Results 161 to 170 of about 525,919 (347)
Ear malformation in a child with Goldenhar syndrome and its appropriate audiological management
Goldenhar syndrome is a rare congenital disorder characterized by defects in the development of structures derived from the first and the second branchial arches. This condition encompasses a range of symptoms, including craniofacial, ocular, vertebral,
Andrés González Fernández +2 more
doaj +1 more source
Hydrothermal synthesis records for rare‐earth compounds are repurposed to learn mineralization rules. An extreme gradient boosting model ingests precursors, additives, and engineered descriptors to predict product phases, crystallization temperature, and pH. Feature importance indicates dominant thermodynamic control with kinetic modulation, suggesting
Juejing Liu +6 more
wiley +1 more source
C5 Dip in Acoustical Trauma and Sound Pressure Amplifying Function of the External Ear
Y Onchi, Y. Ase
openalex +2 more sources
Intrachondral Rupture and Hematoma Formation in the External Ear of Dogs [PDF]
Steen Larsen
openalex +1 more source
Abstract If sexual assault survivors report the assault to the criminal legal system, they often need informal support from family and friends throughout the long and frequently retraumatizing process of investigation and prosecution. This study is part of a long‐term community‐based participatory action research project in a predominately Black ...
Rebecca Campbell +4 more
wiley +1 more source
The Diagnosis That Arrived Decades Late: Living Without and Then With Myhre Syndrome
ABSTRACT Myhre syndrome (MIM #139210) is a rare multisystem disorder first described in 1981, characterized by short stature, neurodevelopmental delay, joint contractures, and cardiopulmonary complications. Its molecular basis, recurrent pathogenic variants in SMAD4, was not discovered until 2011. This narrative is based on a review of medical records,
Abdallah F. Elias
wiley +1 more source
Reconstruction of the external ear using implant-supported alloplasts-Our experience. [PDF]
Malick R, Sham ME, Reddy TJ, Jacob PC.
europepmc +1 more source
ABSTRACT Heterozygous de novo and inherited biallelic pathogenic variants in DNM1 have been reported in association with autosomal dominant (AD) and autosomal recessive (AR) developmental and epileptic encephalopathy, respectively, due to aberrant dynamin function or expression, with each inheritance pattern associated with a different mechanism of ...
Andy Drackley +7 more
wiley +1 more source
Network Representation of the External Ear [PDF]
Mark B. Gardner +2 more
openalex +1 more source

