Results 101 to 110 of about 2,320,202 (301)
INDIVIDUAL APPLICATORS FOR THE TREATMENT OF LIP DISEASES
Recurrent course of most diseases of the lips requires long-term topical use of drugs. To avoid drying and lubrication of drugs, to improve the fixation of applications, various options for individual applicators for the treatment of diseases of the red border and the mucous membrane of the lips are offered. It is possible to manufacture applicators of
Juliya Gennadievna Smerdina +2 more
openaire +1 more source
O Cuidado com a saúde bucal de crianças com fissura labiopalatal sob o olhar e a vivência materna: um estudo exploratório [PDF]
Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Programa de Pós-Graduação em Odontologia, Florianópolis, 2010.A fissura labiopalatal é uma má formação congênita que acarreta para a pessoa uma série de ...
Silva, Cintia Magali da
core
PUS7 Deficiency: Phenotypical Expansion of PUS7‐Related Neurodevelopmental Disorders
ABSTRACT Pathogenic variants in PUS7, encoding pseudouridine synthase 7, cause a rare neurodevelopmental disorder marked by intellectual disability, microcephaly, short stature, and behavioral disturbances. Since the first report in 2018, only 16 patients have been described.
Alice Muda +5 more
wiley +1 more source
Histopatologia da forma labial cicatricial de Keith
O estudo da etiologia das formas congênitas ditas cicatriciais, que incluem bandas cicatriciais congênitas e formas cicatriciais das fissuras labiais, apresenta diversas teorias, que fundamentam seu aparecimento, porém não justificam todos os aspectos ...
Hamilton Aleardo Gonella +1 more
doaj +1 more source
Camouflage Extraction Treatment of Unilateral Cleft Lip and Palate Patient: 4-year Follow-up
Cleft lip and palate is one of the most common congenital abnormalities in the dentofacial region. Orthodontic treatment for adult patients with cleft lip and palate is difficult because of several factors such as dental anomalies, limitations in tooth ...
황순신 +3 more
core +1 more source
ABSTRACT Microdeletions impacting 15q11.2 breakpoint (BP) 1 to BP2, adjacent to the Prader–Willi critical region, have previously described neuropsychiatric associations, with potential low penetrance presentations of congenital heart disease (CHD) also identified.
Morgan B. Wright +10 more
wiley +1 more source
Macrophage metabolism dysregulation, which is exacerbated by persistent stimulation in infectious and inflammatory diseases, such as diabetic infectious bone defects (DIBD), eventually leads to the failure of bone repair.
Jiale Jin +10 more
doaj +1 more source
Spinal Involvement in Charge Syndrome: Implications for Management
ABSTRACT CHARGE syndrome (OMIM #214800) is an autosomal dominant disorder caused by mutations in the CHD7 gene in most cases. Although originally defined by the CHARGE acronym (coloboma, heart defects, choanal atresia, growth restriction, genital hypoplasia, and ear anomalies), the recognized phenotype has expanded considerably to include highly ...
Adriana Gomes +5 more
wiley +1 more source
Premaxillary Reconstruction by Distraction Osteogenesis for Cleft Lip/Palate [PDF]
Patients with cleft lip and palate usually present midfacial depression and anterior cross-bite. This dentofacial deformity has been believed due to the undergrowth of maxilla and/or the collapse of premaxilla.
정영수 +3 more
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p53 and FUT8 regulate the introduction of Fuc-Lip-Cy5.5 into HCC cells.
(A) Expression levels of p53 and FUT8 in HCC cells were examined by western blot. (B) Quantification of AFP-L3 values. (C) Determination of the introduction of Fuc-Lip-Cy5.5 into HCC cells. After siRNA transfection, HepG2 and JHH7 cells were exposed to 1
Hajime Nakamura (3428984) +12 more
core +1 more source

