Results 341 to 350 of about 4,096,588 (418)

Endoscopic remodeling of esophageal stenosis refractory to traditional endoscopic treatment

JPGN Reports, EarlyView.
Abstract Esophageal atresia (EA), with or without tracheoesophageal fistula, is the most common congenital anomaly of the esophagus. Surgical correction is the primary treatment, however, up to 80% of patients experience anastomotic stenosis, with esophageal balloon dilation (EBD) being the first‐line treatment.
María Camila Beltrán‐Ramírez, Jose Fernando Vera‐Chamorro, Ailim Margarita Carias‐Dominguez   +2 more
wiley   +1 more source

Prenatal diagnosis of clinodactyly and its association with genetic syndromes: A case report. [PDF]

Case Rep Womens Health
Loukopoulos T, Zikopoulos A, Vlassis N, Manolakos E, Sotiriou S, Vatopoulou A, Gkrozou F, Potiris A, Stavros S, Skentou C.   +9 more
europepmc   +1 more source

Expanding the Estimated Fetal Weight Definition of Growth Restriction by Adding Small Abdominal Circumference

Journal of Ultrasound in Medicine, EarlyView.
Objective The Society for Maternal‐Fetal Medicine's (SMFM) diagnostic criteria for fetal growth restriction (FGR) recently added abdominal circumference (AC) <10th percentile to estimated fetal weight (EFW) <10th percentile; however, its prediction of neonatal morbidity is unknown.
Ashley Shea, Ashley N. Battarbee, Katherine L. Grantz, Dian He, John Owen   +4 more
wiley   +1 more source

Prenatal diagnosis of isolated fetal hydrometrocolpos: A case report. [PDF]

Radiol Case Rep
Bannour B, Abbassi H, Guerbej E, Bannour I, Boughizane S.   +4 more
europepmc   +1 more source

Construction and Validation of a Risk Prediction Model for Early Severe Intraventricular Hemorrhage in Very Low Birth Weight Infants

The Kaohsiung Journal of Medical Sciences, EarlyView.
ABSTRACT In the past several years, prediction models for severe intraventricular hemorrhage (IVH) in premature infants have emerged. However, few models have considered the importance of predictors related to the clinical course and hemostatic profile in predicting the risk of hemorrhage, such as the FiO2, hematocrit, and platelet count.
Fei Shen, Jie Xu, Hui Rong, Jing Zhang, Yang Yang, Xian‐Wen Li   +5 more
wiley   +1 more source

Prevalence and diagnostic dilemma of chromosomal abnormalities in the Niger Delta area of Nigeria; Is prenatal diagnosis worthwhile? [PDF]

Niger Med J
Abbey M, West BA, Amadi SC, Oloyede OA, Horsfall F, Nonye-Enyidah EI, Okagua KE, Kwosah NJ, Kua PL, Iwo-Amah RS, Ocheche US, Ononuju CN, Briggs NN, Altraide BO, Sapira-Ordu L, Inimgba N.   +15 more
europepmc   +1 more source

A learning health system model for addressing substance use: Denver Health Center for Addiction Medicine

Learning Health Systems, EarlyView.
Abstract Introduction Substance use disorders (SUDs) continue to place heavy burdens on patients, health systems, and communities. Rapidly evolving treatment for SUDs requires health systems that can efficiently and effectively assess data and integrate evidence to practice.
Emily Bacon, Laura J. Podewils, Brooke Bender, Joshua Blum, Christian Thurstone, Alia Al‐Tayyib, John Mills, Alexandra R. Tillman, Judith Shlay   +8 more
wiley   +1 more source

Evaluating Chromosomal Mosaicism in Prenatal Diagnosis: The Complementary Roles of Chromosomal Microarray Analysis and Karyotyping. [PDF]

J Clin Lab Anal
Xu C, Xiong Y, Wang D, Zhang S, Wu X, Li M.   +5 more
europepmc   +1 more source

High Genetic Diagnostic Yield for Patients with Rare Movement Disorders at a Single‐Center Neurogenetics Clinic

Movement Disorders Clinical Practice, EarlyView.
Abstract Background As advanced molecular testing is incorporated into routine clinical practice, accessibility and yield remain limited. Objectives We propose a simplified and effective workup strategy to maximize diagnostic yield based on presented diagnostic yield of rare movement disorders at a tertiary Neurogenetics Clinic.
Dvir Penn, Yam Amir, Gil Ben David, Alina Kuralop, Dalit Barel, Uri Hamiel, Michal Bach, Emil Elhanan, Tali Barkan, Daphna Marom, Adi Mory, Noga Simantov, Gadi Maayan Eshed, Achinoam Faust‐Socher, Vered Livneh, Avner Thaler, Nurit Omer, Tamara Shiner, Nir Giladi, Tanya Gurevich, Hagit Baris Feldman, Roy N. Alcalay, Yuval Yaron, Penina Ponger   +23 more
wiley   +1 more source

Prenatal diagnosis of proboscis lateralis. [PDF]

Arch Gynecol Obstet
Elger T, Wiechers C, Hoopmann M, Kagan KO.   +3 more
europepmc   +1 more source