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Research 481–510 of 1000+
- Quality-of-Life Assessment in Singaporean Children with Alopecia Areata
- Pattern of body fat distribution in patients of PCOS using DEXA-based indices
- Joint Public Review: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Author Response: Touch receptor end-organ innervation and function require sensory neuron expression of the transcription factor Meis2
- Bachmann–Bupp syndrome and treatment
- Hormone replacement therapy and COVID-19 outcomes in solid organ transplant recipients compared with the general population
- Endocrinology
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Editor's evaluation: Lhx2 is a progenitor-intrinsic modulator of Sonic Hedgehog signaling during early retinal neurogenesis
- Prevalence of Cutaneous Disorders in Patients with Polycystic Ovary Syndrome
- Proceedings of the Ninth World Congress for Hair Research (2015)
- The use of microneedling associated to photobiomodulation in the treatment of male androgenetic alopecia: Case series
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Amino Acids Oral Treatment for the Amelioration of Skin, Hair, and Nails Conditions: An Open-Label Study
- Facial Feminization Surgery/Gender Confirming Facial Surgery: Background and State of the Art
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Feasibility of Measuring Hair Glucocorticoids as a Potential Biomarker for Chronic Stress in Older Adults With Intellectual Disabilities
- Importance of a multi-tiered treatment approach for intellectually and developmentally disabled patients with hidradenitis suppurativa
- Importance of a multi-tiered treatment approach for intellectually and developmentally disabled patients with hidradenitis suppurativa
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- DICENTRIC CHROMOSOME 14;18 PLUS TWO ADDITIONAL CNVs IN A GIRL WITH MICROFORM HOLOPROSENCEPHALY AND TURNER STIGMATA
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Tricotiodistrofia. Reporte de un caso
- Down Syndrome and Autoimmune Disease
- An X-traordinary stroke
- The role of AUTS2 in neurodevelopment and human evolution