Results 211 to 220 of about 5,206 (238)
ABSTRACT KBG syndrome is a rare autosomal dominant neurodevelopmental disorder caused by ANKRD11 haploinsufficiency and is characterized by short stature, distinctive facial features, intellectual disability or developmental delay, congenital anomalies and skeletal anomalies.
Marit van der Leij +5 more
wiley +1 more source
El Myotragus de Can Sion: Primer esqueleto completo (no compuesto) del rupicáprido endémico de Baleares [PDF]
Adrover, Rafael, Angel, B.
core
Abstract Notosuchians were key components of western Gondwanan Cretaceous ecosystems in terrestrial predator niches and exhibited remarkable taxonomic and ecological diversity. Previous research has explored their physiology, metabolism, and histology, revealing varied growth patterns and life history strategies.
Tito Aureliano +5 more
wiley +1 more source
ABSTRACT Oropharyngeal food processing exhibits a remarkable diversity among vertebrates, reflecting the evolution of specialised ‘processing centres’ associated with the mandibular, hyoid, and branchial arches. Although studies have detailed various food‐processing strategies and mechanisms across vertebrates, a coherent and comprehensive terminology ...
Daniel Schwarz +6 more
wiley +1 more source
Intradiscal C. acnes injection sustained MC1‐like lesions with persistent neutrophil sustenance in an etiology‐specific lumbar MC rat model. This suggests that patients with bacterial MC etiology may persist in painful MC1, highlighting C. acnes and neutrophils as potential targets to promote MC1‐to‐MC2 conversion and improve pain and disability ...
Irina Heggli +12 more
wiley +1 more source
A Decade of Leadership and Impact: Celebrating 10 Years of the ORS Spine Section
JOR SPINE, Volume 9, Issue 2, June 2026.
Neharika Bhadouria +43 more
wiley +1 more source
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Diagnóstico, manejo y tratamiento de las lesiones cervicales traumáticas
Cirugía Española, 2019Patrizio Petrone
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