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Research 91–120 of 1000+
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Dilated tonic pupils with tabes dorsalis in neurosyphilis as first manifestation of HIV/AIDS: a video report
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence
- Alterations in Corneal Sensitivity, Staining and Biomechanics of Alopecia Areata Patients: Novel Findings in a Case-Control Study
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- COVID-19: Pulmonary and Extra Pulmonary Manifestations
- Epidermal Nevi
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Congenital Trichomegaly of the Eyelashes
- Syphilitic Alopecia: Report of a Challenging Case and Review of the Literature
- Alopecia and Thyroid Disease
- The Influence of Race and Sex on the Side Effect Profile of Methotrexate in the Treatment of Uveitis
- Cutaneous adverse reactions linked to targeted anticancer therapies bortezomib and lenalidomide for multiple myeloma: new drugs, old side effects
- Evaluation of ovarian reserve and function in female patients treated with oral isotretinoin for severe acne: an exploratory study
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Abstracts Pt.30
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Hypothyroidism in Dogs
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Hair Loss in Children
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation