Results 21 to 30 of about 586,591 (251)

A community-based cluster randomized controlled trial (cRCT) to evaluate the impact and operational assessment of “safe motherhood and newborn health promotion package”: study protocol

BMC Public Health, 2018
Background Despite considerable progress in reduction of both under-five and maternal mortality in recent decades, Bangladesh is still one of the low and middle income countries with high burden of maternal and neonatal mortality.
Dewan Md. Emdadul Hoque, Mohiuddin Ahsanul Kabir Chowdhury, Ahmed Ehsanur Rahman, Sk. Masum Billah, Sanwarul Bari, Tazeen Tahsina, Mohammad Mehedi Hasan, Sajia Islam, Tajul Islam, Rintaro Mori, Shams El Arifeen   +10 more
doaj   +1 more source

Retrospective Evaluation of Pediatric Patients with Extremity Pains

Bagcilar Medical Bulletin, 2020
Objective:Recurrent lower extremity pains (growing pains) are the most common non-inflammatory cause of musculoskeletal pain in children. This study aims to investigate musculoskeletal symptoms that may be associated with vitamin D deficiency.
Sezin Naiboğlu, Emrah Naiboğlu, Özden Aksu Sayman, Fatma Gül Demirkan   +3 more
doaj   +1 more source

Awareness levels of teachers of child negligence and abuse: Rural area example

Medicine Science, 2022
It was aimed to determine the frequency of teachers' encounters with child neglect and abuse and their views on this subject in this study. It is a cross-sectional and descriptive study.
Mehmet Emin Parlak, Mehmet Yavuz Ozbey
doaj   +1 more source

A Case of the Perinatal Form Hypophosphatasia Caused by a Novel Large Duplication of the ALPL Gene and Report of One Year Follow-up with Enzyme Replacement Therapy

JCRPE, 2019
Hypophosphatasia (HPP) is a rare disease caused by mutations in the ALPL gene encoding tissue-non-specific isoenzyme of alkaline phosphatase (TNSALP). Duplications of the ALPL gene account for fewer than 1% of the mutations causing HPP. It has been shown
Bülent Hacıhamdioğlu, Gamze Özgürhan, Catarina Pereira, Emre Tepeli, Gülşen Acar, Serdar Cömert   +5 more
doaj   +1 more source

Recurrent Urinary Tract Infection as a Manifestation of Goldenhar Syndrome: Case Report

Van Tıp Dergisi, 2019
Goldenhar syndrome is a rare disease characterized by anomalies of the ear, eye and vertebrae, caused by developmental failure of the first and second brachial arches. Genitourinary, cardiac, skeletal and central nervous system anomalies can also be seen
Ali Güngör, Nilüfer Avunç, Mehmet Orhan Erkan, Emel Isıyel, Esra Kılıç, Bahar Çuhacı Çakır   +5 more
doaj   +1 more source

Pharmacotherapy profiles of children with tic disorders: A cross-sectional retrospective study (tur)

Klinik Psikiyatri Dergisi, 2020
INTRODUCTION[|]In this study, it is aimed to do a cross-sectional evaluation of treatment preferences in tic disorders in a clinical sample.[¤]METHODS[|]The hospital records of cases diagnosed with tic disorders who were admitted to our clinic between ...
Gülser Dinç, Ebru Sekmen, Zeynep Goker, Esra Çöp, Özden Üneri   +4 more
doaj   +1 more source

Distinguishing Kawasaki Disease from Other Febrile Illnesses in Infants

Journal of Pediatric Research, 2022
Aim:Kawasaki disease (KD) is difficult to diagnose in infants, since the disease course is subtle. We aimed to identify whether infants with KD demonstrate significant alterations in laboratory parameters that can be used to distinguish them from other ...
Rumeysa Yalçınkaya, Fatma Nur Öz, Türkan Aydın Teke, Ayşe Kaman, Sevgi Yaşar Durmuş, Utku Arman Örün, Gönül Tanır   +6 more
doaj   +1 more source

Profiles of paediatric patients experiencing stroke-like episodes associated with mitochondrial disease

Frontiers in Neurology
IntroductionStroke-like episodes (SLE) are defined as events characterized by the sudden onset of neurological symptoms with clinical manifestations similar to those of a stroke.
Gülhan Karakaya Molla, Gülhan Karakaya Molla, Özlem Ünal Uzun, Hanım Babazade Agakisili, Emine Genç, Zümrüt Arslan Gülten, Tarık Yıldırım, Aydan Sezgin Ersoy, Belkıs Ak, Aliye Gülbahçe, Sevil Yıldız, Nafiye Emel Çakar, Meryem Karaca, Tanyel Zübarioğlu, Burcu Öztürk Hişmi, Şahin Erdöl, Hasan Önal, Bülent Kara, Gülden Fatma Gökçay   +18 more
doaj   +1 more source

Risk Factors for Invasive Bacterial Infection and Mortality in Febrile Neutropenic Children

Journal of Behçet Uz Children's Hospital, 2019
INTRODUCTION: Febrile neutropenia (FN) is a common and life-threatening complication of therapy for childhood cancer. Serious bacterial illness is a significant cause of morbidity and mortality for neutropenic patients The primary objective was to ...
Belgin Gülhan, Saliha Kanık Yüksek, Aslınur Özkaya Parlakay, Neşe Yaralı, Namık Yaşar Özbek, Hasan Tezer   +5 more
doaj   +1 more source

A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report

Pediatric Rheumatology Online Journal, 2023
Background Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, caused by biallelic pathogenic mutations in the proteoglycan 4 (PRG4) gene, is characterized by early-onset camptodactyly, noninflammatory arthropathy, coxa vara deformity, and ...
İlknur Bağrul, Serdar Ceylaner, Yasemin Tasci Yildiz, Serife Tuncez, Elif Arslanoglu Aydin, Esra Bağlan, Semanur Ozdel, Mehmet Bülbül   +7 more
doaj   +1 more source