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    Research 301–330 of 1000+

    1. Integrative Medicine and Helmet Constructions—A Feature Article about Milestones and Perspectives Sci · 2022 · 1 citations
    2. Dermatologic manifestations of thyroid disease: a literature review Frontiers in Endocrinology · 2023
    3. Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets BoneKEy Reports · 2014 · 107 citations
    4. Real-World Data on Health-Related Quality of Life Assessment in Patients With Breast Cancer Receiving Subcutaneous Trastuzumab Breast Cancer Basic and Clinical Research · 2018 · 12 citations
    5. Common Clinical signs and symptoms observed in Patients diagnosed with Thyrotoxicosis in Gujranwala, Pakistan 2023 · 1 citations
    6. Polyglandular Autoimmune Syndrome Type 3D : A Case Report 2022 · 1 citations
    7. Abstract 4993: A longitudinal examination of nutritional-inflammatory biomarker associations with cancer related cognition, treatment side effects and quality of life in newly diagnosed older adults undergoing chemotherapy Cancer Research · 2025
    8. Vitamin B12 Malabsorption: The Pathophysiological Impacts on Neurological and Hair Physiology The International Journal of Gastroenterology and Hepatology Diseases · 2025
    9. The Pathobiology of Skin Aging American Journal Of Pathology · 2020 · 122 citations
    10. Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing Journal of Investigative Dermatology · 2008 · 99 citations
    11. Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports Journal of neuroendocrinology · 2023 · 1 citations
    12. Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility Molecular and cellular biology · 2002 · 97 citations
    13. Inherited ichthyoses/generalized Mendelian disorders of cornification European journal of human genetics · 2012 · 81 citations
    14. Catalytic Antibodies in Norm and Systemic Lupus Erythematosus InTech eBooks · 2017 · 25 citations
    15. Dicer- and Bulge Stem Cell-Dependent MicroRNAs During Induced Anagen Hair Follicle Development Frontiers in cell and developmental biology · 2020 · 10 citations
    16. Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance? Wiener medizinische Wochenschrift · 2020 · 7 citations
    17. Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease PloS one · 2019 · 5 citations
    18. S100 signaling in hair follicle biology: emerging mechanistic insights and therapeutic opportunities Journal of Molecular Histology · 2026
    19. 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation Journal of the Endocrine Society · 2024
    20. Chemistry, Pharmacology and Therapeutic Potential of Decursin: A Promising Natural Lead for New Drug Discovery and Development Drug Design Development and Therapy · 2024
    21. Identifying critical cell types and gene regulatory pathways for hair and skin disease Nature Genetics · 2023
    22. Quoi de neuf en recherche dermatologique ? Annales de Dermatologie et de Vénéréologie · 2008
    23. Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer Journal of developmental biology · 2017 · 72 citations
    24. The misogyny of iron deficiency Anaesthesia · 2021 · 64 citations
    25. An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess Endocrinology · 2013 · 27 citations
    26. Genetically modified laboratory mice with sebaceous glands abnormalities Cellular and Molecular Life Sciences · 2016 · 22 citations
    27. Ornithine decarboxylase transgenic mice as a model for human atrichia with papular lesions Experimental dermatology · 2000 · 20 citations
    28. Transitional Changes in Fatigue-Related Symptoms Due to Long COVID: A Single-Center Retrospective Observational Study in Japan Medicina-lithuania · 2022 · 8 citations
    29. Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family Journal of clinical laboratory analysis · 2021 · 4 citations
    30. Selenium and its Inorganic Compounds [BAT Value Documentation, 2011] 2019 · 1 citations