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Research 781–810 of 1000+
- "Grievances at the treatment she received": Harriet E. Wilson's Spiritualist Career in Boston, 1868-1900
- MOOEW: Inovasi Hair Tonic Gel Eco-Friendly Berbasis Hydroxyproline Limbah Tulang Ikan Tenggiri dengan Ekstrak Chamomile Solusi Alopesia Kucing
- Hair Fall Count 60-second: Clinic-Based Modified Count Versus Home-Based Count
- The Contribution of Shaykh Abbas Kuta Karang in Malay Medical: A Study on Al-Rahmah fi Al-Tib wa Al-Hikmah Manuscript
- ANDROPAUSE: A MISNOMER FOR A TRUE CLINICAL ENTITY
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Characterization of tiger tail banding and hair shaft abnormalities in trichothiodystrophy
- IMPORTANCE OF ISOLATED GESTATIONAL HYPOTHYROXINEMIA IN THE DEVELOPMENT OF OBSTETRIC AND SOMATIC PATHOLOGIES.
- IJCR Global Summit: Book of Abstracts 2025
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- mTORC1 activity negatively regulates human hair follicle growth and pigmentation
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Southern African HIV Clinicians Society gender-affirming healthcare guideline for South Africa
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- The Reduction of Male Lower Urinary Tract Symptoms Is Associated With a Decreased Risk of Death
- Vitiligo – Study In view of familial occurence
- Industry Updates from the Field of Stem Cell Research and Regenerative Medicine in December 2019
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- HX01 Avicenna: an influence on modern dermatology
- An assessment of the nutritional status of internally displaced school children in the West and Littoral Regions of Cameroon
- Abordagens psicológicas e novas terapêuticas perante as escolhas do paciente portador da Síndrome de Morris
- Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"
- Evidence based medicine: a movement in crisis?
- Investigation, treatment and monitoring of late‐onset hypogonadism in males: ISA, ISSAM, and EAU recommendations
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Investigation, Treatment, and Monitoring of Late‐Onset Hypogonadism in Males: ISA, ISSAM, and EAU Recommendations
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome