Results 131 to 140 of about 1,829,379 (365)
Bilateral supernumerary maxillary lateral incisors: A rare case report
BACKGROUND AND AIM: Supernumerary tooth (ST) is considered as a developmental tooth abnormality in number that most often occurs in the anterior region of the maxilla. They may erupt or remain impacted in the alveolar bone.
Somayeh Hekmatfar +2 more
doaj
Prevalence of the carabelli trait in Iranian adolescents
Aim: The study of dental morphological features is important in anthropological researches, because it can provide information on the dental variations within a specific population.
Ramin Mosharraf
doaj +1 more source
Fluorescent risedronate analogue 800CW-pRIS improves tooth extraction-associated abnormal wound healing in zoledronate-treated mice [PDF]
Hiroko Okawa +11 more
openalex +1 more source
Advances in Triboelectric Nanogenerators With Rotating Structure
The rotating TENG has been widely studied for its superiorities of simple structure, high efficiency, and stable output. This review introduced the four different principles of rotating TENG and offered a thorough summary for performance and application research through three‐level classification. Importantly, the current existing problems, challenges,
Chuguo Zhang +4 more
wiley +1 more source
Consideration for care for your patient with cerebral palsy [PDF]
Cerebral palsy (CP) is a common developmental neurological disorder affecting about 2-3 children out of 1,000. CP is the result of infant brain damage or abnormal development resulting in impaired muscle control, coordination, tone, reflex, posture, and ...
Cannon, Katlin R +2 more
core +1 more source
Metabolic Bone Diseases Affecting Tooth Eruption: A Narrative Review
Tooth eruption is an essential process for the development of the oral and maxillofacial system. Several inherited and acquired diseases might affect this tightly regulated process, resulting in premature, delayed, or even failed tooth eruption.
Christianna Iris Papadopoulou +2 more
doaj +1 more source
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki +6 more
wiley +1 more source
Role of selenium in the pathophysiology of cardiorenal anaemia syndrome
Abstract Chronic kidney disease (CKD) and cardiovascular disease (CVD) have multiple bidirectional mechanisms, and anaemia is one of the critical factors that are associated with the progression of the two disorders [referred to as cardiorenal anaemia syndrome (CRAS)].
Shigeyuki Arai +2 more
wiley +1 more source
Evaluation of coagulation disorders and iron deficiency in women with heavy menstrual bleeding
Abstract Objective To explore the incidence of congenital bleeding disorders (CBD), which may result in anemia, in a large cohort of women referred for heavy menstrual bleeding (HMB) in a specialized gynecologic unit. Methods Between January 2022 and January 2024, all women referred for HMB were screened.
Lucia Rugeri +8 more
wiley +1 more source

