Field-based evaluation of multi-strain PGPR to improve zea mays yield and soil nutrient dynamics in semi-arid of Türkiye. [PDF]
Kurt PO.
europepmc +1 more source
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun+2 more
wiley +1 more source
Longitudinal Evaluation of Listening Effort and Speech Perception in Noise in CROS and BiCROS Hearing Aid Users With Single-Sided Deafness. [PDF]
Kılıç S, Tuz D, Gürses E.
europepmc +1 more source
A Population‐Based Study of Limb Body Wall Complex With Proposed Features for Prenatal Diagnosis
ABSTRACT Limb body wall complex (LBWC) is a lethal condition comprising major congenital anomalies. Although currently diagnosed in the early prenatal period, historical diagnostic criteria are based on detailed pathological assessments. Prenatal and postnatal findings of LBWC and their phenotypic overlap with body stalk anomaly (BSA) and recurrent ...
Mary Ann Thomas+2 more
wiley +1 more source
The Development of Inner Ear Membrane Analog for Experimental Otorhinolaryngology. [PDF]
Riabinin AA+11 more
europepmc +1 more source
ABSTRACT Gastrointestinal (GI) symptoms are common in CHARGE syndrome, but their frequency and characteristics remain poorly documented due to the complex nature of CHARGE syndrome. This study aimed to determine the prevalence of GI issues in CHARGE syndrome and their impact on quality of life (QoL).
Annie Kakamousias, Kim Blake
wiley +1 more source
Awareness and attitudes towards ear health in classical music students-advancing education and care for professional ear users. [PDF]
Fitzlaff M+10 more
europepmc +1 more source
Some observations on the early history of aural surgery, and the nosological arrangement of diseases of the ear [PDF]
W. R. Wilde
openalex +1 more source
ABSTRACT KDM1A‐related neurodevelopmental disorder (CPRF, OMIM #616728) is characterized by cleft palate, global developmental delay, and distinct facial gestalt, but phenotypic knowledge of this ultra‐rare autosomal dominant disorder is limited. Here, we report on a 13‐year‐old boy with a novel heterozygous, likely pathogenic germline missense variant
Sebastian Burkart+6 more
wiley +1 more source
The rarely described association between pseudoaneurysm and aberrant ICA: A case series.
Yousif P+7 more
europepmc +1 more source