Results 251 to 260 of about 238,616 (363)

Maternal gut microbiota‐derived daidzein prevents osteoporosis in female offspring following prenatal prednisone exposure

iMeta, EarlyView.
Prenatal prednisone therapy (PPT)/prenatal prednisone exposure (PPE) induces long bone dysplasia, reduced peak bone mass (PBM), and increased osteoporosis susceptibility in female offspring. Maternal gut microbiota metabolite daidzein (DAI) mediates PPE‐induced osteoporosis susceptibility in female adult offspring.
Chi Ma, Hangyuan He, Kunpeng Wang, Juanjuan Guo, Liang Liu, Yuting Chen, Bin Li, Hao Xiao, Xufeng Li, Xiaoqian Lu, Tingting Wang, Yinxian Wen, Hui Wang, Liaobin Chen   +13 more
wiley   +1 more source

High-flow nasal cannula for stabilisation of very premature infants: A prospective observational study. [PDF]

Acta Paediatr
Jonáš K, Lamberská T, Nguyen TA, Kudrna P, Plavka R.   +4 more
europepmc   +1 more source

Studies on physical growth of premature infants.

, 1960
Miyo Minamii
openalex   +2 more sources

POSTNATAL DEVELOPMENT OF RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM /RAAS/ IN RELATION TO ELECTROLYTE BALANCE IN PREMATURE INFANTS [PDF]

, 1979
Endre Sulyok, F Varga, M Németh, I Tényi, I Csába   +4 more
openalex   +1 more source

Risk Factors Associated With the Development of Late Pulmonary Artery Hypertension in Extremely Premature Infants. [PDF]

Pediatr Pulmonol
Condit PE, Hokanson JS, Balasubramaniam V, McCulley DJ, Lasarev M, Lamers L, McAdams RM, Kaluarachchi DC.   +7 more
europepmc   +1 more source

STATISTICAL RESEARCH ON THE DENTAL HYGIENE OF PREMATURE INFANTS

, 1962
Tetsuro Tsubone
openalex   +2 more sources

Hemoglobin Hasharon in a Premature Infant with Hemolytic Anemia [PDF]

, 1975
Rodney L. Levine, David R. Lincoln, W Buchholz, John T. Gribble, Herbert C. Schwartz   +4 more
openalex   +1 more source

Prenatal Diagnosis and Clinical Phenotypic Heterogeneity of 22q11.2 Microdeletion Syndrome Based on a Single Center Retrospective Study

Journal of Clinical Laboratory Analysis, EarlyView.
Chromosome 22q11.2 microdeletion syndrome (22q11.2DS) is a common congenital disorder with high clinical phenotypic heterogeneity. In this study, we retrospectively investigated the incidence of prenatal diagnosis of 22q11.2DS in a single center and summarized its clinical manifestations to expand the phenotypic database ABSTRACT Objective To ...
Jia‐yan Chen, Mei‐jiao Cai, Yun‐sheng Ge   +2 more
wiley   +1 more source

Efficacy of pulmonary surfactant with budesonide in premature infants: A systematic review and meta-analysis. [PDF]

PLoS One
Phattraprayoon N, Tan B, Na Takuathung M.   +2 more
europepmc   +1 more source

A Statistical Study on Premature Infants in Shirakawa Agricultural Area in Fukushima Prefecture during the Period 1948 to 1956

, 1961
Tadashi MIDORIKAWA
openalex   +2 more sources