Results 221 to 230 of about 43,400 (289)

The Role of the Hyoid Bone in Obstructive Sleep Apnea Severity: A Systematic Review

Journal of Sleep Research, EarlyView.
ABSTRACT Obstructive sleep apnea (OSA) has numerous complications that negatively impact patients' quality of life. Early diagnosis can significantly reduce these complications. The aim of the study was to evaluate the relationship between the hyoid bone position and the severity of apnea, and to determine if hyoid‐related cephalometric variables can ...
Carmen María Correa‐Morillo, Paola Cardil París, Marta Macarena Paz‐Cortés, Andrea Martín‐Vacas, Giovanni Giovannini   +4 more
wiley   +1 more source

Hypodontia in the Korean orthodontic population: Prevalence and characteristics of a nationwide multicenter study. [PDF]

Korean J Orthod
Kim SH, Kim YI, Kim SS, Park SB, Choi DS, Kim HJ, Kim KA, Lee MH, Choi SH, Choi SK, Lee KC, Jeon YM, Jeong S, Choi YK.   +13 more
europepmc   +1 more source

Origin and formation of a chondritic xenolith in Krymka (LL3.2, breccia): Indications for a late formation of the accretionary breccia

Meteoritics &Planetary Science, EarlyView.
Abstract An unusual chondritic xenolith was found in two sequentially prepared thin sections of a sample from the Krymka (LL3.2) chondrite. The xenolith has a rounded, slightly deformed shape of about 5 mm in apparent diameter and is partially surrounded by a double rim made of an inner fine‐grained silicate‐rich rim and an outer sulfide‐rich rim.
Aelita Girich, Addi Bischoff, Samuel Ebert, Kazuhide Nagashima, Andreas Morlok, Harald Hiesinger, Jasper Berndt   +6 more
wiley   +1 more source

Fetal pathology meets clinical genetics – on the value of a comprehensive postmortem examination. [PDF]

Med Genet
Fauth C, Sprung S, BSc MM, BSc RL, Mutz-Dehbalaie I, Döttelmayer P, Freund-Unsinn K.   +6 more
europepmc   +1 more source

Trisomy 18 presenting with complete bilateral radial aplasia: a rare case report. [PDF]

BMC Pediatr
Suboh MW, Atatre MH, Shwieki N, Nassar AA, Awwad MA.   +4 more
europepmc   +1 more source

Erratum: Novel mutation in ABBC9 gene associated with congenital hypertrichosis and acromegaloid facial features, without cardiac or skeletal anomalies: a new phenotype [Corrigendum]. [PDF]

Appl Clin Genet, 2018
europepmc   +1 more source

Severe Progression of Scoliosis Beyond Skeletal Maturity in Partial Trisomy 13: A Case Report Expanding the Phenotypic Spectrum. [PDF]

Cureus
Fabregas A, Lugo E, Nice E, Gupta VP, Samdani AF.   +4 more
europepmc   +1 more source

Explain Yourself: The Ethics of Soliciting Advice

Journal of Social Philosophy, EarlyView.
Jordan Desmond
wiley   +1 more source

Skeletal anomalies and deformities in patients with deletions of 22q11

American Journal of Medical Genetics, 1997
Skeletal anomalies in patients with a 22q11.2 deletion are reported infrequently. We report the skeletal findings in 108 patients with a 22q11.2 deletion, of whom 37 (36%) had a skeletal anomaly. Twenty-two patients (20%) had anomalies of the limbs, 7 of the upper limb, including preaxial or postaxial polydactyly. An anomaly of the lower limb was found
Jeffrey E Ming, Donna M Mcdonald-Mcginn, Deborah A Driscoll   +2 more
exaly   +4 more sources