Halıl Aslan

ORCID: 0000-0003-2004-8522
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Prenatal Screening and Diagnostics
  • Assisted Reproductive Technology and Twin Pregnancy
  • Pregnancy and preeclampsia studies
  • Congenital Anomalies and Fetal Surgery
  • Congenital Heart Disease Studies
  • Urological Disorders and Treatments
  • Congenital Diaphragmatic Hernia Studies
  • Fetal and Pediatric Neurological Disorders
  • Tracheal and airway disorders
  • Maternal and fetal healthcare
  • Gestational Trophoblastic Disease Studies
  • Maternal and Perinatal Health Interventions
  • Genetic and Kidney Cyst Diseases
  • Parvovirus B19 Infection Studies
  • Birth, Development, and Health
  • Gestational Diabetes Research and Management
  • Neonatal Respiratory Health Research
  • Tumors and Oncological Cases
  • Ectopic Pregnancy Diagnosis and Management
  • Cardiac Imaging and Diagnostics
  • Connective tissue disorders research
  • Ureteral procedures and complications
  • Genomic variations and chromosomal abnormalities
  • Coronary Artery Anomalies
  • Reproductive Health and Technologies

Pamukkale University
2019-2025

İstanbul Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi
2012-2019

Ankara Yıldırım Beyazıt University
2017

Atatürk University
2015

University of Health Sciences Antigua
2014

Bakırköy Psychiatric Hospital
2004-2011

Ministry of Health
2011

Boston Children's Hospital
2011

Inonu University
2007

Van Yüzüncü Yıl Üniversitesi
2001

<i>Objective:</i> Our purpose was to find out and compare perinatal outcomes in pregnancies complicated by severe preeclampsia-eclampsia with without HELLP syndrome. <i>Methods:</i> Clinical laboratory findings, perinatal-neonatal of all pregnants preeclampsia, eclampsia have been prospectively recorded. Results were compared means Student’s t test, χ<sup>2</sup> analysis Fisher’s exact test as appropriate. <i>Results:</i> Among 367 consecutive...

10.1159/000082648 article EN Gynecologic and Obstetric Investigation 2004-12-14

Abstract Purpose To investigate the etiology of spontaneous percutaneous nephrostomy (PCN) catheter dislodgements and evaluate factors potentially associated with these dislodgements, including muscle-to-fat composition tissue characteristics traces. Materials methods Data from 92 patients (63 males, 29 females; mean age 63.9 ± 11.4 years, range 28–88) undergoing 151 PCN replacements between January 2016 June 2021 were analyzed. Patients divided into Group 1 (prophylactic every 3 months, n =...

10.1007/s00261-025-04855-6 article EN cc-by Abdominal Radiology 2025-02-26

BACKGROUND: Caudal regression is a rare syndrome which has spectrum of congenital malformations ranging from simple anal atresia to absence sacral, lumbar and possibly lower thoracic vertebrae, the most severe form known as sirenomelia. Maternal diabetes, genetic predisposition vascular hypoperfusion have been suggested possible causative factors. CASE PRESENTATION: We report case caudal diagnosed in utero at 22 weeks' gestation. Prenatal ultrasound examination revealed sudden interruption...

10.1186/1471-2393-1-8 article EN cc-by BMC Pregnancy and Childbirth 2001-12-11

10.1016/s0301-2115(03)00363-4 article EN European Journal of Obstetrics & Gynecology and Reproductive Biology 2003-12-10

This study reviews maternal and fetal outcomes in HELLP syndrome complicated with acute renal failure (ARF), compares clinical laboratory findings of the cases that did not develop ARF.All pregnant women hypertensive disorders admitted or referred to unit were recorded into a perinatal database between January 15, 2002 September 2003. During period, out 615 pregnancy, we followed delivered 347 severe preeclampsia, them 132 diagnosed as syndrome. ARF was defined creatinine level > =1.2 mg/dL...

10.1081/jdi-200031750 article EN Renal Failure 2004-01-01

In this report, we describe 3 cases of pentalogy Cantrell diagnosed prenatally with sonography. All fetuses had an omphalocele and ectopia cordis; 2 them also craniorachischisis, in which the open cranial defect (anencephaly or exencephaly) is continuous completely spine (spinal dysraphism). The association exencephaly rare, to our knowledge, syndrome craniorachischisis has not been reported previously. addition, clubfoot, 1 clubhand, neither previously Cantrell. Finally, polyhydramnios,...

10.1002/jcu.20134 article EN Journal of Clinical Ultrasound 2005-01-01

<i>Objective:</i> The aim of this study was to determine perinatal outcomes twin pregnancies discordant for a major fetal anomaly and compare with twins without anomaly. <i>Methods:</i> All admitted or referred the maternal-fetal unit were prospectively entered into computer database. Chorionicity, anomaly, mean gestational age at delivery, birth weight survival rate reviewed. <i>Main Outcome Measures:</i> Mean <i>Results:</i> There 48 cases...

10.1159/000085078 article EN Fetal Diagnosis and Therapy 2005-01-01

To compare maternal and perinatal outcomes in pregnancies complicated by severe preeclampsia, eclampsia, HELLP (hemolysis, elevated liver enzyme levels, low platelets) syndrome.Maternal neonatal charts of 1,222 consecutive or syndrome at our maternal-perinatal unit were reviewed. Patients divided into three groups: 903 (73.9%) with 123 (10.1%) 196 (16.0%) syndrome.The overall incidence adverse outcome was 5.9%. The rates for women eclampsia higher than preeclampsia (13.8% vs. 11.4% 3.4%,...

