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    Research 751–780 of 1000+

    1. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation Case reports in dermatological medicine · 2023
    2. SAT-293 Novel Presentation Of A Heterozygous INSR Mutation And Markedly Elevated Testosterone Levels In A Pediatric Patient, A Case Report. Journal of the Endocrine Society · 2019
    3. The Skin at Different Ages 2014
    4. Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles BMC Dermatology · 2020 · 4 citations
    5. Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency OPAL (Open@LaTrobe) (La Trobe University) · 2016 · 2 citations
    6. Severe Hypernatremia as Presentation of Netherton Syndrome Global Medical Genetics · 2023
    7. The role of AUTS2 in neurodevelopment and human evolution Trends in Genetics · 2013 · 118 citations
    8. Bachmann–Bupp syndrome and treatment 2023
    9. Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review Egyptian Journal of Medical Human Genetics · 2019 · 49 citations
    10. Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives International Journal of Molecular Sciences · 2024 · 9 citations
    11. Kératose pilaire Pan African Medical Journal · 2019 · 1 citations
    12. Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family Annals of Medicine and Surgery · 2024
    13. Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique American Journal of Dermatopathology · 1997 · 17 citations
    14. Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis Journal of the American Academy of Dermatology · 2018 · 7 citations
    15. Woodhouse-Sakati syndrome (WSS) Saudi medical journal · 2021 · 5 citations
    16. The inflammatory component of androgenetic alopecia Journal of The American Academy of Dermatology · 2021 · 3 citations
    17. Hutchinson-Gilford progeria syndrome - A brief introduction International Journal of Pharmacological Research · 2018 · 2 citations
    18. Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods” Canadian journal of neurological sciences · 2021 · 1 citations
    19. Netherton Syndrome – Responding to Oral Retinoids International Journal of Trichology · 2025
    20. Pharmacotherapy of plexiform neurofibromas in patients with neurofibromatosis type 1. Possible adverse events and their management Russian Journal of Child Neurology · 2024
    21. Review of the Latest Methods of Epidermolysis Bullosa and Other Chronic Wounds Treatment Including BIOOPA Dressing Dermatology and Therapy · 2021 · 9 citations
    22. Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome Indian Journal of Paediatric Dermatology · 2025
    23. Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome The Application of Clinical Genetics · 2022 · 2 citations
    24. Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics Journal of Clinical Medicine · 2023 · 380 citations
    25. 0873 Modeling junctional epidermolysis bullosa using tissue-engineered skin substitutes Journal of Investigative Dermatology · 2025
    26. A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies Zenodo (CERN European Organization for Nuclear Research) · 2026
    27. Male Androgenetic Alopecia - A Review of Current Treatments Zenodo (CERN European Organization for Nuclear Research) · 2026
    28. Male Androgenetic Alopecia - A Review of Current Treatments Zenodo (CERN European Organization for Nuclear Research) · 2026
    29. Hutchinson-Gilford syndrome: History, causes, phenotype and research advances GSC Advanced Research and Reviews · 2023
    30. Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome Frontiers in endocrinology · 2020 · 29 citations