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Research 91–120 of 1000+
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Madarosis
- What does acne genetics teach us about disease pathogenesis?
- The Hair Follicle
- Clinical Approach to the Patient With Alopecia
- Psychotrichology: psychosomatic aspects of hair diseases
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Male fertility and skin diseases
- Dermatologic manifestations of endocrine disorders
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The hair shaft: normality, abnormality, and genetics
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Molecular Genetics of Alopecias
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- The clinical spectrum of parathyroid disease
- Diseases of Periocular Hair
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Diagnosis of an indistinct Leydig cell tumor by positron emission tomography-computed tomography
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Alopecia and Its homoeopathic treatment
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- A rare case of chronic genian fistula with oral mucosal hair follicle inclusion: case report and review of the literature
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Inherited Epidermolysis Bullosa: A Clinical Case