Amniotic Fluid Disorders in Pregnant Women With COVID-19 in Ardabil (Iran): A Descriptive Cross-Sectional Study (2020-2022) [PDF]
Journal of Multidisciplinary CareBackground and aims: Pregnant women faced heightened vulnerability during the coronavirus disease 2019 (COVID-19) pandemic, with evidence suggesting increased risks of adverse outcomes.
Shahla Farzipour +3 more
doaj +1 more source
Fetal Exposure to Lisinopril: Neonatal Manifestations and Management [PDF]
, 1993 Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/90123/1/j.1875-9114.1993.tb04318.x ...
Bhatt‐mehta, Varsha, Deluga, Karl S.
core +1 more source
Expanding Phenotype of GINS1 Deficiency: A Case Report and Review of the Literature
Clinical Genetics, Volume 109, Issue 6, Page 1076-1080, June 2026.The authors present a novel case and review of individuals with GINS1 deficiency, causing severe growth restriction and combined immunodeficiency. Only the ninth case of this ultrarare disorder, it highlights the role of these variants in disease, glaucoma as a feature, and the possibility of immunodeficiency without infections in affected individuals.
Michael P. Mackley +6 more
wiley +1 more source
Peculiarities of Psychoemotional State in Pregnant Women with Oligohydramnios
Galician Medical Journal, 2016 Oligohydramnios is an obstetric pathology being one of the most common perinatal diseases. In 70% of cases, its causes are unclear which requires further improvement of diagnostics and treatment tactics.
Irina Basiuga
doaj +1 more source
Stronger instruments via integer programming in an observational study of late preterm birth outcomes [PDF]
, 2013 In an optimal nonbipartite match, a single population is divided into matched pairs to minimize a total distance within matched pairs. Nonbipartite matching has been used to strengthen instrumental variables in observational studies of treatment effects,
Goyal, Neera K. +4 more
core +3 more sources
Antenatal Presentation of MRPS22‐Related Mitochondrial Disease Confirmed With Rapid Proteomics
JIMD Reports, Volume 67, Issue 3, May 2026.ABSTRACT MRPS22‐related mitochondrial disease (MIM#611719) is a rare autosomal recessive disorder caused by defects in the mitochondrial ribosomal protein S22, a component of the small mitoribosomal subunit essential for mitochondrial translation. Of the few reported cases, most present antenatally with a severe phenotype, conveying a poor prognosis ...
Liana N. Semcesen +43 more
wiley +1 more source
EPIDEMIOLOGY OF URINARY SYSTEM DEFECTS IN CHILDREN OF NORTHERN BUKOVYNA [PDF]
, 2013 The incidence and the dynamics of the frequency of congenital malformations of the urinary organs in the Chernivtsi region over the period from 2004 to 2008 have been studied.
Pishak, Vasiliy, Riznichuk, Marjana
core +2 more sources
Prevalence and risk factors for low birth weight in Ardabil, Iran. [PDF]
Introduction: Low birth weight (LBW) is the most common cause of neonatal death in developing countries. The objective of our study was to determine the prevalence and risk factors associated with low birth weight in Ardabil, Iranfrom 2010 to 2011 ...
احمدی هادی, پیمانه +3 more
core
Maternal Height and Infant Body Mass Index Are Possible Risk Factors for Developmental Dysplasia of the Hip in Female Infants [PDF]
, 2015 Developmental dysplasia of the hip (DDH) is a wide-spectrum disease with a multifactorial etiology and, despite its prevalence, no definitive etiology has yet been established.
Atalar, Hakan +5 more
core +1 more source