10.5152/jtgga.2011.22 article TR Journal of the Turkish-German Gynecological Association 2011-06-01

Abstract Joubert syndrome is a rare, autosomal recessive condition, first described by in 1969. We present case of from consanguineous family which, apart the cerebellar vermis agenesis, ventriculomegaly, bilateral postaxial polydactyly hands and right foot micropenis, episodes fetal breathing pattern with an increased respiratory rate were also demonstrated prenatal ultrasound scan. At birth infant showed odd face fleshy nodules tongue. He had abnormal alternating tachypnea apnea. Cranial...

10.1002/pd.220 article EN Prenatal Diagnosis 2002-01-01

10.1016/j.ijgo.2007.05.047 article EN International Journal of Gynecology & Obstetrics 2007-09-24

Objective. To evaluate the efficacy of membrane sweeping at initiation labor induction in low-risk patients term pregnancy (38–40 gestational weeks).Methods. This prospective study included 351 antenatal women who were randomly assigned to one two groups: a membranes group (n = 181) and no control 170). The primary outcome measure was proportion entered spontaneous within 1 week entry into study. Secondary measures mode delivery maternal fetal complications.Results. Five (two three group)...

10.3109/14767050903387078 article EN The Journal of Maternal-Fetal & Neonatal Medicine 2009-11-09

Placenta percreta is a life-threatening condition that places patients at risk of massive bleeding. It necessitates very complicated surgery and can result in mortality. Caesarean hysterectomy the accepted procedure worldwide; however, recent studies discussing conservative treatment with segmental resections have been published. Foetal extraction resection be performed through same incision (single uterine incision) or two different incisions (double incision). In this study, we aimed to...

10.1186/s12884-017-1262-3 article EN cc-by BMC Pregnancy and Childbirth 2017-04-27

Congenital high airway obstruction syndrome (CHAOS) is an extremely rare life-threatening condition. Laryngeal atresia appears to be the most frequent cause. Generally diagnosis made with severely enlarged and highly echogenic lungs additional ultrasound findings. The prognosis of affected infants often poor. Five cases are reported here that were diagnosed in a tertiary center between 2008 2014.

10.11152/mu.2013.2066.171.haek article EN Medical Ultrasonography 2015-02-27

To compare neonatal outcome after preterm delivery of infants where pregnancy had been complicated by the HELLP syndrome.The maternal and charts 475 consecutive pregnancies hypertensive disorders at our perinatal unit were reviewed. The syndrome was defined previously published laboratory criteria. 93 women fulfilled criteria constituted study group. 188 normotensive patients who delivered because labor comprised control Results compared means chi2 analysis Student's t test appropriate.There...

10.1159/000078679 article EN Gynecologic and Obstetric Investigation 2004-01-01

BACKGROUND: Neu-Laxova syndrome is a rare congenital abnormality involving multiple systems. We report case of (NLS) diagnosed prenatally by ultrasound examination. CASE PRESENTATION: A 29-year-old gravida 3, para 2 woman was first seen in our antenatal clinic at 38 weeks' pregnancy. Except for the consanguinity and two previous abnormal stillborn babies her medical history unremarkable. On examination microcephaly, flat forehead, micrognathia, intrauterine growth restriction, generalized...

10.1186/1471-2393-2-1 article EN cc-by BMC Pregnancy and Childbirth 2002-02-19

The objective of this study was to assess the iodine status pregnant women in a metropolitan city which stated as sufficient area after salt iodination program. This multicenter, cross-sectional carried out on 3543 women. Age, gestational weeks, smoking, consumption iodized salt, dietary restriction, history stillbirth, abortus and congenital malformations were questioned. Spot urine samples analyzed for concentration (UIC). outcomes were: (a) median UIC three trimesters pregnancy (b)...

10.3109/09513590.2015.1101443 article EN Gynecological Endocrinology 2015-10-22

We present a case of esophageal and ileal duplications at 18 weeks gestation. Transabdominal ultrasonography the fetus showed multiple cystic masses 12 to 17 mm in diameter continuity with each other abdomen unilocular mass 15 posterior mediastinum. The filled abdominal cavity signs intestinal obstruction. thoracic was tubular, sausage-shaped behind heart, which displaced antero-lateral wall chest. Amniocentesis revealed normal fetal karyotype 46,XY. Peristaltic movements structure 30...

10.1002/pd.1033 article EN Prenatal Diagnosis 2004-12-15

Abstract Aim: To study the outcome of cases incidental adnexal masses detected during cesarean section. Methods: A total 126 093 live births and 39 115 deliveries performed between 2002 2008 were retrospectively evaluated with additional surgical interventions included in study. Histopathologic assessment related outcomes examined. Results: One hundred nineteen patients had at time delivery; incidence was 1/329. The most common histopathologic diagnoses mature cystic teratoma (32%)...

10.1111/j.1447-0756.2010.01177.x article EN Journal of Obstetrics and Gynaecology Research 2010-06-01

Aretrospective study involving 972 twin births was conducted to evaluate the maternal and fetal outcomes of pregnancies complicated by single death. The incidence death in after 20 weeks 3.3%. Preterm birth rates for 37 32 gestational were 81.3% 41.6% respectively. median interval between diagnosis delivery 11 days (range 1–27 days). Eighteen (56%) infants delivered cesarean 14 (43%) vaginally. Twin–twin transfusion syndrome (TTTS) cause 8 (25%). Ten surviving co-twins lost neonatal period...

10.1375/13690520460741372 article EN Twin Research 2004-02-01
Coming Soon ...