Results 91 to 100 of about 147,441 (298)
Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature
Clinical Genetics, EarlyView.Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi +6 more
wiley +1 more source
Orphanet Journal of Rare DiseasesBackground Osteogenesis Imperfecta (OI) is a rare genetic disorder characterized by bone fragility and susceptibility to fractures. No curative treatment currently exists, and limited data are available on the effects of adapted physical activity (APA ...
Hayssam Al Arab +4 more
doaj +1 more source
Les enfants dans les Ricordi de Giovanni Morelli,de la réalité à l’idéal
Italies, 2018 Tandis que dans les livres de famille les portraits d’enfants obéissent à des stéréotypes, les Ricordi du marchand florentin Giovanni Morelli (1371-1444) sont une exception.
Cécile Terreaux-Scotto
doaj +1 more source
, 2017 Series: Pastorales Published in Le Charivari Original text: Malheureux enfant! ... ça t\u27apprendra à faire ta société des canards!
Daumier, Honoré
core
Developmental Medicine &Child Neurology, EarlyView.The Brain Involvement iN Dystrophinopathies (BIND) screener is an 18‐item questionnaire with strong reliability and validity for identifying potential brain‐related comorbidities in Duchenne muscular dystrophy. It allows rapid, cross‐age and cross‐country screening for both clinical and research purposes, demonstrating good sensitivity and specificity.
Ruben Miranda +46 more
wiley +1 more source
The Pan African Medical Journal, 2012 INTRODUCTION: Les anémies sévères constituent une cause importante de décès d'enfants. Une analyse épidémiologique et clinique permettrait d'estimer la morbidité et mortalité y relatives afin lutter efficacement contre les causes.
Félicitae Nguefack +10 more
doaj +1 more source
Clinical gait analysis use in management of children with cerebral palsy: Qualitative study
Developmental Medicine &Child Neurology, EarlyView.Barriers and facilitators related to the use of clinical gait analysis (CGA), as identified by healthcare professionals working with children with cerebral palsy and by caregivers. The colored triangles represent the different barriers reported at various stages along the CGA care pathway.
Marie Lévesque‐Jalbert +7 more
wiley +1 more source
The Pan African Medical Journal, 2018 La hernie de Claudius Amyand est définie par l'incarcération de l'appendice vermiculaire à travers le sac herniaire. La première appendicectomie fut réalisée en 1735. C'est une pathologie très rare chez l'enfant.
Hind Cherrabi +7 more
doaj +1 more source
Diabetes, Obesity and Metabolism, EarlyView.ABSTRACT Background Although international guidelines provide recommendations for screening and monitoring of early‐stage type 1 diabetes (T1D), navigating the care pathway can still be difficult for individuals, caregivers, and healthcare professionals (HCPs). These challenges are exacerbated by variations in healthcare systems, gaps in communication,
Chantal Mathieu +14 more
wiley +1 more source
Diabetes, Obesity and Metabolism, EarlyView.ABSTRACT Aims Diabetes distress (DD) is common and evolves heterogeneously over time. We aimed to estimate minimal clinically important differences (MCID) for the Problem Areas in Diabetes (PAID) scale and its sub‐dimensions and to identify predictors of worsening over 1 year in people with type 1 diabetes (PwT1D).
Dulce Canha +10 more
wiley +1 more source