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Research 301–330 of 1000+
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Clinical Presentations and Comorbidities of Pediatric Alopecia Areata
- Acne Tarda and Male-Pattern Baldness Unmasking Primary Ovarian Insufficiency: A Case and Review
- Psoriasis and Related Disorders
- A case of acrodermatitis enteropathica misdiagnosed as staphylococcal scalded skin syndrome
- THE IMPACT OF HOMOCYSTEINE IN LUPUS ERYTHEMATOSUS: A LINK OF INFLAMMATION, SKIN AND CARDIOVASCULAR RISK
- Skin Development and Disease: A Molecular Perspective
- The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches
- Ethnopharmacology and hair: Indian perspectives
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Obesity and the skin
- A missense mutation in Lama3 causes androgen alopecia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Hairy tale of signaling in hair follicle development and cycling
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Male Androgenetic Alopecia - A Review of Current Treatments
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Current and Emerging Approaches to Androgenetic Alopecia
- Androgenetic alopecia, hirsutism and hypertrichosis
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Melanocytes: The new Black
- Discreet monilethrix: De novo mutation on the example of polish families
- An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy
- Ether: Fiction or Reality? A Review
- BH03 Lipoedematous scalp occurring in two female siblings: further evidence of a genetic role?