Results 151 to 160 of about 220,488 (308)

Fetal rights from Islamic and contemporary legal perspectives: a scoping review. [PDF]

Reprod Health
Kakrodi SP, Sighaldeh SS, Mosadeghrad MA, Abbassi M.   +3 more
europepmc   +1 more source

Wearable Fetus Monitoring: An IoMT Approach

, 2020
Soumitra Das
openalex   +1 more source

Age‐Related Characteristics of SYT1‐Associated Neurodevelopmental Disorder

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We describe the clinical manifestations and developmental abilities of individuals with SYT1‐associated neurodevelopmental disorder (Baker‐Gordon syndrome) from infancy to adulthood. We further describe the neuroradiological and electrophysiological characteristics of the condition at different ages, and explore the associations ...
Sam G. Norwitz, Josefine Eck, Joel S. Winston, Kate Baker   +3 more
wiley   +1 more source

Whole-genome paternal uniparental disomy identified through prenatal single-nucleotide polymorphism-based cell-free DNA screening. [PDF]

Ultrasound Obstet Gynecol
Benn P, Hashimoto K, Souter V, Dhamankar R, Xu W, Kijacic D.   +5 more
europepmc   +1 more source

The impact of the month pregnant and fetus sex on progesterone and cortisol hormones and lipid profile in the women during the third-trimester pregnancy

, 2019
Wahbi Abdulqader Salman Al-Hamdany, Sanaa Mohammed Morshed   +1 more
openalex   +2 more sources

PSVII-18 Role of azoximer bromid in functional system «mother-fetus» in cows

, 2020
Аndrey Filatov, N. A. Shemuranova, А. Ф. Сапожников, Polina Anipchenko, Sergey Eremin, Georgy Nikitin, Kirill Plemyashov   +6 more
openalex   +2 more sources

Evaluation of the Efficacy and Safety of Satralizumab in a Pregnant NMOSD Patient With AQP4/MOG‐IgG Dual Seropositive: A Case Report

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Neuromyelitis Optica Spectrum Disorder (NMOSD) is a chronic autoimmune neuroinflammatory disease, typically characterized by antibodies against aquaporin 4 (AQP4‐IgG) or myelin oligodendrocyte glycoprotein (MOG‐IgG). Simultaneous seropositivity for both antibodies in a single patient is exceedingly rare.
Yeting Luo, Shuhua Xie, Xianghong Liu
wiley   +1 more source

Fetus in fetu

Pediatric Oncall, 2012
Asok Kumar Datta, Arvind Kumar Singh, Taraknath Ghosh, Narendranath Mukherjee   +3 more
openaire   +2 more sources

Phenotype and genetic variation analysis of primary congenital lymphedema caused by FLT4 gene mutations in a fetus. [PDF]

Front Genet
Zhai S, Yuan L, Li J, Liu L, Hu L, Ban Y, Yang X, Yang J, Ouyang X, Huang N, Tian Y, Wang T, Kong X.   +12 more
europepmc   +1 more source

Placental mammals acquired TRPA1 hypoxia sensitivity to protect the fetus from the insults due to maternal anemia [PDF]

Jiacheng H. Sun, Yasuo Mori, Nobuaki Takahashi   +2 more
openalex   +1 more source