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Research 91–120 of 1000+
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Clinical and laboratory indicators of polycystic ovary syndrome in Chinese Han nationality with different Rotterdam criteria-based phenotypes
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- W locus alleles of the KIT Gene in Turkish Van Cats and Their Association with Certain Phenotypes
- TU55. EXPLORING THE GENOMIC RELATIONSHIP BETWEEN TWO MAJOR DETERMINANT PHENOTYPES OF PSYCHIATRIC DISORDERS: HUMAN GUT MICROBIOME AND SLEEP TRAITS
- Laser therapy on darker ethnic skin
- Translation into Portuguese language (Brazil), transcultural adaptation and validation of the quality of life questionnaire in female pattern hair loss (WAA-QoL-BP)
- Obesity and the skin
- Paradoxical hypertrichosis after laser epilation
- L’effluvium télogène actinique: une facette de la chronobiologie humaine
- Weakly supervised learning of biomedical information extraction from curated data
- Care of the newborn with ichthyosis
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Forensic DNA phenotyping: A promising tool to predict human appearance for forensic purposes
- Forensic DNA phenotyping: A promising tool to predict human appearance for forensic purposes
- Nonablative cutaneous remodeling using radiofrequency devices
- Successful treatment of melasma using a combination of microdermabrasion and Q‐switched Nd:YAG lasers
- Treatment of Pseudofolliculitis With a Pulsed Infrared Laser
- Topical niacinamide 4% and desonide 0.05% for treatment of axillary hyperpigmentation: a randomized, double-blind, placebo-controlled study
- Adverse events of non-ablative fractional laser photothermolysis: a retrospective study of 856 treatments in 362 patients
- Implications of a Clinically Ignored Site of Acanthosis Nigricans: The Knuckles
- VISIA Skin Analysis System as a Tool to Evaluate the Reduction of Pigmented Skin and Vascular Lesions Using the 532 Nm Laser
- Determination of serum 25-hydroxyvitamin D levels in patients with alopecia areata and their comparison with levels in healthy controls: A cross-sectional study
- Antioxidant and photoprotective potential of Polypodium leucotomos
- Skin Semiology and Grading Scales