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Machine Learning and Intelligent Diagnostics in Dental and Orofacial Pain Management: A Systematic Review
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Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi families
Published 2025-12-01“…It is characterized by neurological dysfunction, hypotonia, ocular anomalies, craniofacial abnormalities, and absence of peroxisomes in fibroblasts. …”
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303
Effect of anti-sclerostin antibody on orthodontic tooth movement in ovariectomized rats
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304
Tracheostomy in temporomandibular joint ankylosis – A review of the literature and case report
Published 2025-03-01“…A variety of literature is available for patients with craniofacial anomalies who may require tracheostomy and who may develop TMJ ankylosis from a young age, but no literature is available to provide evidenced-based treatment guidelines for adult patients with ankylosis who may be at increased risk for airway compromise. …”
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PENGARUH PLATELET RICH FIBRIN PADA PROSES EPITELISASI LUKA DONOR SKIN GRAFT: STUDI META ANALISIS
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309
Novel Fast-Setting and Mechanically-Strong Calcium Phosphate Pulp-Capping Cement with Metformin Release to Enhance Dental Pulp Stem Cells
Published 2024-12-01“…Metformin, with its potential in craniofacial regeneration, could enhance dentin synthesis by targeting pulp cells. …”
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Amantadine modulates novel macrophage phenotypes to enhance neural repair following spinal cord injury
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Women Are More Susceptible to Caries but Individuals Born with Clefts Are Not
Published 2011-01-01“…Isolated forms of cleft lip and palate are among the most common craniofacial congenital anomalies in humans. Historically, several reports suggest that individuals born with clefts have a higher risk for caries. …”
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Cellular and immune landscape of chronic liver diseases: insights from immunophenotyping
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TATALAKSANA MANAJEMEN OPERATIF PADA PASIEN SINDROM PARRY-ROMBERG DI RSUD DR. SOETOMO SURABAYA
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Identification and functional analysis of a novel SMARCC2 splicing variant in a family with syndromic neurodevelopmental disorder
Published 2025-02-01“…Results The twin adult males displayed comparable phenotypes, characterized by moderate developmental delay, intellectual and language delays, dense hair, craniofacial anomalies, scoliosis, cryptorchidism, hypotonia, behavioral abnormalities, allergic purpura and eczema, and drug allergies. …”
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Secreted PD-L1 alleviates inflammatory arthritis in mice through local and systemic AAV gene therapy
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Targeted allele-specific FGFR2 knockdown via human recombinant ferritin nanoparticles for personalized treatment of Crouzon syndrome
Published 2025-03-01“…Crouzon syndrome is a rare genetic craniofacial malformation caused by heterozygous gain-of-function mutations in the FGFR2 gene. …”
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