Results 21 to 30 of about 31,475 (257)

Acute Respiratory Distress Syndrome in Preterm Newborns (Morphological Study)

Общая реаниматология, 2020
The aim of the study is to provide a rationale for the morphological diagnostic criteria of respiratory distress syndrome (RDS) and acute respiratory distress syndrome of the newborn (ARDSN) in extremely preterm newborn infants.Materials and methods ...
S. A. Perepelitsa
doaj   +1 more source

Endocrine Disorders in a Newborn with Heterozygous Galactosemia, Down Syndrome and Complex Cardiac Malformation: Case Report

Medicina, 2023
Down syndrome is the most common chromosomal abnormality diagnosed in newborn babies. Infants with Down syndrome have characteristic dysmorphic features and can have neuropsychiatric disorders, cardiovascular diseases, gastrointestinal abnormalities, eye
Ioana Rosca, Alina Turenschi, Alin Nicolescu, Andreea Teodora Constantin, Adina Maria Canciu, Alice Denisa Dica, Elvira Bratila, Ciprian Andrei Coroleuca, Leonard Nastase   +8 more
doaj   +1 more source

Prophylactic Dexamethasone for improving perinatal outcome before elective caesarean section at term pregnancy

Advanced Medical Journal, 2023
Background and objectives: With the increase in the incidence of elective caesarean section, and the absence of onset of labour, the increase in the rate of neonatal respiratory morbidities and admissions to neonatal intensive care unit have also been ...
Parzheen Ibrahim Hamadamin, Ariana Khalis Jawad   +1 more
doaj   +1 more source

Respiratory Distress Syndrome in the Newborn [PDF]

BMJ, 1974
E. O. R. Reynolds, A. Taghizadeh
  +7 more sources

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Factors related to the incident respiratory distress syndrome on neonate at the Harapan and Doa Hospital, Bengkulu City

Jurnal Ners dan Kebidanan Indonesia
Background: Apart from increasing morbidity and motility, respiratory problems in newborn babies are a condition that can result in respiratory arrest and even death.
Febry Kusumawardhani, Diah Eka Nugraheni, Suci Solihat, Lela Hartini, Yuniarti Yuniarti   +4 more
doaj   +1 more source

Malectin Alleviates Endoplasmic Reticulum Stress in Gestational Diabetes Mellitus via Glycoprotein Quality Control Mechanisms

Advanced Science, EarlyView.
Malectin alleviates high glucose‐induced ER stress and damage in placental trophoblasts, a function dependent on its six critical carbohydrate‐binding residues. In a GDM mouse model, administration of TAT‐Malectin ameliorated hyperglycemia and placental ER stress and prevented fetal macrosomia.
Jiahui Zhu, Yumeng Zhang, Ye Wang, Xiaoyu Zhu, Ailin Yuan, Weijing Yin, Huangmin Yu, Xuemin Pang, Yufeng He, Yuchen Wang, Tong Wang, Yong Li, Yunlong Si   +12 more
wiley   +1 more source

Respiratory distress syndrome of the newborn

Sri Lanka Journal of Child Health, 2018
Sri Lanka Journal of Child Health, 2018; 47(4): 295 ...
M Weerasekera, A Y Wimalasiri, K D S K Savithri   +2 more
openaire   +2 more sources

Autoimmune Encephalitis in Acute Care—Pathology, Diagnosis, and Management

Advanced Science, EarlyView.
ABSTRACT Autoimmune encephalitis (AE) is characterized by immune‐mediated inflammation of the brain parenchyma, presenting with various neurological syndromes, including but not limited to seizures, altered consciousness, neuropsychiatric symptoms, and movement disorders.
Suneesh Thilak, David Okoh, William Scotton, Shanika Samarasekera, Vikram Patil, Suresh Renukappa, Andrew Macduff, Subashini Suresh, Rajeev Krishnadas, Tonny Veenith   +9 more
wiley   +1 more source

Netherton Syndrome, a Rare Genetic Disorder—Case Report

Dr. Sulaiman Al Habib Medical Journal, 2023
Netherton syndrome is a rare genetic disorder inherited in an autosomal recessive pattern. Mutations in the serine protease inhibitor Kazal-type 5 (SPINK5) gene are responsible for this disorder.
Yahya Almalki, Faisal Khan, Ammara Naeem, Muhammad Hasan Alabdulghany   +3 more
doaj   +1 more source