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Research 901–930 of 1000+
- The semiotics of breast cancer: Signs, symptoms, and sales
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- THE IMPACT OF HOMOCYSTEINE IN LUPUS ERYTHEMATOSUS: A LINK OF INFLAMMATION, SKIN AND CARDIOVASCULAR RISK
- Drug History and SLE Laboratory Findings Among Iraqi Patients: A Hospital‐Based Study
- The Carcinogenesis of the Human Scalp: An Immunometabolic-Centered View
- Recent Approaches in the Treatment of Polycystic Ovary Syndrome: An Update
- Hypotrichosis in a child with olmsted syndrome
- Book review
- Oral Retinoids in Dermatology
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- <i>Arthroderma vanbreuseghemii</i>infection in three family members with kerion and tinea corporis
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Adverse Events Associated with Azathioprine Treatment in Korean Pediatric Inflammatory Bowel Disease Patients
- Converging physiological roles of the anthrax toxin receptors
- Lepromatous Leprosy in a Renal Transplant Recipient
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- Androgenetic alopecia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Hyperadrenocorticism in Ferrets
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Linking allergy to mercury to HLA and burning mouth syndrome
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Acne Tarda and Male-Pattern Baldness Unmasking Primary Ovarian Insufficiency: A Case and Review
- Isochromosome Mosaic Turner Syndrome: A Case Report