Results 161 to 170 of about 525,919 (347)

Ear malformation in a child with Goldenhar syndrome and its appropriate audiological management

open access: yesAnales del Sistema Sanitario de Navarra
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

Data‐Driven Insights into Rare Earth Mineralization: Machine Learning Applications Using Functional Material Synthesis Data

open access: yesAdvanced Intelligent Systems, EarlyView.
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

“Will you be there for me?” Social support from family and friends during cold case sexual assault prosecutions

open access: yesAmerican Journal of Community Psychology, EarlyView.
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

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
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]

open access: yesNatl J Maxillofac Surg, 2023
Malick R, Sham ME, Reddy TJ, Jacob PC.
europepmc   +1 more source

Long‐Read Genome Sequencing Establishes Biallelic Pathogenic Variants in DNM1 With Distinct Functional Effects as the Cause of Early Infantile Developmental and Epileptic Encephalopathy

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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]

open access: bronze, 1972
Mark B. Gardner   +2 more
openalex   +1 more source

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