Results 101 to 110 of about 20,282 (239)

Prenatal management and perinatal outcome in giant placental chorioangioma complicated with hydrops fetalis, fetal anemia and maternal mirror syndrome

BMC Pregnancy and Childbirth, 2012
Background Giant placental chorioangiomas have been associated with a number of severe fetal complications and high perinatal mortality. Case presentation We report a case of giant chorioangioma with fetal hydrops, additionally complicated by severe ...
García-Díaz Lutgardo, Carreto Práxedes, Costa-Pereira Susana, Antiñolo Guillermo   +3 more
doaj   +1 more source

Observations related to chronologic and gynecologic age in pregnant adolescents. [PDF]

, 1984
A low chronologic age (less than or equal to 15 years) and low gynecologic age (less than or equal to 2 years) have been considered factors that increase medical complications among adolescent pregnant women. Gynecologic age (GA) is defined in this study
Felice, ME, Hollingsworth, DR, James, M, Shragg, P   +3 more
core  

Jefferson Digital Commons quarterly report: January-March 2020 [PDF]

, 2020
This quarterly report includes: New Look for the Jefferson Digital Commons Articles COVID-19 Working Papers Educational Materials From the Archives Grand Rounds and Lectures JeffMD Scholarly Inquiry Abstracts Journals and Newsletters Master of Public ...
Copeland, LIBT, James, Duinkerken, MSI, Kelsey, Gordon, MSLIS, MEd, MA, Larissa   +2 more
core   +1 more source

New cases of δ‐aminolevulinic acid dehydratase deficiency: Functional insights into gene variants using an innovative mouse liver model

Journal of Internal Medicine, Volume 299, Issue 1, Page 126-142, January 2026.
Abstract Background Dysfunction of δ‐aminolevulinic acid dehydratase (ALAD), the second enzyme involved in heme biosynthesis, leads to two pathologies: genetic and acquired. The genetic form is an ultrarare, severe childhood‐onset disease inherited in an autosomal recessive manner, whereas the acquired form usually affects adults due to enzyme ...
Elena Di Pierro, Isabel Solares, Daniel Jericó, Francisco J. Castelbón, Javier Tomás Solera, Antoni Riera‐Mestre, María Barreda‐Sánchez, Carlo Poci, Annamaria Nicolli, Francesco Urigo, Ana Sampedro, Rafael Enríquez de Salamanca, Matteo Marcacci, Matías A. Ávila, Pauline Harper, Marta G. Fanlo‐Maresma, Encarna Guillén‐Navarro, Giovanna Graziadei, Andrea Wenzel, Bodo B. Beck, Paolo Ventura, Montserrat Morales‐Conejo, Antonio Fontanellas   +22 more
wiley   +1 more source

Management of late-preterm and term infants with hyperbilirubinaemia in resource-constrained settings. [PDF]

, 2015
Hyperbilirubinaemia is a ubiquitous transitional morbidity in the vast majority of newborns and a leading cause of hospitalisation in the first week of life worldwide.
Boo, Nem-Yun, de Almeida, Maria Fernanda B, Iskander, Iman F, Kumar, Praveen, Ogunlesi, Tinuade A, Olusanya, Bolajoko O, Slusher, Tina M, Vaucher, Yvonne E   +7 more
core   +2 more sources

[Intrauterine blood transfusion in case of placental chorangioma].

Ginekologia polska, 2011
The paper presents a case of placental tumor causing hemodynamic changes. Doppler studies and fetal echocardiography allowed the diagnosis of hyperkinetic circulation in the course of fetal anemia. Cordocentesis has been performed and confirmed fetal anemia. The treatment used, intrauterine blood transfusion, allowed the compensation of hemodynamic and
Karolina, Gruca-Stryjak, Mariola, Ropacka-Lesiak, Grzegorz, Breborowicz   +2 more
openaire   +1 more source

Genotype–Phenotype Correlation in TTC7A ‐Associated Gastrointestinal Defects and Immunodeficiency Syndrome 1

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff, Hans Christian Schmidt, Matthias Hans Belau, Johanna Hagens, Mario Lange, Daniel Tegtmeyer, Konrad Reinshagen, Frederike Leonie Harms, Christian Tomuschat   +8 more
wiley   +1 more source

Different Types of Minor Blood Group Incompatibility Causing Haemolytic Disease of Neonates in one of the National Children’s Medical Centre in China

Journal of Blood Medicine, 2021
Mingchun Lin,1,2 Meixiu Liu,3 Shulian Zhang,1 Chao Chen,1 Jin Wang1 1Neonatal Department, Children’s Hospital of Fudan University, Shanghai, 201102, People’s Republic of China; 2Neonatal Fellowship Training at Children’s Hospital of Fudan University ...
Lin M, Liu M, Zhang S, Chen C, Wang J
doaj  

Mitochondrial Disease Diagnosed Following Preterm Birth at 29 Weeks of Gestation and Postpartum Heart Failure: A Case Report and Literature Review

Clinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT In some cases, mitochondrial disease can remain undiagnosed until pregnancy reveals systemic symptoms. Clinicians should therefore consider this diagnosis in young patients presenting with diabetes, kidney disease, and hearing loss. Early diagnosis can improve maternal and fetal outcomes, particularly in high‐risk pregnancies complicated by ...
Tomoyuki Watanabe, Gen Ishikawa, Tsutomu Tabata   +2 more
wiley   +1 more source

Major obstetric haemorrhage: portrait of "near miss" and risk management-based optimisation of obstetric techniques and telemedicine technologies

Фундаментальная и клиническая медицина, 2019
Aim. To identify measures for the improvement of obstetric techniques and telemedicine technologies in women with major obstetric haemorrhage.Materials and Methods.
O. V. Remneva, E. G. Ershova, A. E. Chernova, A. I. Galchenko, V. A. Borovko   +4 more
doaj   +1 more source