Results 171 to 180 of about 20,697 (308)
Morphological indicators of puberty in 3/4 and 5/8 Girolando heifers. [PDF]
Böck MJ +6 more
europepmc +1 more source
Abstract Background and Purpose Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with limited therapeutic options. This study compared the therapeutic effects of bone marrow mesenchymal stem cell‐derived extracellular vesicles (BM‐MSC‐EVs) with an IPF treatment, pirfenidone (PFD), in mature adult mice with established pulmonary ...
Jennie S. Charoenphannathon +4 more
wiley +1 more source
Acute Megakaryoblastic Leukemia With Myeloid Sarcoma in the Temporal Bone: A Case Report. [PDF]
Fujisawa N +4 more
europepmc +1 more source
Ilium Hydroelectric Plant, San Miguel County, Colorado [04] [PDF]
Photo of the power plant located at Ilium, San Miguel County, Colorado, "altitude 8,097 ...
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Using data from 17,093 participants in the 2022 Australian National Health Survey, this study is the first to report nationwide prevalence estimates for allergic rhinitis (23.9%), food allergy (7.0%), drug allergy (5.2%), eczema (1.6%) and diagnosed asthma (10.8%) across Australia.
Yichao Wang +14 more
wiley +1 more source
Isolated Osteochondromas of the Inner and Outer Tables of the Ilium: A Report of two Rare Cases. [PDF]
Singapanga RS +5 more
europepmc +1 more source
ABSTRACT A hive of recent policy and legislative activity in Australian family law has emphasized the importance of children's right to participate in decision‐making following parental separation. Yet a powerful tension persists between supporting children's right to participation and protecting children from parental conflict.
Georgina Dimopoulos +3 more
wiley +1 more source
An Atypical Hip Pain in a Recreational Athlete: A Case Report. [PDF]
Milan Q, Adelheid S, Karel W.
europepmc +1 more source
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi +6 more
wiley +1 more source
On-Scanner Correction of Gradient Nonlinearity Bias for Accurate Assessment of Diffusion Heterogeneity Across Bone Sites in Myelofibrosis Patients. [PDF]
Malyarenko D +9 more
europepmc +1 more source

