Results 61 to 70 of about 896 (147)

TRMT10A‐Related Neurodevelopmental Disorder Without Metabolic Findings

open access: yesHuman Mutation, Volume 2026, Issue 1, 2026.
TRMT10A is a tRNA methyltransferase gene associated with a rare autosomal recessive disorder characterized by microcephaly, intellectual disability, epilepsy, short stature, and abnormalities in glucose metabolism. Although an increasing number of patients have been reported, the extent of phenotypic variability and genotype–phenotype correlations ...
Döndü Ülker Üstebay   +5 more
wiley   +1 more source

Relationship between three methods for the evaluation of skeletal maturation with sexual maturation

open access: yesRevista Facultad de Odontología Universidad de Antioquia, 2006
The objective of this study was to determine which of the methods used to establish the skeletal maturation is better related with the maturity of the patient, and for that reason is more practical and applicable to the clinical practice.
Óscar Zapata   +3 more
doaj  

Predıctıon Of The Skeletal Age By Usıng The Cervıcal Vertebral Dımensıons

open access: yesTurkish Journal of Orthodontics, 1996
The purpose of this study is to develop a new method to predict the skeletal age by using the dimentional changes of the cervical vertebrae due to the growth and development on the routinely taken lateral cephalometric radiographs before the orthodontic ...
Sönmez Fıratlı, Evren Öztaş
doaj   +1 more source

Enhancing the Evaluation of Central Precocious Puberty in Female Patients via Age‐Specific Models Incorporating Clinical Biomarkers

open access: yesInternational Journal of Clinical Practice, Volume 2026, Issue 1, 2026.
Objective This investigation sought to develop and prospectively validate age‐specific diagnostic models based on routinely accessible clinical biomarkers. These models differentiate central precocious puberty (CPP) from peripheral precocious puberty (PPP) in girls, providing a pragmatic strategy to reduce superfluous gonadotropin‐releasing hormone ...
Shuyu Xie   +10 more
wiley   +1 more source

Artificial Intelligence-Based Models for Automated Bone Age Assessment from Posteroanterior Wrist X-Rays: A Systematic Review

open access: yesApplied Sciences
Introduction: Bone-age assessment using posteroanterior left hand–wrist radiographs is indispensable in pediatric endocrinology and forensic age determination.
Isidro Miguel Martín Pérez   +2 more
doaj   +1 more source

The “blind age assessment”: applicability of Greulich & Pyle, Demirjian and Mincer aging methods on a population of unknown ethnic origin

open access: yes, 2011
Purpose: Age estimation is one of the most crucial issues in case of unknown deceased as well as in the living and is very frequently of radiological interest.
D. Gibelli   +4 more
core   +1 more source

Congenital Hypothyroidism: Long‐Term Growth and Intellectual Outcomes With a Lower Initial Levothyroxine Dose

open access: yesClinical Endocrinology, Volume 103, Issue 6, Page 895-905, December 2025.
ABSTRACT Objectives This study aims to review the long‐term outcome of congenital hypothyroidism (CH) and whether patient‐ or treatment‐related factors impact the outcomes, especially focusing on the initial Levothyroxine dose. Methods This is a retrospective, cross‐sectional study of the children diagnosed with CH who received Levothyroxine at Ajou ...
Jun‐Hong Park   +4 more
wiley   +1 more source

Is Greulich and Pyle standards of skeletal maturation applicable for age estimation in South Indian Andhra children?

open access: yesJournal of Pharmacy and Bioallied Sciences, 2015
Introduction: Now-a-day age determination has gained importance for various forensic and legal reasons. Skeletal age (SA) of a test population can be estimated by comparing with established standards of Greulich and Pyle (G-P).
Rezwana Begum Mohammed   +5 more
doaj   +1 more source

Phenotypic Spectrum and Diagnostic Challenges in Klippel‐Trenaunay Syndrome: A Case Series

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Klippel‐Trénaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, venous varicosities, and soft tissue or bony hypertrophy. This case series highlights rare and atypical presentations of KTS, emphasizing the importance of a multidisciplinary diagnostic approach.
Marya Hameed, Tooba Ali, Md Ariful Haque
wiley   +1 more source

Avaliação da idade óssea em crianças de 9 a 12 anos de idade na cidade de Manaus-AM Evaluation of the bone age in 9-12 years old children in Manaus-AM city

open access: yesDental Press Journal of Orthodontics, 2011
OBJETIVO: o presente estudo teve como objetivo avaliar a idade óssea pelo método de Greulich & Pyle (1959) e o período do crescimento puberal, de acordo com o trabalho de Martins (1979).
Carlos Eduardo da Silva Nossa Tuma   +5 more
doaj   +1 more source

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