, and that children with chronic kidney disease are in the highest risk group for the development of cardiovascular disease...
December 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062258/re-hla-genes-as-a-predictive-screening-tool-for-celiac-disease
#15
Hale Tuhan, Sakine Işık, Ayhan Abacı, Erdem Şimşek, Ahmet Anık, Özden Anal, Ece Böber
No abstract text is available yet for this article.
September 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062257/hla-genes-as-a-predictive-screening-tool-for-celiac-disease
#16
COMMENT
Hakim Rahmoune, Nada Boutrid, Mounira Amrane, Belkacem Bioud
No abstract text is available yet for this article.
September 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062256/re-epidemiology-of-hepatitis-e-virus-in-children
#17
Gülsüm İclal Bayhan, Kaan Demirören, Hüseyin Güdücüoğlu
No abstract text is available yet for this article.
September 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062255/epidemiology-of-hepatitis-e-virus-in-children
#18
COMMENT
Anirban Mandal, Amitabh Singh
No abstract text is available yet for this article.
September 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062254/erroneous-diagnosis-of-rickets
#19
Stepan Kutilek, Sylva Skalova
No abstract text is available yet for this article.
September 2017: Türk Pediatri Arşivi
https://www.readbyqxmd.com/read/29062253/gorlin-goltz-syndrome
#20
Betül Şereflican, Bengü Tuman, Murat Şereflican, Sıddıka Halıcıoğlu, Gülzade Özyalvaçlı, Seval Bayrak
Gorlin-Goltz syndrome is a rare multisystemic disease inherited in an autosomal dominant pattern. It is characterized by numerous basal cell carcinoma of the skin, jaw cysts, and skeletal anomalies such as frontal bossing, vertebral anomalies, palmoplantar pits, and falx cerebri calcification. There is a tendency to tumors including medullablastoma, fibroma, rabdomyoma, leiomyosarcoma etc.. The diagnosis is based on major and minor clinical and radiologic criteria. Early diagnosis and treatment are of utmost importance in reducing the severity of long-term sequelae of this syndrome...
September 2017: Türk Pediatri Arşivi
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