A Narrative Review of Bertolotti's Syndrome: Etiology, Classification, Diagnosis, and Treatment. [PDF]
Tsegaye MA, Muffly A.
europepmc +1 more source
ABSTRACT This study focuses on two terracotta incense burners discovered in the Daba Al‐Bayah necropolis in the Musandam Peninsula (Oman), associated with an Iron Age collective tomb (LCG‐2). Through gas chromatography–mass spectrometry (GC‐MS), the organic residues preserved within these artifacts were analyzed to investigate their use and ...
Francesco Genchi +3 more
wiley +1 more source
A positioning method for the transiliac-transsacral screw bone channel based on a manual tracing of a transparent overlay of preoperative computed tomography images in patients with pelvic fracture and a unilateral trans-sacroiliac corridor. [PDF]
Ye G +6 more
europepmc +1 more source
Mortars From Punic and Hellenistic–Roman Solunto: Materials, Formulations, and Technology
ABSTRACT This study presents an archaeometric investigation of 18 hydraulic rendering and bedding mortars from Punic and Hellenistic–Roman Solunto (NW Sicily). The research aimed to characterize raw materials, reconstruct manufacturing sequences, and evaluate technological proficiency through mineralogical and petrochemical analyses.
G. Montana +4 more
wiley +1 more source
Comparison of PSMA/FAPI Bispecific Tracer ¹⁸F-ALF-NOTA-PSFA-1 and ¹⁸F-FDG PET/CT in the Detection of Primary Clear Cell Sarcoma of Bone. [PDF]
Wu J, Gao H, He L, Liu N, Zhang W.
europepmc +1 more source
ECSU Concert Choir - O Sacrum Convivium - 2012
ECSU Concert Choir - O Sacrum Convivium ...
Swan, Walter +1 more
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“Now we don't have that freedom to not work”: Childhood and parenting in insecurity culture
The British Journal of Sociology, EarlyView.
Allison J. Pugh
wiley +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
Recognizing Sacral Insufficiency Fractures Hidden in Plain Sight: An Illustrative Case Report. [PDF]
Valerio J +4 more
europepmc +1 more source
Beatissimis Manibus Theologi-Principis Tu Pany Welleri Sacrum
BEATISSIMIS MANIBUS THEOLOGI-PRINCIPIS TU PANY WELLERI SACRUM Beatissimis Manibus Theologi-Principis Tu Pany Welleri Sacrum ([1 ...
Alberti, Valentin, Weller, Jacob
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